1VM1 の概要
エントリーDOI | 10.2210/pdb1vm1/pdb |
関連するPDBエントリー | 1SHV |
分子名称 | BETA-LACTAMASE SHV-1, CYCLOHEXYL-HEXYL-BETA-D-MALTOSIDE, TAZOBACTAM INTERMEDIATE, ... (6 entities in total) |
機能のキーワード | beta-lactamase, beta-lactam hydrolase, penicillinase, detergent binding, inhibitor design, hydrolase |
由来する生物種 | Klebsiella pneumoniae |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 30598.88 |
構造登録者 | Kuzin, A.P.,Nukaga, M.,Nukaga, Y.,Hujer, A.,Bonomo, R.A.,Knox, J.R. (登録日: 2004-08-27, 公開日: 2004-09-07, 最終更新日: 2025-05-07) |
主引用文献 | Kuzin, A.P.,Nukaga, M.,Nukaga, Y.,Hujer, A.,Bonomo, R.A.,Knox, J.R. Inhibition of the SHV-1 beta-lactamase by sulfones: crystallographic observation of two reaction intermediates with tazobactam. Biochemistry, 40:1861-1866, 2001 Cited by PubMed Abstract: Two species resulting from the reaction of the SHV-1 class A beta-lactamase with the sulfone inhibitor tazobactam have been trapped at 100 K and mapped by X-ray crystallography at 2.0 A resolution. An acyclic form of tazobactam is covalently bonded to the catalytic Ser70 side chain, and a second species, a five-atom vinyl carboxylic acid fragment of tazobactam, is bonded to Ser130. It is proposed that the electron density map of the crystal is a composite picture of two complexes, each with only a single bound species. It is estimated that the two complexes exist in the crystal in approximately equal populations. Results are discussed in relation to the mechanism-based inhibition of class A beta-lactamases by the similar inhibitors sulbactam and clavulanic acid. PubMed: 11327849DOI: 10.1021/bi0022745 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.02 Å) |
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