|
1RY7
Crystal Structure of the 3 Ig form of FGFR3c in complex with FGF1
提交 2003-12-19
|
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 B
33–365(333 aa)
片段:FGFR-3c
|
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 7.5;293 K;Peg 4000, glycerol, MPD, cadmium chloride, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 293K
|
分辨率 3.20 Å
R-free 0.341
|
|
2LZL
FGFR3tm
提交 2012-10-04
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验方法不同
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 × 2
PDB 声明:dimeric
|
链 A
357–399(43 aa)
片段:UNP residues 357-399
链 B
357–399(43 aa)
片段:UNP residues 357-399
|
未记录
|
未记录非水小分子
|
SOLUTION NMR
NMR测量条件
pH 5.7;313 K;离子强度(mmCIF原始值)50;压力 ambient
NMR样品组成
0.75 mM [U-99% 13C; U-99% 15N] FGFR3tm, 0.75 mM FGFR3tm, 88 mM [U-99% 2H] DPC, 10 mM [U-99% 2H] SDS, 0.3 mM sodium azide, 6 mM TCEP, 5 mM citric acid, 15 mM Na2HPO4, 95% H2O/5% D2O | 95% H2O/5% D2O
|
分辨率未提供
|
|
4K33
Crystal Structure of FGF Receptor 3 (FGFR3) Kinase Domain Harboring the K650E Mutation, a Gain-of-Function Mutation Responsible for Thanatophoric Dysplasia Type II and Spermatocytic Seminoma
提交 2013-04-10
|
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
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 A
449–759(311 aa)
片段:Human FGF Receptor 3 Kinase Domain
|
突变:C482A, C582S, K650E
|
ACP PHOSPHOMETHYLPHOSPHONIC ACID ADENYLATE ESTER × 1
MG MAGNESIUM ION × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.5;298 K;100mM HEPES pH7.5, 19% PEG 4000, 4% C4H10O2, VAPOR DIFFUSION, HANGING DROP, temperature 298K
|
分辨率 2.34 Å
R-free 0.228
|
|
6LVM
Crystal structure of FGFR3 in complex with pyrimidine derivative
提交 2020-02-04
|
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
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 A
472–759(288 aa)
|
非标准单体:是(mmCIF未提供具体位点)
|
EVR 2-[[5-[2-(3,5-dimethoxyphenyl)ethyl]-2-[[3-methoxy-4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]phenyl]amino]pyrimidin-4-yl]amino]-N-ethyl-benzenesulfonamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 5;296 K;Citric Acid, PEG 8000
|
分辨率 2.53 Å
R-free 0.279
|
|
6PNX
Crystal Structure of an Asymmetric Dimer of FGF Receptor 3 Kinases Trapped in A-loop Tyrosine Transphosphorylation Reaction
提交 2019-07-03
|
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 × 2
PDB 声明:dimeric
|
链 A
451–759(309 aa)
链 B
451–759(309 aa)
|
突变:C482A, C582S, R669E
突变:C482A, C582S, R669E
|
ACP PHOSPHOMETHYLPHOSPHONIC ACID ADENYLATE ESTER × 2
SO4 SULFATE ION × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;292 K;0.1 M Hepes, pH 7.5, and 1.8 M (NH4)2SO4
|
分辨率 2.20 Å
R-free 0.230
|
|
7DHL
Crystal structure of FGFR3 in complex with pyrimidine derivative
提交 2020-11-16
|
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
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 A
472–759(288 aa)
|
非标准单体:是(mmCIF未提供具体位点)
|
H6X 5-[2-(3,5-dimethoxyphenyl)ethyl]-N-[3-methoxy-4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]phenyl]pyrimidin-2-amine × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 5;293 K;Citric Acid, Ammonium dihydrogen phosphate, PEG 3350
|
分辨率 2.57 Å
R-free 0.254
|
|
7YSU
Cryo-EM Structure of FGF23-FGFR3c-aKlotho-HS Quaternary Complex
提交 2022-08-13
|
构建体不同
突变/修饰不同
聚集状态不同
配体/离子不同
实验方法不同
实验环境不同
结构质量不同
|
Assembly 1
其他组合
异源复合物;蛋白 × 4
PDB 声明:tetrameric
|
链 C
148–358(211 aa)
链 E
148–358(211 aa)
|
未记录
|
ZN ZINC ION × 1
CU COPPER (II) ION × 1
|
ELECTRON MICROSCOPY
cryo-EM缓冲液
pH 7.5
cryo-EM玻璃化条件
冷冻剂 ETHANE
|
分辨率 3.20 Å
|
|
8UDT
The X-RAY co-crystal structure of human FGFR3 and KIN-3248
提交 2023-09-29
|
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
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 A
455–756(302 aa)
片段:kinase domain
|
突变:residues 572-585 replaced by Ser-Gly
|
MLT D-MALATE × 2
WGF 3-[(1-cyclopropyl-4,6-difluoro-1H-benzimidazol-5-yl)ethynyl]-1-[(3R,5R)-5-(methoxymethyl)-1-propanoylpyrrolidin-3-yl]-5-(methylamino)-1H-pyrazole-4-carboxamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;0.20 M DL-Malic acid pH 5.00,
18.00 % (w/v) PEG 4000
|
分辨率 2.83 Å
R-free 0.274
|
|
8UDT
The X-RAY co-crystal structure of human FGFR3 and KIN-3248
提交 2023-09-29
|
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 2
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 B
455–756(302 aa)
片段:kinase domain
|
突变:residues 572-585 replaced by Ser-Gly
|
WGF 3-[(1-cyclopropyl-4,6-difluoro-1H-benzimidazol-5-yl)ethynyl]-1-[(3R,5R)-5-(methoxymethyl)-1-propanoylpyrrolidin-3-yl]-5-(methylamino)-1H-pyrazole-4-carboxamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;0.20 M DL-Malic acid pH 5.00,
18.00 % (w/v) PEG 4000
|
分辨率 2.83 Å
R-free 0.274
|
|
8UDT
The X-RAY co-crystal structure of human FGFR3 and KIN-3248
提交 2023-09-29
|
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 3
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 C
455–756(302 aa)
片段:kinase domain
|
突变:residues 572-585 replaced by Ser-Gly
|
WGF 3-[(1-cyclopropyl-4,6-difluoro-1H-benzimidazol-5-yl)ethynyl]-1-[(3R,5R)-5-(methoxymethyl)-1-propanoylpyrrolidin-3-yl]-5-(methylamino)-1H-pyrazole-4-carboxamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;0.20 M DL-Malic acid pH 5.00,
18.00 % (w/v) PEG 4000
|
分辨率 2.83 Å
R-free 0.274
|
|
8UDU
The X-RAY co-crystal structure of human FGFR3 and Compound 17
提交 2023-09-29
|
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
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 A
455–756(302 aa)
片段:kinase domain
|
突变:residues 572-585 replaced by Ser-Gly
|
CL CHLORIDE ION × 1
WIQ 3-[(6-chloro-1-cyclopropyl-1H-benzimidazol-5-yl)ethynyl]-1-[(3S,5S)-5-(methoxymethyl)-1-(prop-2-enoyl)pyrrolidin-3-yl]-5-(methylamino)-1H-pyrazole-4-carboxamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;0.10 M Magnesium Chloride,
0.10 M TRIS/HCl pH 8.10,
0.20 M Sodium Chloride,
20.00 % (w/v) PEG 3350
|
分辨率 1.74 Å
R-free 0.256
|
|
8UDU
The X-RAY co-crystal structure of human FGFR3 and Compound 17
提交 2023-09-29
|
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 2
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 B
455–756(302 aa)
片段:kinase domain
|
突变:residues 572-585 replaced by Ser-Gly
|
CL CHLORIDE ION × 1
WIQ 3-[(6-chloro-1-cyclopropyl-1H-benzimidazol-5-yl)ethynyl]-1-[(3S,5S)-5-(methoxymethyl)-1-(prop-2-enoyl)pyrrolidin-3-yl]-5-(methylamino)-1H-pyrazole-4-carboxamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;0.10 M Magnesium Chloride,
0.10 M TRIS/HCl pH 8.10,
0.20 M Sodium Chloride,
20.00 % (w/v) PEG 3350
|
分辨率 1.74 Å
R-free 0.256
|
|
8UDV
The X-RAY co-crystal structure of human FGFR3 V555M and Compound 17
提交 2023-09-29
|
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
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 A
455–756(302 aa)
片段:kinase domain
|
突变:V555M and residues 572-585 (Uniprot numbering) replaced by Ser-Gly
|
SO4 SULFATE ION × 3
WIQ 3-[(6-chloro-1-cyclopropyl-1H-benzimidazol-5-yl)ethynyl]-1-[(3S,5S)-5-(methoxymethyl)-1-(prop-2-enoyl)pyrrolidin-3-yl]-5-(methylamino)-1H-pyrazole-4-carboxamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;0.10 M BIS-TRIS/HCl pH 6.50,
0.20 M (NH4)2SO4,
25.00 % (w/v) PEG 3350
|
分辨率 2.35 Å
R-free 0.261
|
|
8UDV
The X-RAY co-crystal structure of human FGFR3 V555M and Compound 17
提交 2023-09-29
|
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 2
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 B
455–756(302 aa)
片段:kinase domain
|
突变:V555M and residues 572-585 (Uniprot numbering) replaced by Ser-Gly
|
SO4 SULFATE ION × 2
WIQ 3-[(6-chloro-1-cyclopropyl-1H-benzimidazol-5-yl)ethynyl]-1-[(3S,5S)-5-(methoxymethyl)-1-(prop-2-enoyl)pyrrolidin-3-yl]-5-(methylamino)-1H-pyrazole-4-carboxamide × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;0.10 M BIS-TRIS/HCl pH 6.50,
0.20 M (NH4)2SO4,
25.00 % (w/v) PEG 3350
|
分辨率 2.35 Å
R-free 0.261
|
|
8UDV
The X-RAY co-crystal structure of human FGFR3 V555M and Compound 17
提交 2023-09-29
|
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 3
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 C
455–756(302 aa)
片段:kinase domain
|
突变:V555M and residues 572-585 (Uniprot numbering) replaced by Ser-Gly
|
SO4 SULFATE ION × 2
WIQ 3-[(6-chloro-1-cyclopropyl-1H-benzimidazol-5-yl)ethynyl]-1-[(3S,5S)-5-(methoxymethyl)-1-(prop-2-enoyl)pyrrolidin-3-yl]-5-(methylamino)-1H-pyrazole-4-carboxamide × 1
EDO 1,2-ETHANEDIOL × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;293 K;0.10 M BIS-TRIS/HCl pH 6.50,
0.20 M (NH4)2SO4,
25.00 % (w/v) PEG 3350
|
分辨率 2.35 Å
R-free 0.261
|
|
9CD7
FGFR3 Kinase Domain with Inhibitor TYRA-300
提交 2024-06-24
|
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
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 A
448–759(312 aa)
|
突变:C482A, C582S, K650E
|
A1AV2 (3P)-5-[(1R)-1-(3,5-dichloropyridin-4-yl)ethoxy]-3-{6-[6-(methanesulfonyl)-2,6-diazaspiro[3.3]heptan-2-yl]pyridin-3-yl}-1H-indazole × 1
GOL GLYCEROL × 4
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 5.25;291 K;17% PEG Smear Medium
10% Tacsimate pH 5.25
0.2M Ammonium Sulfate
|
分辨率 2.53 Å
R-free 0.267
|
|
9CD7
FGFR3 Kinase Domain with Inhibitor TYRA-300
提交 2024-06-24
|
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 2
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 B
448–759(312 aa)
|
突变:C482A, C582S, K650E
|
A1AV2 (3P)-5-[(1R)-1-(3,5-dichloropyridin-4-yl)ethoxy]-3-{6-[6-(methanesulfonyl)-2,6-diazaspiro[3.3]heptan-2-yl]pyridin-3-yl}-1H-indazole × 1
GOL GLYCEROL × 6
SO4 SULFATE ION × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 5.25;291 K;17% PEG Smear Medium
10% Tacsimate pH 5.25
0.2M Ammonium Sulfate
|
分辨率 2.53 Å
R-free 0.267
|
|
9CD7
FGFR3 Kinase Domain with Inhibitor TYRA-300
提交 2024-06-24
|
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 3
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 C
448–759(312 aa)
|
突变:C482A, C582S, K650E
|
A1AV2 (3P)-5-[(1R)-1-(3,5-dichloropyridin-4-yl)ethoxy]-3-{6-[6-(methanesulfonyl)-2,6-diazaspiro[3.3]heptan-2-yl]pyridin-3-yl}-1H-indazole × 1
GOL GLYCEROL × 6
SO4 SULFATE ION × 2
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 5.25;291 K;17% PEG Smear Medium
10% Tacsimate pH 5.25
0.2M Ammonium Sulfate
|
分辨率 2.53 Å
R-free 0.267
|
|
9D1X
Crystal structure of FGFR3 bound to indazole inhibitor
提交 2024-08-08
|
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
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 A
455–756(302 aa)
片段:kinase domain
|
突变:P572S, P573G
|
A1A6M (3P)-N-(2,6-dimethylphenyl)-6-methoxy-3-(1-methyl-1H-pyrazol-4-yl)-1H-indazole-5-carboxamide × 1
CL CHLORIDE ION × 1
MG MAGNESIUM ION × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, SITTING DROP;pH 8.1;293 K;0.2 M magnesium chloride, 0.3 M sodium chloride, 23% (w/v) PEG 3350, 0.1 M Tris-HCl pH 8.1
|
分辨率 1.60 Å
R-free 0.190
|
|
9EKO
A chimeric hybrid protein fused with the FGFR3 Transmembrane Domain
提交 2024-12-03
|
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
信息不足
同源多聚体;蛋白 × 2
PDB 声明:dimeric
|
链 A
371–399(29 aa)
|
未记录
|
未记录非水小分子
|
X-RAY DIFFRACTION
mmCIF 未提供已读取条件
|
分辨率 2.90 Å
R-free 0.287
|
|
9KFU
Human FGFR3 in complex with inhibitor F1
提交 2024-11-07
|
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
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 A
448–756(309 aa)
|
未记录
|
A1L5T (7~{S})-2-azanyl-7-(4-fluorophenyl)-6,7-dihydro-4~{H}-[1,3]thiazolo[4,5-b]pyridin-5-one × 1
SO4 SULFATE ION × 4
CO COBALT (II) ION × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.5;293.15 K;25mM HEPES pH7.5, 1.8-2.0 M LiSO4, 10 Mm CoCl2
|
分辨率 1.40 Å
R-free 0.251
|
|
9VMB
The X-RAY co-crystal structure of human FGFR3 and Compound 10t
提交 2025-06-27
|
配体/离子不同
结构质量不同
|
Assembly 1
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 A
455–756(302 aa)
|
未记录
|
A1ESX ~{N}-[1-methyl-3-[2-[[3-methyl-1-(2-morpholin-4-ylethyl)pyrazol-4-yl]amino]pyrimidin-4-yl]indol-6-yl]propanamide × 1
MG MAGNESIUM ION × 1
GOL GLYCEROL × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.5;293 K;25% (w/v) PEG 3350, 0.2 M MgCl2, and 0.1 M HEPES, pH 7.5
|
分辨率 1.97 Å
R-free 0.237
|
|
9VMB
The X-RAY co-crystal structure of human FGFR3 and Compound 10t
提交 2025-06-27
|
配体/离子不同
结构质量不同
|
Assembly 2
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 B
455–756(302 aa)
|
未记录
|
A1ESX ~{N}-[1-methyl-3-[2-[[3-methyl-1-(2-morpholin-4-ylethyl)pyrazol-4-yl]amino]pyrimidin-4-yl]indol-6-yl]propanamide × 1
MG MAGNESIUM ION × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.5;293 K;25% (w/v) PEG 3350, 0.2 M MgCl2, and 0.1 M HEPES, pH 7.5
|
分辨率 1.97 Å
R-free 0.237
|
|
9VMB
The X-RAY co-crystal structure of human FGFR3 and Compound 10t
提交 2025-06-27
|
配体/离子不同
结构质量不同
|
Assembly 3
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 C
455–756(302 aa)
|
未记录
|
A1ESX ~{N}-[1-methyl-3-[2-[[3-methyl-1-(2-morpholin-4-ylethyl)pyrazol-4-yl]amino]pyrimidin-4-yl]indol-6-yl]propanamide × 1
MG MAGNESIUM ION × 1
GOL GLYCEROL × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.5;293 K;25% (w/v) PEG 3350, 0.2 M MgCl2, and 0.1 M HEPES, pH 7.5
|
分辨率 1.97 Å
R-free 0.237
|
|
9VMB
The X-RAY co-crystal structure of human FGFR3 and Compound 10t
提交 2025-06-27
|
配体/离子不同
结构质量不同
|
Assembly 4
蛋白单体
单体;蛋白 × 1
PDB 声明:monomeric
|
链 D
455–756(302 aa)
|
未记录
|
A1ESX ~{N}-[1-methyl-3-[2-[[3-methyl-1-(2-morpholin-4-ylethyl)pyrazol-4-yl]amino]pyrimidin-4-yl]indol-6-yl]propanamide × 1
MG MAGNESIUM ION × 1
GOL GLYCEROL × 1
|
X-RAY DIFFRACTION
X-ray结晶条件
VAPOR DIFFUSION, HANGING DROP;pH 7.5;293 K;25% (w/v) PEG 3350, 0.2 M MgCl2, and 0.1 M HEPES, pH 7.5
|
分辨率 1.97 Å
R-free 0.237
|