PDB ID: 5V9P
Hetero Atom Contents
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Color scheme of protein:
Code | Name | Style | Show | Link | |
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90S | [(3s)-3-(4-bromo-1h-pyrazol-1-yl)pyrrolidin-1-yl][3-(propan-2-yl)-1h-pyrazol-5-yl]methanone | PoSSuM | |||
NI | Nickel (II) ion | PoSSuM | |||
SO4 | Sulfate ion | PoSSuM | |||
ZN | Zinc ion | PoSSuM |
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Download interaction data: 5V9P
Structure summary
Code : | 5V9P PDBj RCSB PDB PDBe | ||||||||||||||||||||||||
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Header : | OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR | ||||||||||||||||||||||||
Title : | Crystal structure of pyrrolidine amide inhibitor [(3S)-3-(4-bromo-1H-pyrazol-1-yl)pyrrolidin-1-yl][3-(propan-2-yl)-1H-pyrazol-5-yl]methanone (compound 35) in complex with KDM5A | ||||||||||||||||||||||||
Release Data : | 2017-05-10 | ||||||||||||||||||||||||
Compound : |
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Source : |
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Authors : | Kiefer, J.R., Liang, J., Vinogradova, M. | ||||||||||||||||||||||||
Keywords : | epigenetics, histone demethylase, cancer, inhibitor, selective, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR complex | ||||||||||||||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 3.0 Å ) | ||||||||||||||||||||||||
Citation : |
From a novel HTS hit to potent, selective, and orally bioavailable KDM5 inhibitors.
Liang, J.,Labadie, S.,Zhang, B.
et al.
PubMed: 28512031 |
Reaction
Chain : | A | ||||||||
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UniProt : | P29375 (KDM5A_HUMAN) | ||||||||
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