7BHV

Crystal structure of MAT2a bound to allosteric inhibitor and in vivo tool compound 28

7BHV の概要

• エントリーDOI: 10.2210/pdb7bhv/pdb
• 分子名称: S-adenosylmethionine synthase isoform type-2, 7-chloranyl-4-(dimethylamino)-1-phenyl-quinazolin-2-one, S-ADENOSYLMETHIONINE, ... (4 entities in total)
• 機能のキーワード: allosteric inhibitor, fragment-based drug design, synthetic lethal therapy, oncology, transferase
• 由来する生物種: Homo sapiens (Human)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 44634.02

構造登録者

Schimpl, M.,De Fusco, C.,Borjesson, U.,Cheung, T.,Collie, I.,Evans, L.,Narasimhan, P.,Stubbs, C.,Vazquez-Chantada, M.,Wagner, D.J.,Grondine, M.,Tentarelli, S.,Underwood, E.,Argyrou, A.,Bagal, S.,Chiarparin, E.,Robb, G.,Scott, J.S. (登録日: 2021-01-11, 公開日: 2021-04-21, 最終更新日: 2024-05-01)

• 主引用文献: De Fusco, C.,Schimpl, M.,Borjesson, U.,Cheung, T.,Collie, I.,Evans, L.,Narasimhan, P.,Stubbs, C.,Vazquez-Chantada, M.,Wagner, D.J.,Grondine, M.,Sanders, M.G.,Tentarelli, S.,Underwood, E.,Argyrou, A.,Smith, J.M.,Lynch, J.T.,Chiarparin, E.,Robb, G.,Bagal, S.K.,Scott, J.S.; Fragment-Based Design of a Potent MAT2a Inhibitor and in Vivo Evaluation in an MTAP Null Xenograft Model.; J.Med.Chem., 64:6814-6826, 2021; PubMed: 33900758; DOI: 10.1021/acs.jmedchem.1c00067

実験手法

X-RAY DIFFRACTION (1.16 Å)