|
1GWQ
HUMAN OESTROGEN RECEPTOR ALPHA LIGAND-BINDING DOMAIN IN COMPLEX WITH RALOXIFENE CORE AND TIF2 NRBOX2 PEPTIDE
提交 2002-03-22
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
688–696(9 aa)
片段:NUCLEAR RECEPTOR BOX II, RESIDUES 688-696
链 D
688–696(9 aa)
片段:NUCLEAR RECEPTOR BOX II, RESIDUES 688-696
|
未记录
|
ZTW RALOXIFENE CORE × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
pH 8.5;6-11% (W/V) PEG 1500, 4% (V/V) DMF, pH 8.50
|
分辨率 2.45 Å
R-free 0.269
|
|
1GWR
HUMAN OESTROGEN RECEPTOR ALPHA LIGAND-BINDING DOMAIN IN COMPLEX WITH 17BETA-OESTRADIOL AND TIF2 NRBOX3 PEPTIDE
提交 2002-03-22
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
742–750(9 aa)
片段:NUCLEAR RECEPTOR BOX III RESIDUES 742-750
|
未记录
|
EST ESTRADIOL × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
pH 7.8;2-2.5% (W/V) PEG 20000 0.1M HEPES PH7.8, pH 7.80
|
分辨率 2.40 Å
R-free 0.288
|
|
1GWR
HUMAN OESTROGEN RECEPTOR ALPHA LIGAND-BINDING DOMAIN IN COMPLEX WITH 17BETA-OESTRADIOL AND TIF2 NRBOX3 PEPTIDE
提交 2002-03-22
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
742–750(9 aa)
片段:NUCLEAR RECEPTOR BOX III RESIDUES 742-750
|
未记录
|
EST ESTRADIOL × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
pH 7.8;2-2.5% (W/V) PEG 20000 0.1M HEPES PH7.8, pH 7.80
|
分辨率 2.40 Å
R-free 0.288
|
|
1M2Z
Crystal structure of a dimer complex of the human glucocorticoid receptor ligand-binding domain bound to dexamethasone and a TIF2 coactivator motif
提交 2002-06-26
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
734–754(21 aa)
片段:TIF2 coactivator motif, residues 734-754
链 E
734–754(21 aa)
片段:TIF2 coactivator motif, residues 734-754
|
未记录
|
BOG octyl beta-D-glucopyranoside × 3
DEX DEXAMETHASONE × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8;293 K;salts, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 293K
|
分辨率 2.50 Å
R-free 0.267
|
|
1MV9
Crystal Structure of the human RXR alpha ligand binding domain bound to the eicosanoid DHA (Docosa Hexaenoic Acid) and a coactivator peptide
提交 2002-09-24
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:NR box
|
未记录
|
HXA DOCOSA-4,7,10,13,16,19-HEXAENOIC ACID × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;295 K;PEG 4000, glycerol, NaCl, Pipes or BisTris, pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 295K
|
分辨率 1.90 Å
R-free 0.249
|
|
1MVC
Crystal structure of the human RXR alpha ligand binding domain bound to the synthetic agonist compound BMS 649 and a coactivator peptide
提交 2002-09-24
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:NR box
|
未记录
|
BM6 4-[2-(5,5,8,8-TETRAMETHYL-5,6,7,8-TETRAHYDRO-NAPHTHALEN-2-YL)-[1,3]DIOXOLAN-2-YL]-BENZOIC ACID × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;295 K;PEG 4000, NaCl, Glycerol, BisTris, Pipes, pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 295.0K
|
分辨率 1.90 Å
R-free 0.228
|
|
1MZN
CRYSTAL STRUCTURE at 1.9 ANGSTROEMS RESOLUTION OF THE HOMODIMER OF HUMAN RXR ALPHA LIGAND BINDING DOMAIN BOUND TO THE SYNTHETIC AGONIST COMPOUND BMS 649 AND A COACTIVATOR PEPTIDE
提交 2002-10-09
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:NR box
链 D
686–698(13 aa)
片段:NR box
|
未记录
|
BM6 4-[2-(5,5,8,8-TETRAMETHYL-5,6,7,8-TETRAHYDRO-NAPHTHALEN-2-YL)-[1,3]DIOXOLAN-2-YL]-BENZOIC ACID × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;295 K;PEG 4000, NaCl, Pipes, BisTris, glycerol, pH 7, VAPOR DIFFUSION, HANGING DROP, temperature 295K
|
分辨率 1.90 Å
R-free 0.232
|
|
1MZN
CRYSTAL STRUCTURE at 1.9 ANGSTROEMS RESOLUTION OF THE HOMODIMER OF HUMAN RXR ALPHA LIGAND BINDING DOMAIN BOUND TO THE SYNTHETIC AGONIST COMPOUND BMS 649 AND A COACTIVATOR PEPTIDE
提交 2002-10-09
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 F
686–698(13 aa)
片段:NR box
链 H
686–698(13 aa)
片段:NR box
|
未记录
|
BM6 4-[2-(5,5,8,8-TETRAMETHYL-5,6,7,8-TETRAHYDRO-NAPHTHALEN-2-YL)-[1,3]DIOXOLAN-2-YL]-BENZOIC ACID × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;295 K;PEG 4000, NaCl, Pipes, BisTris, glycerol, pH 7, VAPOR DIFFUSION, HANGING DROP, temperature 295K
|
分辨率 1.90 Å
R-free 0.232
|
|
1P93
CRYSTAL STRUCTURE OF THE AGONIST FORM OF GLUCOCORTICOID RECEPTOR
提交 2003-05-09
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 E
740–751(12 aa)
片段:TIF PEPTIDE 12mer
|
未记录
|
DEX DEXAMETHASONE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.5;281 K;PEG 400, MgCl2, Dioxane, Tris, pH 8.5, VAPOR DIFFUSION, HANGING DROP
|
分辨率 2.70 Å
R-free 0.363
|
|
1P93
CRYSTAL STRUCTURE OF THE AGONIST FORM OF GLUCOCORTICOID RECEPTOR
提交 2003-05-09
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 F
740–751(12 aa)
片段:TIF PEPTIDE 12mer
|
未记录
|
DEX DEXAMETHASONE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.5;281 K;PEG 400, MgCl2, Dioxane, Tris, pH 8.5, VAPOR DIFFUSION, HANGING DROP
|
分辨率 2.70 Å
R-free 0.363
|
|
1P93
CRYSTAL STRUCTURE OF THE AGONIST FORM OF GLUCOCORTICOID RECEPTOR
提交 2003-05-09
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 3
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 G
740–751(12 aa)
片段:TIF PEPTIDE 12mer
|
未记录
|
DEX DEXAMETHASONE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.5;281 K;PEG 400, MgCl2, Dioxane, Tris, pH 8.5, VAPOR DIFFUSION, HANGING DROP
|
分辨率 2.70 Å
R-free 0.363
|
|
1P93
CRYSTAL STRUCTURE OF THE AGONIST FORM OF GLUCOCORTICOID RECEPTOR
提交 2003-05-09
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 4
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 H
740–751(12 aa)
片段:TIF PEPTIDE 12mer
|
未记录
|
DEX DEXAMETHASONE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.5;281 K;PEG 400, MgCl2, Dioxane, Tris, pH 8.5, VAPOR DIFFUSION, HANGING DROP
|
分辨率 2.70 Å
R-free 0.363
|
|
1T63
Crystal Structure of the Androgen Receptor Ligand Binding Domain with DHT and a peptide derived from its physiological coactivator GRIP1 NR box3
提交 2004-05-05
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
|
未记录
|
DHT 5-ALPHA-DIHYDROTESTOSTERONE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7.5;298 K;hepes, Na-citrate, pH 7.5, VAPOR DIFFUSION, SITTING DROP, temperature 298K
|
分辨率 2.07 Å
R-free 0.230
|
|
1T65
Crystal structure of the androgen receptor ligand binding domain with DHT and a peptide derived form its physiological coactivator GRIP1 NR box 2 bound in a non-helical conformation
提交 2004-05-05
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
686–698(13 aa)
|
未记录
|
DHT 5-ALPHA-DIHYDROTESTOSTERONE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7.5;298 K;hepes, Na-citrate, pH 7.5, VAPOR DIFFUSION, SITTING DROP, temperature 298K
|
分辨率 1.66 Å
R-free 0.270
|
|
1UHL
Crystal structure of the LXRalfa-RXRbeta LBD heterodimer
提交 2003-07-03
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
687–696(10 aa)
链 D
687–696(10 aa)
|
未记录
|
MEI (2E,4E)-11-METHOXY-3,7,11-TRIMETHYLDODECA-2,4-DIENOIC ACID × 1
444 N-(2,2,2-TRIFLUOROETHYL)-N-{4-[2,2,2-TRIFLUORO-1-HYDROXY-1-(TRIFLUOROMETHYL)ETHYL]PHENYL}BENZENESULFONAMIDE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;305 K;MES, PEG, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 305K
|
分辨率 2.90 Å
R-free 0.326
|
|
1YOK
crystal structure of human LRH-1 bound with TIF-2 peptide and phosphatidylglycerol
提交 2005-01-27
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 3
PDB 声明:trimeric
|
链 B
740–753(14 aa)
片段:sequence database residues 740-753
链 C
740–753(14 aa)
片段:sequence database residues 740-753
|
未记录
|
P6L (2S)-3-{[{[(2S)-2,3-DIHYDROXYPROPYL]OXY}(HYDROXY)PHOSPHORYL]OXY}-2-[(6E)-HEXADEC-6-ENOYLOXY]PROPYL (8E)-OCTADEC-8-ENOATE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 4.9;298 K;Sodium potassium phosphate, glycerol, ethylene glycol, pH 4.9, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
分辨率 2.50 Å
R-free 0.290
|
|
1ZDT
The Crystal Structure of Human Steroidogenic Factor-1
提交 2005-04-14
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 P
741–752(12 aa)
片段:residues 741-752
|
未记录
|
PEF DI-PALMITOYL-3-SN-PHOSPHATIDYLETHANOLAMINE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 5.5;277 K;PEG3350, ammonium sulfate, sucrose, pH 5.5, temperature 277K, VAPOR DIFFUSION, SITTING DROP
|
分辨率 2.10 Å
R-free 0.265
|
|
1ZDT
The Crystal Structure of Human Steroidogenic Factor-1
提交 2005-04-14
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 Q
741–752(12 aa)
片段:residues 741-752
|
未记录
|
PEF DI-PALMITOYL-3-SN-PHOSPHATIDYLETHANOLAMINE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 5.5;277 K;PEG3350, ammonium sulfate, sucrose, pH 5.5, temperature 277K, VAPOR DIFFUSION, SITTING DROP
|
分辨率 2.10 Å
R-free 0.265
|
|
1ZDT
The Crystal Structure of Human Steroidogenic Factor-1
提交 2005-04-14
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 3
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 P
741–752(12 aa)
片段:residues 741-752
链 Q
741–752(12 aa)
片段:residues 741-752
|
未记录
|
PEF DI-PALMITOYL-3-SN-PHOSPHATIDYLETHANOLAMINE × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 5.5;277 K;PEG3350, ammonium sulfate, sucrose, pH 5.5, temperature 277K, VAPOR DIFFUSION, SITTING DROP
|
分辨率 2.10 Å
R-free 0.265
|
|
1ZDU
The Crystal Structure of Human Liver Receptor Homologue-1
提交 2005-04-14
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 3
PDB 声明:trimeric
|
链 P
741–751(11 aa)
片段:residues 741-751
链 Q
741–751(11 aa)
片段:residues 741-751
|
未记录
|
P3A PHOSPHATIDYLGLYCEROL-PHOSPHOGLYCEROL × 1
TRS 2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7.5;293 K;NaH2PO4, K2HPO4, pH 7.5, temperature 293K, VAPOR DIFFUSION, SITTING DROP
|
分辨率 2.50 Å
R-free 0.281
|
|
1ZKY
Human Estrogen Receptor Alpha Ligand-Binding Domain In Complex With OBCP-3M and A Glucocorticoid Receptor Interacting Protein 1 Nr Box II Peptide
提交 2005-05-04
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Residues 686 - 698
链 D
686–698(13 aa)
片段:Residues 686 - 698
|
未记录
|
689 4-[(1S,2S,5S)-5-(HYDROXYMETHYL)-6,8,9-TRIMETHYL-3-OXABICYCLO[3.3.1]NON-7-EN-2-YL]PHENOL × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;289 K;0.2M sodium malonate, 20% PEG 3350, pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 289K
|
分辨率 2.25 Å
R-free 0.231
|
|
2AO6
Crystal structure of the human androgen receptor ligand binding domain bound with TIF2(iii) 740-753 peptide and R1881
提交 2005-08-12
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
片段:BOX 3, RESIDUES 740-753
|
未记录
|
R18 (17BETA)-17-HYDROXY-17-METHYLESTRA-4,9,11-TRIEN-3-ONE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.9;293 K;100mM BTP, 0.6 M Na/K Tartrate, pH 7.90, VAPOR DIFFUSION, HANGING DROP, temperature 293K
|
分辨率 1.89 Å
R-free 0.242
|
|
2B1V
Human estrogen receptor alpha ligand-binding domain in complex with OBCP-1M and a glucocorticoid receptor interacting protein 1 NR box II peptide
提交 2005-09-16
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:RESIDUES 686 - 698
链 D
686–698(13 aa)
片段:RESIDUES 686 - 698
|
未记录
|
458 4-[(1S,2S,5S)-5-(HYDROXYMETHYL)-8-METHYL-3-OXABICYCLO[3.3.1]NON-7-EN-2-YL]PHENOL × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
pH 8.5;pH 8.50
|
分辨率 1.80 Å
R-free 0.238
|
|
2B1Z
Human estrogen receptor alpha ligand-binding domain in complex with 17methyl-17alpha-dihydroequilenin and a glucoc interacting protein 1 NR box II peptide
提交 2005-09-16
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:RESIDUES 686 - 698
链 D
686–698(13 aa)
片段:RESIDUES 686 - 698
|
未记录
|
17M 17-METHYL-17-ALPHA-DIHYDROEQUILENIN × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
pH 8.5;pH 8.50
|
分辨率 1.78 Å
R-free 0.238
|
|
2B23
Human estrogen receptor alpha ligand-binding domain and a glucocorticoid receptor-interacting protein 1 NR box II peptide
提交 2005-09-16
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:RESIDUES 686 - 698
链 D
686–698(13 aa)
片段:RESIDUES 686 - 698
|
未记录
|
未记录非水小分子
|
X-RAY DIFFRACTION
X-ray结晶条件
pH 4.5;pH 4.50
|
分辨率 2.10 Å
R-free 0.272
|
|
2FAI
Human Estrogen Receptor Alpha Ligand-Binding Domain In Complex With OBCP-2M and A Glucocorticoid Receptor Interacting Protein 1 NR Box II Peptide
提交 2005-12-07
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
链 D
686–698(13 aa)
|
未记录
|
459 4-[(1S,2S,5S,9R)-5-(HYDROXYMETHYL)-8,9-DIMETHYL-3-OXABICYCLO[3.3.1]NON-7-EN-2-YL]PHENOL × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.5;289 K;0.2M Ammonium Sulfate
0.1M Tris pH 8.5
25% PEG 3350, VAPOR DIFFUSION, HANGING DROP, temperature 289K
|
分辨率 2.10 Å
R-free 0.240
|
|
2G44
Human Estrogen Receptor Alpha Ligand-Binding Domain In Complex With OBCP-1M-G and A Glucocorticoid Receptor Interacting Protein 1 NR Box II Peptide
提交 2006-02-21
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:GRIP PEPTIDE
链 D
686–698(13 aa)
片段:GRIP PEPTIDE
|
未记录
|
T3O 4-[(1S,2R,5S)-4,4,8-TRIMETHYL-3-OXABICYCLO[3.3.1]NON-7-EN-2-YL]PHENOL × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
pH 7;0.2M AMMONIUM SULFATE 0.1M TRIS PH 7.0 25% PEG 3350, VAPOR DIFFUSION, HANGING DROP, TEMPERATURE 289K
|
分辨率 2.65 Å
R-free 0.256
|
|
2G5O
Human estrogen receptor alpha ligand-binding domain in complex with 2-(but-1-enyl)-17beta-estradiol and a glucocorticoid receptor interacting protein 1 NR BOX II Peptide
提交 2006-02-23
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:GRIP PEPTIDE
链 D
686–698(13 aa)
片段:GRIP PEPTIDE
|
未记录
|
DRQ (9ALPHA,13BETA,17BETA)-2-[(1Z)-BUT-1-EN-1-YL]ESTRA-1,3,5(10)-TRIENE-3,17-DIOL × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8;289 K;0.2M MAGENESIUM CHLORIDE 0.1M TRIS P 8.0 25% PEG 3350, VAPOR DIFFUSION, HANGING DROP, temperature 289K
|
分辨率 2.30 Å
R-free 0.264
|
|
2P15
Crystal structure of the ER alpha ligand binding domain with the agonist ortho-trifluoromethylphenylvinyl estradiol
提交 2007-03-02
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
链 D
686–698(13 aa)
|
未记录
|
EZT (17BETA)-17-{(E)-2-[2-(TRIFLUOROMETHYL)PHENYL]VINYL}ESTRA-1(10),2,4-TRIENE-3,17-DIOL × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 8.5;293 K;20% PEG 4000, 0.2M Ammonium sulfate, pH 8.5, VAPOR DIFFUSION, SITTING DROP, temperature 293K
|
分辨率 1.94 Å
R-free 0.216
|
|
2P1T
Crystal structure of the ligand binding domain of the retinoid X receptor alpha in complex with 3-(2'-methoxy)-tetrahydronaphtyl cinnamic acid and a fragment of the coactivator TIF-2
提交 2007-03-06
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:nuclear receptor interaction motif 2 (residues 686-698)
|
未记录
|
3TN (2E)-3-[4-HYDROXY-3-(3-METHOXY-5,5,8,8-TETRAMETHYL-5,6,7,8-TETRAHYDRONAPHTHALEN-2-YL)PHENYL]ACRYLIC ACID × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.5;298 K;16% PEG 3350, 0.1M Tris, 1M ammonium acetate, pH 8.5, VAPOR DIFFUSION, HANGING DROP, temperature 298.0K
|
分辨率 1.80 Å
R-free 0.218
|
|
2P1U
Crystal structure of the ligand binding domain of the retinoid X receptor alpha in complex with 3-(2'-ethoxy)-tetrahydronaphtyl cinnamic acid and a fragment of the coactivator TIF-2
提交 2007-03-06
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:nuclear receptor interaction motif 2 (residues 686-698)
|
未记录
|
4TN (2E)-3-[3-(3-ETHOXY-5,5,8,8-TETRAMETHYL-5,6,7,8-TETRAHYDRONAPHTHALEN-2-YL)-4-HYDROXYPHENYL]ACRYLIC ACID × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 8.5;298 K;14% PEG 10000, 0.1M Tris, 1M ammonium chloride, pH 8.5, VAPOR DIFFUSION, SITTING DROP, temperature 298K
|
分辨率 2.20 Å
R-free 0.251
|
|
2P1V
Crystal structure of the ligand binding domain of the retinoid X receptor alpha in complex with 3-(2'-propoxy)-tetrahydronaphtyl cinnamic acid and a fragment of the coactivator TIF-2
提交 2007-03-06
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:nuclear receptor interaction motif 2 (residues 686-698)
|
未记录
|
5TN (2E)-3-[4-HYDROXY-3-(5,5,8,8-TETRAMETHYL-3-PROPOXY-5,6,7,8-TETRAHYDRONAPHTHALEN-2-YL)PHENYL]ACRYLIC ACID × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.5;298 K;24% PEG 4000, 0.1M Tris, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
分辨率 2.20 Å
R-free 0.232
|
|
2Q7J
The Wild Type Androgen Receptor Ligand Binding Domain Bound with Testosterone and a TIF2 box 3 Coactivator Peptide 740-753
提交 2007-06-07
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
|
未记录
|
SO4 SULFATE ION × 1
TES TESTOSTERONE × 1
GOL GLYCEROL × 1
|
X-RAY DIFFRACTION
mmCIF 未提供已读取条件
|
分辨率 1.90 Å
R-free 0.220
|
|
2Q7L
The Androgen Receptor Prostate Cancer Mutant H874Y Ligand Binding Domain Bound with Testosterone and a TIF2 box3 Coactivator Peptide 740-753
提交 2007-06-07
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
|
未记录
|
TES TESTOSTERONE × 1
GOL GLYCEROL × 1
|
X-RAY DIFFRACTION
mmCIF 未提供已读取条件
|
分辨率 1.92 Å
R-free 0.221
|
|
2ZXZ
Crystal structure of the human RXR alpha ligand binding domain bound to a synthetic agonist compound and a coactivator peptide
提交 2009-01-09
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
P26 4-[2-(1,1,3,3-tetramethyl-2,3-dihydro-1H-inden-5-yl)-1,3-dioxolan-2-yl]benzoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8;290 K;10mM Tris-HCl, 250mM NaCl, 5mM DTT, 50mM calcium acetate, 18% PEG3350, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 290K
|
分辨率 3.00 Å
R-free 0.278
|
|
2ZY0
Crystal structure of the human RXR alpha ligand binding domain bound to a synthetic agonist compound and a coactivator peptide
提交 2009-01-09
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
链 D
686–698(13 aa)
|
未记录
|
21P 4-[2-(1,1,3,3-tetramethyl-2,3-dihydro-1H-1,3-benzodisilol-5-yl)-1,3-dioxolan-2-yl]benzoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8;290 K;10mM Tris-HCl, 250mM NaCl, 5mM DTT, 50mM calcium acetate, 18% PEG3350, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 290K
|
分辨率 2.90 Å
R-free 0.289
|
|
3A9E
Crystal structure of a mixed agonist-bound RAR-alpha and antagonist-bound RXR-alpha heterodimer ligand binding domains
提交 2009-10-24
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 3
PDB 声明:trimeric
|
链 I
686–698(13 aa)
|
未记录
|
754 (2E,4E,6Z)-3-methyl-7-(5,5,8,8-tetramethyl-3-propoxy-5,6,7,8-tetrahydronaphthalen-2-yl)octa-2,4,6-trienoic acid × 1
REA RETINOIC ACID × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 8;290 K;200mM potassium thiocyanate, 20% PEG 3350, pH 8.0, VAPOR DIFFUSION, SITTING DROP, temperature 290K
|
分辨率 2.75 Å
R-free 0.264
|
|
3A9E
Crystal structure of a mixed agonist-bound RAR-alpha and antagonist-bound RXR-alpha heterodimer ligand binding domains
提交 2009-10-24
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 6
PDB 声明:hexameric
|
链 I
686–698(13 aa)
|
未记录
|
754 (2E,4E,6Z)-3-methyl-7-(5,5,8,8-tetramethyl-3-propoxy-5,6,7,8-tetrahydronaphthalen-2-yl)octa-2,4,6-trienoic acid × 2
REA RETINOIC ACID × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 8;290 K;200mM potassium thiocyanate, 20% PEG 3350, pH 8.0, VAPOR DIFFUSION, SITTING DROP, temperature 290K
|
分辨率 2.75 Å
R-free 0.264
|
|
3DZU
Intact PPAR gamma - RXR alpha Nuclear Receptor Complex on DNA bound with BVT.13, 9-cis Retinoic Acid and NCOA2 Peptide
提交 2008-07-30
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白–DNA
异源复合物;蛋白 × 4
PDB 声明:hexameric
|
链 E
685–697(13 aa)
链 G
685–697(13 aa)
|
未记录
|
ZN ZINC ION × 4
9CR (9cis)-retinoic acid × 1
PLB 2-[(2,4-DICHLOROBENZOYL)AMINO]-5-(PYRIMIDIN-2-YLOXY)BENZOIC ACID × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;277 K;15-18% PEG 3350, 25mM MgCl2, 100mM NH4Cl, 5mM DTT and 0.1M MES, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 277K
|
分辨率 3.20 Å
R-free 0.272
|
|
3DZY
Intact PPAR gamma - RXR alpha Nuclear Receptor Complex on DNA bound with Rosiglitazone, 9-cis Retinoic Acid and NCOA2 Peptide
提交 2008-07-30
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白–DNA
异源复合物;蛋白 × 4
PDB 声明:hexameric
|
链 E
685–697(13 aa)
链 G
685–697(13 aa)
|
未记录
|
9CR (9cis)-retinoic acid × 1
ZN ZINC ION × 4
BRL 2,4-THIAZOLIDIINEDIONE, 5-[[4-[2-(METHYL-2-PYRIDINYLAMINO)ETHOXY]PHENYL]METHYL]-(9CL) × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;277 K;15-18% PEG 3350, 25mM MgCl2, 100mM NH4Cl, 5mM DTT and 0.1M MES, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 277K
|
分辨率 3.10 Å
R-free 0.268
|
|
3E00
Intact PPAR gamma - RXR alpha Nuclear Receptor Complex on DNA bound with GW9662, 9-cis Retinoic Acid and NCOA2 Peptide
提交 2008-07-30
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白–DNA
异源复合物;蛋白 × 4
PDB 声明:hexameric
|
链 E
685–697(13 aa)
链 G
685–697(13 aa)
|
未记录
|
ZN ZINC ION × 4
9CR (9cis)-retinoic acid × 1
GW9 2-chloro-5-nitro-N-phenylbenzamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;277 K;15-18% PEG 3350, 25mM MgCl2, 100mM NH4Cl, 5mM DTT and 0.1M MES, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 277K
|
分辨率 3.10 Å
R-free 0.276
|
|
3E7C
Glucocorticoid Receptor LBD bound to GSK866
提交 2008-08-18
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 D
741–751(11 aa)
片段:UNP RESIDUES 741-751
链 H
741–751(11 aa)
片段:UNP RESIDUES 741-751
|
未记录
|
866 5-amino-N-[(2S)-2-({[(2,6-dichlorophenyl)carbonyl](ethyl)amino}methyl)-3,3,3-trifluoro-2-hydroxypropyl]-1-(4-fluorophenyl)-1H-pyrazole-4-carboxamide × 2
GOL GLYCEROL × 3
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;295 K;0.1M MES pH 6.5, 1.6M MgSO4,
0.1% betahexaglucoside, VAPOR DIFFUSION, HANGING DROP, temperature 295K
|
分辨率 2.15 Å
R-free 0.266
|
|
3E7C
Glucocorticoid Receptor LBD bound to GSK866
提交 2008-08-18
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 H
741–751(11 aa)
片段:UNP RESIDUES 741-751
|
未记录
|
866 5-amino-N-[(2S)-2-({[(2,6-dichlorophenyl)carbonyl](ethyl)amino}methyl)-3,3,3-trifluoro-2-hydroxypropyl]-1-(4-fluorophenyl)-1H-pyrazole-4-carboxamide × 1
GOL GLYCEROL × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;295 K;0.1M MES pH 6.5, 1.6M MgSO4,
0.1% betahexaglucoside, VAPOR DIFFUSION, HANGING DROP, temperature 295K
|
分辨率 2.15 Å
R-free 0.266
|
|
3E7C
Glucocorticoid Receptor LBD bound to GSK866
提交 2008-08-18
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 3
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
741–751(11 aa)
片段:UNP RESIDUES 741-751
|
未记录
|
866 5-amino-N-[(2S)-2-({[(2,6-dichlorophenyl)carbonyl](ethyl)amino}methyl)-3,3,3-trifluoro-2-hydroxypropyl]-1-(4-fluorophenyl)-1H-pyrazole-4-carboxamide × 1
GOL GLYCEROL × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;295 K;0.1M MES pH 6.5, 1.6M MgSO4,
0.1% betahexaglucoside, VAPOR DIFFUSION, HANGING DROP, temperature 295K
|
分辨率 2.15 Å
R-free 0.266
|
|
3E94
Crystal structure of RXRalpha ligand binding domain in complex with tributyltin and a coactivator fragment
提交 2008-08-21
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:Nuclear Receptor box 2 (UNP residues 686-698)
|
未记录
|
TBY tributylstannanyl × 2
ACT ACETATE ION × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION;pH 7.5;293 K;PEG 4000, ammonium acetate, pH 7.5, VAPOR DIFFUSION, temperature 293K
|
分辨率 1.90 Å
R-free 0.225
|
|
3FUG
Crystal Structure of the Retinoid X Receptor Ligand Binding Domain Bound to the Synthetic Agonist 3-[4-Hydroxy-3-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-phenyl]acrylic Acid
提交 2009-01-14
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
686–698(13 aa)
片段:NUCLEAR RECEPTOR INTERACTION MOTIF 2 (RESIDUES 686-698)
|
未记录
|
2E3 (2E)-3-[4-hydroxy-3-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)phenyl]prop-2-enoic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;20% PEG 4000, 0.1M TRIS, 1M AMMONIUM ACETATE, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
分辨率 2.00 Å
R-free 0.241
|
|
3FUG
Crystal Structure of the Retinoid X Receptor Ligand Binding Domain Bound to the Synthetic Agonist 3-[4-Hydroxy-3-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)-phenyl]acrylic Acid
提交 2009-01-14
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:NUCLEAR RECEPTOR INTERACTION MOTIF 2 (RESIDUES 686-698)
|
未记录
|
2E3 (2E)-3-[4-hydroxy-3-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)phenyl]prop-2-enoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;20% PEG 4000, 0.1M TRIS, 1M AMMONIUM ACETATE, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
分辨率 2.00 Å
R-free 0.241
|
|
3GN8
X-ray Crystal Structure of AncGR2 in Complex with Dexamethasone
提交 2009-03-16
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
734–754(21 aa)
片段:sequence database residues 734-754
|
未记录
|
DEX DEXAMETHASONE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.4;298 K;0.5-0.75M ammonium acetate, pH 7.4, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
分辨率 2.50 Å
R-free 0.255
|
|
3GN8
X-ray Crystal Structure of AncGR2 in Complex with Dexamethasone
提交 2009-03-16
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 E
734–754(21 aa)
片段:sequence database residues 734-754
|
未记录
|
DEX DEXAMETHASONE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.4;298 K;0.5-0.75M ammonium acetate, pH 7.4, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
分辨率 2.50 Å
R-free 0.255
|
|
3K23
Glucocorticoid Receptor with Bound D-prolinamide 11
提交 2009-09-29
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
740–751(12 aa)
片段:UNP residues 740-751
|
未记录
|
JZN 1-{[3-(4-{[(2R)-4-(5-fluoro-2-methoxyphenyl)-2-hydroxy-4-methyl-2-(trifluoromethyl)pentyl]amino}-6-methyl-1H-indazol-1-yl)phenyl]carbonyl}-D-prolinamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;298 K;0.1M MES 6.5, 28% PEG 5K MME, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
分辨率 3.00 Å
R-free 0.289
|
|
3K23
Glucocorticoid Receptor with Bound D-prolinamide 11
提交 2009-09-29
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 E
740–751(12 aa)
片段:UNP residues 740-751
|
未记录
|
JZN 1-{[3-(4-{[(2R)-4-(5-fluoro-2-methoxyphenyl)-2-hydroxy-4-methyl-2-(trifluoromethyl)pentyl]amino}-6-methyl-1H-indazol-1-yl)phenyl]carbonyl}-D-prolinamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;298 K;0.1M MES 6.5, 28% PEG 5K MME, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
分辨率 3.00 Å
R-free 0.289
|
|
3K23
Glucocorticoid Receptor with Bound D-prolinamide 11
提交 2009-09-29
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 3
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 F
740–751(12 aa)
片段:UNP residues 740-751
|
未记录
|
JZN 1-{[3-(4-{[(2R)-4-(5-fluoro-2-methoxyphenyl)-2-hydroxy-4-methyl-2-(trifluoromethyl)pentyl]amino}-6-methyl-1H-indazol-1-yl)phenyl]carbonyl}-D-prolinamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;298 K;0.1M MES 6.5, 28% PEG 5K MME, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
分辨率 3.00 Å
R-free 0.289
|
|
3KWY
Crystal structure of RXRalpha ligand binding domain in complex with triphenyltin and a coactivator fragment
提交 2009-12-02
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:Nuclear Receptor box 2 (UNP residue 686-698)
|
未记录
|
T9T triphenylstannanyl × 2
ACT ACETATE ION × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION;pH 7.5;293 K;PEG 4000, acetate ammonium, Tris-HCl, pH 7.5, VAPOR DIFFUSION, temperature 293K
|
分辨率 2.30 Å
R-free 0.244
|
|
3KYT
Crystal structure of orphan nuclear receptor RORgamma in complex with natural ligand
提交 2009-12-07
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
686–697(12 aa)
片段:SCR2-2
|
未记录
|
HC2 20-HYDROXYCHOLESTEROL × 1
|
X-RAY DIFFRACTION
mmCIF 未提供已读取条件
|
分辨率 2.35 Å
R-free 0.298
|
|
3L03
Crystal Structure of human Estrogen Receptor alpha Ligand-Binding Domain in complex with a Glucocorticoid Receptor Interacting Protein 1 Nr Box II peptide and Estetrol (Estra-1,3,5(10)-triene-3,15 alpha,16alpha,17beta-tetrol)
提交 2009-12-09
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
链 D
686–698(13 aa)
|
未记录
|
CL CHLORIDE ION × 1
GOL GLYCEROL × 1
4OH (14beta,15alpha,16alpha,17alpha)-estra-1,3,5(10)-triene-3,15,16,17-tetrol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7.5;289 K;15% (v/v) ethanol, HEPES pH 7.5, MgCl2 , VAPOR DIFFUSION, SITTING DROP, temperature 289K
|
分辨率 1.90 Å
R-free 0.220
|
|
3L0E
X-ray crystal structure of a Potent Liver X Receptor Modulator
提交 2009-12-09
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–751(12 aa)
片段:UNP residues 740-751
|
未记录
|
G58 N-(2-chloro-6-fluorobenzyl)-1-methyl-N-{[3'-(methylsulfonyl)biphenyl-4-yl]methyl}-1H-imidazole-4-sulfonamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8;277 K;1:1 (v/v) ratio of the protein complex and PEG 2K MME 20%, 0.2mM MgCl2, 0.1mM TRIS HCl, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 277K
|
分辨率 2.30 Å
R-free 0.237
|
|
3L0E
X-ray crystal structure of a Potent Liver X Receptor Modulator
提交 2009-12-09
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
740–751(12 aa)
片段:UNP residues 740-751
|
未记录
|
G58 N-(2-chloro-6-fluorobenzyl)-1-methyl-N-{[3'-(methylsulfonyl)biphenyl-4-yl]methyl}-1H-imidazole-4-sulfonamide × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8;277 K;1:1 (v/v) ratio of the protein complex and PEG 2K MME 20%, 0.2mM MgCl2, 0.1mM TRIS HCl, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 277K
|
分辨率 2.30 Å
R-free 0.237
|
|
3L0J
Crystal structure of orphan nuclear receptor RORgamma in complex with natural ligand
提交 2009-12-10
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
688–697(10 aa)
片段:SRC2-2
|
未记录
|
HC9 (3alpha,8alpha,22R)-cholest-5-ene-3,22-diol × 1
|
X-RAY DIFFRACTION
mmCIF 未提供已读取条件
|
分辨率 2.40 Å
R-free 0.283
|
|
3L0L
Crystal structure of orphan nuclear receptor RORgamma in complex with natural ligand
提交 2009-12-10
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
685–697(13 aa)
片段:SRC2-2
|
未记录
|
HC3 25-HYDROXYCHOLESTEROL × 1
|
X-RAY DIFFRACTION
mmCIF 未提供已读取条件
|
分辨率 1.74 Å
R-free 0.252
|
|
3L0L
Crystal structure of orphan nuclear receptor RORgamma in complex with natural ligand
提交 2009-12-10
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 E
685–697(13 aa)
片段:SRC2-2
|
未记录
|
HC3 25-HYDROXYCHOLESTEROL × 1
|
X-RAY DIFFRACTION
mmCIF 未提供已读取条件
|
分辨率 1.74 Å
R-free 0.252
|
|
3O1D
Structure-function study of Gemini derivatives with two different side chains at C-20, Gemini-0072 and Gemini-0097.
提交 2010-07-21
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
G72 (1R,3R,7E,17beta)-17-[(1S)-6,6,6-trifluoro-5-hydroxy-1-(4-hydroxy-4-methylpentyl)-5-(trifluoromethyl)hex-3-yn-1-yl]-9,10-secoestra-5,7-diene-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;297 K;50 mM BIS-TRIS pH6.5, 1.6 M lithium sulfate, 50 mM magnesium sulfate, VAPOR DIFFUSION, HANGING DROP, temperature 297K
|
分辨率 2.40 Å
R-free 0.267
|
|
3O1E
Structure-function of Gemini derivatives with two different side chains at C-20, Gemini-0072 and Gemini-0097.
提交 2010-07-21
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
H97 (1R,3R,7E,17beta)-17-[(1R)-6,6,6-trifluoro-5-hydroxy-1-(4-hydroxy-4-methylpentyl)-5-(trifluoromethyl)hex-3-yn-1-yl]-9,1 0-secoestra-5,7-diene-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;297 K;50 mM BIS-TRIS pH6.5, 1.6 M lithium sulfate, 50 mM magnesium sulfate, VAPOR DIFFUSION, HANGING DROP, temperature 297K
|
分辨率 2.50 Å
R-free 0.272
|
|
3OAP
Crystal structure of human Retinoid X Receptor alpha-ligand binding domain complex with 9-cis retinoic acid and the coactivator peptide GRIP-1
提交 2010-08-05
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–696(11 aa)
片段:GRIP-1, UNP residues 686-696
|
未记录
|
9CR (9cis)-retinoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;296 K;4-20% PEG4000, 4-16% glycerol, 0.1M Bis-Tris, pH7.0, VAPOR DIFFUSION, HANGING DROP, temperature 296K
|
分辨率 2.05 Å
R-free 0.244
|
|
3OZJ
Crystal structure of human retinoic X receptor alpha complexed with bigelovin and coactivator SRC-1
提交 2010-09-25
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–696(11 aa)
片段:UNP residues 686-696
链 D
686–696(11 aa)
片段:UNP residues 686-696
|
未记录
|
BGV (3aR,4S,4aR,7aR,8R,9aS)-4a,8-dimethyl-3-methylidene-2,5-dioxo-2,3,3a,4,4a,5,7a,8,9,9a-decahydroazuleno[6,5-b]furan-4-yl acetate × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.5;277 K;8% v/v Tacsimate pH7.5, 20% w/v PEG3350, VAPOR DIFFUSION, HANGING DROP, temperature 277K
|
分辨率 2.10 Å
|
|
3PCU
Crystal structure of human retinoic X receptor alpha ligand-binding domain complexed with LX0278 and SRC1 peptide
提交 2010-10-22
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
687–696(10 aa)
片段:SRC-1 peptide (UNP residues 687-696)
|
未记录
|
LX8 2-[(2S)-6-(2-methylbut-3-en-2-yl)-7-oxo-2,3-dihydro-7H-furo[3,2-g]chromen-2-yl]propan-2-yl acetate × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8;277 K;8% v/v Tacsimate pH8.0, 20% w/v PEG 3350, VAPOR DIFFUSION, HANGING DROP, temperature 277K
|
分辨率 2.00 Å
|
|
3PLZ
Human LRH1 LBD bound to GR470
提交 2010-11-15
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
740–753(14 aa)
片段:UNP residues 740-753
|
未记录
|
470 (3aS,6aR)-5-[(4E)-oct-4-en-4-yl]-N,4-diphenyl-2,3,6,6a-tetrahydropentalen-3a(1H)-amine × 1
EDO 1,2-ETHANEDIOL × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 4.6;298 K;0.2M ammonium sulfate, 0.1M sodium acetate trihydrate, 25% w/v polyethylene glycol 4000, pH 4.6, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
分辨率 1.75 Å
R-free 0.214
|
|
3PLZ
Human LRH1 LBD bound to GR470
提交 2010-11-15
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
740–753(14 aa)
片段:UNP residues 740-753
|
未记录
|
470 (3aS,6aR)-5-[(4E)-oct-4-en-4-yl]-N,4-diphenyl-2,3,6,6a-tetrahydropentalen-3a(1H)-amine × 1
EDO 1,2-ETHANEDIOL × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 4.6;298 K;0.2M ammonium sulfate, 0.1M sodium acetate trihydrate, 25% w/v polyethylene glycol 4000, pH 4.6, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
分辨率 1.75 Å
R-free 0.214
|
|
3Q95
Crystal structure of human estrogen receptor alpha LBD in complex with GRIP peptide and estriol
提交 2011-01-07
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
686–698(13 aa)
|
未记录
|
ESL ESTRIOL × 1
CL CHLORIDE ION × 4
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 8.5;289 K;0.2 M Lithium sulfate monohydrate, 0.1 M Tris pH 8.5, 25% w/v Polyethylene glycol 3,350, VAPOR DIFFUSION, SITTING DROP, temperature 289K
|
分辨率 2.05 Å
R-free 0.241
|
|
3Q95
Crystal structure of human estrogen receptor alpha LBD in complex with GRIP peptide and estriol
提交 2011-01-07
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
686–698(13 aa)
|
未记录
|
ESL ESTRIOL × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 8.5;289 K;0.2 M Lithium sulfate monohydrate, 0.1 M Tris pH 8.5, 25% w/v Polyethylene glycol 3,350, VAPOR DIFFUSION, SITTING DROP, temperature 289K
|
分辨率 2.05 Å
R-free 0.241
|
|
3R5M
Crystal structure of RXRalphaLBD complexed with the agonist magnolol
提交 2011-03-18
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
687–696(10 aa)
片段:UNP residues 687-696
链 D
687–696(10 aa)
片段:UNP residues 687-696
|
未记录
|
MLO 5,5'-di(prop-2-en-1-yl)biphenyl-2,2'-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.5;277 K;20% PEG3350, 100 mM Tris, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 277K
|
分辨率 2.80 Å
R-free 0.293
|
|
3UP0
Nuclear receptor DAF-12 from hookworm Ancylostoma ceylanicum in complex with (25S)-delta7-dafachronic acid
提交 2011-11-17
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 P
740–753(14 aa)
片段:nuclear receptor binding motif (UNP residues 740-753)
|
未记录
|
D7S (5beta,14beta,17alpha,25S)-3-oxocholest-7-en-26-oic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
SITTING DROP;pH 5.1;293 K;26% w/v PEG2000, 0.2 M ammonium acetate, pH 5.1, SITTING DROP, temperature 293K
|
分辨率 1.60 Å
R-free 0.202
|
|
3UP0
Nuclear receptor DAF-12 from hookworm Ancylostoma ceylanicum in complex with (25S)-delta7-dafachronic acid
提交 2011-11-17
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 Q
740–753(14 aa)
片段:nuclear receptor binding motif (UNP residues 740-753)
|
未记录
|
D7S (5beta,14beta,17alpha,25S)-3-oxocholest-7-en-26-oic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
SITTING DROP;pH 5.1;293 K;26% w/v PEG2000, 0.2 M ammonium acetate, pH 5.1, SITTING DROP, temperature 293K
|
分辨率 1.60 Å
R-free 0.202
|
|
3UP3
Nuclear receptor DAF-12 from hookworm Ancylostoma ceylanicum in complex with (25S)-cholestenoic acid
提交 2011-11-17
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 P
741–754(14 aa)
片段:nuclear receptor binding motif (UNP residues 741-754)
|
未记录
|
XCA (8alpha,10alpha,25S)-3-hydroxycholesta-3,5-dien-26-oic acid × 1
EDO 1,2-ETHANEDIOL × 6
|
X-RAY DIFFRACTION
X-ray结晶条件
293 K;20% w/v PEG3350, 0.2 M diammonium tartrate, SITTING DROP, temperature 293K
|
分辨率 1.25 Å
R-free 0.180
|
|
4DOS
Human Nuclear Receptor Liver Receptor Homologue-1, LRH-1, Bound to DLPC and a Fragment of TIF-2
提交 2012-02-10
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 3
PDB 声明:trimeric
|
链 B
740–753(14 aa)
片段:NR Box 3, UNP residues 740-753
链 C
740–753(14 aa)
片段:NR Box 3, UNP residues 740-753
|
未记录
|
1PE PENTAETHYLENE GLYCOL × 3
PLC DIUNDECYL PHOSPHATIDYL CHOLINE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
hanging drop vapor diffusion;pH 5.2;298 K;18%-24% PEG 400, 5% glycerol, 0.1M lithium sulfate, and 0.1M sodium acetate pH 5.2, hanging drop vapor diffusion, temperature 298K
|
分辨率 2.00 Å
R-free 0.238
|
|
4DOS
Human Nuclear Receptor Liver Receptor Homologue-1, LRH-1, Bound to DLPC and a Fragment of TIF-2
提交 2012-02-10
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 3
PDB 声明:trimeric
|
链 B
740–753(14 aa)
片段:NR Box 3, UNP residues 740-753
链 C
740–753(14 aa)
片段:NR Box 3, UNP residues 740-753
|
未记录
|
1PE PENTAETHYLENE GLYCOL × 3
PLC DIUNDECYL PHOSPHATIDYL CHOLINE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
hanging drop vapor diffusion;pH 5.2;298 K;18%-24% PEG 400, 5% glycerol, 0.1M lithium sulfate, and 0.1M sodium acetate pH 5.2, hanging drop vapor diffusion, temperature 298K
|
分辨率 2.00 Å
R-free 0.238
|
|
4DOS
Human Nuclear Receptor Liver Receptor Homologue-1, LRH-1, Bound to DLPC and a Fragment of TIF-2
提交 2012-02-10
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 3
蛋白异源复合物
异源复合物;蛋白 × 6
PDB 声明:hexameric
|
链 B
740–753(14 aa)
片段:NR Box 3, UNP residues 740-753
链 C
740–753(14 aa)
片段:NR Box 3, UNP residues 740-753
|
未记录
|
1PE PENTAETHYLENE GLYCOL × 6
PLC DIUNDECYL PHOSPHATIDYL CHOLINE × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
hanging drop vapor diffusion;pH 5.2;298 K;18%-24% PEG 400, 5% glycerol, 0.1M lithium sulfate, and 0.1M sodium acetate pH 5.2, hanging drop vapor diffusion, temperature 298K
|
分辨率 2.00 Å
R-free 0.238
|
|
4E2J
X-Ray Crystal Structure of the Ancestral Glucocorticoid Receptor 2 ligand binding domain in complex with mometasone furoate and TIF-2 coactivator fragment
提交 2012-03-08
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
741–752(12 aa)
片段:nuclear receptor box 3, UNP residues 741-752
|
未记录
|
GOL GLYCEROL × 1
MOF MOMETASONE FUROATE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.4;277 K;1.5-3 M ammonium formate, pH 7.4, VAPOR DIFFUSION, HANGING DROP, temperature 277K
|
分辨率 2.50 Å
R-free 0.255
|
|
4E2J
X-Ray Crystal Structure of the Ancestral Glucocorticoid Receptor 2 ligand binding domain in complex with mometasone furoate and TIF-2 coactivator fragment
提交 2012-03-08
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 E
741–752(12 aa)
片段:nuclear receptor box 3, UNP residues 741-752
|
未记录
|
GOL GLYCEROL × 1
MOF MOMETASONE FUROATE × 1
FMT FORMIC ACID × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.4;277 K;1.5-3 M ammonium formate, pH 7.4, VAPOR DIFFUSION, HANGING DROP, temperature 277K
|
分辨率 2.50 Å
R-free 0.255
|
|
4FHH
Development of synthetically accessible non-secosteroidal hybrid molecules combining vitamin D receptor agonism and histone deacetylase inhibition
提交 2012-06-06
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:UNP RESIDUES 686-698
|
未记录
|
0U3 N-hydroxy-2-{4-[3-(4-{[(2S)-2-hydroxy-3,3-dimethylbutyl]oxy}-3-methylphenyl)pentan-3-yl]-2-methylphenoxy}acetamide × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;291 K;Bis Tris 0.1M, lithium sulfate 1.6M and magnesium sulfate 50 mM, VAPOR DIFFUSION, HANGING DROP, temperature 291K, pH 6.5
|
分辨率 2.33 Å
R-free 0.258
|
|
4IA1
Diastereotopic and Deuterium Effects in Gemini
提交 2012-12-06
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:unp residues 686-698
|
未记录
|
BIV 21-NOR-9,10-SECOCHOLESTA-5,7,10(19)-TRIENE-1,3,25-TRIOL, 20-(4-HYDROXY-4-METHYLPENTYL)-, (1A,3B,5Z,7E) × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 6.5;293 K;Bis Tris 0.1M, lithium sulfate 1.6M and magnesium sulfate 50 mM , pH 6.5, VAPOR DIFFUSION, SITTING DROP, temperature 293K
|
分辨率 2.44 Å
R-free 0.260
|
|
4IA2
Diastereotopic and Deuterium Effects in Gemini
提交 2012-12-06
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:LXXLL peptide unp residues 686-698
|
未记录
|
BIV 21-NOR-9,10-SECOCHOLESTA-5,7,10(19)-TRIENE-1,3,25-TRIOL, 20-(4-HYDROXY-4-METHYLPENTYL)-, (1A,3B,5Z,7E) × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 6.5;293 K;Bis-Tris 0.1 M, lithium sulfate 1.6 M and magnesium sulfate 50 mM , pH 6.5, VAPOR DIFFUSION, SITTING DROP, temperature 293K
|
分辨率 2.95 Å
R-free 0.256
|
|
4IA3
Diastereotopic and Deuterium Effects in Gemini
提交 2012-12-06
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:LXXLL peptide (unp residues 686-698)
|
未记录
|
BIV 21-NOR-9,10-SECOCHOLESTA-5,7,10(19)-TRIENE-1,3,25-TRIOL, 20-(4-HYDROXY-4-METHYLPENTYL)-, (1A,3B,5Z,7E) × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 6.5;293 K;Bis-Tris 0.1 M, lithium sulfate 1.6 M and magnesium sulfate 50 mM , pH 6.5, VAPOR DIFFUSION, SITTING DROP, temperature 293K
|
分辨率 2.70 Å
R-free 0.260
|
|
4IA7
Diastereotopic and Deuterium Effects in Gemini
提交 2012-12-06
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:LXXLL peptide (unp residues 686-698)
|
未记录
|
BIV 21-NOR-9,10-SECOCHOLESTA-5,7,10(19)-TRIENE-1,3,25-TRIOL, 20-(4-HYDROXY-4-METHYLPENTYL)-, (1A,3B,5Z,7E) × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 6.5;293 K;Bis-Tris 0.1 M, lithium sulfate 1.6 M and magnesium sulfate 50 mM , pH 6.5, VAPOR DIFFUSION, SITTING DROP, temperature 293K
|
分辨率 2.70 Å
R-free 0.255
|
|
4IQR
Multi-Domain Organization of the HNF4alpha Nuclear Receptor Complex on DNA
提交 2013-01-13
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白–DNA
异源复合物;蛋白 × 4
PDB 声明:hexameric
|
链 I
685–697(13 aa)
片段:LxxLL motif peptide (unp residues 685-697)
链 J
685–697(13 aa)
片段:LxxLL motif peptide (unp residues 685-697)
|
未记录
|
MYR MYRISTIC ACID × 2
ZN ZINC ION × 4
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;277 K;0.1M MES, 25mM NH4Cl, 25mM MgCl2 and PEG 3350 , pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 277K
|
分辨率 2.90 Å
R-free 0.278
|
|
4IQR
Multi-Domain Organization of the HNF4alpha Nuclear Receptor Complex on DNA
提交 2013-01-13
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白–DNA
异源复合物;蛋白 × 4
PDB 声明:hexameric
|
链 K
685–697(13 aa)
片段:LxxLL motif peptide (unp residues 685-697)
链 L
685–697(13 aa)
片段:LxxLL motif peptide (unp residues 685-697)
|
未记录
|
MYR MYRISTIC ACID × 2
ZN ZINC ION × 4
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;277 K;0.1M MES, 25mM NH4Cl, 25mM MgCl2 and PEG 3350 , pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 277K
|
分辨率 2.90 Å
R-free 0.278
|
|
4IU7
Crystal Structure of the Estrogen Receptor alpha Ligand-binding Domain in Complex with Constrained WAY-derivative, 2b
提交 2013-01-20
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
|
未记录
|
1GM 4-[2-ethyl-7-(trifluoromethyl)-2H-indazol-3-yl]benzene-1,3-diol × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M magnesium chloride, 0.067M sodium chloride, 0.1M Tris, pH 8.3, VAPOR DIFFUSION, HANGING DROP, temperature 294K
|
分辨率 2.29 Å
R-free 0.237
|
|
4IU7
Crystal Structure of the Estrogen Receptor alpha Ligand-binding Domain in Complex with Constrained WAY-derivative, 2b
提交 2013-01-20
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
|
未记录
|
1GM 4-[2-ethyl-7-(trifluoromethyl)-2H-indazol-3-yl]benzene-1,3-diol × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M magnesium chloride, 0.067M sodium chloride, 0.1M Tris, pH 8.3, VAPOR DIFFUSION, HANGING DROP, temperature 294K
|
分辨率 2.29 Å
R-free 0.237
|
|
4IU7
Crystal Structure of the Estrogen Receptor alpha Ligand-binding Domain in Complex with Constrained WAY-derivative, 2b
提交 2013-01-20
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 3
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
链 D
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
|
未记录
|
1GM 4-[2-ethyl-7-(trifluoromethyl)-2H-indazol-3-yl]benzene-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M magnesium chloride, 0.067M sodium chloride, 0.1M Tris, pH 8.3, VAPOR DIFFUSION, HANGING DROP, temperature 294K
|
分辨率 2.29 Å
R-free 0.237
|
|
4IUI
Crystal Structure of the Estrogen Receptor alpha Ligand-binding Domain in Complex with Dynamic WAY derivative, 4a
提交 2013-01-21
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
链 D
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
|
未记录
|
1GQ 4-[1-butyl-7-(trifluoromethyl)-1H-indazol-3-yl]benzene-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M magnesium chloride, 0.067M sodium chloride, 0.1M Tris, pH 8.3, VAPOR DIFFUSION, HANGING DROP, temperature 294K
|
分辨率 2.30 Å
R-free 0.312
|
|
4IV2
Crystal Structure of the Estrogen Receptor alpha Ligand-binding Domain in Complex with Dynamic WAY-derivative, 5a
提交 2013-01-22
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
链 D
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
|
未记录
|
1GR 4-[1-(2-methylpropyl)-7-(trifluoromethyl)-1H-indazol-3-yl]benzene-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M magnesium chloride, 0.067M sodium chloride, 0.1M Tris, pH 8.3, VAPOR DIFFUSION, HANGING DROP, temperature 294K
|
分辨率 2.14 Å
R-free 0.226
|
|
4IV4
Crystal Structure of the Estrogen Receptor alpha Ligand-binding Domain in Complex with Constrained WAY-derivative, 5b
提交 2013-01-22
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
链 D
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
|
未记录
|
1GS 4-[2-(2-methylpropyl)-7-(trifluoromethyl)-2H-indazol-3-yl]benzene-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M magnesium chloride, 0.067M sodium chloride, 0.1M Tris, pH 8.3, VAPOR DIFFUSION, HANGING DROP, temperature 294K
|
分辨率 2.30 Å
R-free 0.237
|
|
4IVW
Crystal Structure of the Estrogen Receptor alpha Ligand-binding Domain in Complex with Constrained WAY-derivative, 6b
提交 2013-01-23
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
|
未记录
|
1GJ 4-[2-benzyl-7-(trifluoromethyl)-2H-indazol-3-yl]benzene-1,3-diol × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M magnesium chloride, 0.067M sodium chloride, 0.1M Tris, pH 8.3, VAPOR DIFFUSION, HANGING DROP, temperature 294K
|
分辨率 2.06 Å
R-free 0.230
|
|
4IVW
Crystal Structure of the Estrogen Receptor alpha Ligand-binding Domain in Complex with Constrained WAY-derivative, 6b
提交 2013-01-23
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
|
未记录
|
1GJ 4-[2-benzyl-7-(trifluoromethyl)-2H-indazol-3-yl]benzene-1,3-diol × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M magnesium chloride, 0.067M sodium chloride, 0.1M Tris, pH 8.3, VAPOR DIFFUSION, HANGING DROP, temperature 294K
|
分辨率 2.06 Å
R-free 0.230
|
|
4IVW
Crystal Structure of the Estrogen Receptor alpha Ligand-binding Domain in Complex with Constrained WAY-derivative, 6b
提交 2013-01-23
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 3
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
链 D
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
|
未记录
|
1GJ 4-[2-benzyl-7-(trifluoromethyl)-2H-indazol-3-yl]benzene-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M magnesium chloride, 0.067M sodium chloride, 0.1M Tris, pH 8.3, VAPOR DIFFUSION, HANGING DROP, temperature 294K
|
分辨率 2.06 Å
R-free 0.230
|
|
4IVY
Crystal Structure of the Estrogen Receptor alpha Ligand-binding Domain in Complex with Dynamic WAY-derivative, 7a
提交 2013-01-23
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
链 D
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
|
未记录
|
1GT 4-[1-(but-3-en-1-yl)-7-(trifluoromethyl)-1H-indazol-3-yl]benzene-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M magnesium chloride, 0.067M sodium chloride, 0.1M Tris, pH 8.3, VAPOR DIFFUSION, HANGING DROP, temperature 294K
|
分辨率 1.95 Å
R-free 0.232
|
|
4IW6
Crystal Structure of the Estrogen Receptor alpha Ligand-binding Domain in Complex with Constrained WAY-derivative, 7b
提交 2013-01-23
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
链 D
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
|
未记录
|
1GU 4-[2-(but-3-en-1-yl)-7-(trifluoromethyl)-2H-indazol-3-yl]benzene-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M magnesium chloride, 0.067M sodium chloride, 0.1M Tris, pH 8.3, VAPOR DIFFUSION, HANGING DROP, temperature 294K
|
分辨率 1.98 Å
R-free 0.227
|
|
4IW8
Crystal Structure of the Estrogen Receptor alpha Ligand-binding Domain in Complex with Dynamic WAY-derivative, 9a
提交 2013-01-23
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
链 D
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
|
未记录
|
KN3 4-[1-(3-methylbut-2-en-1-yl)-7-(trifluoromethyl)-1H-indazol-3-yl]benzene-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M magnesium chloride, 0.067M sodium chloride, 0.1M Tris, pH 8.3, VAPOR DIFFUSION, HANGING DROP, temperature 294K
|
分辨率 2.04 Å
R-free 0.247
|
|
4IWC
Crystal Structure of the Estrogen Receptor alpha Ligand-binding Domain in Complex with a Dynamic Thiophene-derivative
提交 2013-01-23
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
链 D
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
|
未记录
|
1GV 4,4'-thiene-2,5-diylbis(3-methylphenol) × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M magnesium chloride, 0.067M sodium chloride, 0.1M Tris, pH 8.3, VAPOR DIFFUSION, HANGING DROP, temperature 294K
|
分辨率 2.24 Å
R-free 0.227
|
|
4IWF
Crystal Structure of the Estrogen Receptor alpha Ligand-binding Domain in Complex with a Dynamic Oxime-derivative
提交 2013-01-23
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
链 D
687–696(10 aa)
片段:Receptor-interacting peptide, UNP residues 687-696
|
未记录
|
15Q 2-chloro-3'-fluoro-3-[(E)-(hydroxyimino)methyl]biphenyl-4,4'-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M magnesium chloride, 0.067M sodium chloride, 0.1M Tris, pH 8.3, VAPOR DIFFUSION, HANGING DROP, temperature 294K
|
分辨率 1.93 Å
R-free 0.209
|
|
4K4J
Crystal structure of human Retinoid X Receptor alpha-ligand binding domain complex with 9cUAB30 and the coactivator peptide GRIP-1
提交 2013-04-12
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:coactivator peptide, UNP residues 686-698
|
未记录
|
1O8 (2E,4E,6Z,8E)-8-(3,4-dihydronaphthalen-1(2H)-ylidene)-3,7-dimethylocta-2,4,6-trienoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;295 K;5-10% PEG4000, 2-5% Glycerol, 0.1M Bis-Tris, pH 7, VAPOR DIFFUSION, HANGING DROP, temperature 295K
|
分辨率 2.00 Å
R-free 0.283
|
|
4K6I
Crystal structure of human retinoid X receptor alpha-ligand binding domain complex with Targretin and the coactivator peptide GRIP-1
提交 2013-04-15
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:coactivator peptide, UNP residues 686-698
|
未记录
|
9RA 4-[1-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)ethenyl]benzoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;295 K;5-15% PEG4000, 6-12% Glycerol, 0.1M Bis-Tris pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 295K
|
分辨率 2.10 Å
R-free 0.288
|
|
4M8E
CRYSTAL STRUCTURE OF HUMAN RETINOID X RECEPTOR ALPHA-LIGAND BINDING DOMAIN COMPLEX WITH (S) 4-Methyl 9cUAB30 COACTIVATOR PEPTIDE GRIP-1
提交 2013-08-13
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–696(11 aa)
片段:GRIP-1, UNP RESIDUES 686-696
|
未记录
|
29V (3E,6Z,8E)-3,7-dimethyl-8-[(4S)-4-methyl-3,4-dihydronaphthalen-1(2H)-ylidene]octa-3,6-dienoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;295 K;4-20% PEG4000, 4-16% GLYCEROL, 0.1M BIS-TRIS, PH7.0, VAPOR DIFFUSION, HANGING DROP, TEMPERATURE 295K
|
分辨率 2.40 Å
R-free 0.247
|
|
4M8H
CRYSTAL STRUCTURE OF HUMAN RETINOID X RECEPTOR ALPHA-LIGAND BINDING DOMAIN COMPLEX WITH (R)4-METHYL 9cUAB30 AND COACTIVATOR PEPTIDE GRIP-1
提交 2013-08-13
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–696(11 aa)
片段:GRIP-1, UNP RESIDUES 686-696
|
未记录
|
R4M (2E,6Z,8E)-3,7-dimethyl-8-[(4R)-4-methyl-3,4-dihydronaphthalen-1(2H)-ylidene]octa-2,6-dienoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;295 K;4-20% PEG4000, 4-16% GLYCEROL, 0.1M BIS-TRIS, PH7.0, VAPOR DIFFUSION, HANGING DROP, TEMPERATURE 295K
|
分辨率 2.20 Å
R-free 0.265
|
|
4NQA
Crystal structure of liganded hRXR-alpha/hLXR-beta heterodimer on DNA
提交 2013-11-24
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白–DNA
异源复合物;蛋白 × 4
PDB 声明:hexameric
|
链 C
686–698(13 aa)
片段:peptide (UNP residues 686-698)
链 D
686–698(13 aa)
片段:peptide (UNP residues 686-698)
|
未记录
|
9CR (9cis)-retinoic acid × 1
ZN ZINC ION × 4
965 [3-(3-{[2-chloro-3-(trifluoromethyl)benzyl](2,2-diphenylethyl)amino}propoxy)phenyl]acetic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8;295 K;6% PEG8000, 18% isopropanol, 0.05 M Tris, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 295K
|
分辨率 3.10 Å
R-free 0.218
|
|
4NQA
Crystal structure of liganded hRXR-alpha/hLXR-beta heterodimer on DNA
提交 2013-11-24
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白–DNA
异源复合物;蛋白 × 4
PDB 声明:hexameric
|
链 J
686–698(13 aa)
片段:peptide (UNP residues 686-698)
链 K
686–698(13 aa)
片段:peptide (UNP residues 686-698)
|
未记录
|
9CR (9cis)-retinoic acid × 1
ZN ZINC ION × 4
965 [3-(3-{[2-chloro-3-(trifluoromethyl)benzyl](2,2-diphenylethyl)amino}propoxy)phenyl]acetic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8;295 K;6% PEG8000, 18% isopropanol, 0.05 M Tris, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 295K
|
分辨率 3.10 Å
R-free 0.218
|
|
4OC7
Retinoic acid receptor alpha in complex with (E)-3-(3'-allyl-6-hydroxy-[1,1'-biphenyl]-3-yl)acrylic acid and a fragment of the coactivator TIF2
提交 2014-01-08
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:nuclear receptor interaction motif 2 (residues 686-698)
|
未记录
|
2QO (2E)-3-[6-hydroxy-3'-(prop-2-en-1-yl)biphenyl-3-yl]prop-2-enoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.5;277 K;0.1 M Na HEPES pH 7.5, 20% PEG 2000 MME, VAPOR DIFFUSION, HANGING DROP, temperature 277K
|
分辨率 2.50 Å
R-free 0.242
|
|
4P6W
Crystal Structure of mometasone furoate-bound glucocorticoid receptor ligand binding domain
提交 2014-03-25
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
741–752(12 aa)
片段:SRC2-3 peptide (UNP residues 741-752)
|
未记录
|
MOF MOMETASONE FUROATE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;295 K;0.1 M imidazole, pH6.5, and 1 M sodium acetate trihydrate. 30% sucrose
|
分辨率 1.95 Å
R-free 0.225
|
|
4P6X
Crystal Structure of cortisol-bound glucocorticoid receptor ligand binding domain
提交 2014-03-25
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
片段:SRC2-3 peptide longer version (UNP residues 740-753)
|
未记录
|
HCY (11alpha,14beta)-11,17,21-trihydroxypregn-4-ene-3,20-dione × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;295 K;0.1 M imidazole, pH6.5, and 1 M sodium acetate trihydrate. 30% sucrose
|
分辨率 2.50 Å
R-free 0.276
|
|
4P6X
Crystal Structure of cortisol-bound glucocorticoid receptor ligand binding domain
提交 2014-03-25
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
740–753(14 aa)
片段:SRC2-3 peptide longer version (UNP residues 740-753)
|
未记录
|
HCY (11alpha,14beta)-11,17,21-trihydroxypregn-4-ene-3,20-dione × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;295 K;0.1 M imidazole, pH6.5, and 1 M sodium acetate trihydrate. 30% sucrose
|
分辨率 2.50 Å
R-free 0.276
|
|
4P6X
Crystal Structure of cortisol-bound glucocorticoid receptor ligand binding domain
提交 2014-03-25
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 3
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 F
740–753(14 aa)
片段:SRC2-3 peptide longer version (UNP residues 740-753)
|
未记录
|
HCY (11alpha,14beta)-11,17,21-trihydroxypregn-4-ene-3,20-dione × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;295 K;0.1 M imidazole, pH6.5, and 1 M sodium acetate trihydrate. 30% sucrose
|
分辨率 2.50 Å
R-free 0.276
|
|
4P6X
Crystal Structure of cortisol-bound glucocorticoid receptor ligand binding domain
提交 2014-03-25
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 4
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 H
740–753(14 aa)
片段:SRC2-3 peptide longer version (UNP residues 740-753)
|
未记录
|
HCY (11alpha,14beta)-11,17,21-trihydroxypregn-4-ene-3,20-dione × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;295 K;0.1 M imidazole, pH6.5, and 1 M sodium acetate trihydrate. 30% sucrose
|
分辨率 2.50 Å
R-free 0.276
|
|
4P6X
Crystal Structure of cortisol-bound glucocorticoid receptor ligand binding domain
提交 2014-03-25
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 5
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 J
740–753(14 aa)
片段:SRC2-3 peptide longer version (UNP residues 740-753)
|
未记录
|
HCY (11alpha,14beta)-11,17,21-trihydroxypregn-4-ene-3,20-dione × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;295 K;0.1 M imidazole, pH6.5, and 1 M sodium acetate trihydrate. 30% sucrose
|
分辨率 2.50 Å
R-free 0.276
|
|
4P6X
Crystal Structure of cortisol-bound glucocorticoid receptor ligand binding domain
提交 2014-03-25
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 6
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 L
740–753(14 aa)
片段:SRC2-3 peptide longer version (UNP residues 740-753)
|
未记录
|
HCY (11alpha,14beta)-11,17,21-trihydroxypregn-4-ene-3,20-dione × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;295 K;0.1 M imidazole, pH6.5, and 1 M sodium acetate trihydrate. 30% sucrose
|
分辨率 2.50 Å
R-free 0.276
|
|
4PLD
Human Nuclear Receptor Liver Receptor Homologue-1, LRH-1, in its apo State Bound to a Fragment of Human TIF-2
提交 2014-05-16
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
片段:UNP RESIDUES 740-753
|
未记录
|
CPS 3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.4;293 K;0.7-1 M di-Sodium Malonate, 0.1 M HEPES pH 7.4, 0.5% Jeffamine ED-2001
|
分辨率 1.75 Å
R-free 0.225
|
|
4PLE
Human Nuclear Receptor Liver Receptor Homologue-1, LRH-1, Bound to an E. Coli Phospholipid and a Fragment of TIF-2
提交 2014-05-16
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
片段:UNP residues 740-753
|
未记录
|
EPH L-ALPHA-PHOSPHATIDYL-BETA-OLEOYL-GAMMA-PALMITOYL-PHOSPHATIDYLETHANOLAMINE × 1
CPS 3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE × 3
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.4;293 K;0.7-1 M di-Sodium Malonate, 0.1 M HEPES pH 7.4, 0.5% Jeffamine ED-2001
|
分辨率 1.75 Å
R-free 0.236
|
|
4PLE
Human Nuclear Receptor Liver Receptor Homologue-1, LRH-1, Bound to an E. Coli Phospholipid and a Fragment of TIF-2
提交 2014-05-16
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
740–753(14 aa)
片段:UNP residues 740-753
|
未记录
|
EPH L-ALPHA-PHOSPHATIDYL-BETA-OLEOYL-GAMMA-PALMITOYL-PHOSPHATIDYLETHANOLAMINE × 1
CPS 3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.4;293 K;0.7-1 M di-Sodium Malonate, 0.1 M HEPES pH 7.4, 0.5% Jeffamine ED-2001
|
分辨率 1.75 Å
R-free 0.236
|
|
4PLE
Human Nuclear Receptor Liver Receptor Homologue-1, LRH-1, Bound to an E. Coli Phospholipid and a Fragment of TIF-2
提交 2014-05-16
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 3
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 F
740–753(14 aa)
片段:UNP residues 740-753
|
未记录
|
EPH L-ALPHA-PHOSPHATIDYL-BETA-OLEOYL-GAMMA-PALMITOYL-PHOSPHATIDYLETHANOLAMINE × 1
CPS 3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE × 5
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.4;293 K;0.7-1 M di-Sodium Malonate, 0.1 M HEPES pH 7.4, 0.5% Jeffamine ED-2001
|
分辨率 1.75 Å
R-free 0.236
|
|
4PLE
Human Nuclear Receptor Liver Receptor Homologue-1, LRH-1, Bound to an E. Coli Phospholipid and a Fragment of TIF-2
提交 2014-05-16
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 4
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 H
740–753(14 aa)
片段:UNP residues 740-753
|
未记录
|
EPH L-ALPHA-PHOSPHATIDYL-BETA-OLEOYL-GAMMA-PALMITOYL-PHOSPHATIDYLETHANOLAMINE × 1
CPS 3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.4;293 K;0.7-1 M di-Sodium Malonate, 0.1 M HEPES pH 7.4, 0.5% Jeffamine ED-2001
|
分辨率 1.75 Å
R-free 0.236
|
|
4POH
Crystal structure of human Retinoid X Receptor alpha-ligand binding domain complex with 8-methyl UAB30 and the coactivator peptide GRIP-1
提交 2014-02-25
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:Coactivator peptide, UNP residues 686-698
|
未记录
|
2VR (2E,4E,6Z,8E)-3,7-dimethyl-8-(8-methyl-3,4-dihydronaphthalen-1(2H)-ylidene)octa-2,4,6-trienoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;295 K;4-12% PEG4000, 3-12% Glycerol, 0.1M Bis-Tris, pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 295K
|
分辨率 2.30 Å
R-free 0.265
|
|
4POJ
Crystal structure of human Retinoid X Receptor alpha-ligand binding domain complex with 7-methyl UAB30 and the coactivator peptide GRIP-1
提交 2014-02-25
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:Coactivator peptide, UNP residues 686-698
|
未记录
|
2VP (2E,4E,6Z,8E)-3,7-dimethyl-8-(7-methyl-3,4-dihydronaphthalen-1(2H)-ylidene)octa-2,4,6-trienoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;4-12% PEG4000, 3-12% Glycerol, 0.1M Bis-Tris, pH 7.0 , VAPOR DIFFUSION, HANGING DROP
|
分辨率 2.00 Å
R-free 0.261
|
|
4PP3
Crystal structure of human Retinoid X Receptor alpha-ligand binding domain complex with 6-methyl UAB30 and the coactivator peptide GRIP-1
提交 2014-02-26
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:Coactivator peptide, UNP residues 686-698
|
未记录
|
2VZ (2E,4E,6Z,8E)-3,7-dimethyl-8-(6-methyl-3,4-dihydronaphthalen-1(2H)-ylidene)octa-2,4,6-trienoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;295 K;4-12% PEG4000, 3-12% Glycerol, 0.1M Bis-Tris, pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 295K
|
分辨率 2.00 Å
R-free 0.275
|
|
4PP5
Crystal structure of human Retinoid X Receptor alpha-ligand binding domain complex with 5-methyl UAB30 and the coactivator peptide GRIP-1
提交 2014-02-26
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:Coactivator peptide, UNP residues 686-698
|
未记录
|
2W0 (2E,4E,6Z,8E)-3,7-dimethyl-8-(5-methyl-3,4-dihydronaphthalen-1(2H)-ylidene)octa-2,4,6-trienoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;295 K;4-12% PEG4000, 3-12% Glycerol, 0.1M Bis-Tris, pH 7.0 , VAPOR DIFFUSION, HANGING DROP, temperature 295K
|
分辨率 2.00 Å
R-free 0.250
|
|
4PP6
Crystal Structure of the Estrogen Receptor alpha Ligand-binding Domain in Complex with Resveratrol
提交 2014-02-26
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
688–696(9 aa)
片段:receptor-interacting peptide (UNP residues 688-696)
链 D
688–696(9 aa)
片段:receptor-interacting peptide (UNP residues 688-696)
|
未记录
|
STL RESVERATROL × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG3350, 0.05 M magnesium chloride, 0.067 M sodium chloride, 0.1 M Tris, pH 8.3, VAPOR DIFFUSION, HANGING DROP, temperature 294K
|
分辨率 2.20 Å
R-free 0.221
|
|
4PPP
Crystal Structure of the Estrogen Receptor alpha Ligand-binding Domain in Complex with Fluoro-Resveratrol
提交 2014-02-27
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
688–696(9 aa)
片段:receptor-interacting peptide (UNP residues 688-696)
链 D
688–696(9 aa)
片段:receptor-interacting peptide (UNP residues 688-696)
|
未记录
|
FSV 5-[(E)-2-(3-fluoro-4-hydroxyphenyl)ethenyl]benzene-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG3350, 0.05 M magnesium chloride, 0.067 M sodium chloride, 0.1 M Tris, pH 8.3, VAPOR DIFFUSION, HANGING DROP, temperature 294K
|
分辨率 2.69 Å
R-free 0.247
|
|
4PPS
Crystal Structure of the Estrogen Receptor alpha Ligand-binding Domain in Complex with an A-CD ring estrogen derivative
提交 2014-02-27
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
687–698(12 aa)
片段:receptor-interacting peptide (UNP residues 687-698)
链 D
687–698(12 aa)
片段:receptor-interacting peptide (UNP residues 687-698)
|
未记录
|
ESE (1S,3aR,5R,7aS)-5-(4-hydroxyphenyl)-7a-methyloctahydro-1H-inden-1-ol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG3350, 0.05 M magnesium chloride, 0.067 M sodium chloride, 0.1 M Tris, pH 8.3, VAPOR DIFFUSION, HANGING DROP, temperature 294K
|
分辨率 1.93 Å
R-free 0.202
|
|
4PXM
The Estrogen Receptor Alpha Ligand Binding Domain D538G Mutant in Complex with Estradiol and a glucocorticoid receptor-interacting protein 1 NR box II peptide
提交 2014-03-24
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
链 D
686–698(13 aa)
|
未记录
|
EST ESTRADIOL × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8;298.15 K;20% PEG 3,350, 1 mM Phenylalanine, 64 mM NaCl, 50 mM MgCl2, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 298.15K
|
分辨率 1.90 Å
R-free 0.214
|
|
4Q0A
Vitamin D Receptor complex with lithocholic acid
提交 2014-04-01
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 D
687–695(9 aa)
片段:peptide
|
未记录
|
4OA (3beta,5beta,14beta,17alpha)-3-hydroxycholan-24-oic acid × 4
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7;290 K;BTP 0.1M, NaOAc 3M, pH 7, VAPOR DIFFUSION, SITTING DROP, temperature 290K
|
分辨率 1.90 Å
R-free 0.244
|
|
4QE8
FXR with DM175 and NCoA-2 peptide
提交 2014-05-15
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
740–752(13 aa)
片段:unp residues 740-752
|
未记录
|
31D 4-({2-[(4-tert-butylbenzoyl)amino]benzoyl}amino)benzoic acid × 1
EDO 1,2-ETHANEDIOL × 4
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION;pH 7;277 K;300 mM MgCl2, 100 mM Bis-Tris, 15-20% PEG 3350, pH 7, VAPOR DIFFUSION, temperature 277K
|
分辨率 2.62 Å
R-free 0.273
|
|
4QE8
FXR with DM175 and NCoA-2 peptide
提交 2014-05-15
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
740–752(13 aa)
片段:unp residues 740-752
|
未记录
|
31D 4-({2-[(4-tert-butylbenzoyl)amino]benzoyl}amino)benzoic acid × 1
EDO 1,2-ETHANEDIOL × 3
MRD (4R)-2-METHYLPENTANE-2,4-DIOL × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION;pH 7;277 K;300 mM MgCl2, 100 mM Bis-Tris, 15-20% PEG 3350, pH 7, VAPOR DIFFUSION, temperature 277K
|
分辨率 2.62 Å
R-free 0.273
|
|
4RFW
Crystal structure of human retinoid X Receptor alpha-ligand binding domain complex with 9cUAB70 and the coactivator peptide GRIP-1
提交 2014-09-28
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 G
686–698(13 aa)
片段:coactivator peptide LXXLL motif 2, residues 686-698
|
未记录
|
3RB (2E,4E,6Z,8E)-3,7-dimethyl-8-(6,7,8,9-tetrahydro-5H-benzo[7]annulen-5-ylidene)octa-2,4,6-trienoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;295 K;5-12% PEG4000, 3-12 Glycerol, 0.1 Bis-Tris pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 295K
|
分辨率 2.40 Å
R-free 0.261
|
|
4RMC
Crystal Structure of human retinoid X receptor alpha-ligand binding domain complex with 9cUAB76 and the coactivator peptide GRIP-1
提交 2014-10-21
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:coactivator peptide residues 686-698
|
未记录
|
3SV (3S,7S,8E)-8-[3-ethyl-2-(3-methylbutyl)cyclohex-2-en-1-ylidene]-3,7-dimethyloctanoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;295 K;5-15% PEG4000, 4-12% Glycerol, 0.1M Bis-Tris, pH=7.0, VAPOR DIFFUSION, HANGING DROP, temperature 295K
|
分辨率 2.70 Å
R-free 0.265
|
|
4RMD
Crystal structure of human Retinoid X receptor alpha ligand binding domain complex with 9cUAB110 and coactivator peptide GRIP-1
提交 2014-10-21
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:coactivator peptide residues 686-698
|
未记录
|
3SW (2E,4E,6Z,8E)-8-[3-cyclopropyl-2-(3-methylbutyl)cyclohex-2-en-1-ylidene]-3,7-dimethylocta-2,4,6-trienoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;295 K;5-15% PEG4000, 4-12% Glycerol, 0.1M Bis-Tris pH=7.0, VAPOR DIFFUSION, HANGING DROP, temperature 295K
|
分辨率 1.90 Å
R-free 0.239
|
|
4RME
Crystal structure of human Retinoid X receptor alpha ligand binding domain complex with 9cUAB111 and coactivator peptide GRIP-1
提交 2014-10-21
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:coactivator peptide residues 686-698
|
未记录
|
3T2 (2E,4E,6Z,8E)-3,7-dimethyl-8-[2-(3-methylbutyl)-3-(propan-2-yl)cyclohex-2-en-1-ylidene]octa-2,4,6-trienoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;295 K;5-15% PEG4000, 4-12% Glycerol, 0.1M Bis-Tris pH=7.0, VAPOR DIFFUSION, HANGING DROP, temperature 295K
|
分辨率 2.30 Å
R-free 0.273
|
|
4RUO
Crystal structure of zVDR L337H mutant-gemini complex
提交 2014-11-21
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
片段:UNP residues 686-698
|
未记录
|
BIV 21-NOR-9,10-SECOCHOLESTA-5,7,10(19)-TRIENE-1,3,25-TRIOL, 20-(4-HYDROXY-4-METHYLPENTYL)-, (1A,3B,5Z,7E) × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 6.5;295 K;Bis-Tris 0.1 M, lithium sulfate 1.6 M and magnesium sulfate 50 mM, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 295K
|
分辨率 2.81 Å
R-free 0.261
|
|
4UDC
GR in complex with dexamethasone
提交 2014-12-09
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
片段:RESIDUES 740-753
|
未记录
|
CPS 3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE × 1
DEX DEXAMETHASONE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
pH 7.5;10% PEG8000, 10% ETHYLENE GLYCOL, 0.1 M HEPES PH 7.5
|
分辨率 2.50 Å
R-free 0.253
|
|
4UDD
GR in complex with desisobutyrylciclesonide
提交 2014-12-09
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
片段:RESIDUES 740-753
|
未记录
|
CPS 3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE × 3
EDO 1,2-ETHANEDIOL × 1
CV7 DESISOBUYTYRYL CICLESONIDE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
pH 7.5;10% PEG8000, 20% ETHYLENE GLYCOL, 0.1 M HEPES PH 7.5
|
分辨率 1.80 Å
R-free 0.224
|
|
4WG0
Crystal structure of a tridecameric superhelix
提交 2014-09-17
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白同源多聚体
同源多聚体;蛋白 × 13
PDB 声明:tridecameric
|
链 A
740–752(13 aa)
片段:UNP Residues 740-752
链 B
740–752(13 aa)
片段:UNP Residues 740-752
链 C
740–752(13 aa)
片段:UNP Residues 740-752
链 D
740–752(13 aa)
片段:UNP Residues 740-752
链 E
740–752(13 aa)
片段:UNP Residues 740-752
链 F
740–752(13 aa)
片段:UNP Residues 740-752
链 G
740–752(13 aa)
片段:UNP Residues 740-752
链 H
740–752(13 aa)
片段:UNP Residues 740-752
链 I
740–752(13 aa)
片段:UNP Residues 740-752
链 J
740–752(13 aa)
片段:UNP Residues 740-752
链 K
740–752(13 aa)
片段:UNP Residues 740-752
链 L
740–752(13 aa)
片段:UNP Residues 740-752
链 M
740–752(13 aa)
片段:UNP Residues 740-752
|
非标准单体:是(mmCIF未提供具体位点)
非标准单体:是(mmCIF未提供具体位点)
非标准单体:是(mmCIF未提供具体位点)
非标准单体:是(mmCIF未提供具体位点)
非标准单体:是(mmCIF未提供具体位点)
非标准单体:是(mmCIF未提供具体位点)
非标准单体:是(mmCIF未提供具体位点)
非标准单体:是(mmCIF未提供具体位点)
非标准单体:是(mmCIF未提供具体位点)
非标准单体:是(mmCIF未提供具体位点)
非标准单体:是(mmCIF未提供具体位点)
非标准单体:是(mmCIF未提供具体位点)
非标准单体:是(mmCIF未提供具体位点)
|
SO4 SULFATE ION × 24
CHD CHOLIC ACID × 13
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 3.5;298 K;2M ammonium sulfate,
5-10% glycerol,
0.1 M citric acid pH 3.5
|
分辨率 1.82 Å
R-free 0.218
|
|
4ZN7
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in complex with Diethylstilbestrol
提交 2015-05-04
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
|
未记录
|
DES DIETHYLSTILBESTROL × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 1.93 Å
R-free 0.226
|
|
4ZN9
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in complex with Oxabicyclic Heptene Sulfonate (OBHS)
提交 2015-05-04
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:UNP residues 686-698
链 D
686–698(13 aa)
片段:UNP residues 686-698
|
未记录
|
OBH cyclohexa-2,5-dien-1-yl (1S,2R,4S)-5,6-bis(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-5-ene-2-sulfonate × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.21 Å
R-free 0.242
|
|
4ZNH
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in complex with a 2-Fluoro-substituted OBHS derivative
提交 2015-05-04
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:UNP residues 686-698
链 D
686–698(13 aa)
片段:UNP residues 686-698
|
未记录
|
OBC 2-fluorophenyl (1S,2R,4S)-5,6-bis(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-5-ene-2-sulfonate × 3
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 1.93 Å
R-free 0.251
|
|
4ZNS
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in complex with a 3-Fluoro-substituted OBHS derivative
提交 2015-05-05
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:UNP residues 686-698
链 D
686–698(13 aa)
片段:UNP residues 686-698
|
未记录
|
OFB 3-fluorophenyl (1S,2R,4S)-5,6-bis(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-5-ene-2-sulfonate × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 1.86 Å
R-free 0.236
|
|
4ZNT
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in complex with a 3-Bromo-substituted OBHS derivative
提交 2015-05-05
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:UNP residues 686-698
链 D
686–698(13 aa)
片段:UNP residues 686-698
|
未记录
|
OBB 3-bromophenyl (1S,2R,4S)-5,6-bis(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-5-ene-2-sulfonate × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 1.90 Å
R-free 0.214
|
|
4ZNU
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in complex with a 2-Methyl-substituted OBHS derivative
提交 2015-05-05
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:UNP residues 686-698
链 D
686–698(13 aa)
片段:UNP residues 686-698
|
未记录
|
4Q9 2-methylphenyl (1S,2R,4S)-5,6-bis(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-5-ene-2-sulfonate × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.40 Å
R-free 0.245
|
|
4ZNV
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in complex with a 2-Methoxy-substituted OBHS derivative
提交 2015-05-05
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:UNP residues 686-698
链 D
686–698(13 aa)
片段:UNP residues 686-698
|
未记录
|
4Q7 2-methoxyphenyl (1S,2R,4S)-5,6-bis(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-5-ene-2-sulfonate × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 1.77 Å
R-free 0.197
|
|
4ZNW
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in complex with a 4-Bromo-substituted OBHS derivative
提交 2015-05-05
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:UNP residues 686-698
链 D
686–698(13 aa)
片段:UNP residues 686-698
|
未记录
|
OBM 4-bromophenyl (1S,2R,4S)-5,6-bis(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-5-ene-2-sulfonate × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.31 Å
R-free 0.236
|
|
5DI7
Crystal Structure of the ER-alpha Ligand-binding Domain in complex with an methyl-substituted A-CD ring estrogen derivative (1S,3aR,5S,7aS)-5-(4-hydroxy-2-methylphenyl)-7a-methyloctahydro-1H-inden-1-ol
提交 2015-08-31
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5CQ (1S,3aR,5S,7aS)-5-(4-hydroxy-2-methylphenyl)-7a-methyloctahydro-1H-inden-1-ol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.24 Å
R-free 0.213
|
|
5DID
Crystal Structure of the ER-alpha Ligand-binding Domain in complex with a difluoro-substituted A-CD ring estrogen derivative (1S,3aR,5S,7aS)-5-(2,3-difluoro-4-hydroxyphenyl)-7a-methyloctahydro-1H-inden-1-ol
提交 2015-08-31
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
链 D
686–699(14 aa)
|
未记录
|
5CK (1S,3aR,5S,7aS)-5-(2,3-difluoro-4-hydroxyphenyl)-7a-methyloctahydro-1H-inden-1-ol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.24 Å
R-free 0.228
|
|
5DIE
Crystal Structure of the ER-alpha Ligand-binding Domain in complex with a trifluoro-substituted A-CD ring estrogen derivative (1S,3aR,5S,7aS)-7a-methyl-5-(2,3,5-trifluoro-4-hydroxyphenyl)octahydro-1H-inden-1-ol
提交 2015-08-31
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5CJ (1S,3aR,5S,7aS)-7a-methyl-5-(2,3,5-trifluoro-4-hydroxyphenyl)octahydro-1H-inden-1-ol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.24 Å
R-free 0.247
|
|
5DIG
Crystal Structure of the ER-alpha Ligand-binding Domain in complex with a trifluoromethyl-substituted A-CD ring estrogen derivative (1S,3aR,5S,7aS)-5-[4-hydroxy-2-(trifluoromethyl)phenyl]-7a-methyloctahydro-1H-inden-1-ol
提交 2015-09-01
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5CE (1S,3aR,5S,7aS)-5-[4-hydroxy-2-(trifluoromethyl)phenyl]-7a-methyloctahydro-1H-inden-1-ol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.24 Å
R-free 0.212
|
|
5DK9
Crystal Structure of the ER-alpha Ligand-binding Domain in complex with a phenylamino-substituted ethyl triaryl-ethylene derivative 4,4'-{2-[3-(phenylamino)phenyl]but-1-ene-1,1-diyl}diphenol
提交 2015-09-03
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5CC 4,4'-{2-[3-(phenylamino)phenyl]but-1-ene-1,1-diyl}diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.28 Å
R-free 0.238
|
|
5DKB
Crystal Structure of the ER-alpha Ligand-binding Domain in complex with a 3-methylphenylamino-substituted ethyl triaryl-ethylene derivative 4,4'-(2-{3-[(3-methylphenyl)amino]phenyl}but-1-ene-1,1-diyl)diphenol
提交 2015-09-03
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5C9 4,4'-(2-{3-[(3-methylphenyl)amino]phenyl}but-1-ene-1,1-diyl)diphenol × 3
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.40 Å
R-free 0.226
|
|
5DKG
Crystal Structure of the ER-alpha Ligand-binding Domain in complex with a t-butyl-substituted, methyl, triaryl-ethylene derivative 4,4'-[2-(4-tert-butylphenyl)prop-1-ene-1,1-diyl]diphenol
提交 2015-09-03
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5C7 4,4'-[2-(4-tert-butylphenyl)prop-1-ene-1,1-diyl]diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.15 Å
R-free 0.233
|
|
5DKS
Crystal Structure of the ER-alpha Ligand-binding Domain in complex with a 2-naphthylamino-substituted, ethyl, triaryl-ethylene derivative 4,4'-{2-[3-(naphthalen-1-ylamino)phenyl]but-1-ene-1,1-diyl}diphenol
提交 2015-09-03
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5C6 4,4'-{2-[3-(naphthalen-1-ylamino)phenyl]but-1-ene-1,1-diyl}diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.60 Å
R-free 0.260
|
|
5DL4
Crystal Structure of the ER-alpha Ligand-binding Domain in complex with a phenylamino-substituted, methyl, triaryl-ethylene derivative 4,4'-{2-[3-(phenylamino)phenyl]prop-1-ene-1,1-diyl}diphenol
提交 2015-09-04
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5C4 4,4'-{2-[3-(phenylamino)phenyl]prop-1-ene-1,1-diyl}diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.10 Å
R-free 0.214
|
|
5DLR
Crystal Structure of the ER-alpha Ligand-binding Domain in complex with a triaryl-ethylene compound 4,4'-(2-phenylethene-1,1-diyl)diphenol
提交 2015-09-07
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5DJ 4,4'-(2-phenylethene-1,1-diyl)diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.26 Å
R-free 0.232
|
|
5DMC
Crystal Structure of the ER-alpha Ligand-binding Domain in complex with a nitrile-substituted triaryl-ethylene derivative 3,3-bis(4-hydroxyphenyl)-2-phenylprop-2-enenitrile
提交 2015-09-08
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5DH 3,3-bis(4-hydroxyphenyl)-2-phenylprop-2-enenitrile × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.40 Å
R-free 0.246
|
|
5DMF
Crystal Structure of the ER-alpha Ligand-binding Domain in complex with a 4-fluorophenylamino-substituted, methyl triaryl-ethylene derivative 4,4'-(2-{3-[(4-fluorophenyl)amino]phenyl}prop-1-ene-1,1-diyl)diphenol
提交 2015-09-08
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5DG 4,4'-(2-{3-[(4-fluorophenyl)amino]phenyl}prop-1-ene-1,1-diyl)diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.40 Å
R-free 0.254
|
|
5DRM
Crystal Structure of the ER-alpha Ligand-binding Domain in complex with a dichloro-substituted, 2,5-diarylthiophene-core ligand 4,4'-thiene-2,5-diylbis(3-chlorophenol)
提交 2015-09-16
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
链 D
686–699(14 aa)
|
未记录
|
5ET 4,4'-thiene-2,5-diylbis(3-chlorophenol) × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.24 Å
R-free 0.215
|
|
5DTV
Crystal Structure of the ER-alpha Ligand-binding Domain in complex with a dimethyl-substituted, 3,4-diarylthiophene dioxide core ligand
提交 2015-09-18
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
链 D
686–699(14 aa)
|
未记录
|
5FS 3,4-bis(4-hydroxy-2-methylphenyl)-1H-1lambda~6~-thiophene-1,1-dione × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.29 Å
R-free 0.247
|
|
5DU5
Crystal Structure of the ER-alpha Ligand-binding Domain in complex with a dichloro-substituted, 3,4-diarylthiophene dioxide core ligand
提交 2015-09-18
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
链 D
686–699(14 aa)
|
未记录
|
5G2 3,4-bis(2-chloro-4-hydroxyphenyl)-1H-1lambda~6~-thiophene-1,1-dione × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.19 Å
R-free 0.250
|
|
5DUE
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with a para-Hydroxyl-substituted, Sulfoxide-bridged Oxabicyclic Heptene Sulfonate (SOBHS)-2 Analog 4-hydroxyphenyl (1S,2S,4S,5S,6R,7S)-5,6-bis(4-hydroxy-2-methylphenyl)-7-thiabicyclo[2.2.1]heptane-2-sulfonate 7-oxide
提交 2015-09-18
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5FY 4-hydroxyphenyl (1S,2S,4S,7S)-5,6-bis(4-hydroxy-2-methylphenyl)-7-thiabicyclo[2.2.1]hept-5-ene-2-sulfonate 7-oxide × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.09 Å
R-free 0.238
|
|
5DUG
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with a Sulfoxide-bridged Oxabicyclic Heptene Sulfonate (SOBHS)-2 analog phenyl (1S,2S,4S,7S)-5,6-bis(4-hydroxy-2-methylphenyl)-7-thiabicyclo[2.2.1]hept-5-ene-2-sulfonate 7-oxide
提交 2015-09-18
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5FV phenyl (1S,2S,4S,7S)-5,6-bis(4-hydroxy-2-methylphenyl)-7-thiabicyclo[2.2.1]hept-5-ene-2-sulfonate 7-oxide × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.25 Å
R-free 0.233
|
|
5DUH
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with a Sulfoxide-bridged Oxabicyclic Heptene Sulfonate (SOBHS)-3 analog phenyl (1S,2S,4S,7S)-5,6-bis(4-hydroxy-3-methylphenyl)-7-thiabicyclo[2.2.1]hept-5-ene-2-sulfonate 7-oxide
提交 2015-09-18
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5FT phenyl (1S,2S,4S,7S)-5,6-bis(4-hydroxy-3-methylphenyl)-7-thiabicyclo[2.2.1]hept-5-ene-2-sulfonate 7-oxide × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.24 Å
R-free 0.239
|
|
5DVS
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with a 2-Methyl-substituted Triaryl-imine 4,4'-[(2-methylphenyl)carbonimidoyl]diphenol
提交 2015-09-21
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5G7 4,4'-[(2-methylphenyl)carbonimidoyl]diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.28 Å
R-free 0.263
|
|
5DVV
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with a Triaryl-imine analog 4,4'-(phenylcarbonimidoyl)diphenol
提交 2015-09-21
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5G6 4,4'-(phenylcarbonimidoyl)diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.50 Å
R-free 0.258
|
|
5DWE
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with a 2-Chloro-substituted Triaryl-imine analog 4,4'-[(2-chlorophenyl)carbonimidoyl]diphenol
提交 2015-09-22
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5G5 4,4'-[(2-chlorophenyl)carbonimidoyl]diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 1.92 Å
R-free 0.238
|
|
5DWG
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with the Triaryl-substituted Imine Analog, 4-{(E)-(4-hydroxyphenyl)[(2-methylphenyl)imino]methyl}benzene-1,3-diol
提交 2015-09-22
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5G4 4-{(E)-(4-hydroxyphenyl)[(2-methylphenyl)imino]methyl}benzene-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.30 Å
R-free 0.254
|
|
5DWI
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with a Resorcinyl 2-Chloro-substituted Diaryl-imine analog 4-[(E)-[(2-chlorophenyl)imino](4-hydroxyphenyl)methyl]benzene-1,3-diol
提交 2015-09-22
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5G3 4-[(E)-[(2-chlorophenyl)imino](4-hydroxyphenyl)methyl]benzene-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.43 Å
R-free 0.231
|
|
5DWJ
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with a Resorcinyl 4-Fluoro-substituted Diaryl-imine analog 4-[(E)-[(4-fluorophenyl)imino](4-hydroxyphenyl)methyl]benzene-1,3-diol
提交 2015-09-22
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5J2 4-[(E)-[(4-fluorophenyl)imino](4-hydroxyphenyl)methyl]benzene-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.00 Å
R-free 0.232
|
|
5DX3
Estrogen Receptor Alpha Ligand Binding Domain Y537S Mutant in Complex with Stapled Peptide SRC2-P3 and Estradiol
提交 2015-09-23
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
687–697(11 aa)
链 D
687–697(11 aa)
|
非标准单体:是(mmCIF未提供具体位点)
非标准单体:是(mmCIF未提供具体位点)
|
EST ESTRADIOL × 2
CL CHLORIDE ION × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;15% PEG 3,350, 200 mM MgCl2, 100 mM Tris pH 8.0
|
分辨率 2.09 Å
R-free 0.257
|
|
5DXB
Estrogen Receptor Alpha Ligand Binding Domain Y537S Mutant in Complex with Stapled Peptide SRC2-P1 and Estradiol
提交 2015-09-23
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 D
687–697(11 aa)
链 E
687–697(11 aa)
|
非标准单体:是(mmCIF未提供具体位点)
非标准单体:是(mmCIF未提供具体位点)
|
EST ESTRADIOL × 2
GOL GLYCEROL × 2
CL CHLORIDE ION × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;20% PEG 3,350, 200 mM MgCl2, 100 mM Tris pH 8.0
|
分辨率 2.08 Å
R-free 0.210
|
|
5DXE
Estrogen Receptor Alpha Ligand Binding Domain Y537S Mutant in Complex with Stapled Peptide SRC2-P4 and Estradiol
提交 2015-09-23
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
687–697(11 aa)
链 D
687–697(11 aa)
|
非标准单体:是(mmCIF未提供具体位点)
非标准单体:是(mmCIF未提供具体位点)
|
EST ESTRADIOL × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;298 K;20% PEG 3,350, 200 mM MgCl2, 100 mM Tris pH 8.0
|
分辨率 1.50 Å
R-free 0.201
|
|
5DXK
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with the Cyclofenil Derivative 4,4'-[(9s)-bicyclo[3.3.1]non-9-ylmethanediyl]diphenol
提交 2015-09-23
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5J1 4,4'-[(9s)-bicyclo[3.3.1]non-9-ylmethanediyl]diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.23 Å
R-free 0.226
|
|
5DXM
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with the Cyclofenil Derivative 3-[(E)-(1s,5s)-bicyclo[3.3.1]non-9-ylidene(4-hydroxyphenyl)methyl]phenol
提交 2015-09-23
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5J0 3-[(E)-(1s,5s)-bicyclo[3.3.1]non-9-ylidene(4-hydroxyphenyl)methyl]phenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.37 Å
R-free 0.232
|
|
5DXP
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with the Cyclofenil Derivative 4-[(E)-(1s,5s)-bicyclo[3.3.1]non-9-ylidene(phenyl)methyl]phenol
提交 2015-09-23
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5HX 4-[(E)-(1s,5s)-bicyclo[3.3.1]non-9-ylidene(phenyl)methyl]phenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.20 Å
R-free 0.235
|
|
5DXQ
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with the Cyclofenil Derivative 4,4'-[(1s,5s)-bicyclo[3.3.1]non-9-ylidenemethanediyl]diphenol
提交 2015-09-23
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5HZ 4,4'-[(1s,5s)-bicyclo[3.3.1]non-9-ylidenemethanediyl]diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.40 Å
R-free 0.239
|
|
5DXR
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with the Cyclofenil Derivative 4,4'-{[(3R)-3-methylcyclohexylidene]methanediyl}diphenol
提交 2015-09-23
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5HW 4,4'-{[(3R)-3-methylcyclohexylidene]methanediyl}diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.28 Å
R-free 0.235
|
|
5DY8
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with the Cyclofenil Derivative 4,4'-{[(3S)-3-ethylcyclohexylidene]methanediyl}diphenol
提交 2015-09-24
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5K4 4,4'-{[(3S)-3-ethylcyclohexylidene]methanediyl}diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.03 Å
R-free 0.243
|
|
5DYB
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with the Cyclofenil Derivative 4,4'-(3,4-dihydronaphthalen-2(1H)-ylidenemethanediyl)diphenol
提交 2015-09-24
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5K2 4,4'-(3,4-dihydronaphthalen-2(1H)-ylidenemethanediyl)diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.27 Å
R-free 0.238
|
|
5DZ1
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with the Cyclofenil Derivative 4,4'-[(4-ethylcyclohexylidene)methanediyl]diphenol
提交 2015-09-25
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5JY 4,4'-[(4-ethylcyclohexylidene)methanediyl]diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.20 Å
R-free 0.239
|
|
5DZ3
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with the Cyclofenil Derivative 4,4'-{[4-(fluoromethyl)cyclohexylidene]methanediyl}diphenol
提交 2015-09-25
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5JX 4,4'-{[4-(fluoromethyl)cyclohexylidene]methanediyl}diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.15 Å
R-free 0.234
|
|
5DZH
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with the Cyclofenil Derivative 4,4'-{[4-(2-hydroxyethyl)cyclohexylidene]methanediyl}diphenol
提交 2015-09-25
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5KG 4,4'-{[4-(2-hydroxyethyl)cyclohexylidene]methanediyl}diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.11 Å
R-free 0.220
|
|
5DZI
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with the Cyclofenil Derivative 4,4'-{[(3S)-3-(2-hydroxyethyl)cyclohexylidene]methanediyl}diphenol
提交 2015-09-25
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5KF 4,4'-{[(3S)-3-(2-hydroxyethyl)cyclohexylidene]methanediyl}diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 1.90 Å
R-free 0.214
|
|
5E0W
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with the Cyclofenil Derivative 4,4'-{[(3S)-3-(4-hydroxyphenyl)cyclohexylidene]methanediyl}diphenol
提交 2015-09-29
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5KE 4,4'-{[(3S)-3-(4-hydroxyphenyl)cyclohexylidene]methanediyl}diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.00 Å
R-free 0.226
|
|
5E0X
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with the Cyclofenil Derivative 4,4'-{[(3S)-3-(4-methoxyphenyl)cyclohexylidene]methanediyl}diphenol
提交 2015-09-29
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5KD 4,4'-{[(3S)-3-(4-methoxyphenyl)cyclohexylidene]methanediyl}diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.01 Å
R-free 0.237
|
|
5E14
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with the Cyclofenil Derivative 4,4'-{[(3R)-3-phenylcyclohexylidene]methanediyl}diphenol
提交 2015-09-29
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5KB 4,4'-{[(3R)-3-phenylcyclohexylidene]methanediyl}diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.22 Å
R-free 0.255
|
|
5E19
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with the Cyclofenil Derivative methyl {4-[bis(4-hydroxyphenyl)methylidene]cyclohexyl}acetate
提交 2015-09-29
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5K7 methyl {4-[bis(4-hydroxyphenyl)methylidene]cyclohexyl}acetate × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.24 Å
R-free 0.233
|
|
5E1C
Crystal Structure of the ER-alpha Ligand-binding Domain in Complex with the Cyclofenil Derivative dimethyl {(1S)-3-[bis(4-hydroxyphenyl)methylidene]cyclohexyl}propanedioate
提交 2015-09-29
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–699(14 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
5K8 dimethyl {(1S)-3-[bis(4-hydroxyphenyl)methylidene]cyclohexyl}propanedioate × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 1.98 Å
R-free 0.214
|
|
5G3J
Discovery of New Selective Glucocorticoid Receptor Agonist Leads
提交 2016-04-27
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
片段:RESIDUES 740-753
|
未记录
|
CPS 3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE × 1
EDO 1,2-ETHANEDIOL × 1
E7T 5-[[(1S,2R,4R)-4-ethyl-6,7-bis(fluoranyl)-2,5-bis(oxidanyl)-2-(trifluoromethyl)-3,4-dihydro-1H-naphthalen-1-yl]amino]-1H-quinolin-2-one × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
pH 7.5;8% PEG8000, 15% ETHYLENE GLYCOL AND 0.1 M HEPES PH 7.5
|
分辨率 2.40 Å
R-free 0.235
|
|
5G5W
Structure guided design and discovery of Indazole ethers as highly potent, non-steroidal Glucocorticoid receptor modulators
提交 2016-06-08
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
片段:RESIDUES 740-753
|
未记录
|
EDO 1,2-ETHANEDIOL × 1
R8C 2,2,2-trifluoro-N-[(1R,2S)-1-{[1-(4-fluorophenyl)-1H-indazol-5-yl]oxy}-1-phenylpropan-2-yl]acetamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
pH 7.5;12% PEG8000, 20% ETHYLENE GLYCOL AND 0.1 M HEPES PH 7.5
|
分辨率 2.20 Å
R-free 0.210
|
|
5H1E
Interaction between vitamin D receptor and coactivator peptide SRC2-3
提交 2016-10-08
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
740–752(13 aa)
片段:UNP RESIDUES 740-752
|
未记录
|
VDX 5-{2-[1-(5-HYDROXY-1,5-DIMETHYL-HEXYL)-7A-METHYL-OCTAHYDRO-INDEN-4-YLIDENE]-ETHYLIDENE}-4-METHYLENE-CYCLOHEXANE-1,3-DIOL × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;MOP-Na, Na-Formate, PEG 4000, Ethleneglycol
|
分辨率 2.60 Å
R-free 0.248
|
|
5I4V
Discovery of novel, orally efficacious Liver X Receptor (LXR) beta agonists
提交 2016-02-12
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
信息不足
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 A
687–699(13 aa)
链 B
687–699(13 aa)
|
突变:Q259A, R261G, D262S, R264S,Q259A, R261G, D262S, R264S,Q259A, R261G, D262S, R264S,Q259A, R261G, D262S, R264S
|
67S {2-[(2R)-4-[4-(hydroxymethyl)-3-(methylsulfonyl)phenyl]-2-(propan-2-yl)piperazin-1-yl]-4-(trifluoromethyl)pyrimidin-5-yl}methanol × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;1uL of scLXRbeta-LBD/scRXRbeta-LBD @ 10 mg protein/ml in 20 mM Tris-HCl pH 8.0, 150 mM NaCl, 5 mM DTT containing 1mM ligand and less than 2%(v/v) DMSO was mixed with 1uL of reservoir solution (0.2M LiCl, 16-20%(w/v) PEG3350, 7-10%(v/v) ethylene glycol, 0.01M Strontium chloride) on a circular, silanized glass cover slide and inverted and sealed with silicon grease over a well of 200uL of reservoir solution. Crystallization plates were incubated at 23 deg C for 2-5 days before rods would appear measuring 50 to 100um long.
|
分辨率 2.61 Å
R-free 0.248
|
|
5I4V
Discovery of novel, orally efficacious Liver X Receptor (LXR) beta agonists
提交 2016-02-12
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
信息不足
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 E
687–699(13 aa)
链 F
687–699(13 aa)
|
突变:Q259A, R261G, D262S, R264S,Q259A, R261G, D262S, R264S,Q259A, R261G, D262S, R264S,Q259A, R261G, D262S, R264S
|
67S {2-[(2R)-4-[4-(hydroxymethyl)-3-(methylsulfonyl)phenyl]-2-(propan-2-yl)piperazin-1-yl]-4-(trifluoromethyl)pyrimidin-5-yl}methanol × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;1uL of scLXRbeta-LBD/scRXRbeta-LBD @ 10 mg protein/ml in 20 mM Tris-HCl pH 8.0, 150 mM NaCl, 5 mM DTT containing 1mM ligand and less than 2%(v/v) DMSO was mixed with 1uL of reservoir solution (0.2M LiCl, 16-20%(w/v) PEG3350, 7-10%(v/v) ethylene glycol, 0.01M Strontium chloride) on a circular, silanized glass cover slide and inverted and sealed with silicon grease over a well of 200uL of reservoir solution. Crystallization plates were incubated at 23 deg C for 2-5 days before rods would appear measuring 50 to 100um long.
|
分辨率 2.61 Å
R-free 0.248
|
|
5ICK
A unique binding model of FXR LBD with feroline
提交 2016-02-23
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
742–752(11 aa)
片段:UNP residues 742-752
|
未记录
|
FEZ (1S,2S,3Z,5S,8Z)-5-hydroxy-5,9-dimethyl-2-(propan-2-yl)cyclodeca-3,8-dien-1-yl 4-hydroxybenzoate × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293.15 K;20% polyethylene glycol 3350 and 0.2 M ammonia acetate
|
分辨率 2.47 Å
R-free 0.277
|
|
5ICK
A unique binding model of FXR LBD with feroline
提交 2016-02-23
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
742–752(11 aa)
片段:UNP residues 742-752
|
未记录
|
FEZ (1S,2S,3Z,5S,8Z)-5-hydroxy-5,9-dimethyl-2-(propan-2-yl)cyclodeca-3,8-dien-1-yl 4-hydroxybenzoate × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293.15 K;20% polyethylene glycol 3350 and 0.2 M ammonia acetate
|
分辨率 2.47 Å
R-free 0.277
|
|
5KCE
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with an N-methyl, 2-chlorobenzyl OBHS-N derivative
提交 2016-06-06
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
|
未记录
|
OB3 (1S,2R,4S)-N-(2-chlorophenyl)-5,6-bis(4-hydroxyphenyl)-N-methyl-7-oxabicyclo[2.2.1]hept-5-ene-2-sulfonamide × 3
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 1.85 Å
R-free 0.250
|
|
5MK4
Crystal structure of the Retinoid X Receptor alpha in complex with synthetic honokiol derivative 7 and a fragment of the TIF2 co-activator.
提交 2016-12-02
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–696(11 aa)
片段:UNP residues 686-696
链 D
686–696(11 aa)
片段:UNP residues 686-696
|
未记录
|
I5W (~{E})-3-[3-(2-methyl-5-phenyl-phenyl)-4-oxidanyl-phenyl]prop-2-enoic acid × 2
CL CHLORIDE ION × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;277 K;0.1M PIPES, pH 7.0, 0.1M NaCl, 22% PEG 2K MME
|
分辨率 2.00 Å
R-free 0.229
|
|
5NFP
Glucocorticoid Receptor in complex with budesonide
提交 2017-03-15
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
|
未记录
|
CPS 3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE × 1
EDO 1,2-ETHANEDIOL × 1
GOL GLYCEROL × 1
8W5 (1~{S},2~{S},4~{R},6~{R},8~{S},9~{S},11~{S},12~{S},13~{R})-9,13-dimethyl-11-oxidanyl-8-(2-oxidanylethanoyl)-6-propyl-5,7-dioxapentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icosa-14,17-dien-16-one × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;277 K;2 ul of protein, 0.2ul of Polypropylene Glycol 400 and 0.8ul of well solution (10-12% PEG8000, 20% ethylene glycol and 0.1 M Hepes pH 7.5).
|
分辨率 2.10 Å
R-free 0.202
|
|
5NFT
Glucocorticoid Receptor in complex with AZD5423
提交 2017-03-15
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
|
未记录
|
EDO 1,2-ETHANEDIOL × 3
8W8 2,2,2-tris(fluoranyl)-~{N}-[(1~{R},2~{S})-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2-yl]ethanamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;277 K;2 ul of protein and 1ul of well solution (8-12% PEG8000, 10-20% ethylene glycol and 0.1 M Hepes pH 7.5)
|
分辨率 2.30 Å
R-free 0.215
|
|
5SYZ
Human Liver Receptor Homologue-1 (LRH-1) Bound to a RJW100 stereoisomer and a Fragment of TIF-2
提交 2016-08-12
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
740–754(15 aa)
片段:UNP Rresidues 740-754
|
未记录
|
71W (1S,3aR,6aR)-5-hexyl-4-phenyl-3a-(1-phenylethenyl)-1,2,3,3a,6,6a-hexahydropentalen-1-ol × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;Sodium acetate, PEG4000, glycerol
|
分辨率 1.93 Å
R-free 0.228
|
|
5T1Z
Estrogen Receptor Alpha Ligand Binding Domain Y537S Mutant in Complex with Ethoxytriphenylethylene and GRIP Peptide
提交 2016-08-22
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
链 D
686–698(13 aa)
|
未记录
|
Q97 4,4'-[(1Z)-1-(4-ethoxyphenyl)but-1-ene-1,2-diyl]diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;293 K;0.15 M KBr, 30% w/v MPEG 2,000, 100 mM Tris pH 8.3
|
分辨率 2.10 Å
R-free 0.246
|
|
5TLV
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with 4,4'-(thiophene-2,3-diyl)bis(3-fluorophenol)
提交 2016-10-12
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
|
未记录
|
7ES 4,4'-(thiene-2,3-diyl)bis(3-fluorophenol) × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.32 Å
R-free 0.236
|
|
5TLX
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with 3,4-bis(4-hydroxyphenyl)thiophene 1,1-dioxide
提交 2016-10-12
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
|
未记录
|
7EH 3-methyl-6-phenyl-3H-imidazo[4,5-b]pyridin-2-amine × 2
7G5 3,4-bis(4-hydroxyphenyl)-2,5-dihydro-1H-1lambda~6~-thiophene-1,1-dione × 4
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.10 Å
R-free 0.226
|
|
5TLY
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with 3,4-bis(2-fluoro-4-hydroxyphenyl)thiophene 1,1-dioxide
提交 2016-10-12
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
|
未记录
|
7ER 3,4-bis(2-fluoro-4-hydroxyphenyl)-1H-1lambda~6~-thiophene-1,1-dione × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.14 Å
R-free 0.221
|
|
5TM1
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with 2,5-bis(2-fluoro-4-hydroxyphenyl)thiophene 1-oxide
提交 2016-10-12
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
|
未记录
|
7EQ 2,5-bis(2-fluoro-4-hydroxyphenyl)-1H-1lambda~4~-thiophen-1-one × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.23 Å
R-free 0.236
|
|
5TM2
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with 2,5-bis(2-chloro-4-hydroxyphenyl)thiophene 1-oxide
提交 2016-10-12
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
|
未记录
|
7EO 2,5-bis(2-chloro-4-hydroxyphenyl)-1H-1lambda~4~-thiophen-1-one × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.60 Å
R-free 0.244
|
|
5TM3
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with 2,3-bis(2-chloro-4-hydroxyphenyl)thiophene 1-oxide
提交 2016-10-12
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
|
未记录
|
7EN (1S)-2,3-bis(2-chloro-4-hydroxyphenyl)-1H-1lambda~4~-thiophen-1-one × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.19 Å
R-free 0.234
|
|
5TM4
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the OBHS-ASC Analog, 5-(4-((1R,4S,6R)-6-((3-chlorophenoxy)sulfonyl)-3-(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-2-en-2-yl)phenoxy)pentanoic acid
提交 2016-10-12
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
|
未记录
|
7E3 5-{4-[(1S,4S,6R)-6-[(3-chlorophenoxy)sulfonyl]-3-(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-2-en-2-yl]phenoxy}pentanoic acid × 4
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.25 Å
R-free 0.236
|
|
5TM5
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the OBHS-ASC compound, 5-(4-((1R,4S,6R)-6-((4-bromophenoxy)sulfonyl)-3-(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-2-en-2-yl)phenoxy)pentanoic acid
提交 2016-10-12
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
|
未记录
|
7EV 5-{4-[(1S,4S,5R)-5-[(4-bromophenoxy)sulfonyl]-3-(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-2-en-2-yl]phenoxy}pentanoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.24 Å
R-free 0.232
|
|
5TM6
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the OBHS-ASC compound, 6-(4-((1R,4S,6R)-6-((4-bromophenoxy)sulfonyl)-3-(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-2-en-2-yl)phenoxy)hexanoic acid
提交 2016-10-12
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
7J9 6-{4-[(1S,4S,6R)-6-[(4-bromophenoxy)sulfonyl]-3-(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-2-en-2-yl]phenoxy}hexanoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.54 Å
R-free 0.245
|
|
5TM7
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the OBHS-ASC compound, 7-(4-((1R,4S,6R)-6-((3-chlorophenoxy)sulfonyl)-3-(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-2-en-2-yl)phenoxy)heptanoic acid
提交 2016-10-12
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
|
未记录
|
7JY 7-{4-[(1S,4S,6R)-6-[(3-chlorophenoxy)sulfonyl]-3-(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-2-en-2-yl]phenoxy}heptanoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.40 Å
R-free 0.231
|
|
5TM8
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the OBHS-ASC compound, 7-(4-((1R,4S,6R)-6-((4-bromophenoxy)sulfonyl)-3-(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-2-en-2-yl)phenoxy)heptanoic acid
提交 2016-10-12
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
|
未记录
|
7K6 7-{4-[(1S,4S,6R)-6-[(4-bromophenoxy)sulfonyl]-3-(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-2-en-2-yl]phenoxy}heptanoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 1.99 Å
R-free 0.222
|
|
5TM9
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the OBHS-ASC Analog, (E)-3-(4-((1R,4S,6R)-6-((3-chlorophenoxy)sulfonyl)-3-(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-2-en-2-yl)phenyl)acrylic acid
提交 2016-10-12
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
|
未记录
|
7KL 3-{4-[(1S,4S,6R)-6-[(3-chlorophenoxy)sulfonyl]-3-(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-2-en-2-yl]phenyl}prop-2-enoic acid × 5
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.50 Å
R-free 0.237
|
|
5TML
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the OBHS-ASC compound, (E)-6-(4-((1R,4S,6R)-6-((3-chlorophenoxy)sulfonyl)-3-(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-2-en-2-yl)phenyl)hex-5-enoic acid
提交 2016-10-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
|
未记录
|
7E1 6-{4-[(1S,4S,6R)-6-[(3-chlorophenoxy)sulfonyl]-3-(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-2-en-2-yl]phenyl}hex-5-enoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.25 Å
R-free 0.233
|
|
5TMM
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the OBHS-ASC analog, (E)-6-(4-((1R,4S,6R)-6-((4-bromophenoxy)sulfonyl)-3-(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-2-en-2-yl)phenyl)hex-5-enoic acid
提交 2016-10-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
|
未记录
|
7M4 6-{4-[(1S,4S,6S)-6-[(4-bromophenoxy)sulfonyl]-3-(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-2-en-2-yl]phenyl}hex-5-enoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.20 Å
R-free 0.251
|
|
5TMO
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the Arene Core OBHS derivative, phenyl 4,4''-dihydroxy-[1,1':2',1''-terphenyl]-4'-sulfonate
提交 2016-10-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
|
未记录
|
7M1 phenyl 4,4''-dihydroxy-[1,1':2',1''-terphenyl]-4'-sulfonate × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.17 Å
R-free 0.233
|
|
5TMQ
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the Arene Core OBHS derivative, 4-bromophenyl 4,4''-dihydroxy-[1,1':2',1''-terphenyl]-4'-sulfonate
提交 2016-10-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide, UNP residues 686-698
|
未记录
|
7M7 4-bromophenyl 4,4''-dihydroxy-[1,1':2',1''-terphenyl]-4'-sulfonate × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.24 Å
R-free 0.242
|
|
5TMR
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the Cyclofenil-ASC derivative, ethyl (E)-3-(4-(cyclohexylidene(4-hydroxyphenyl)methyl)phenyl)acrylate
提交 2016-10-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
|
未记录
|
7FD ethyl 3-{4-[cyclohexylidene(4-hydroxyphenyl)methyl]phenyl}prop-2-enoate × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.30 Å
R-free 0.238
|
|
5TMS
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the Cyclofenil-ASC derivative, ethyl (E)-3-(4-(bicyclo[3.3.1]nonan-9-ylidene(4-hydroxyphenyl)methyl)phenyl)acrylate
提交 2016-10-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
|
未记录
|
7FG ethyl 3-(4-{[(1s,5s)-bicyclo[3.3.1]nonan-9-ylidene](4-hydroxyphenyl)methyl}phenyl)prop-2-enoate × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.24 Å
R-free 0.241
|
|
5TMT
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with 4,4'-((1,3-dihydro-2H-inden-2-ylidene)methylene)diphenol
提交 2016-10-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
|
未记录
|
7FJ 4,4'-[(1,3-dihydro-2H-inden-2-ylidene)methylene]diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.05 Å
R-free 0.247
|
|
5TMU
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with 4,4'-(cycloheptylidenemethylene)diphenol
提交 2016-10-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
|
未记录
|
7FL 4,4'-(cycloheptylidenemethylene)diphenol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.43 Å
R-free 0.237
|
|
5TMV
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the OBHS analog, 4-iodophenyl (1S,2R,4S)-5,6-bis(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-5-ene-2-sulfonate
提交 2016-10-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
|
未记录
|
7FO 4-iodophenyl (1S,2R,4S)-5,6-bis(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-5-ene-2-sulfonate × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.38 Å
R-free 0.252
|
|
5TMW
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the OBHS derivative, 4-acetamidophenyl (1S,2R,4S)-5,6-bis(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-5-ene-2-sulfonate
提交 2016-10-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
|
未记录
|
7FP 4-(acetylamino)phenyl (1S,2R,4S)-5,6-bis(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-5-ene-2-sulfonate × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.29 Å
R-free 0.245
|
|
5TMZ
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the estradiol derivative, (8S,9S,13S,14S,17S)-16-(3-methoxybenzyl)-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthrene-3,17-diol
提交 2016-10-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
|
未记录
|
7FQ (9beta,13alpha,14beta,16alpha,17alpha)-16-[(4-methoxyphenyl)methyl]estra-1,3,5(10)-triene-3,17-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.21 Å
R-free 0.242
|
|
5TN1
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the estradiol derivative, (8S,9S,13S,14S,E)-17-((4-isopropylphenyl)imino)-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-3-ol
提交 2016-10-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
|
未记录
|
7FR (9beta,13alpha,17Z)-17-{[4-(propan-2-yl)phenyl]imino}estra-1,3,5(10)-trien-3-ol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.06 Å
R-free 0.215
|
|
5TN3
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the estradiol derivative, (8S,9S,13S,14S)-17-((4-isopropylphenyl)amino)-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-3-ol
提交 2016-10-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
|
未记录
|
7FS (9beta,13alpha,17beta)-17-{[4-(propan-2-yl)phenyl]amino}estra-1(10),2,4-trien-3-ol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.54 Å
R-free 0.256
|
|
5TN4
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the ACD-ring estrogen, (S)-5-(4-hydroxy-3,5-dimethylphenyl)-2,3-dihydro-1H-inden-1-ol
提交 2016-10-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
|
未记录
|
7FZ (1S)-5-(4-hydroxy-3,5-dimethylphenyl)-2,3-dihydro-1H-inden-1-ol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 1.86 Å
R-free 0.218
|
|
5TN5
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the AC-ring estrogen, (1S,3aS,5S,7aS)-5-(4-hydroxyphenyl)-7a-methyloctahydro-1H-inden-1-ol
提交 2016-10-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
|
未记录
|
7G0 (1S,3aS,5S,7aS)-5-(4-hydroxyphenyl)-7a-methyloctahydro-1H-inden-1-ol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 1.89 Å
R-free 0.233
|
|
5TN6
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with the Spiro BC-estradiol, (1S,1'S,3a'S,7a'S)-7a'-methyl-1',2,2',3,3',3a',4',6',7',7a'-decahydro-1,5'-spirobi[indene]-1',5-diol
提交 2016-10-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
|
未记录
|
7G1 (1S,1'S,3a'S,7a'S)-7a'-methyl-1',2,2',3,3',3a',4',6',7',7a'-decahydro-1,5'-spirobi[indene]-1',5-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.09 Å
R-free 0.225
|
|
5TN7
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with (E)-3'-fluoro-4'-hydroxy-3-((hydroxyiminio)methyl)-[1,1'-biphenyl]-4-olate
提交 2016-10-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
|
未记录
|
7G2 3-fluoro-3'-[(E)-(hydroxyimino)methyl][1,1'-biphenyl]-4,4'-diol × 3
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.24 Å
R-free 0.235
|
|
5TN8
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in Complex with (E)-4'-hydroxy-3-((hydroxyiminio)methyl)-[1,1'-biphenyl]-4-olate
提交 2016-10-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide (UNP residues 686-698)
|
未记录
|
7G3 3-[(Z)-(hydroxyimino)methyl][1,1'-biphenyl]-4,4'-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 2.65 Å
R-free 0.259
|
|
5U2D
Crystal Structure of the ER-alpha Ligand-binding Domain (Y537S) in complex with Oxabicyclic Heptene Sulfonate (OBHS)
提交 2016-11-30
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
片段:Nuclear receptor-interacting peptide
链 D
686–698(13 aa)
片段:Nuclear receptor-interacting peptide
|
未记录
|
OBH cyclohexa-2,5-dien-1-yl (1S,2R,4S)-5,6-bis(4-hydroxyphenyl)-7-oxabicyclo[2.2.1]hept-5-ene-2-sulfonate × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 8.3;294 K;15% PEG 3350, 0.05M MgCl2, 0.067M NaCl, 0.1M Tris
|
分辨率 1.86 Å
R-free 0.215
|
|
5WZX
Structural basis for a pentacyclic oleanane-type triterpenoid as a ligand of FXR
提交 2017-01-19
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
741–752(12 aa)
|
未记录
|
7VX (4aR,6aR,6aS,6bS,8aS,9R,12aR,14bR)-2,2,6a,6b,9,12a-hexamethyl-10-oxidanylidene-1,3,4,5,6,6a,7,8,8a,9,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid × 1
BU3 (R,R)-2,3-BUTANEDIOL × 3
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293.15 K;0.1 M HEPES, 10% w/v Polyethylene glycol 6000, 5% v/v (+/-)-2-Methyl-2,4-pentanediol
|
分辨率 2.95 Å
R-free 0.263
|
|
5WZX
Structural basis for a pentacyclic oleanane-type triterpenoid as a ligand of FXR
提交 2017-01-19
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
741–752(12 aa)
|
未记录
|
7VX (4aR,6aR,6aS,6bS,8aS,9R,12aR,14bR)-2,2,6a,6b,9,12a-hexamethyl-10-oxidanylidene-1,3,4,5,6,6a,7,8,8a,9,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293.15 K;0.1 M HEPES, 10% w/v Polyethylene glycol 6000, 5% v/v (+/-)-2-Methyl-2,4-pentanediol
|
分辨率 2.95 Å
R-free 0.263
|
|
5XPL
Crystal structure of VDR-LBD complexed with 22S-butyl-25-hydroxyphenyl-2-methylidene-19,26,27-trinor-25-oxo-1-hydroxyvitamin D3
提交 2017-06-03
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
740–752(13 aa)
片段:UNP residues 740-752
|
未记录
|
8C9 (4~{S})-4-[(1~{R})-1-[(1~{R},3~{a}~{S},4~{E},7~{a}~{R})-7~{a}-methyl-4-[2-[(3~{R},5~{R})-4-methylidene-3,5-bis(oxidanyl )cyclohexylidene]ethylidene]-2,3,3~{a},5,6,7-hexahydro-1~{H}-inden-1-yl]ethyl]-1-(4-hydroxyphenyl)octan-1-one × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;293 K;MOPS-Na, Na-Formate, PEG 4000, Ethylenglycol
|
分辨率 2.05 Å
R-free 0.242
|
|
5Y1J
Crystal structure of human FXR in complex with a functional drug ligand
提交 2017-07-20
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 U
742–751(10 aa)
|
未记录
|
D5H 2-[[2-fluoranyl-4-(3-methoxyphenyl)phenyl]carbamoyl]cyclopentene-1-carboxylic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293.15 K;0.1M MgSO4, 25% w/v polyethylene glycol 8000
|
分辨率 2.00 Å
R-free 0.238
|
|
5Y49
A moderator XD22 binding to bile acid receptor
提交 2017-08-02
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
741–751(11 aa)
|
未记录
|
XD5 [(1R,2S,4S)-2-bicyclo[2.2.1]heptanyl] 4-azanylbenzoate × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293.15 K;0.1M Magnesium sulfate, 12% w/v polyethylene glycol 8000
|
分辨率 2.40 Å
R-free 0.253
|
|
5Y49
A moderator XD22 binding to bile acid receptor
提交 2017-08-02
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 E
741–751(11 aa)
|
未记录
|
XD5 [(1R,2S,4S)-2-bicyclo[2.2.1]heptanyl] 4-azanylbenzoate × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293.15 K;0.1M Magnesium sulfate, 12% w/v polyethylene glycol 8000
|
分辨率 2.40 Å
R-free 0.253
|
|
6EL6
Glucocorticoid Receptor in complex with compound 4
提交 2017-09-28
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
|
未记录
|
EDO 1,2-ETHANEDIOL × 1
B9Q ~{N}-[(1~{R},2~{S})-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(6-methoxypyridin-3-yl)propan-2-yl]cyclopropanecarboxamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;277 K;8-10% PEG8000, 10-19% Ethylene Glycol, 0.1 M HEPES pH 7.5
|
分辨率 2.40 Å
R-free 0.283
|
|
6EL7
Glucocorticoid Receptor in complex with compound 31
提交 2017-09-28
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
|
未记录
|
EDO 1,2-ETHANEDIOL × 1
B9T ~{N}-[(1~{R},2~{S})-1-(2-bromanyl-4-cyano-phenoxy)-1-(2-cyclopropylpyrimidin-5-yl)propan-2-yl]-2,2-bis(fluoranyl)propanamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;277 K;8-10% PEG8000, 10-19% Ethylene Glycol, 0.1 M HEPES pH 7.5
|
分辨率 2.18 Å
R-free 0.225
|
|
6EL9
Glucocorticoid Receptor in complex with AZD9567
提交 2017-09-28
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
|
未记录
|
EDO 1,2-ETHANEDIOL × 1
B9W 2,2-bis(fluoranyl)-~{N}-[(1~{R},2~{S})-3-methyl-1-[1-(1-methyl-6-oxidanylidene-pyridin-3-yl)indazol-5-yl]oxy-1-phenyl-butan-2-yl]propanamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;277 K;8-10% PEG8000, 10-19% Ethylene Glycol, 0.1 M HEPES pH 7.5
|
分辨率 2.19 Å
R-free 0.224
|
|
6KNU
THRb mutation with a novel agonist
提交 2019-08-07
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
741–751(11 aa)
|
未记录
|
8HO 2-[(1-methyl-4-oxidanyl-7-phenoxy-isoquinolin-3-yl)carbonylamino]ethanoic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 4.6;293 K;0.1M Sodium acetate trihydrate pH 4.6, 2.0M Sodium formate
|
分辨率 2.70 Å
R-free 0.231
|
|
6KNV
THRb mutation with a novel agonist
提交 2019-08-07
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
741–751(11 aa)
|
未记录
|
8HO 2-[(1-methyl-4-oxidanyl-7-phenoxy-isoquinolin-3-yl)carbonylamino]ethanoic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;2% v/v Tacsimate pH 5.0, 0.1 M Sodium citrate tribasic dihydrate pH 5.6, 16% w/v Polyethylene glycol 3,350
|
分辨率 2.80 Å
R-free 0.265
|
|
6KNW
THRb mutation with a novel agonist
提交 2019-08-07
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
741–751(11 aa)
|
未记录
|
8HO 2-[(1-methyl-4-oxidanyl-7-phenoxy-isoquinolin-3-yl)carbonylamino]ethanoic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;100mM Nacl 20% PEG 4000
|
分辨率 2.67 Å
R-free 0.244
|
|
6LB4
Crystal structure of dimeric RXR-LBD complexed with NEt-3ME and TIF2 co-activator
提交 2019-11-13
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
E8L 6-[ethyl-[3-(2-methoxyethoxy)-4-propan-2-yl-phenyl]amino]pyridine-3-carboxylic acid × 2
EDO 1,2-ETHANEDIOL × 8
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;293 K;0.2 M Sodium Acetate
18 % PEG3350
0.1 M Spermine tetrahydrochroride
|
分辨率 1.50 Å
R-free 0.201
|
|
6LB5
Crystal structure of dimeric RXR-LBD complexed with full agonist NEt-3IB and TIF2 co-activator
提交 2019-11-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
链 D
686–698(13 aa)
|
未记录
|
E80 6-[ethyl-[3-(2-methylpropoxy)-4-propan-2-yl-phenyl]amino]pyridine-3-carboxylic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7;293 K;0.1 M Imidazole
20 % PEG 6000
|
分辨率 2.40 Å
R-free 0.240
|
|
6LB6
Crystal structure of dimeric RXR-LBD complexed with partial agonist NEt-4IB and TIF2 co-activator
提交 2019-11-13
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
E8O 6-[ethyl-[4-(2-methylpropoxy)-3-propan-2-yl-phenyl]amino]pyridine-3-carboxylic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7;293 K;0.1 M Imidazole
20 % PEG6000
|
分辨率 2.40 Å
R-free 0.257
|
|
6LIT
Estrogen-related receptor beta(ERR2) in complex with BPA
提交 2019-12-13
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 D
686–696(11 aa)
链 E
686–696(11 aa)
|
未记录
|
2OH 4,4'-PROPANE-2,2-DIYLDIPHENOL × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;300mM NH4Cl, 10% PEG 4000
|
分辨率 2.00 Å
R-free 0.238
|
|
6OQX
Human Liver Receptor Homolog-1 bound to the agonist 5N and a fragment of the Tif2 coregulator
提交 2019-04-29
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
740–754(15 aa)
片段:UNP Residues 740-754
|
未记录
|
N1V (8beta,11alpha,12alpha)-8-(1-phenylethenyl)-1,6:7,14-dicycloprosta-1,3,5,7(14)-tetraen-11-yl sulfamate × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;291 K;Sodium acetate (pH 4.6), PEG4000, glycerol
|
分辨率 2.00 Å
R-free 0.245
|
|
6OQY
Human LRH-1 bound to the agonist 6N and a fragment of the Tif2 coregulator
提交 2019-04-29
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
740–754(15 aa)
|
突变:UNP Residues 740-754
|
N2J N-[(1S,3aR,6aR)-5-hexyl-4-phenyl-3a-(1-phenylethenyl)-1,2,3,3a,6,6a-hexahydropentalen-1-yl]sulfuric diamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;291 K;Sodium acetate (pH 4.6), PEG4000, glycerol
|
分辨率 2.23 Å
R-free 0.269
|
|
6OR1
Human LRH-1 bound to the agonist 2N and a fragment of the Tif2 coregulator
提交 2019-04-29
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
740–754(15 aa)
片段:UNP Residues 740-754
|
未记录
|
N27 N-[(1S,3aR,6aR)-5-hexyl-4-phenyl-3a-(1-phenylethenyl)-1,2,3,3a,6,6a-hexahydropentalen-1-yl]acetamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;291 K;0.05M sodium acetate (pH 4.6), 5-11% PEG4000, 0-10% glycerol. Microseeding with LRH-1-RJW100 crystals.
|
分辨率 2.17 Å
R-free 0.239
|
|
6SJM
Crystal structure of the Retinoic Acid Receptor alpha in complex with compound 24 (JP175)
提交 2019-08-13
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–699(14 aa)
|
未记录
|
LFZ 2-[4-[3,5-bis(trifluoromethyl)phenyl]phenyl]ethanoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7.5;293.15 K;21% PEG 4000, 0.2 M ammonium acetate and 0.1 M tris, pH 7.5
|
分辨率 2.52 Å
R-free 0.247
|
|
6STI
Crystal structure of RXRalpha LBD in complex with LG 100754 and a coactivator peptide
提交 2019-09-10
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
754 (2E,4E,6Z)-3-methyl-7-(5,5,8,8-tetramethyl-3-propoxy-5,6,7,8-tetrahydronaphthalen-2-yl)octa-2,4,6-trienoic acid × 2
ACT ACETATE ION × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;17.5% PEG3350, 0.7 M CH3COONH4, 30 mM CH3COONa pH4.6
|
分辨率 1.89 Å
R-free 0.172
|
|
6VC2
LRH-1 bound to SS-RJW100 and a fragment of the Tif2 Coactivator
提交 2019-12-20
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
740–754(15 aa)
|
未记录
|
QU7 (1S,3aS,6aS)-5-hexyl-4-phenyl-3a-(1-phenylethenyl)-1,2,3,3a,6,6a-hexahydropentalen-1-ol × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;291 K;Sodium acetate, PEG 4000, glycerol
|
分辨率 1.70 Å
R-free 0.228
|
|
6VIF
Human LRH-1 ligand-binding domain bound to agonist cpd 15 and fragment of coregulator TIF-2
提交 2020-01-13
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
|
未记录
|
QY4 N-[(8beta,11alpha,12alpha)-8-{[methyl(phenyl)amino]methyl}-1,6:7,14-dicycloprosta-1(6),2,4,7(14)-tetraen-11-yl]sulfuric diamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;291.15 K;Na acetate (pH 4.6), PEG 4000, glycerol
|
分辨率 2.26 Å
R-free 0.284
|
|
7A77
Crystal structure of RXR alpha LBD in complexes with palmitic acid and GRIP-1 peptide
提交 2020-08-27
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–699(14 aa)
|
未记录
|
EDO 1,2-ETHANEDIOL × 8
PLM PALMITIC ACID × 2
CL CHLORIDE ION × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 8;293.15 K;17% PEG 3350, 0.2M ammonium actetate, 0.1M tris, pH 8.0
|
分辨率 1.50 Å
R-free 0.180
|
|
7A78
Crystal structure of RXR beta LBD in complexes with palmitic acid and GRIP-1 peptide
提交 2020-08-27
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–699(14 aa)
|
未记录
|
PLM PALMITIC ACID × 2
CL CHLORIDE ION × 2
EDO 1,2-ETHANEDIOL × 10
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7.5;293.15 K;16% low molecular weight PEG smears, 0.1M HEPES, pH 7.5, 5% ethylene glycol, 0.1M KCl
|
分辨率 1.72 Å
R-free 0.204
|
|
7A79
Crystal structure of RXR gamma LBD in complexes with palmitic acid and GRIP-1 peptide
提交 2020-08-27
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
链 D
686–699(14 aa)
|
未记录
|
PLM PALMITIC ACID × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;293.15 K;17% PEG 3350, 0.1M potassium citrate
|
分辨率 2.05 Å
R-free 0.248
|
|
7B88
Crystal structure of Retinoic Acid Receptor alpha (RXRA) in complexed with S99 inhibitor
提交 2020-12-12
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–699(14 aa)
|
未记录
|
T2K 3-[5-[3,5-bis(chloranyl)phenyl]-4-phenyl-1,3-oxazol-2-yl]propanoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7.5;293.15 K;21% PEG 3350, 0.1 M Ammomium Acetate, 0.1 M tris 7.5
|
分辨率 2.38 Å
R-free 0.259
|
|
7B9O
Crystal structure of Retinoic Acid Receptor alpha (RXRA) in complexed with S169 inhibitor
提交 2020-12-14
|
构建体不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
|
未记录
|
T72 3-(5-(3,5-bis(trifluoromethyl)phenyl)-4-phenyloxazol-2-yl)propanoic acid × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;293 K;24% PEG 4000
0.2M Ammonium acetate
0.1M Tris pH7.5
|
分辨率 2.05 Å
R-free 0.236
|
|
7D42
Structural basis of tropifexor as a potent and selective agonist for farnesoid X receptor
提交 2020-09-22
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
|
未记录
|
GWF Tropifexor × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;291 K;100mM Sodium acetate pH 4.7, 2.3-2.6M Sodium formate
|
分辨率 2.70 Å
R-free 0.269
|
|
7JHD
Estrogen Receptor Alpha Ligand Binding Domain Y537S in Complex with TTC-352 and GRIP Peptide
提交 2020-07-20
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
链 D
686–698(13 aa)
|
未记录
|
V9J 3-(4-fluorophenyl)-2-(4-hydroxyphenoxy)-1-benzothiophene-6-ol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;298.15 K;PEG 3350, MgCl2, Tris HCl
|
分辨率 2.40 Å
R-free 0.265
|
|
7JYD
Human Liver Receptor Homolog-1 in Complex with 10CA and a Fragment of Tif2
提交 2020-08-30
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
740–751(12 aa)
片段:residues 740-751
|
未记录
|
VQA 10-[(3aR,6R,6aR)-6-hydroxy-3-phenyl-3a-(1-phenylethenyl)-1,3a,4,5,6,6a-hexahydropentalen-2-yl]decanoic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;291 K;0.4 M sodium/potassium tartrate
|
分辨率 2.30 Å
R-free 0.227
|
|
7JYE
Human Liver Receptor Homolog-1 in Complex with 9ChoP and a Fragment of Tif2
提交 2020-08-30
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构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
740–751(12 aa)
片段:residues 740-751
|
未记录
|
VQY 9-[(3~{a}~{R},6~{R},6~{a}~{R})-6-oxidanyl-3-phenyl-3~{a}-(1-phenylethenyl)-4,5,6,6~{a}-tetrahydro-1~{H}-pentalen-2-yl]nonyl 2-(trimethyl-$l^{4}-azanyl)ethyl hydrogen phosphate × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 4.6;277 K;9-19% tert-butanol, 0-6 % glycerol, 0.1 M tri-sodium citrate pH 4.6
|
分辨率 2.55 Å
R-free 0.187
|
|
7NEL
ER-PRS*(+) (Y537S) in complex with estradiol and SRC-2 coactivator peptide
提交 2021-02-04
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构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
链 D
686–699(14 aa)
|
非标准单体:是(mmCIF未提供具体位点)
非标准单体:是(mmCIF未提供具体位点)
|
EST ESTRADIOL × 2
EDO 1,2-ETHANEDIOL × 14
GOL GLYCEROL × 5
NA SODIUM ION × 1
CL CHLORIDE ION × 1
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X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION;292 K;200 mM NaCl, 100 mM Tris pH 8.5 and 25% polyethylene glycol 3,350
|
分辨率 1.45 Å
R-free 0.186
|
|
7NFB
ER-PRS*(+) (Y537S) in complex with genistein and SRC-2 coactivator peptide
提交 2021-02-05
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构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–699(14 aa)
链 D
686–699(14 aa)
|
非标准单体:是(mmCIF未提供具体位点)
非标准单体:是(mmCIF未提供具体位点)
|
GEN GENISTEIN × 2
NA SODIUM ION × 3
EDO 1,2-ETHANEDIOL × 16
CL CHLORIDE ION × 3
GOL GLYCEROL × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION;292 K;200 mM NaCl, 100 mM Tris pH 8.5 and 25% polyethylene glycol 3,350
|
分辨率 1.33 Å
R-free 0.178
|
|
7NKE
Crystal structure of human RXRalpha ligand binding domain in complex with 2,4-di-tert-butylphenol and a coactivator fragment
提交 2021-02-17
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构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
链 D
686–698(13 aa)
|
未记录
|
UGW 2,4-di~{tert}-butylphenol × 2
FMT FORMIC ACID × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION;293 K;20% PEG 3350
0.2 M sodium formate
|
分辨率 2.35 Å
R-free 0.246
|
|
7OFI
Ligand complex of RORg LBD
提交 2021-05-05
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构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
684–698(15 aa)
|
未记录
|
VCK (2~{R})-2-(4-ethylsulfonylphenyl)-~{N}-[4-[1,1,1,3,3,3-hexakis(fluoranyl)-2-oxidanyl-propan-2-yl]phenyl]-~{N}'-methyl-butanediamide × 1
NA SODIUM ION × 1
DMS DIMETHYL SULFOXIDE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;295 K;soaking
|
分辨率 1.95 Å
R-free 0.227
|
|
7OFK
Ligand complex of RORg LBD
提交 2021-05-05
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
684–698(15 aa)
|
未记录
|
VCH (1~{R})-2-ethanoyl-~{N}-[4-[1,1,1,3,3,3-hexakis(fluoranyl)-2-oxidanyl-propan-2-yl]phenyl]-5-methylsulfonyl-1,3-dihydroisoindole-1-carboxamide × 1
DMS DIMETHYL SULFOXIDE × 2
NA SODIUM ION × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;295 K;soaking
|
分辨率 1.61 Å
R-free 0.230
|
|
7PDQ
Crystal structure of a mutated form of RXRalpha ligand binding domain in complex with LG100268 and a coactivator fragment
提交 2021-08-06
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
LG2 6-[1-(3,5,5,8,8-PENTAMETHYL-5,6,7,8-TETRAHYDRONAPHTHALEN-2-YL)CYCLOPROPYL]PYRIDINE-3-CARBOXYLIC ACID × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;26% PEG3350, 0.2M NaF
|
分辨率 1.58 Å
R-free 0.195
|
|
7PDT
Crystal structure of a mutated form of RXRalpha ligand binding domain in complex with BMS649 and a coactivator fragment
提交 2021-08-07
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构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 U
686–698(13 aa)
链 V
686–698(13 aa)
|
未记录
|
BM6 4-[2-(5,5,8,8-TETRAMETHYL-5,6,7,8-TETRAHYDRO-NAPHTHALEN-2-YL)-[1,3]DIOXOLAN-2-YL]-BENZOIC ACID × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;18% PEG3350, 0.2M Na Nitrate, 0.1M BisTris propane pH6.5
|
分辨率 3.30 Å
R-free 0.207
|
|
7T2X
Estrogen Receptor Alpha Ligand Binding Domain Y537S in Complex with 2-chloro-4-((4-hydroxybenzyl)amino)-5-phenylthieno[2,3-d]pyrimidin-6-ol and GRIP Peptide
提交 2021-12-06
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
686–698(13 aa)
|
未记录
|
EMY S-(2-chloro-6-{[(4-hydroxyphenyl)methyl]amino}pyrimidin-4-yl) phenylethanethioate × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;298 K;PEG 3,350, MgCl2, HEPES pH 8
|
分辨率 2.60 Å
R-free 0.277
|
|
7T2X
Estrogen Receptor Alpha Ligand Binding Domain Y537S in Complex with 2-chloro-4-((4-hydroxybenzyl)amino)-5-phenylthieno[2,3-d]pyrimidin-6-ol and GRIP Peptide
提交 2021-12-06
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
686–698(13 aa)
|
未记录
|
EMY S-(2-chloro-6-{[(4-hydroxyphenyl)methyl]amino}pyrimidin-4-yl) phenylethanethioate × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;298 K;PEG 3,350, MgCl2, HEPES pH 8
|
分辨率 2.60 Å
R-free 0.277
|
|
7TT8
Human LRH-1 LBD bound to agonist 6N-10CA and fragment of Tif2 coactivator
提交 2022-01-31
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
740–753(14 aa)
|
未记录
|
IUW 10-[(3aR,6S,6aR)-3-phenyl-3a-(1-phenylethenyl)-6-(sulfamoylamino)-1,3a,4,5,6,6a-hexahydropentalen-2-yl]decanoic acid (non-preferred name) × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;277.15 K;tri-Na citrate (4.6), tert-butanol, glycerol
|
分辨率 2.80 Å
R-free 0.276
|
|
7UW2
Crystal structure of human Retinoid X receptor alpha ligand binding domain complex with UAB116 and coactivator peptide GRIP-1
提交 2022-05-02
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
686–698(13 aa)
|
未记录
|
OI2 (2E,4E,6Z,8E)-8-{3-[(2S)-butan-2-yl]-2-(3-methylbutyl)cyclohex-2-en-1-ylidene}-3,7-dimethylocta-2,4,6-trienoic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;295 K;100 mM Bis-Tris, pH 7.0, 8% PEG4000, 25% ethylene glycol. The drop contained 2 ul protein + 1 ul well solution
|
分辨率 1.88 Å
R-free 0.218
|
|
7UW4
Crystal structure of human Retinoid X receptor alpha ligand binding domain complex with UAB113 and coactivator peptide GRIP-1
提交 2022-05-02
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
686–698(13 aa)
|
未记录
|
OI5 (2E,4E,6Z,8E)-3,7-dimethyl-8-[2-(3-methylbutyl)-3-propylcyclohex-2-en-1-ylidene]octa-2,4,6-trienoic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;295 K;100 mM Bis-Tris, pH 7.0, 7% PEG4000, 5% ethylene glycol
|
分辨率 2.10 Å
R-free 0.243
|
|
7VUE
Structural insight of the molecular mechanism of cilofexor bound to FXR
提交 2021-11-02
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
|
未记录
|
811 2-[3-[4-[[3-[2,6-bis(chloranyl)phenyl]-5-cyclopropyl-1,2-oxazol-4-yl]methoxy]-2-chloranyl-phenyl]-3-oxidanyl-azetidin-1-yl]pyridine-4-carboxylic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;291 K;100mM sodium acetate pH 4.7, and 2.4-2.6M sodium formate
|
分辨率 2.60 Å
R-free 0.269
|
|
7W3P
Crystal structure of RORgamma in complex with natural inverse agonist
提交 2021-11-25
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
686–698(13 aa)
|
未记录
|
88K (3S,5R,8R,9R,10R,12R,13R,14R,17S)-4,4,8,10,14-pentamethyl-17-[(2R)-2,6,6-trimethyloxan-2-yl]-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,12-diol × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293.15 K;0.1M BIS-TRIS pH 5.5, 3.0M Sodium chloride
|
分辨率 1.77 Å
R-free 0.234
|
|
7W3Q
Crystal structure of RORgamma in complex with natural inverse agonist
提交 2021-11-25
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
686–698(13 aa)
|
未记录
|
97I (3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-4,4,8,10,14-pentamethyl-17-[(2R)-6-methyl-2-oxidanyl-hept-5-en-2-yl]-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,6,12-triol × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293.15 K;0.2M Magnesium chloride hexahydrate, 0.1M BIS-TRIS pH 5.5, 25% w/v Polyethylene glycol 3350
|
分辨率 2.00 Å
R-free 0.265
|
|
7WLX
A novel chemical derivative(53) of THRB agonist
提交 2022-01-14
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
741–751(11 aa)
|
未记录
|
9GC 2-[[1-methoxy-4-oxidanyl-7-[4-(phenylmethyl)phenoxy]isoquinolin-3-yl]carbonylamino]ethanoic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;2% v/v tacsimate pH 5.0, 0.1 M sodium citrate tribasic dihydrate pH 5.6 and 16% w/v polyethylene glycol 3,350.
|
分辨率 2.39 Å
R-free 0.270
|
|
7WMG
A novel chemical derivative(52) of THRB agonist
提交 2022-01-14
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
741–751(11 aa)
|
未记录
|
9IF 2-[[1-methoxy-4-oxidanyl-7-(4-phenoxyphenoxy)isoquinolin-3-yl]carbonylamino]ethanoic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;0.2 M sodium formate pH 7.0 and 20% w/v polyethylene glycol 3,350.
|
分辨率 2.93 Å
R-free 0.298
|
|
7WMH
A novel chemical derivative(56) of THRB agonist
提交 2022-01-14
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
741–751(11 aa)
|
未记录
|
9II 2-[[1-methoxy-4-oxidanyl-7-(4-phenylphenoxy)isoquinolin-3-yl]carbonylamino]ethanoic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;0.1M MgSO4 and 5% PEG 8000
|
分辨率 1.97 Å
R-free 0.253
|
|
7WMJ
A novel chemical derivative(71) of THRB agonist
提交 2022-01-14
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
741–751(11 aa)
|
未记录
|
9IL 2-[[7-[2,6-dimethyl-4-(phenylcarbonyl)phenoxy]-1-methoxy-4-oxidanyl-isoquinolin-3-yl]carbonylamino]ethanoic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;25% v/v ethylene glycol.
|
分辨率 2.81 Å
R-free 0.274
|
|
7WML
A novel chemical derivative(85) of THRB agonist
提交 2022-01-15
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
741–751(11 aa)
|
未记录
|
9IQ 2-[[7-[4-(3,5-dimethylphenyl)carbonyl-2,6-dimethyl-phenoxy]-1-ethoxy-4-oxidanyl-isoquinolin-3-yl]carbonylamino]ethanoic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;0.1 M MgSO4 and 12% PEG 6000.
|
分辨率 2.67 Å
R-free 0.245
|
|
7WMN
A novel chemical derivative(89) of THRB agonist
提交 2022-01-15
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
741–751(11 aa)
|
未记录
|
9IT 2-[[7-[2,6-dimethyl-4-(3-methylphenyl)carbonyl-phenoxy]-1-methoxy-4-oxidanyl-isoquinolin-3-yl]carbonylamino]ethanoic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;0.1 M MgSO4 and 12% PEG 6000.
|
分辨率 2.57 Å
R-free 0.261
|
|
7WMO
A novel chemical derivative(92) of THRB agonist
提交 2022-01-15
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
741–751(11 aa)
|
未记录
|
9IW 2-[[1-ethoxy-7-[4-(3-fluoranyl-5-methoxy-phenyl)carbonyl-2,6-dimethyl-phenoxy]-4-oxidanyl-isoquinolin-3-yl]carbonylamino]ethanoic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;0.2 M sodium malonate pH 6.0 and 20% w/v Polyethylene glycol 3,350
|
分辨率 2.56 Å
R-free 0.241
|
|
8C1L
Crystal structure of HNF4 alpha LBD in complexes with palmitic acid and GRIP-1 peptide
提交 2022-12-20
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 D
687–695(9 aa)
链 E
687–695(9 aa)
|
未记录
|
PLM PALMITIC ACID × 2
EDO 1,2-ETHANEDIOL × 3
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;284 K;20% PEG3350 -- 10% ethylene glycol -- 0.1M bis-tris-propane pH 8.5 -- 0.2M sodium nitrate
|
分辨率 2.00 Å
R-free 0.237
|
|
8DAF
Human SF-1 LBD bound to synthetic agonist 6N-10CA and bacterial phospholipid
提交 2022-06-13
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
740–753(14 aa)
|
未记录
|
IUW 10-[(3aR,6S,6aR)-3-phenyl-3a-(1-phenylethenyl)-6-(sulfamoylamino)-1,3a,4,5,6,6a-hexahydropentalen-2-yl]decanoic acid (non-preferred name) × 1
PEF DI-PALMITOYL-3-SN-PHOSPHATIDYLETHANOLAMINE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION;277.15 K;Na acetate (pH 4.6), glycerol, PEG 4000
|
分辨率 2.59 Å
R-free 0.281
|
|
8DAF
Human SF-1 LBD bound to synthetic agonist 6N-10CA and bacterial phospholipid
提交 2022-06-13
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
740–753(14 aa)
|
未记录
|
IUW 10-[(3aR,6S,6aR)-3-phenyl-3a-(1-phenylethenyl)-6-(sulfamoylamino)-1,3a,4,5,6,6a-hexahydropentalen-2-yl]decanoic acid (non-preferred name) × 1
PEF DI-PALMITOYL-3-SN-PHOSPHATIDYLETHANOLAMINE × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION;277.15 K;Na acetate (pH 4.6), glycerol, PEG 4000
|
分辨率 2.59 Å
R-free 0.281
|
|
8EV1
Dual Modulators
提交 2022-10-19
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
686–698(13 aa)
|
未记录
|
WVW (3aS,4R,9bR)-4-(4-hydroxyphenyl)-2,3,3a,4,5,9b-hexahydro-1H-cyclopenta[c]quinoline-8-sulfonamide × 1
WVR (3aR,4S,9bS)-4-(4-hydroxyphenyl)-2,3,3a,4,5,9b-hexahydro-1H-cyclopenta[c]quinoline-8-sulfonamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
EVAPORATION;298 K;20-25% PEG 3350, 200 mM MgCl2, 200 mM NaCl, 0.1 M Hepes pH 7
|
分辨率 1.83 Å
R-free 0.224
|
|
8EV1
Dual Modulators
提交 2022-10-19
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
686–698(13 aa)
|
未记录
|
WVW (3aS,4R,9bR)-4-(4-hydroxyphenyl)-2,3,3a,4,5,9b-hexahydro-1H-cyclopenta[c]quinoline-8-sulfonamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
EVAPORATION;298 K;20-25% PEG 3350, 200 mM MgCl2, 200 mM NaCl, 0.1 M Hepes pH 7
|
分辨率 1.83 Å
R-free 0.224
|
|
8EV2
Dual Modulators
提交 2022-10-19
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
686–698(13 aa)
|
未记录
|
LYQ (3~{a}~{R},4~{S},9~{b}~{S})-4-(2-chloranyl-4-oxidanyl-phenyl)-2,3,3~{a},4,5,9~{b}-hexahydro-1~{H}-cyclopenta[c]quinoline-8-sulfonamide × 2
WVE (3aS,4R,9bR)-4-(2-chloro-4-hydroxyphenyl)-2,3,3a,4,5,9b-hexahydro-1H-cyclopenta[c]quinoline-8-sulfonamide × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
EVAPORATION;298 K;20-25% PEG 3350, 200 mM MgCl2, 200 mM NaCl, 0.1 M Hepes pH 7
|
分辨率 2.01 Å
R-free 0.248
|
|
8EV2
Dual Modulators
提交 2022-10-19
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
686–698(13 aa)
|
未记录
|
LYQ (3~{a}~{R},4~{S},9~{b}~{S})-4-(2-chloranyl-4-oxidanyl-phenyl)-2,3,3~{a},4,5,9~{b}-hexahydro-1~{H}-cyclopenta[c]quinoline-8-sulfonamide × 2
WVE (3aS,4R,9bR)-4-(2-chloro-4-hydroxyphenyl)-2,3,3a,4,5,9b-hexahydro-1H-cyclopenta[c]quinoline-8-sulfonamide × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
EVAPORATION;298 K;20-25% PEG 3350, 200 mM MgCl2, 200 mM NaCl, 0.1 M Hepes pH 7
|
分辨率 2.01 Å
R-free 0.248
|
|
8F8M
LRH-1 bound to small molecule Tet and fragment of coactivator Tif2
提交 2022-11-22
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
740–753(14 aa)
|
未记录
|
XKE (1~{R},3~{a}~{R},6~{a}~{R})-4-phenyl-3~{a}-(1-phenylethenyl)-5-[9-(1~{H}-1,2,3,4-tetrazol-5-yl)nonyl]-2,3,6,6~{a}-tetrahydro-1~{H}-pentalen-1-ol × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;277.15 K;tri-Na citrate, tert-butanol, glycerol
|
分辨率 2.60 Å
R-free 0.220
|
|
8GL7
AncAR1 - progesterone - Tif2
提交 2023-03-21
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
743–751(9 aa)
|
未记录
|
STR PROGESTERONE × 1
GOL GLYCEROL × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;20% PEG 4000, 0.1M Tris pH 8.9, 4% glycerol
|
分辨率 2.40 Å
R-free 0.253
|
|
8P9X
Vitamin D receptor complex with Xe4Me agonist ligand
提交 2023-06-06
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
686–698(13 aa)
|
未记录
|
ACT ACETATE ION × 1
FO6 (1~{R},3~{S},5~{Z})-5-[(2~{E})-2-[(1~{S},3~{a}~{S},7~{a}~{S})-1,7~{a}-dimethyl-1-(5-methyl-5-oxidanyl-hexa-1,3-diynyl)-2,3,3~{a},5,6,7-hexahydroinden-4-ylidene]ethylidene]-4-methylidene-cyclohexane-1,3-diol × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;293 K;0.1 M BTP pH 7.0, 3 M NaOAc
|
分辨率 2.15 Å
R-free 0.241
|
|
8PP0
Crystal structure of Retinoic Acid Receptor alpha (RXRA) in complexed with JP147
提交 2023-07-05
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
686–699(14 aa)
|
未记录
|
7QJ 3-[4-[2,3-dihydro-1H-inden-4-yl(methyl)amino]-6-(trifluoromethyl)pyrimidin-2-yl]oxypropanoic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;293.15 K;23% PEG 3350, 0.1 M Ammonium actetate, 0.1 M tris pH 7.5
|
分辨率 1.90 Å
R-free 0.223
|
|
8PWD
Crystal structure of VDR in complex Des-C-Ring and Aromatic-D-Ring analog 3c
提交 2023-07-20
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
FT9 (1R,3S,5Z)-4-methylidene-5-[(E)-3-[3-[7,7,7-tris(fluoranyl)-6-oxidanyl-6-(trifluoromethyl)hept-3-ynyl]phenyl]pent-2-enylidene]cyclohexane-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7;293 K;NH4SO4 1.5M, BisTris 0.1M pH 7
|
分辨率 2.80 Å
R-free 0.274
|
|
8PWE
Crystal structure of VDR complex with Novel Des-C-Ring and Aromatic-D-Ring analog 3a
提交 2023-07-20
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
ACT ACETATE ION × 2
FUW (1~{R},3~{S},5~{Z})-4-methylidene-5-[(~{E})-3-[3-(6-methyl-6-oxidanyl-hept-3-ynyl)phenyl]pent-2-enylidene]cyclohexane-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7;293 K;NaAcetate 2.5M, BisTris 0.1M pH 7
|
分辨率 2.00 Å
R-free 0.233
|
|
8PWF
crystal structure of VDR in complex with Des-C-Ring and Aromatic-D-Ring analog 2
提交 2023-07-20
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
FVB (1R,3S,5Z)-4-methylidene-5-[(E)-3-[3-[7,7,7-tris(fluoranyl)-6-oxidanyl-6-(trifluoromethyl)heptyl]phenyl]pent-2-enylidene]cyclohexane-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7.5;293 K;LiSO4 1.6M, Hepes 0.1M pH 7.5
|
分辨率 2.30 Å
R-free 0.265
|
|
8PWM
Crystal structure of VDR in complex with Des-C-Ring and Aromatic-D-Ring analog 3b
提交 2023-07-20
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
ACT ACETATE ION × 2
HXI (1R,3S,5Z)-4-methylidene-5-[(E)-3-[3-[7,7,7-tris(fluoranyl)-6-oxidanyl-6-(trifluoromethyl)hept-3-ynyl]phenyl]but-2-enylidene]cyclohexane-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7;293 K;NaAcetate 2.5M, BisTris 0.1M pH 7
|
分辨率 2.30 Å
R-free 0.252
|
|
8PZ7
crystal structure of VDR complex with D-Bishomo-1a,25-dihydroxyvitamin D3 Analog 57
提交 2023-07-27
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
IG0 (1~{R},3~{R})-5-[(2~{E})-2-[(4~{a}~{R},5~{R},9~{a}~{S})-4~{a}-methyl-5-[(2~{R})-6-methyl-6-oxidanyl-heptan-2-yl]-3,4,5,8,9,9~{a}-hexahydro-2~{H}-benzo[7]annulen-1-ylidene]ethylidene]-2-methyl-cyclohexane-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7;293 K;NH4Acetate 3.5M, BisTrisPropane 0.1M pH 7
|
分辨率 2.93 Å
R-free 0.257
|
|
8PZ8
crystal structure of VDR in complex with D-Bishomo-1a,25-dihydroxyvitamin D3 Analog 54
提交 2023-07-27
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
IFU (1~{R},3~{R})-5-[(2~{E})-2-[(4~{a}~{R},5~{S},9~{a}~{S})-4~{a}-methyl-5-[(2~{R})-6-methyl-6-oxidanyl-heptan-2-yl]-3,4,5,6,7,8,9,9~{a}-octahydro-2~{H}-benzo[7]annulen-1-ylidene]ethylidene]cyclohexane-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;293 K;(NH4)2SO4 1.5M
|
分辨率 2.64 Å
R-free 0.261
|
|
8PZ9
Crystal structure of VDR in complex with D-Bishomo-1a,25-dihydroxyvitamin D3 Analog 55
提交 2023-07-27
|
配体/离子不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
IFK (1~{R},3~{R})-5-[(2~{E})-2-[(4~{a}~{R},5~{R},9~{a}~{S})-4~{a}-methyl-5-[(2~{R})-6-methyl-6-oxidanyl-heptan-2-yl]-3,4,5,8,9,9~{a}-hexahydro-2~{H}-benzo[7]annulen-1-ylidene]ethylidene]-2-methylidene-cyclohexane-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7.5;293 K;NaAcetate 3M, Hepes 0.1M pH 7.5
|
分辨率 2.74 Å
R-free 0.278
|
|
8PZB
crystal structure of VDR in complex with D-Bishomo-1a,25-dihydroxyvitamin D3 Analog 49
提交 2023-07-27
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
I72 (1~{R},3~{S},5~{Z})-5-[(2~{E})-2-[(4~{a}~{R},5~{S},9~{a}~{S})-4~{a}-methyl-5-[(2~{R})-6-methyl-6-oxidanyl-heptan-2-yl]-3,4,5,6,7,8,9,9~{a}-octahydro-2~{H}-benzo[7]annulen-1-ylidene]ethylidene]-4-methylidene-cyclohexane-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 6;293 K;(NH4)2SO4 1.6M, Mes 0.1M pH 6
|
分辨率 2.73 Å
R-free 0.275
|
|
8VKZ
Crystal structure of Glucocorticoid Receptor in complex with an inhibitor
提交 2024-01-10
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 D
740–753(14 aa)
链 E
740–753(14 aa)
|
未记录
|
A1ACE (4aR,4bS,5R,6aS,6bS,8R,9aR,10aR,10bR)-8-{4-[(3-aminophenyl)methyl]phenyl}-5-hydroxy-6b-(hydroxyacetyl)-4a,6a-dimethyl-4a,4b,5,6,6a,6b,9a,10,10a,10b,11,12-dodecahydro-2H,8H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-2-one × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION;pH 5.5;296 K;24% (w/v) PEG 400, 200 mM ammonium acetate, 100 mM sodium citrate pH 5.5
|
分辨率 2.13 Å
R-free 0.245
|
|
9D8Q
Crystal structure of Estrogen Receptor alpha from Melanotaenia fluviatilis bound to estradiol and human SRC2 peptide
提交 2024-08-20
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
EST ESTRADIOL × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7;290 K;9-10% Tacsimate pH 7.0, 22% PEG3000
|
分辨率 2.75 Å
R-free 0.261
|
|
9EBG
Crystal structure of the hERalpha LBD complexed with androstenediol and SRC 2-2 peptide
提交 2024-11-12
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
链 D
686–698(13 aa)
|
未记录
|
B81 (3alpha,8alpha,17beta)-androst-5-ene-3,17-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;289.15 K;.1 M PIPES pH 7, 7% w/v PEG 8000
|
分辨率 2.02 Å
R-free 0.248
|
|
9EBL
Crystal structure of the hERbeta LBD complexed with androstenediol and SRC 2-2 peptide (crystal form 1)
提交 2024-11-12
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 16
PDB 声明:octameric
|
链 C
686–698(13 aa)
链 D
686–698(13 aa)
链 G
686–698(13 aa)
链 H
686–698(13 aa)
|
未记录
|
B81 (3alpha,8alpha,17beta)-androst-5-ene-3,17-diol × 8
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;289.15 K;0.1 M sodium HEPES pH 7.5, 22% w/v PEG 5000 MME
|
分辨率 2.20 Å
R-free 0.277
|
|
9ECF
Crystal structure of the hERbeta LBD complexed with androstenediol and SRC 2-2 peptide (crystal form 2)
提交 2024-11-14
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 G
686–698(13 aa)
链 H
686–698(13 aa)
|
未记录
|
B81 (3alpha,8alpha,17beta)-androst-5-ene-3,17-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;289.15 K;0.2 M ammonium acetate, 0.1 M Bis-Tris pH 5.5, 25% w/v PEG 3350
|
分辨率 2.00 Å
R-free 0.278
|
|
9ECF
Crystal structure of the hERbeta LBD complexed with androstenediol and SRC 2-2 peptide (crystal form 2)
提交 2024-11-14
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
686–698(13 aa)
链 D
686–698(13 aa)
|
未记录
|
B81 (3alpha,8alpha,17beta)-androst-5-ene-3,17-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;289.15 K;0.2 M ammonium acetate, 0.1 M Bis-Tris pH 5.5, 25% w/v PEG 3350
|
分辨率 2.00 Å
R-free 0.278
|
|
9ECF
Crystal structure of the hERbeta LBD complexed with androstenediol and SRC 2-2 peptide (crystal form 2)
提交 2024-11-14
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 3
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 K
686–698(13 aa)
链 L
686–698(13 aa)
|
未记录
|
B81 (3alpha,8alpha,17beta)-androst-5-ene-3,17-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;289.15 K;0.2 M ammonium acetate, 0.1 M Bis-Tris pH 5.5, 25% w/v PEG 3350
|
分辨率 2.00 Å
R-free 0.278
|
|
9ECF
Crystal structure of the hERbeta LBD complexed with androstenediol and SRC 2-2 peptide (crystal form 2)
提交 2024-11-14
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 4
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 O
686–698(13 aa)
链 P
686–698(13 aa)
|
未记录
|
B81 (3alpha,8alpha,17beta)-androst-5-ene-3,17-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;289.15 K;0.2 M ammonium acetate, 0.1 M Bis-Tris pH 5.5, 25% w/v PEG 3350
|
分辨率 2.00 Å
R-free 0.278
|
|
9EZ1
Vitamin D receptor in complex with 1,4a,25-trihydroxyvitamin D3
提交 2024-04-10
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
A1H9P 1,4a,25-trihydroxyvitamin D3 × 2
ACT ACETATE ION × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;293 K;0.1 M MES pH 6.0,2.5 M NaOAc
|
分辨率 1.95 Å
R-free 0.258
|
|
9EZ2
Vitamin D receptor complex with 1,4b,25-trihydroxyvitamin D3
提交 2024-04-10
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
A1H72 1,4b,25-trihydroxyvitamin D3 × 2
ACT ACETATE ION × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;293 K;0.1 M MES pH 6.0,2.5 M NaOAc
|
分辨率 1.80 Å
R-free 0.230
|
|
9FW8
VDR complex with UG-650
提交 2024-06-28
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
A1IGV (1~{R},3~{S},5~{Z})-5-[(2~{E})-2-[(1~{R},3~{a}~{S},7~{a}~{R})-7~{a}-methyl-1-[(2~{S})-7-methyl-4-methylidene-7-oxidanyl-octan-2-yl]-2,3,3~{a},5,6,7-hexahydro-1~{H}-inden-4-ylidene]ethylidene]-4-methylidene-cyclohexane-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7;290 K;(NH4)2SO4 1.5 M, BisTris 0.1 M pH 7
|
分辨率 2.42 Å
R-free 0.261
|
|
9GY8
Vitamin D Receptor complex with Sila-A
提交 2024-10-01
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
A1IQM (1~{R},3~{S},5~{Z})-5-[(2~{E})-2-[(1~{R},3~{a}~{S},7~{a}~{R})-7~{a}-methyl-1-[(2~{R})-5-trimethylsilylpentan-2-yl]-2,3,3~{a},5,6,7-hexahydro-1~{H}-inden-4-ylidene]ethylidene]-4-methylidene-cyclohexane-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 8;293 K;(NH4)2SO4 1.5M, Tris 0.1M pH 8
|
分辨率 2.20 Å
R-free 0.262
|
|
9GYA
Vitamin D Receptor in complex with Sila-e
提交 2024-10-01
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
ACT ACETATE ION × 2
A1IQQ (1~{R},3~{S},5~{Z})-5-[(2~{E})-2-[(1~{R},3~{a}~{S},7~{a}~{R})-1-[(2~{R})-5-dimethylsilylpent-4-yn-2-yl]-7~{a}-methyl-2,3,3~{a},5,6,7-hexahydro-1~{H}-inden-4-ylidene]ethylidene]-4-methylidene-cyclohexane-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;293 K;NaAcetate 2.5M, Hepes 0.1M pH 7.5
|
分辨率 1.85 Å
R-free 0.232
|
|
9GYC
Vitamin D receptor in complex with Sila-d
提交 2024-10-01
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
686–698(13 aa)
|
未记录
|
ACT ACETATE ION × 1
A1IQP (1~{R},3~{S},5~{Z})-5-[(2~{E})-2-[(1~{R},3~{a}~{S},7~{a}~{R})-1-[(2~{R})-5-[~{tert}-butyl(dimethyl)silyl]pent-4-yn-2-yl]-7~{a}-methyl-2,3,3~{a},5,6,7-hexahydro-1~{H}-inden-4-ylidene]ethylidene]-4-methylidene-cyclohexane-1,3-diol × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;293 K;NaAcetate 2.5M, Hepes 0.1M pH 7.5
|
分辨率 2.20 Å
R-free 0.246
|
|
9GYJ
Vitamin D receptor in complex with Sila-c
提交 2024-10-02
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
ACT ACETATE ION × 2
A1IQN (1~{R},3~{S},5~{Z})-5-[(2~{E})-2-[(1~{R},3~{a}~{S},7~{a}~{R})-7~{a}-methyl-1-[(2~{R})-5-trimethylsilylpent-4-yn-2-yl]-2,3,3~{a},5,6,7-hexahydro-1~{H}-inden-4-ylidene]ethylidene]-4-methylidene-cyclohexane-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;293 K;NaAcetate 2.5M
|
分辨率 1.90 Å
R-free 0.239
|
|
9GYK
Vitamin D receptor in complex with Sila-f
提交 2024-10-02
|
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 B
686–698(13 aa)
|
未记录
|
ACT ACETATE ION × 2
A1IQO (1~{R},3~{S},5~{Z})-5-[(2~{E})-2-[(1~{S},3~{a}~{S},7~{a}~{S})-7~{a}-methyl-1-(4-trimethylsilylbuta-1,3-diynyl)-2,3,3~{a},5,6,7-hexahydro-1~{H}-inden-4-ylidene]ethylidene]-4-methylidene-cyclohexane-1,3-diol × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;293 K;NaAcetate 2.5M, Hepes 0.1M pH 7.5
|
分辨率 2.20 Å
R-free 0.255
|
|
9H65
Steroidal Selective Modulators of FXR with Therapeutic Potential
提交 2024-10-23
|
构建体不同
突变/修饰不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
740–752(13 aa)
链 D
740–752(13 aa)
|
未记录
|
RJC 1-[(3R)-3-[(3R,4R,5S,6R,7R,8S,9S,10R,13R,14S,17R)-6-ethyl-4-fluoranyl-10,13-dimethyl-3,7-bis(oxidanyl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]butyl]-3-(phenylsulfonyl)urea × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7;295 K;0.1M HEPES, 0.1M magnesium chloride hexahydrate, 20% PEG 6000, 10% ethylene glycol
|
分辨率 3.10 Å
R-free 0.323
|
|
9H66
Steroidal Selective Modulators of FXR with Therapeutic Potential
提交 2024-10-23
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 5
PDB 声明:pentameric
|
链 E
740–752(13 aa)
链 F
740–752(13 aa)
链 G
740–752(13 aa)
|
未记录
|
R3U (4~{R})-4-[(3~{R},4~{R},5~{S},6~{R},7~{R},8~{S},9~{S},10~{R},13~{R},14~{R},17~{R})-6-ethyl-4-fluoranyl-10,13-dimethyl-3,7-bis(oxidanyl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1~{H}-cyclopenta[a]phenanthren-17-yl]-~{N}-[4-(trifluoromethyloxy)phenyl]sulfonyl-pentanamide × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 4.2;295 K;0.1M sodium phosphate dibasic, 0.2M lithium sulphate pH4.2, 20% PEG2000 MME
|
分辨率 2.60 Å
R-free 0.312
|
|
9H66
Steroidal Selective Modulators of FXR with Therapeutic Potential
提交 2024-10-23
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 5
PDB 声明:pentameric
|
链 H
740–752(13 aa)
链 I
740–752(13 aa)
链 J
740–752(13 aa)
|
未记录
|
R3U (4~{R})-4-[(3~{R},4~{R},5~{S},6~{R},7~{R},8~{S},9~{S},10~{R},13~{R},14~{R},17~{R})-6-ethyl-4-fluoranyl-10,13-dimethyl-3,7-bis(oxidanyl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1~{H}-cyclopenta[a]phenanthren-17-yl]-~{N}-[4-(trifluoromethyloxy)phenyl]sulfonyl-pentanamide × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 4.2;295 K;0.1M sodium phosphate dibasic, 0.2M lithium sulphate pH4.2, 20% PEG2000 MME
|
分辨率 2.60 Å
R-free 0.312
|
|
9H66
Steroidal Selective Modulators of FXR with Therapeutic Potential
提交 2024-10-23
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 3
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 J
740–752(13 aa)
|
未记录
|
R3U (4~{R})-4-[(3~{R},4~{R},5~{S},6~{R},7~{R},8~{S},9~{S},10~{R},13~{R},14~{R},17~{R})-6-ethyl-4-fluoranyl-10,13-dimethyl-3,7-bis(oxidanyl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1~{H}-cyclopenta[a]phenanthren-17-yl]-~{N}-[4-(trifluoromethyloxy)phenyl]sulfonyl-pentanamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 4.2;295 K;0.1M sodium phosphate dibasic, 0.2M lithium sulphate pH4.2, 20% PEG2000 MME
|
分辨率 2.60 Å
R-free 0.312
|
|
9IX5
An agonist(compound 15n) of Thyroid Hormone Receptor B
提交 2024-07-26
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
741–752(12 aa)
|
未记录
|
A1EAC 2-[(1-methoxy-7-naphthalen-2-yloxy-4-oxidanyl-isoquinolin-3-yl)carbonylamino]ethanoic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;0.35 M Sodium citrate tribasic dihydrate, 22%(w/v) Polyethylene glycol 3,350
|
分辨率 2.65 Å
R-free 0.277
|
|
9J0K
An agonist(compound 14e)of Thyroid Hormone Receptor B
提交 2024-08-02
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
741–752(12 aa)
|
未记录
|
A1EAE 2-[[7-[3-(aminomethyl)phenoxy]-1-methoxy-4-oxidanyl-isoquinolin-3-yl]carbonylamino]ethanoic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;1.3 M ammonium sulfate, 0.1 M MES monohydrate pH 6.7 and 13% v/v 1,4-Dioxane
|
分辨率 2.70 Å
R-free 0.275
|
|
9J0K
An agonist(compound 14e)of Thyroid Hormone Receptor B
提交 2024-08-02
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 2
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 D
741–752(12 aa)
|
未记录
|
A1EAE 2-[[7-[3-(aminomethyl)phenoxy]-1-methoxy-4-oxidanyl-isoquinolin-3-yl]carbonylamino]ethanoic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;1.3 M ammonium sulfate, 0.1 M MES monohydrate pH 6.7 and 13% v/v 1,4-Dioxane
|
分辨率 2.70 Å
R-free 0.275
|
|
9LQ3
Crystal structure of Linafexor-FXR complex
提交 2025-01-27
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 C
687–697(11 aa)
|
未记录
|
A1ELK Linafexor × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION;291 K;0.2 M Sodium malonate pH 7.0, 20% Polyethylene glycol 3,350
|
分辨率 2.80 Å
R-free 0.293
|
|
9QX6
Crystal structure of RXR alpha LBD bound to a synthetic agonist FN537 and a coactivator fragment
提交 2025-04-15
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
687–696(10 aa)
|
未记录
|
A1JAT (6R,6aR,7S,10R,10aS)-6-(3,5-bis(trifluoromethyl)phenyl)-5,6,6a,7,8,9,10,10a-octahydro-7,10-methanophenanthridine-3-carboxylic acid × 1
A1JHO 6S,6aS,7R,10S,10aR)-6-(3,5-bis(trifluoromethyl)phenyl)-5,6,6a,7,8,9,10,10a-octahydro-7,10-methanophenanthridine-3-carboxylic acid × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;289 K;20% PEG3350, 0.2M calcium acetate
|
分辨率 1.46 Å
R-free 0.213
|
|
9RAP
VDR complex with UG-635
提交 2025-05-21
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
686–698(13 aa)
|
未记录
|
ACT ACETATE ION × 1
A1JD0 (1~{R},3~{S},5~{Z})-5-[(2~{E})-2-[(1~{R},3~{a}~{S},7~{a}~{R})-1-[(2~{S})-6-[bis(oxidanyl)amino]-6-methyl-heptan-2-yl]-7~{a}-methyl-2,3,3~{a},5,6,7-hexahydro-1~{H}-inden-4-ylidene]ethylidene]-4-methylidene-cyclohexane-1,3-diol × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7;290 K;3M Na Acetate 0.1M Tris HCl pH8
|
分辨率 2.20 Å
R-free 0.249
|
|
9RCG
Vitamin D receptor complex with a vitamin D receptor agonist/histone deacetylase inhibitor hybrid molecule
提交 2025-05-28
|
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
686–698(13 aa)
|
未记录
|
A1JD5 4-[4-[3-[5-[(3~{S})-4,4-dimethyl-3-oxidanyl-pentyl]-4-methyl-1,3-thiazol-2-yl]pentan-3-yl]phenoxy]-~{N}-oxidanyl-butanamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 7.5;293 K;Na2 Tartrate 1.1M, MgCl2 0.2M, Hepes 0.1M pH7.5
|
分辨率 2.10 Å
R-free 0.206
|
|
9RMR
Crystal structure of RXR alpha LBD bound to a synthetic agonist FN558 and a coactivator fragment
提交 2025-06-18
|
构建体不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
|
Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 2
PDB 声明:dimeric
|
链 B
687–696(10 aa)
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未记录
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A1JH6 FN558 × 1
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X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;277 K;20% PEG 3350, 0.1 M magnesium actetate
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分辨率 1.65 Å
R-free 0.215
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9SMQ
Crystal structure of LRH-1/TIF-2 peptide in complex with CP4
提交 2025-09-08
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构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验环境不同
结构质量不同
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Assembly 1
蛋白异源复合物
异源复合物;蛋白 × 3
PDB 声明:trimeric
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链 C
740–753(14 aa)
链 E
740–753(14 aa)
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未记录
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A1JOT 3-[5-phenyl-1-[3-(trifluoromethyl)phenyl]pyrazol-3-yl]propanoic acid × 1
PO4 PHOSPHATE ION × 2
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X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;293 K;1.25 M Ammonium phosphate monobasic
0.9 Ammonium phosphate dibasic
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分辨率 2.20 Å
R-free 0.244
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