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7ZZR

HDAC2 in complex with inhibitory ligand

Summary for 7ZZR
Entry DOI10.2210/pdb7zzr/pdb
DescriptorHistone deacetylase 2, ZINC ION, CALCIUM ION, ... (10 entities in total)
Functional Keywordschromatin binding, transcription regulation, protein de-acetylation, transcription
Biological sourceHomo sapiens (human)
Total number of polymer chains3
Total formula weight172240.96
Authors
Cleasby, A.,Tisi, D. (deposition date: 2022-05-26, release date: 2022-09-21, Last modification date: 2024-06-19)
Primary citationTamanini, E.,Miyamura, S.,Buck, I.M.,Cons, B.D.,Dawson, L.,East, C.,Futamura, T.,Goto, S.,Griffiths-Jones, C.,Hashimoto, T.,Heightman, T.D.,Ishikawa, S.,Ito, H.,Kaneko, Y.,Kawato, T.,Kondo, K.,Kurihara, N.,McCarthy, J.M.,Mori, Y.,Nagase, T.,Nakaishi, Y.,Reeks, J.,Sato, A.,Schopf, P.,Tai, K.,Tamai, T.,Tisi, D.,Woolford, A.J.
Fragment-Based Discovery of a Novel, Brain Penetrant, Orally Active HDAC2 Inhibitor.
Acs Med.Chem.Lett., 13:1591-1597, 2022
Cited by
PubMed: 36262388
DOI: 10.1021/acsmedchemlett.2c00272
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.168 Å)
Structure validation

222415

數據於2024-07-10公開中

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