9JWJ
Structure of Human HDAC2 in complex with inhibitor N-(2-amino-5-(furan-2-yl)phenyl)-4-(1-((phenylsulfonyl)methyl)-1H-1,2,3-triazol-4-yl)benzamid
This is a non-PDB format compatible entry.
Summary for 9JWJ
Entry DOI | 10.2210/pdb9jwj/pdb |
Descriptor | Histone deacetylase 2, ZINC ION, CALCIUM ION, ... (10 entities in total) |
Functional Keywords | histone deacetylase 2, transcription |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 3 |
Total formula weight | 141649.14 |
Authors | Tojo, T.,Itoh, Y.,Kurohara, T.,Li, Y.,Singh, R.,Narozny, R.,Wiel, A.,Miyake, Y.,Yamashita, Y.,Kusakabe, K.,Uchida, S.,Suzuki, T. (deposition date: 2024-10-10, release date: 2025-10-15) |
Primary citation | Tojo, T.,Itoh, Y.,Kurohara, T.,Li, Y.,Singh, R.,Narozny, R.,Wiel, A.,Miyake, Y.,Yamashita, Y.,Kusakabe, K.,Uchida, S.,Suzuki, T. Discovery of an HDAC2-selective inhibitor based on enzyme-inhibitor binding thermodynamics and kinetics, and its potential as a therapeutic drug for neurological disorders To Be Published, |
Experimental method | X-RAY DIFFRACTION (1.78 Å) |
Structure validation
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