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6C9V

Mycobacterium tuberculosis adenosine kinase bound to (2R,3S,4R,5R)-2-(hydroxymethyl)-5-(6-(4-phenylpiperazin-1-yl)-9H-purin-9-yl)tetrahydrofuran-3,4-diol

6C9V の概要
エントリーDOI10.2210/pdb6c9v/pdb
分子名称Adenosine kinase, (2R,3S,4R,5R)-2-(hydroxymethyl)-5-[6-(4-phenylpiperazin-1-yl)-9H-purin-9-yl]tetrahydrofuran-3,4-diol, SULFATE ION, ... (6 entities in total)
機能のキーワードnucleoside analog, complex, inhibitor, structural genomics, psi-2, protein structure initiative, tb structural genomics consortium, tbsgc, transferase-transferase inhibitor complex, transferase/transferase inhibitor
由来する生物種Mycobacterium tuberculosis
タンパク質・核酸の鎖数2
化学式量合計70162.99
構造登録者
Crespo, R.A.,TB Structural Genomics Consortium (TBSGC) (登録日: 2018-01-28, 公開日: 2019-05-01, 最終更新日: 2023-10-04)
主引用文献Crespo, R.A.,Dang, Q.,Zhou, N.E.,Guthrie, L.M.,Snavely, T.C.,Dong, W.,Loesch, K.A.,Suzuki, T.,You, L.,Wang, W.,O'Malley, T.,Parish, T.,Olsen, D.B.,Sacchettini, J.C.
Structure-Guided Drug Design of 6-Substituted Adenosine Analogues as Potent Inhibitors of Mycobacterium tuberculosis Adenosine Kinase.
J.Med.Chem., 62:4483-4499, 2019
Cited by
PubMed: 31002508
DOI: 10.1021/acs.jmedchem.9b00020
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.7 Å)
構造検証レポート
Validation report summary of 6c9v
検証レポート(詳細版)ダウンロードをダウンロード

217705

件を2024-03-27に公開中

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