首页/数据集/HUMAN ALPHA-THROMBIN TERNARY COMPLEX WITH THE EXOSITE INHIBITOR HIRUGEN AND ACTIVE SITE INHIBITOR PHCH2OCO-D-DPA-PRO-BOROMPG

HUMAN ALPHA-THROMBIN TERNARY COMPLEX WITH THE EXOSITE INHIBITOR HIRUGEN AND ACTIVE SITE INHIBITOR PHCH2OCO-D-DPA-PRO-BOROMPG

NIAID Data Ecosystem2026-05-02 收录

抑制剂结构

蛋白质-药物复合物

数据链接：

https://www.rcsb.org/structure/1AI8 数据链接链接失效反馈

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资源简介：

HUMAN ALPHA-THROMBIN TERNARY COMPLEX WITH THE EXOSITE INHIBITOR HIRUGEN AND ACTIVE SITE INHIBITOR PHCH2OCO-D-DPA-PRO-BOROMPG

应用场景：

创建时间：

2024-12-25

抑制剂结构

TAK1靶点药物发现

Structure of TAK1 in complex with compound 22 Descriptor: DIMETHYL SULFOXIDE, GLYCEROL, Mitogen-activated protein kinase 7,TGF-beta-activated kinase 1 and MAP3K7-binding protein 1, ... Authors: Veerma

Protein Data Bank Japan2024-06-19 更新100

Crystal Structure of ITK kinase bound to an inhibitor

抑制剂结构

药物靶点复合物晶体学

Crystal Structure of ITK kinase bound to an inhibitor Descriptor: 3-[(8-phenylthieno[2,3-h]quinazolin-2-yl)amino]benzenesulfonamide, N-(6-oxo-1,6-dihydro-3,4'-bipyridin-5-yl)benzamide, Tyrosine-protei

Protein Data Bank Japan2024-03-20 更新80

Coccomyxa beta-carbonic anhydrase in complex with azide

蛋白质-配体共结晶

抑制剂结构

Coccomyxa beta-carbonic anhydrase in complex with azide Descriptor: AZIDE ION, CHLORIDE ION, Carbonic anhydrase, ... Authors: Huang, S, Hainzl, T, Sauer-Eriksson, A.E. Deposit date: 2011-10-27 Release

Protein Data Bank Japan2023-09-13 更新50

Co-crytsal Structure of MNK2 in Complex With an Inhibitor

抑制剂结构

靶点药物设计

Co-crytsal Structure of MNK2 in Complex With an Inhibitor Descriptor: (3R)-3-methyl-5-[(pyrimidin-4-yl)amino]-2,3-dihydro-1H-isoindol-1-one, CHLORIDE ION, MAP kinase-interacting serine/threonine-prote

Protein Data Bank Japan2024-10-09 更新90

The Jak1 kinase domain in complex with compound 37

抑制剂结构

药物靶点复合物

The Jak1 kinase domain in complex with compound 37 Descriptor: (1R,2S)-2-{[8-oxo-2-(1H-pyrazol-4-yl)-5,8-dihydropyrido[3,4-d]pyrimidin-4-yl]amino}cyclopentanecarbonitrile, Tyrosine-protein kinase JAK1

Protein Data Bank Japan2024-11-27 更新60

HUMAN ALPHA-THROMBIN TERNARY COMPLEX WITH THE EXOSITE INHIBITOR HIRUGEN AND ACTIVE SITE INHIBITOR PHCH2OCO-D-DPA-PRO-BOROMPG

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