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7BHT

Crystal structure of MAT2a with quinazolinone fragment 5 bound in the allosteric site

7BHT の概要
エントリーDOI10.2210/pdb7bht/pdb
分子名称S-adenosylmethionine synthase isoform type-2, DIMETHYL SULFOXIDE, 7-chloranyl-4-(dimethylamino)-1~{H}-quinazolin-2-one, ... (6 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44671.51
構造登録者
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
Cited by
PubMed Abstract: MAT2a is a methionine adenosyltransferase that synthesizes the essential metabolite -adenosylmethionine (SAM) from methionine and ATP. Tumors bearing the co-deletion of p16 and MTAP genes have been shown to be sensitive to MAT2a inhibition, making it an attractive target for treatment of MTAP-deleted cancers. A fragment-based lead generation campaign identified weak but efficient hits binding in a known allosteric site. By use of structure-guided design and systematic SAR exploration, the hits were elaborated through a merging and growing strategy into an arylquinazolinone series of potent MAT2a inhibitors. The selected tool compound reduced SAM-dependent methylation events in cells and inhibited proliferation of MTAP-null cells . studies showed that was able to induce antitumor response in an MTAP knockout HCT116 xenograft model.
PubMed: 33900758
DOI: 10.1021/acs.jmedchem.1c00067
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.052 Å)
構造検証レポート
Validation report summary of 7bht
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-12-31に公開中

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