当前蛋白身份:O75469 重新检索
本组结构的主要差异维度
构建体不同 突变/修饰不同 组装状态不同 配体/离子不同 实验环境不同 结构质量指标不同

差异标签只比较当前检索结果;所有PDB和assembly原始记录仍分别保留。

相关结构差异明细

一行代表一个 PDB 条目中的一个 biological assembly;同一蛋白的多个单体会分别列出。

PDB 条目 Assembly / 聚集状态 构建体 突变与修饰 配体、离子与非聚合物 实验方法 实验环境 结构质量
1ILG Crystal Structure of Apo Human Pregnane X Receptor Ligand Binding Domain 提交 2001-05-08 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa) 片段:LIGAND BINDING DOMAIN
未记录 未记录非水小分子 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.2;298 K;isopropanol, imidazole, sodium chloride, glycerol, Tris-HCl, , pH 7.2, VAPOR DIFFUSION, HANGING DROP, temperature 298K
分辨率 2.52 Å R-free 0.279
1ILH Crystal Structure of Human Pregnane X Receptor Ligand Binding Domain Bound to SR12813 提交 2001-05-08 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa) 片段:LIGAND BINDING DOMAIN
未记录 SRL [2-(3,5-DI-TERT-BUTYL-4-HYDROXY-PHENYL)-1-(DIETHOXY-PHOSPHORYL)-VINYL]-PHOSPHONIC ACID DIETHLYL ESTER × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.2;298 K;isopropanol, imidazole, glycerol, sodium chloride, Tris-HCl, pH 7.2, VAPOR DIFFUSION, HANGING DROP, temperature 298K
分辨率 2.76 Å R-free 0.282
1M13 Crystal Structure of the Human Pregane X Receptor Ligand Binding Domain in Complex with Hyperforin, a Constituent of St. John's Wort 提交 2002-06-17 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa) 片段:Includes Ligand Binding Domain (Residues 130-434)
未记录 HYF 4-HYDROXY-5-ISOBUTYRYL-6-METHYL-1,3,7-TRIS-(3-METHYL-BUT-2-ENYL)-6-(4-METHYL-PENT-3-ENYL)-BICYCLO[3.3.1]NON-3-ENE-2,9-DIONE × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.6;295 K;isopropanol, tris-HCl, sodium chloride, glycerol, EDTA, DTT, sodium azide, pH 7.6, VAPOR DIFFUSION, HANGING DROP, temperature 295K
分辨率 2.15 Å R-free 0.246
1NRL Crystal Structure of the human PXR-LBD in complex with an SRC-1 coactivator peptide and SR12813 提交 2003-01-25 Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa) 片段:Ligand Binding Domain
未记录 SRL [2-(3,5-DI-TERT-BUTYL-4-HYDROXY-PHENYL)-1-(DIETHOXY-PHOSPHORYL)-VINYL]-PHOSPHONIC ACID DIETHLYL ESTER × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.2;295 K;isopropanol, imidazole, sodium chloride, Tris-HCl, glycerol, EDTA, pH 7.2, VAPOR DIFFUSION, HANGING DROP, temperature 295.0K
分辨率 2.00 Å R-free 0.240
1NRL Crystal Structure of the human PXR-LBD in complex with an SRC-1 coactivator peptide and SR12813 提交 2003-01-25 Assembly 2 蛋白异源复合物 异源复合物;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 B 130–434(305 aa) 片段:Ligand Binding Domain
未记录 SRL [2-(3,5-DI-TERT-BUTYL-4-HYDROXY-PHENYL)-1-(DIETHOXY-PHOSPHORYL)-VINYL]-PHOSPHONIC ACID DIETHLYL ESTER × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.2;295 K;isopropanol, imidazole, sodium chloride, Tris-HCl, glycerol, EDTA, pH 7.2, VAPOR DIFFUSION, HANGING DROP, temperature 295.0K
分辨率 2.00 Å R-free 0.240
1NRL Crystal Structure of the human PXR-LBD in complex with an SRC-1 coactivator peptide and SR12813 提交 2003-01-25 Assembly 3 蛋白异源复合物 异源复合物;蛋白 × 4 PDB 声明:tetrameric(4) 与蛋白数一致
链 A 130–434(305 aa) 片段:Ligand Binding Domain
链 B 130–434(305 aa) 片段:Ligand Binding Domain
未记录 SRL [2-(3,5-DI-TERT-BUTYL-4-HYDROXY-PHENYL)-1-(DIETHOXY-PHOSPHORYL)-VINYL]-PHOSPHONIC ACID DIETHLYL ESTER × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.2;295 K;isopropanol, imidazole, sodium chloride, Tris-HCl, glycerol, EDTA, pH 7.2, VAPOR DIFFUSION, HANGING DROP, temperature 295.0K
分辨率 2.00 Å R-free 0.240
1SKX Structural Disorder in the Complex of Human PXR and the Macrolide Antibiotic Rifampicin 提交 2004-03-05 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–431(302 aa) 片段:PXR Ligand Binding Domain; residues 130-431
未记录 RFP RIFAMPICIN × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.2;298 K;50mM imidizole, 9% 2-propanol, pH 7.2, VAPOR DIFFUSION, HANGING DROP, temperature 298K
分辨率 2.80 Å R-free 0.266
2O9I Crystal Structure of the Human Pregnane X Receptor LBD in complex with an SRC-1 coactivator peptide and T0901317 提交 2006-12-13 Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 142–434(293 aa) 片段:Ligand Binding Domain
未记录 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 7.1;295 K;50 mM Imidizole, 10% 2-propanol (v/v), pH 7.1, VAPOR DIFFUSION, HANGING DROP, temperature 295K
分辨率 2.80 Å R-free 0.240
2O9I Crystal Structure of the Human Pregnane X Receptor LBD in complex with an SRC-1 coactivator peptide and T0901317 提交 2006-12-13 Assembly 2 蛋白异源复合物 异源复合物;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 B 1142–1434(293 aa) 片段:Ligand Binding Domain
未记录 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 7.1;295 K;50 mM Imidizole, 10% 2-propanol (v/v), pH 7.1, VAPOR DIFFUSION, HANGING DROP, temperature 295K
分辨率 2.80 Å R-free 0.240
2O9I Crystal Structure of the Human Pregnane X Receptor LBD in complex with an SRC-1 coactivator peptide and T0901317 提交 2006-12-13 Assembly 3 蛋白异源复合物 异源复合物;蛋白 × 4 PDB 声明:tetrameric(4) 与蛋白数一致
链 A 142–434(293 aa) 片段:Ligand Binding Domain
链 B 1142–1434(293 aa) 片段:Ligand Binding Domain
未记录 444 N-(2,2,2-TRIFLUOROETHYL)-N-{4-[2,2,2-TRIFLUORO-1-HYDROXY-1-(TRIFLUOROMETHYL)ETHYL]PHENYL}BENZENESULFONAMIDE × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.1;295 K;50 mM Imidizole, 10% 2-propanol (v/v), pH 7.1, VAPOR DIFFUSION, HANGING DROP, temperature 295K
分辨率 2.80 Å R-free 0.240
2QNV Crystal Structure of the Pregnane X Receptor bound to Colupulone 提交 2007-07-19 Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa) 片段:PXR Ligand Binding Domain; residues 130-434
未记录 CDZ 3,5-dihydroxy-4,6,6-tris(3-methylbut-2-en-1-yl)-2-(2-methylpropanoyl)cyclohexa-2,4-dien-1-one × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;Precipitant: 10% Isopropanol; Cryoprotectant: done by serial dipping into 15%, 25% and 35% ethylene glycol, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K
分辨率 2.80 Å R-free 0.284
3CTB Tethered PXR-LBD/SRC-1p apoprotein 提交 2008-04-11 Assembly 1 信息不足 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa) 片段:PXR, residues 130-434, linker, SRC-1, residues 678-700
未记录 未记录非水小分子 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION;pH 7;277 K;10-30% MPD or isopropanol, 100 mM imidazole, pH 7, VAPOR DIFFUSION, temperature 277K
分辨率 2.00 Å R-free 0.244
3CTB Tethered PXR-LBD/SRC-1p apoprotein 提交 2008-04-11 Assembly 2 信息不足 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 B 130–434(305 aa) 片段:PXR, residues 130-434, linker, SRC-1, residues 678-700
未记录 未记录非水小分子 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION;pH 7;277 K;10-30% MPD or isopropanol, 100 mM imidazole, pH 7, VAPOR DIFFUSION, temperature 277K
分辨率 2.00 Å R-free 0.244
3CTB Tethered PXR-LBD/SRC-1p apoprotein 提交 2008-04-11 Assembly 3 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa) 片段:PXR, residues 130-434, linker, SRC-1, residues 678-700
链 B 130–434(305 aa) 片段:PXR, residues 130-434, linker, SRC-1, residues 678-700
未记录 未记录非水小分子 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION;pH 7;277 K;10-30% MPD or isopropanol, 100 mM imidazole, pH 7, VAPOR DIFFUSION, temperature 277K
分辨率 2.00 Å R-free 0.244
3HVL Tethered PXR-LBD/SRC-1p complexed with SR-12813 提交 2009-06-16 Assembly 1 信息不足 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa) 片段:PXR, residues 130-434, linker, SRC-1, residues 678-700
未记录 SRL [2-(3,5-DI-TERT-BUTYL-4-HYDROXY-PHENYL)-1-(DIETHOXY-PHOSPHORYL)-VINYL]-PHOSPHONIC ACID DIETHLYL ESTER × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION;pH 7;277 K;10-30% MPD OR ISOPROPANOL, 100 mM IMIDAZOLE, 1 mM SR12813, pH 7, VAPOR DIFFUSION, temperature 277K
分辨率 2.10 Å R-free 0.265
3HVL Tethered PXR-LBD/SRC-1p complexed with SR-12813 提交 2009-06-16 Assembly 2 信息不足 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 B 130–434(305 aa) 片段:PXR, residues 130-434, linker, SRC-1, residues 678-700
未记录 SRL [2-(3,5-DI-TERT-BUTYL-4-HYDROXY-PHENYL)-1-(DIETHOXY-PHOSPHORYL)-VINYL]-PHOSPHONIC ACID DIETHLYL ESTER × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION;pH 7;277 K;10-30% MPD OR ISOPROPANOL, 100 mM IMIDAZOLE, 1 mM SR12813, pH 7, VAPOR DIFFUSION, temperature 277K
分辨率 2.10 Å R-free 0.265
3HVL Tethered PXR-LBD/SRC-1p complexed with SR-12813 提交 2009-06-16 Assembly 3 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa) 片段:PXR, residues 130-434, linker, SRC-1, residues 678-700
链 B 130–434(305 aa) 片段:PXR, residues 130-434, linker, SRC-1, residues 678-700
未记录 SRL [2-(3,5-DI-TERT-BUTYL-4-HYDROXY-PHENYL)-1-(DIETHOXY-PHOSPHORYL)-VINYL]-PHOSPHONIC ACID DIETHLYL ESTER × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION;pH 7;277 K;10-30% MPD OR ISOPROPANOL, 100 mM IMIDAZOLE, 1 mM SR12813, pH 7, VAPOR DIFFUSION, temperature 277K
分辨率 2.10 Å R-free 0.265
3R8D Activation of the Human Nuclear Xenobiotic Receptor PXR by the Reverse Transcriptase-Targeted Anti-HIV Drug PNU-142721 提交 2011-03-23 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa) 片段:PXR Ligand binding domain (residues 130-434)
未记录 PNU 6-CHLORO-2-(1-FURO[2,3-C]PYRIDIN-5-YL-ETHYLSULFANYL)-PYRIMIDIN-4-YLAMINE × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.8;295 K;50 mM imidazole, 16% 2-propanol (v/v), pH 7.8, VAPOR DIFFUSION, HANGING DROP, temperature 295K
分辨率 2.80 Å R-free 0.289
4J5W Crystal Structure of the apo-PXR/RXRalpha LBD Heterotetramer Complex 提交 2013-02-10 Assembly 1 信息不足 异源复合物;蛋白 × 4 PDB 声明:tetrameric(4) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
未记录 MG MAGNESIUM ION × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7;277.15 K;16-20% PEG 8000, 0.1-0.2 M MgCl, 0.1 M bis-tris proprane, 0.02% sodium azide, pH 7.0, vapor diffusion, hanging drop, temperature 277.15K
分辨率 2.80 Å R-free 0.298
4J5X Crystal Structure of the SR12813-bound PXR/RXRalpha LBD Heterotetramer Complex 提交 2013-02-10 Assembly 1 信息不足 异源复合物;蛋白 × 4 PDB 声明:tetrameric(4) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
未记录 SRL [2-(3,5-DI-TERT-BUTYL-4-HYDROXY-PHENYL)-1-(DIETHOXY-PHOSPHORYL)-VINYL]-PHOSPHONIC ACID DIETHLYL ESTER × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7;277.15 K;16-20% PEG 8000, 0.1-0.2 M MgCl, 0.1 M bis-tris proprane, 0.02% sodium azide, pH 7.0, vapor diffusion, hanging drop, temperature 277.15K
分辨率 2.80 Å R-free 0.298
4NY9 Crystal Structure Of the Human PXR-LBD In Complex With N-{(2R)-1-[(4S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl]-3-methyl-1-oxobutan-2-yl}-3-hydroxy-3-methylbutanamide 提交 2013-12-10 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 142–431(290 aa) 片段:unp residues 142-431
未记录 2Q4 N-{(2R)-1-[(4S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl]-3-methyl-1-oxobutan-2-yl}-3-hydroxy-3-methylbutanamide × 1 GOL GLYCEROL × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.8;296 K;0.1M imidazole, 8-10%(V/V)isopropanol. Apo crystal was soaked with 5 mM compound and Crystals harvested next day using 32% ethylene glycol as cryoprotectant, pH 7.8, VAPOR DIFFUSION, HANGING DROP, temperature 296K
分辨率 2.80 Å R-free 0.298
4NY9 Crystal Structure Of the Human PXR-LBD In Complex With N-{(2R)-1-[(4S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl]-3-methyl-1-oxobutan-2-yl}-3-hydroxy-3-methylbutanamide 提交 2013-12-10 Assembly 2 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 142–431(290 aa) 片段:unp residues 142-431
未记录 2Q4 N-{(2R)-1-[(4S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl]-3-methyl-1-oxobutan-2-yl}-3-hydroxy-3-methylbutanamide × 2 GOL GLYCEROL × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.8;296 K;0.1M imidazole, 8-10%(V/V)isopropanol. Apo crystal was soaked with 5 mM compound and Crystals harvested next day using 32% ethylene glycol as cryoprotectant, pH 7.8, VAPOR DIFFUSION, HANGING DROP, temperature 296K
分辨率 2.80 Å R-free 0.298
4S0S STRUCTURE OF HUMAN PREGNANE X RECEPTOR LIGAND BINDING DOMAIN with ADNECTIN-1 提交 2015-01-05 Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
未记录 未记录非水小分子 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;293 K;0.1M HEPES pH 7.0, 18%(V/V)1,6 hexanediol, and 3% (V/V) MPD. Crystals harvested next day using mother liquor supplemented with 21%(V/V) 1,6 hexanediol and 3%(V/V) MPD as cryoprotectant, vapor diffusion, hanging drop, temperature 293K
分辨率 2.80 Å R-free 0.229
4S0S STRUCTURE OF HUMAN PREGNANE X RECEPTOR LIGAND BINDING DOMAIN with ADNECTIN-1 提交 2015-01-05 Assembly 2 蛋白异源复合物 异源复合物;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 B 130–434(305 aa)
未记录 未记录非水小分子 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;293 K;0.1M HEPES pH 7.0, 18%(V/V)1,6 hexanediol, and 3% (V/V) MPD. Crystals harvested next day using mother liquor supplemented with 21%(V/V) 1,6 hexanediol and 3%(V/V) MPD as cryoprotectant, vapor diffusion, hanging drop, temperature 293K
分辨率 2.80 Å R-free 0.229
4S0T STRUCTURE OF HUMAN PREGNANE X RECEPTOR LIGAND BINDING DOMAIN BOUND WITH ADNECTIN-1 AND COMPOUND-1 提交 2015-01-05 Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 4 PDB 声明:tetrameric(4) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
未记录 40U N-{(2R)-1-[(4S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl]-3-methyl-1-oxobutan-2-yl}-2-cyclopropylacetamide × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.5;293 K;0.1M Tris pH 7.5, 10%(V/V)isopropanol, 3.5% (V/V) MPD. Apo crystal was soaked with 5 mM compound 1 and Crystals harvested next day using Paratone-N as cryoprotectant, VAPOR DIFFUSION, HANGING DROP, temperature 293K
分辨率 3.14 Å R-free 0.247
4S0T STRUCTURE OF HUMAN PREGNANE X RECEPTOR LIGAND BINDING DOMAIN BOUND WITH ADNECTIN-1 AND COMPOUND-1 提交 2015-01-05 Assembly 2 蛋白异源复合物 异源复合物;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
未记录 40U N-{(2R)-1-[(4S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl]-3-methyl-1-oxobutan-2-yl}-2-cyclopropylacetamide × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.5;293 K;0.1M Tris pH 7.5, 10%(V/V)isopropanol, 3.5% (V/V) MPD. Apo crystal was soaked with 5 mM compound 1 and Crystals harvested next day using Paratone-N as cryoprotectant, VAPOR DIFFUSION, HANGING DROP, temperature 293K
分辨率 3.14 Å R-free 0.247
4S0T STRUCTURE OF HUMAN PREGNANE X RECEPTOR LIGAND BINDING DOMAIN BOUND WITH ADNECTIN-1 AND COMPOUND-1 提交 2015-01-05 Assembly 3 蛋白异源复合物 异源复合物;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 B 130–434(305 aa)
未记录 40U N-{(2R)-1-[(4S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl]-3-methyl-1-oxobutan-2-yl}-2-cyclopropylacetamide × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.5;293 K;0.1M Tris pH 7.5, 10%(V/V)isopropanol, 3.5% (V/V) MPD. Apo crystal was soaked with 5 mM compound 1 and Crystals harvested next day using Paratone-N as cryoprotectant, VAPOR DIFFUSION, HANGING DROP, temperature 293K
分辨率 3.14 Å R-free 0.247
4X1F Crystal structure of the hPXR-LBD in complex with the synthetic estrogen 17alpha-ethinylestradiol 提交 2014-11-24 Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa) 片段:UNP residues 130-434
未记录 3WF Ethinyl estradiol × 2 MPD (4S)-2-METHYL-2,4-PENTANEDIOL × 4 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.1;291 K;100 mM NaCl, 100 mM Imidazole, 10% Isopropanol
分辨率 2.00 Å R-free 0.210
4X1G Crystal structure of the hPXR-LBD in complex with the synthetic estrogen 17alpha-ethinylestradiol and the pesticide trans-nonachlor 提交 2014-11-24 Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:Dimeric(2) 与蛋白数一致
链 A 130–434(305 aa) 片段:UNP residues 130-434
未记录 3WF Ethinyl estradiol × 2 3WG Trans-nonachlor × 2 MPD (4S)-2-METHYL-2,4-PENTANEDIOL × 2 IPA ISOPROPYL ALCOHOL × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.1;291 K;50 mM NaCl, 50 mM LiCl, 100 mM Imidazole, 10% Isopropanol
分辨率 2.25 Å R-free 0.218
4XAO Crystal structure of the hPXR-LBD obtained in presence of the pesticide trans-nonachlor 提交 2014-12-15 Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa) 片段:UNP residues 130-434
未记录 IPA ISOPROPYL ALCOHOL × 2 MPD (4S)-2-METHYL-2,4-PENTANEDIOL × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.1;291 K;100 mM Imidazole, 10% Isopropanol
分辨率 2.58 Å R-free 0.239
4XHD STRUCTURE OF HUMAN PREGNANE X RECEPTOR LIGAND BINDING DOMAIN WITH COMPOUND-1 提交 2015-01-05 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 153–457(305 aa)
未记录 GOL GLYCEROL × 1 40U N-{(2R)-1-[(4S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl]-3-methyl-1-oxobutan-2-yl}-2-cyclopropylacetamide × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.8;293 K;0.1M imidazole pH 7.8, 8-10%(V/V)isopropanol. Apo crystal was soaked with 5 mM compound 1 and Crystals harvested next day using 32% ethylene glycol as cryoprotectant
分辨率 2.40 Å R-free 0.242
4XHD STRUCTURE OF HUMAN PREGNANE X RECEPTOR LIGAND BINDING DOMAIN WITH COMPOUND-1 提交 2015-01-05 Assembly 2 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 153–457(305 aa)
未记录 GOL GLYCEROL × 2 40U N-{(2R)-1-[(4S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl]-3-methyl-1-oxobutan-2-yl}-2-cyclopropylacetamide × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.8;293 K;0.1M imidazole pH 7.8, 8-10%(V/V)isopropanol. Apo crystal was soaked with 5 mM compound 1 and Crystals harvested next day using 32% ethylene glycol as cryoprotectant
分辨率 2.40 Å R-free 0.242
5A86 Structure of pregnane X receptor in complex with a Sphingosine 1- Phosphate Receptor 1 Antagonist 提交 2015-07-13 Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 4 PDB 声明:tetrameric(4) 与蛋白数一致
链 A 130–432(303 aa)
链 B 130–432(303 aa)
未记录 D7E 4-chloro-N-[(1R)-1-[1-ethyl-6-(trifluoromethyl)benzimidazol-2-yl]ethyl]benzenesulfonamide × 2 X-RAY DIFFRACTION mmCIF 未提供已读取条件 分辨率 2.25 Å R-free 0.256
5X0R Crystal Structure of PXR LBD Complexed with SJB7 提交 2017-01-23 Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 4 PDB 声明:tetrameric(4) 与蛋白数一致
链 A 153–457(305 aa) 片段:UNP residues 153-457
链 B 153–457(305 aa) 片段:UNP residues 153-457
未记录 4WH 4-[(4-tert-butylphenyl)sulfonyl]-1-(2,4-dimethoxy-5-methylphenyl)-5-methyl-1H-1,2,3-triazole × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.8;291 K;Tris-HCl, imidazole, isopropanol,sodium chloride, glycerol, EDTA, pH 7.2-7.8, VAPOR DIFFUSION, HANGING DROP, temperature 291.0K
分辨率 2.67 Å R-free 0.252
6BNS STRUCTURE OF HUMAN PREGNANE X RECEPTOR LIGAND BINDING DOMAIN BOUND TETHERED WITH SRC co-activator peptide and Compound 25a AKA BICYCLIC HEXAFLUOROISOPROPYL 2 ALCOHOL SULFONAMIDES 提交 2017-11-17 Assembly 1 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
未记录 XGH 2-[(2S)-4-[(4-fluorophenyl)sulfonyl]-7-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-3,4-dihydro-2H-1,4-benzothiazin-2-yl]-N-(2-hydroxy-2-methylpropyl)acetamide × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;296 K;0.1M Hepes pH 7.5, 150mM NaCl, 10-15%(V/V)PEG10K.Crystals were cryoprotected by supplementing the mother liquor with 15% (v/v) ethylene glycol and harvested by flash-cooling in liquid nitrogen
分辨率 2.56 Å R-free 0.246
6DUP CRYSTAL STRUCTURE OF PXR IN COMPLEX WITH COMPOUND 7 提交 2018-06-21 Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 153–449(297 aa)
链 B 153–449(297 aa)
未记录 HCJ (2S)-2-({[3'-(trifluoromethyl)[1,1'-biphenyl]-4-yl]oxy}methyl)-2,3-dihydro-7H-[1,3]oxazolo[3,2-a]pyrimidin-7-one × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION;pH 8;278 K;imidazole 100mM, NaCl 100M, Jeffamine M-600 5%,isopropanol 20%, pH8
分辨率 2.30 Å R-free 0.266
6HJ2 Crystal structure of hPXR in complex with dabrafenib 提交 2018-08-31 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 P06 Dabrafenib × 1 IPA ISOPROPYL ALCOHOL × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7;291 K;100 mM Imidazole 10% Isopropanol (dry co-crystallization with ligand)
分辨率 2.28 Å R-free 0.232
6HTY PXR in complex with P2X4 inhibitor compound 25 提交 2018-10-05 Assembly 1 信息不足 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 129–434(306 aa)
突变:K129G,K129G GOL GLYCEROL × 1 DMS DIMETHYL SULFOXIDE × 3 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 8;277 K;1 microliter protein at 12.1 mg/ml (in 20 millimolar Tris pH 7.8, 250 millimolar NaCl, 2.5 millimolar EDTA, 5% (v/v) glycerol, 5 mM DTT), preincubated with 10 millimolar compound 15 (from 200 millimolar stock in DMSO), mixed with 1 microliter of reservoir (100 mM imidazole pH 8.0, 17 % (v/v) MPD). Crystals additionally soaked in 20 millimolar compound 15 prior to data collection. cryo buffer 34% (v/v) MPD supplemented with 20 millimolar compound 15
分辨率 2.22 Å R-free 0.226
6HTY PXR in complex with P2X4 inhibitor compound 25 提交 2018-10-05 Assembly 2 信息不足 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 B 129–434(306 aa)
突变:K129G,K129G DMS DIMETHYL SULFOXIDE × 2 GRH (2~{R})-~{N}-[4-(3-chloranylphenoxy)-3-sulfamoyl-phenyl]-2-phenyl-propanamide × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 8;277 K;1 microliter protein at 12.1 mg/ml (in 20 millimolar Tris pH 7.8, 250 millimolar NaCl, 2.5 millimolar EDTA, 5% (v/v) glycerol, 5 mM DTT), preincubated with 10 millimolar compound 15 (from 200 millimolar stock in DMSO), mixed with 1 microliter of reservoir (100 mM imidazole pH 8.0, 17 % (v/v) MPD). Crystals additionally soaked in 20 millimolar compound 15 prior to data collection. cryo buffer 34% (v/v) MPD supplemented with 20 millimolar compound 15
分辨率 2.22 Å R-free 0.226
6NX1 STRUCTURE OF HUMAN PREGNANE X RECEPTOR LIGAND BINDING DOMAIN BOUND TETHERED WITH SRC CO-ACTIVATOR PEPTIDE AND COMPOUND-3 AKA 1,1,1,3,3,3-HEXAFLUORO-2-{4-[1-(4- LUOROBENZENESULFONYL)CYCLOPENTYL]PHENYL}PROPAN-2-OL 提交 2019-02-07 Assembly 1 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa) 片段:LIGAND BINDING DOMAIN
链 B 130–434(305 aa) 片段:LIGAND BINDING DOMAIN
未记录 L7D 1,1,1,3,3,3-hexafluoro-2-(4-{1-[(4-fluorophenyl)sulfonyl]cyclopentyl}phenyl)propan-2-ol × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;296 K;0.1M Hepes pH 7.5, 150mM NaCl, 10-15%(V/V)PEG10K, Crystals were cryoprotected by supplementing the mother liquor with 15% (v/v) ethylene glycol and harvested by flash-cooling in liquid nitrogen
分辨率 2.27 Å R-free 0.240
6NX1 STRUCTURE OF HUMAN PREGNANE X RECEPTOR LIGAND BINDING DOMAIN BOUND TETHERED WITH SRC CO-ACTIVATOR PEPTIDE AND COMPOUND-3 AKA 1,1,1,3,3,3-HEXAFLUORO-2-{4-[1-(4- LUOROBENZENESULFONYL)CYCLOPENTYL]PHENYL}PROPAN-2-OL 提交 2019-02-07 Assembly 2 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa) 片段:LIGAND BINDING DOMAIN
链 B 130–434(305 aa) 片段:LIGAND BINDING DOMAIN
未记录 L7D 1,1,1,3,3,3-hexafluoro-2-(4-{1-[(4-fluorophenyl)sulfonyl]cyclopentyl}phenyl)propan-2-ol × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;296 K;0.1M Hepes pH 7.5, 150mM NaCl, 10-15%(V/V)PEG10K, Crystals were cryoprotected by supplementing the mother liquor with 15% (v/v) ethylene glycol and harvested by flash-cooling in liquid nitrogen
分辨率 2.27 Å R-free 0.240
6P2B Tethered PXR-LBD/SRC-1p bound to Garcinoic Acid 提交 2019-05-21 Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 169–473(305 aa)
链 B 169–473(305 aa)
未记录 NQD (2Z,6E,10E)-13-[(2R)-6-hydroxy-2,8-dimethyl-3,4-dihydro-2H-1-benzopyran-2-yl]-2,6,10-trimethyltrideca-2,6,10-trienoic acid × 2 DMS DIMETHYL SULFOXIDE × 3 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;277 K;30% MPD, 100mM Imidazole, pH 7
分辨率 2.30 Å R-free 0.227
6S41 CRYSTAL STRUCTURE OF PXR IN COMPLEX WITH XPC-7455 提交 2019-06-26 Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 138–434(297 aa) 片段:LIGAND BINDING DOMAIN
链 B 138–434(297 aa) 片段:LIGAND BINDING DOMAIN
未记录 KUB 4-[[(1~{S})-1-[2,5-bis(fluoranyl)phenyl]ethyl]amino]-5-chloranyl-2-fluoranyl-~{N}-(1,3-thiazol-4-yl)benzenesulfonamide × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, SITTING DROP;277 K
分辨率 2.70 Å R-free 0.259
6TFI PXR IN COMPLEX WITH THROMBIN INHIBITOR COMPOUND 17 提交 2019-11-14 Assembly 1 信息不足 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 129–434(306 aa)
突变:K129G GOL GLYCEROL × 2 MPD (4S)-2-METHYL-2,4-PENTANEDIOL × 1 PO4 PHOSPHATE ION × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 8;277 K;1 MICROLITER PROTEIN AT 12.1 MG/ML (IN 20 MILLIMOLAR TRIS PH 7.8, 250 MILLIMOLAR NACL, 2.5 MILLIMOLAR EDTA, 5% (V/V) GLYCEROL, 5 MM DTT), PREINCUBATED WITH 25 MILLIMOLAR COMPOUND 17 (FROM 500 MILLIMOLAR STOCK IN DMSO) for 24 hours at 277 K, MIXED WITH 1 MICROLITER OF RESERVOIR (100 MILLIMOLAR IMIDAZOLE PH 8.0, 20 % (V/V) MPD). CRYO BUFFER 100 MILLIMOLAR IMIDAZOLE PH 8.0, 30 % (V/V) MPD
分辨率 1.85 Å R-free 0.199
6TFI PXR IN COMPLEX WITH THROMBIN INHIBITOR COMPOUND 17 提交 2019-11-14 Assembly 2 信息不足 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 B 129–434(306 aa)
突变:K129G GOL GLYCEROL × 3 MPD (4S)-2-METHYL-2,4-PENTANEDIOL × 1 DMS DIMETHYL SULFOXIDE × 2 N6H [2-[(3-chlorophenyl)methylamino]-7-methoxy-1,3-benzoxazol-5-yl]-(2,2-dimethylmorpholin-4-yl)methanone × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 8;277 K;1 MICROLITER PROTEIN AT 12.1 MG/ML (IN 20 MILLIMOLAR TRIS PH 7.8, 250 MILLIMOLAR NACL, 2.5 MILLIMOLAR EDTA, 5% (V/V) GLYCEROL, 5 MM DTT), PREINCUBATED WITH 25 MILLIMOLAR COMPOUND 17 (FROM 500 MILLIMOLAR STOCK IN DMSO) for 24 hours at 277 K, MIXED WITH 1 MICROLITER OF RESERVOIR (100 MILLIMOLAR IMIDAZOLE PH 8.0, 20 % (V/V) MPD). CRYO BUFFER 100 MILLIMOLAR IMIDAZOLE PH 8.0, 30 % (V/V) MPD
分辨率 1.85 Å R-free 0.199
6XP9 STRUCTURE OF HUMAN PREGNANE X RECEPTOR LIGAND BINDING DOMAIN BOUND TETHERED WITH SRC co-activator peptide IN COMPLEX WITH (S,S)-1 提交 2020-07-08 Assembly 1 信息不足 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa) 片段:Ligand Binding Domain tethered with SRC co-activator peptide
未记录 QCG (2S)-tert-butoxy[7-(8-fluoro-5-methyl-3,4-dihydro-2H-1-benzopyran-6-yl)-5-methyl-2-phenylpyrazolo[1,5-a]pyrimidin-6-yl]acetic acid × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, SITTING DROP;296 K;0.1 M Ammonium acetate, 0.1 M Sodium HEPES pH 7.5, 18-20 % w/v PEG 4000.Crystals were cryoprotected by supplementing the mother liquor with 20% (v/v) Glycerol and harvested by flash-cooling in liquid nitrogen
分辨率 2.27 Å R-free 0.220
6XP9 STRUCTURE OF HUMAN PREGNANE X RECEPTOR LIGAND BINDING DOMAIN BOUND TETHERED WITH SRC co-activator peptide IN COMPLEX WITH (S,S)-1 提交 2020-07-08 Assembly 2 信息不足 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 B 130–434(305 aa) 片段:Ligand Binding Domain tethered with SRC co-activator peptide
未记录 QCG (2S)-tert-butoxy[7-(8-fluoro-5-methyl-3,4-dihydro-2H-1-benzopyran-6-yl)-5-methyl-2-phenylpyrazolo[1,5-a]pyrimidin-6-yl]acetic acid × 1 GOL GLYCEROL × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, SITTING DROP;296 K;0.1 M Ammonium acetate, 0.1 M Sodium HEPES pH 7.5, 18-20 % w/v PEG 4000.Crystals were cryoprotected by supplementing the mother liquor with 20% (v/v) Glycerol and harvested by flash-cooling in liquid nitrogen
分辨率 2.27 Å R-free 0.220
7AX8 Crystal structure of the hPXR-LBD in apo form (P43212 SG) 提交 2020-11-09 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 EDO 1,2-ETHANEDIOL × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.15 Å R-free 0.224
7AX8 Crystal structure of the hPXR-LBD in apo form (P43212 SG) 提交 2020-11-09 Assembly 2 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
未记录 EDO 1,2-ETHANEDIOL × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.15 Å R-free 0.224
7AX9 Crystal structure of the hPXR-LBD in complex with cis-chlordane 提交 2020-11-09 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 S6H (+)cis-chlordane × 1 IPA ISOPROPYL ALCOHOL × 3 GOL GLYCEROL × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.25 Å R-free 0.228
7AX9 Crystal structure of the hPXR-LBD in complex with cis-chlordane 提交 2020-11-09 Assembly 2 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
未记录 S6H (+)cis-chlordane × 2 IPA ISOPROPYL ALCOHOL × 6 GOL GLYCEROL × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.25 Å R-free 0.228
7AXA Crystal structure of the hPXR-LBD in complex with clotrimazole 提交 2020-11-09 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 CL6 1-[(2-CHLOROPHENYL)(DIPHENYL)METHYL]-1H-IMIDAZOLE × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.26 Å R-free 0.234
7AXA Crystal structure of the hPXR-LBD in complex with clotrimazole 提交 2020-11-09 Assembly 2 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
未记录 CL6 1-[(2-CHLOROPHENYL)(DIPHENYL)METHYL]-1H-IMIDAZOLE × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.26 Å R-free 0.234
7AXB Crystal structure of the hPXR-LBD in complex with endosulfan 提交 2020-11-09 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 MPD (4S)-2-METHYL-2,4-PENTANEDIOL × 1 S68 endosulfan × 1 GOL GLYCEROL × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.55 Å R-free 0.219
7AXB Crystal structure of the hPXR-LBD in complex with endosulfan 提交 2020-11-09 Assembly 2 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
未记录 MPD (4S)-2-METHYL-2,4-PENTANEDIOL × 2 S68 endosulfan × 2 GOL GLYCEROL × 4 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.55 Å R-free 0.219
7AXC Crystal structure of the hPXR-LBD in complex with ferutinine 提交 2020-11-09 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 27H ferutinine × 1 GOL GLYCEROL × 1 IPA ISOPROPYL ALCOHOL × 4 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.05 Å R-free 0.251
7AXD Crystal structure of the hPXR-LBD in complex with fipronil 提交 2020-11-09 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 S6W fipronil × 1 IPA ISOPROPYL ALCOHOL × 5 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.65 Å R-free 0.237
7AXE Crystal structure of the hPXR-LBD in complex with oxadiazon 提交 2020-11-09 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 GOL GLYCEROL × 1 S6Z oxadiazon × 1 IPA ISOPROPYL ALCOHOL × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 1.90 Å R-free 0.230
7AXE Crystal structure of the hPXR-LBD in complex with oxadiazon 提交 2020-11-09 Assembly 2 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
未记录 GOL GLYCEROL × 2 S6Z oxadiazon × 2 IPA ISOPROPYL ALCOHOL × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 1.90 Å R-free 0.230
7AXF Crystal structure of the hPXR-LBD in complex with pretilachlor 提交 2020-11-09 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 S6T pretilachlor × 2 IPA ISOPROPYL ALCOHOL × 5 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.45 Å R-free 0.246
7AXF Crystal structure of the hPXR-LBD in complex with pretilachlor 提交 2020-11-09 Assembly 2 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
未记录 S6T pretilachlor × 4 IPA ISOPROPYL ALCOHOL × 10 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.45 Å R-free 0.246
7AXG Crystal structure of the hPXR-LBD in complex with tributyltin 提交 2020-11-09 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 TBY tributylstannanyl × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.70 Å R-free 0.238
7AXG Crystal structure of the hPXR-LBD in complex with tributyltin 提交 2020-11-09 Assembly 2 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
未记录 TBY tributylstannanyl × 4 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.70 Å R-free 0.238
7AXH Crystal structure of the hPXR-LBD in complex with alpha-zearalanol 提交 2020-11-09 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 IPA ISOPROPYL ALCOHOL × 2 MPD (4S)-2-METHYL-2,4-PENTANEDIOL × 1 27J alpha-zearalanol × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.55 Å R-free 0.214
7AXH Crystal structure of the hPXR-LBD in complex with alpha-zearalanol 提交 2020-11-09 Assembly 2 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
未记录 IPA ISOPROPYL ALCOHOL × 4 MPD (4S)-2-METHYL-2,4-PENTANEDIOL × 2 27J alpha-zearalanol × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.55 Å R-free 0.214
7AXI Crystal structure of the hPXR-LBD in complex with estradiol and cis-chlordane 提交 2020-11-09 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 EST ESTRADIOL × 1 MPD (4S)-2-METHYL-2,4-PENTANEDIOL × 1 S6E (-)cis-chlordane × 1 S6H (+)cis-chlordane × 1 IPA ISOPROPYL ALCOHOL × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.15 Å R-free 0.203
7AXI Crystal structure of the hPXR-LBD in complex with estradiol and cis-chlordane 提交 2020-11-09 Assembly 2 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
未记录 EST ESTRADIOL × 2 MPD (4S)-2-METHYL-2,4-PENTANEDIOL × 2 S6E (-)cis-chlordane × 2 S6H (+)cis-chlordane × 2 IPA ISOPROPYL ALCOHOL × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.15 Å R-free 0.203
7AXJ Crystal structure of the hPXR-LBD in complex with estradiol and clotrimazole 提交 2020-11-09 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 CL6 1-[(2-CHLOROPHENYL)(DIPHENYL)METHYL]-1H-IMIDAZOLE × 1 EST ESTRADIOL × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.30 Å R-free 0.222
7AXJ Crystal structure of the hPXR-LBD in complex with estradiol and clotrimazole 提交 2020-11-09 Assembly 2 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
未记录 CL6 1-[(2-CHLOROPHENYL)(DIPHENYL)METHYL]-1H-IMIDAZOLE × 2 EST ESTRADIOL × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.30 Å R-free 0.222
7AXK Crystal structure of the hPXR-LBD in complex with estradiol and endosulfan 提交 2020-11-09 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 EST ESTRADIOL × 1 MPD (4S)-2-METHYL-2,4-PENTANEDIOL × 1 S68 endosulfan × 1 GOL GLYCEROL × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.00 Å R-free 0.212
7AXK Crystal structure of the hPXR-LBD in complex with estradiol and endosulfan 提交 2020-11-09 Assembly 2 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
未记录 EST ESTRADIOL × 2 MPD (4S)-2-METHYL-2,4-PENTANEDIOL × 2 S68 endosulfan × 2 GOL GLYCEROL × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.00 Å R-free 0.212
7AXL Crystal structure of the hPXR-LBD in complex with estradiol and heptachlor endo-epoxide 提交 2020-11-09 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 EST ESTRADIOL × 1 S65 heptachlor endo-epoxide × 1 MPD (4S)-2-METHYL-2,4-PENTANEDIOL × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.50 Å R-free 0.232
7AXL Crystal structure of the hPXR-LBD in complex with estradiol and heptachlor endo-epoxide 提交 2020-11-09 Assembly 2 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
未记录 EST ESTRADIOL × 2 S65 heptachlor endo-epoxide × 2 MPD (4S)-2-METHYL-2,4-PENTANEDIOL × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.50 Å R-free 0.232
7N2A human PXR LBD bound to compound 2 提交 2021-05-28 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 160–457(298 aa) 片段:ligand binding domain
未记录 07F 5-benzyl-2-(3-fluoro-2-hydroxyphenyl)-6-methyl-3-(2-phenylethyl)pyrimidin-4(3H)-one × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.2;277 K;50mM Imidazole pH7.2, 12% 2-propanol
分辨率 2.26 Å R-free 0.255
7RIO human PXR LBD bound to GSK003 提交 2021-07-20 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 160–457(298 aa) 片段:ligand binding domain
未记录 5YX N-[3-(2-tert-butyl-5-{2-[2-(methanesulfonyl)ethyl]pyrimidin-4-yl}-1,3-thiazol-4-yl)-2-fluorophenyl]-2,5-difluorobenzene-1-sulfonamide × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.2;277 K;50mM Imidazole pH7.2, 12% 2-propanol
分辨率 2.48 Å R-free 0.273
7RIU human PXR LBD bound to GSK002 提交 2021-07-20 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 160–457(298 aa) 片段:ligand binding domain
未记录 5YU N-{3-[5-(2-aminopyrimidin-4-yl)-2-tert-butyl-1,3-thiazol-4-yl]-2-fluorophenyl}thiophene-3-sulfonamide × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.2;277 K;50mM Imidazole pH7.2, 12% 2-propanol
分辨率 2.05 Å R-free 0.241
7RIV human PXR LBD bound to GSK001 提交 2021-07-20 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 160–457(298 aa) 片段:ligand binding domain
未记录 P06 Dabrafenib × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.2;277 K;50mM Imidazole pH7.2, 12% 2-propanol
分辨率 2.20 Å R-free 0.238
7YFK The structure of human pregnane X receptor in complex with an SRC-1 coactivator peptide and a limonoid compound, nomilin 提交 2022-07-08 Assembly 1 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
未记录 G3L Nomilin × 2 X-RAY DIFFRACTION
X-ray结晶条件 EVAPORATION;pH 8;277.15 K;10% (v/v) 2-propanol, 100 mM Imidazole/ Hydrochloric acid, pH 8.0
分辨率 2.10 Å
8CCT Crystal structure of the human PXR ligand-binding domain in complex with 2,2'-dichloro bisphenol A 提交 2023-01-27 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 UAI 2-chloranyl-4-[2-(3-chloranyl-4-oxidanyl-phenyl)propan-2-yl]phenol × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50-100 mM IMIDAZOLE 8-14% ISOPROPANOL
分辨率 2.90 Å R-free 0.261
8CF9 Crystal structure of the human PXR ligand-binding domain in complex with sclareol 提交 2023-02-03 Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
未记录 UK6 sclareol × 2 GOL GLYCEROL × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION;291 K;50-100 mM IMIDAZOLE, 8-14% ISOPROPANOL
分辨率 2.00 Å R-free 0.247
8CH8 Crystal structure of the human PXR ligand-binding domain in complex with liranaftate 提交 2023-02-07 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 ULC ~{O}-(5,6,7,8-tetrahydronaphthalen-2-yl) ~{N}-(6-methoxypyridin-2-yl)-~{N}-methyl-carbamothioate × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION;291 K;50-100 mM IMIDAZOLE, 8-14% ISOPROPANOL
分辨率 2.15 Å R-free 0.228
8E3N Crystal structure of pregnane X receptor ligand binding domain complexed with rifamycin S 提交 2022-08-17 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 153–457(305 aa) 片段:UNP residues 153-457
未记录 VA0 Rifamycin S × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.2;293 K;100 mM imidazole (pH 7.2), 14% isopropanol
分辨率 2.25 Å R-free 0.235
8EQZ Crystal structure of pregnane X receptor ligand binding domain complexed with T0901317 analog T0-C6 提交 2022-10-11 Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
未记录 WQB N-[4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]-N-hexylbenzenesulfonamide × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 5.8;293 K;100 mM Bis-Tris (pH 5.8), 9% MPD
分辨率 2.37 Å R-free 0.228
8F5Y Crystal structure of pregnane X receptor ligand binding domain complexed with JQ1 提交 2022-11-15 Assembly 1 蛋白异源复合物 异源复合物;蛋白 × 4 PDB 声明:tetrameric(4) 与蛋白数一致
链 A 153–457(305 aa) 片段:UNP residues 153-457
链 B 153–457(305 aa) 片段:UNP residues 153-457
未记录 JQ1 (6S)-6-(2-tert-butoxy-2-oxoethyl)-4-(4-chlorophenyl)-2,3,9-trimethyl-6,7-dihydrothieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-10-ium × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7;293 K;50 mM imidazole pH 7.0, 8% isopropanol
分辨率 2.15 Å R-free 0.215
8FPE Crystal structure of pregnane X receptor ligand binding domain complexed with T0901317 analog T0-BP 提交 2023-01-04 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 153–457(305 aa) 片段:UNP residues 153-457
未记录 Y5B N-[([1,1'-biphenyl]-4-yl)methyl]-N-[4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]benzenesulfonamide × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7;293 K;50 mM imidazole pH 7, 12% isopropanol
分辨率 2.30 Å R-free 0.239
8R00 Crystal structure of the human PXR ligand-binding domain in complex with furanodienone 提交 2023-10-30 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 XFQ furanodienone × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;291 K;50-100 mM IMIDAZOLE, 8-14% ISOPROPANOL
分辨率 1.95 Å R-free 0.215
8R81 Crystal structure of the hPXR-LBD in complex with compound JMV6845 提交 2023-11-27 Assembly 1 蛋白同源多聚体 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
未记录 IPA ISOPROPYL ALCOHOL × 2 Y8B 2,4,6-trimethyl-~{N}-[1-(phenylmethyl)benzimidazol-5-yl]benzenesulfonamide × 2 GOL GLYCEROL × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;293 K;50-100 mM Imidazole 8-16% Isopropanol
分辨率 2.45 Å R-free 0.221
8R82 Crystal structure of the hPXR-LBD in complex with compound JMV6944 提交 2023-11-27 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
非标准单体:是(mmCIF未提供具体位点) IPA ISOPROPYL ALCOHOL × 1 GOL GLYCEROL × 3 EDO 1,2-ETHANEDIOL × 2 Y7Q ~{N}-[2-(7-azanylheptyl)-1-(phenylmethyl)benzimidazol-5-yl]-2,4,6-trimethyl-benzenesulfonamide × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.4;293 K;75 mM Imidazole 13% Isopropanol
分辨率 2.10 Å R-free 0.236
8SVN Crystal structure of the apo form of pregnane X receptor ligand binding domain 提交 2023-05-17 Assembly 1 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
未记录 未记录非水小分子 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7;277 K;in 0.1 M HEPES pH 7.0, and 14% Isopropanol
分辨率 2.20 Å R-free 0.235
8SVO Crystal structure of pregnane X receptor ligand binding domain in complex with SJPYT-310 提交 2023-05-17 Assembly 1 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
未记录 WSO (1P)-N-(5-tert-butyl-2-{[(2S)-pentan-2-yl]oxy}phenyl)-1-(2-methoxy-5-methylphenyl)-5-methyl-1H-1,2,3-triazole-4-carboxamide × 2 DMS DIMETHYL SULFOXIDE × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;293 K;50 mM Bis-Tris pH 6.0-7.0, 9-16% (v/v) 2-Methyl-2,4-pentanediol
分辨率 2.35 Å R-free 0.238
8SVP Crystal structure of pregnane X receptor ligand binding domain in complex with SJPYT-278 提交 2023-05-17 Assembly 1 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
未记录 WSX (1P)-N-(5-tert-butyl-2-{[(3S)-hexan-3-yl]oxy}phenyl)-1-(2,5-dimethoxyphenyl)-5-methyl-1H-1,2,3-triazole-4-carboxamide × 2 YGO (1P)-N-(5-tert-butyl-2-{[(3R)-hexan-3-yl]oxy}phenyl)-1-(2,5-dimethoxyphenyl)-5-methyl-1H-1,2,3-triazole-4-carboxamide × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;293 K;50 mM Bis-Tris pH 6.0-7.0, 9-16% (v/v) 2-Methyl-2,4-pentanediol
分辨率 3.32 Å R-free 0.252
8SVQ Crystal structure of pregnane X receptor ligand binding domain in complex with SJPYT-312 提交 2023-05-17 Assembly 1 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
未记录 WSX (1P)-N-(5-tert-butyl-2-{[(3S)-hexan-3-yl]oxy}phenyl)-1-(2,5-dimethoxyphenyl)-5-methyl-1H-1,2,3-triazole-4-carboxamide × 2 DMS DIMETHYL SULFOXIDE × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;293 K;50 mM Bis-Tris pH 6.0-7.0, 9-16% (v/v) 2-Methyl-2,4-pentanediol
分辨率 2.75 Å R-free 0.262
8SVR Crystal structure of pregnane X receptor ligand binding domain in complex with SJPYT-326 提交 2023-05-17 Assembly 1 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
未记录 DMS DIMETHYL SULFOXIDE × 1 WT1 (1P)-N-(5-tert-butyl-2-{[(3S)-hexan-3-yl]oxy}phenyl)-5-methyl-1-(2,4,5-trimethoxyphenyl)-1H-1,2,3-triazole-4-carboxamide × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;293 K;50 mM Bis-Tris pH 6.0-7.0, 9-16% (v/v) 2-Methyl-2,4-pentanediol
分辨率 2.92 Å R-free 0.258
8SVS Crystal structure of pregnane X receptor ligand binding domain in complex with SJPYT-328 提交 2023-05-17 Assembly 1 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
未记录 WU2 (1P)-N-(5-tert-butyl-2-{[(3S)-hexan-3-yl]oxy}phenyl)-1-(2,4-dimethoxy-5-methylphenyl)-5-methyl-1H-1,2,3-triazole-4-carboxamide × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;293 K;50 mM Bis-Tris pH 6.0-7.0, 9-16% (v/v) 2-Methyl-2,4-pentanediol
分辨率 2.68 Å R-free 0.250
8SVT Crystal structure of pregnane X receptor ligand binding domain in complex with SJPYT-331 提交 2023-05-17 Assembly 1 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
未记录 WU6 methyl 3-{[(1P)-1-(2,5-dimethoxyphenyl)-5-methyl-1H-1,2,3-triazole-4-carbonyl]amino}-4-{[(3S)-hexan-3-yl]oxy}benzoate × 2 DMS DIMETHYL SULFOXIDE × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;293 K;50 mM Bis-Tris pH 6.0-7.0, 9-16% (v/v) 2-Methyl-2,4-pentanediol
分辨率 2.39 Å R-free 0.237
8SVU Crystal structure of the L428V mutant of pregnane X receptor ligand binding domain in apo form 提交 2023-05-17 Assembly 1 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
突变:L428V 突变:L428V GOL GLYCEROL × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;293 K;50 mM Bis-Tris pH 6.0-7.0, 9-16% (v/v) 2-Methyl-2,4-pentanediol
分辨率 2.89 Å R-free 0.244
8SVX Crystal structure of the L428V mutant of pregnane X receptor ligand binding domain in complex with SJPYT-331 提交 2023-05-17 Assembly 1 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
突变:L428V 突变:L428V WU6 methyl 3-{[(1P)-1-(2,5-dimethoxyphenyl)-5-methyl-1H-1,2,3-triazole-4-carbonyl]amino}-4-{[(3S)-hexan-3-yl]oxy}benzoate × 2 DMS DIMETHYL SULFOXIDE × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;293 K;50 mM Bis-Tris pH 6.0-7.0, 9-16% (v/v) 2-Methyl-2,4-pentanediol
分辨率 2.14 Å R-free 0.235
8SZV Crystal structure of pregnane X receptor ligand binding domain complexed with T0901317 analog SJPYT-318 提交 2023-05-30 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 153–457(305 aa) 片段:UNP residues 153-457
未记录 X1D N-[4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]-N-[(4-phenoxyphenyl)methyl]benzenesulfonamide × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 6.8;293 K;50 mM imidazole (pH 6.8), 10% isopropanol
分辨率 2.20 Å R-free 0.223
9BEQ Crystal structure of pregnane X receptor ligand binding domain complexed with AP1867 提交 2024-04-16 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 153–457(305 aa) 片段:UNP residues 153-457
未记录 AP1 {3-[3-(3,4-DIMETHOXY-PHENYL)-1-(1-{1-[2-(3,4,5-TRIMETHOXY-PHENYL)-BUTYRYL]-PIPERIDIN-2YL}-VINYLOXY)-PROPYL]-PHENOXY}-ACETIC ACID × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;pH 7.8;293 K;50 mM imidazole pH 7.8, 12% isopropanol
分辨率 2.60 Å R-free 0.246
9FZG Crystal structure of the hPXR-LBD in complex with compound JMV7035 提交 2024-07-05 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 A1IHA 2-(1-adamantyl)-~{N}-[2-[2-[2-oxidanylidene-2-[7-[1-(phenylmethyl)-5-[(2,4,6-trimethylphenyl)sulfonylamino]benzimidazol-2-yl]heptylamino]ethoxy]ethoxy]ethyl]ethanamide × 1 GOL GLYCEROL × 2 IPA ISOPROPYL ALCOHOL × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION;293 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.00 Å R-free 0.237
9FZH Crystal structure of the hPXR-LBD in complex with compound JMV6995 提交 2024-07-05 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 A1IHB 2-(1-adamantyl)-~{N}-[7-[1-(phenylmethyl)-5-[(2,4,6-trimethylphenyl)sulfonylamino]benzimidazol-2-yl]heptyl]ethanamide × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION;291 K;50 - 100 mM imidazole 8 - 14% isopropanol
分辨率 2.50 Å R-free 0.257
9FZI A new crystal structure of the hPXR-LBD in fusion with an SRC1 co-activator peptide and in complex with SR12813 (P212121 form) 提交 2024-07-05 Assembly 1 信息不足 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 SRL [2-(3,5-DI-TERT-BUTYL-4-HYDROXY-PHENYL)-1-(DIETHOXY-PHOSPHORYL)-VINYL]-PHOSPHONIC ACID DIETHLYL ESTER × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION;277 K;100 mM Imidazole 25 - 30% MPD
分辨率 2.70 Å R-free 0.237
9FZI A new crystal structure of the hPXR-LBD in fusion with an SRC1 co-activator peptide and in complex with SR12813 (P212121 form) 提交 2024-07-05 Assembly 2 信息不足 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 B 130–434(305 aa)
未记录 SRL [2-(3,5-DI-TERT-BUTYL-4-HYDROXY-PHENYL)-1-(DIETHOXY-PHOSPHORYL)-VINYL]-PHOSPHONIC ACID DIETHLYL ESTER × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION;277 K;100 mM Imidazole 25 - 30% MPD
分辨率 2.70 Å R-free 0.237
9FZJ A new crystal structure of the hPXR-LBD in complex with SR12813 (P43212 form) 提交 2024-07-05 Assembly 1 蛋白单体 单体;蛋白 × 1 PDB 声明:monomeric(1) 与蛋白数一致
链 A 130–434(305 aa)
未记录 EDO 1,2-ETHANEDIOL × 2 GOL GLYCEROL × 1 IPA ISOPROPYL ALCOHOL × 1 SRL [2-(3,5-DI-TERT-BUTYL-4-HYDROXY-PHENYL)-1-(DIETHOXY-PHOSPHORYL)-VINYL]-PHOSPHONIC ACID DIETHLYL ESTER × 1 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION;291 K;50 - 100 mM imidazole / 8 - 14% isopropanol
分辨率 1.60 Å R-free 0.209
9O41 Crystal structure of the L411A mutant of pregnane X receptor ligand binding domain (apo form) 提交 2025-04-08 Assembly 1 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
突变:L411A 突变:L411A 未记录非水小分子 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;293 K;50 mM Bis-Tris (pH 6-7), 9-16% (v/v) 2-methyl-2,4-pentanediol
分辨率 2.05 Å R-free 0.222
9O42 Crystal structure of the L411A mutant of pregnane X receptor ligand binding domain in complex with SJPYT-328 提交 2025-04-08 Assembly 1 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
突变:L411A 突变:L411A WU2 (1P)-N-(5-tert-butyl-2-{[(3S)-hexan-3-yl]oxy}phenyl)-1-(2,4-dimethoxy-5-methylphenyl)-5-methyl-1H-1,2,3-triazole-4-carboxamide × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;293 K;50 mM Bis-Tris (pH 6-7), 9-16% (v/v) 2-methyl-2,4-pentanediol
分辨率 2.51 Å R-free 0.219
9O43 Crystal structure of the L411A mutant of pregnane X receptor ligand binding domain in complex with SJPYT-331 提交 2025-04-08 Assembly 1 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
突变:L411A 突变:L411A WU6 methyl 3-{[(1P)-1-(2,5-dimethoxyphenyl)-5-methyl-1H-1,2,3-triazole-4-carbonyl]amino}-4-{[(3S)-hexan-3-yl]oxy}benzoate × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;293 K;50 mM Bis-Tris (pH 6-7), 9-16% (v/v) 2-methyl-2,4-pentanediol
分辨率 2.76 Å R-free 0.239
9O44 Crystal structure of the L411W mutant of pregnane X receptor ligand binding domain (apo form) 提交 2025-04-08 Assembly 1 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
突变:L411W 突变:L411W 未记录非水小分子 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;293 K;50 mM Bis-Tris (pH 6-7), 9-16% (v/v) 2-methyl-2,4-pentanediol
分辨率 2.30 Å R-free 0.228
9O45 Crystal structure of the L411W mutant of pregnane X receptor ligand binding domain in complex with SJPYT-328 提交 2025-04-08 Assembly 1 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
突变:L411W 突变:L411W WU2 (1P)-N-(5-tert-butyl-2-{[(3S)-hexan-3-yl]oxy}phenyl)-1-(2,4-dimethoxy-5-methylphenyl)-5-methyl-1H-1,2,3-triazole-4-carboxamide × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;293 K;50 mM Bis-Tris (pH 6-7), 9-16% (v/v) 2-methyl-2,4-pentanediol
分辨率 2.56 Å R-free 0.241
9O46 Crystal structure of the L411W mutant of pregnane X receptor ligand binding domain in complex with SJPYT-331 提交 2025-04-08 Assembly 1 信息不足 同源多聚体;蛋白 × 2 PDB 声明:dimeric(2) 与蛋白数一致
链 A 130–434(305 aa)
链 B 130–434(305 aa)
突变:L411W 突变:L411W WU6 methyl 3-{[(1P)-1-(2,5-dimethoxyphenyl)-5-methyl-1H-1,2,3-triazole-4-carbonyl]amino}-4-{[(3S)-hexan-3-yl]oxy}benzoate × 2 X-RAY DIFFRACTION
X-ray结晶条件 VAPOR DIFFUSION, HANGING DROP;293 K;50 mM Bis-Tris (pH 6-7), 9-16% (v/v) 2-methyl-2,4-pentanediol
分辨率 3.02 Å R-free 0.232