PDB ID: 4LY1
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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ZN | Zinc ion | PoSSuM | |||
CA | Calcium ion | PoSSuM | |||
NA | Sodium ion | PoSSuM | |||
PG4 | Tetraethylene glycol | PoSSuM | |||
20Y | 4-(acetylamino)-N-[2-amino-5-(thiophen-2-yl)phenyl]benzamide | PoSSuM |
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Download interaction data: 4LY1
Structure summary
Code : | 4LY1 PDBj RCSB PDB PDBe | ||||||||||||
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Header : | HYDROLASE/HYDROLASE INHIBITOR | ||||||||||||
Title : | Structure of Human HDAC2 in complex with inhibitor 4-(acetylamino)-N-[2-amino-5-(thiophen-2-yl)phenyl]benzamide | ||||||||||||
Release Data : | 2013-08-21 | ||||||||||||
Compound : |
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Authors : | Fong, R., Lupardus, P.J. | ||||||||||||
Keywords : | deacetylase, Histone, HYDROLASE-HYDROLASE INHIBITOR complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.57 Å ) | ||||||||||||
Citation : |
Histone Deacetylase (HDAC) Inhibitor Kinetic Rate Constants Correlate with Cellular Histone Acetylation but Not Transcription and Cell Viability.
Lauffer, B.E.,Mintzer, R.,Fong, R.
et al.
PubMed: 23897821 |
Reaction
Chain : | A, B, C | ||||||||||||||||||||
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UniProt : | Q92769 (HDAC2_HUMAN) | ||||||||||||||||||||
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