7Q11
Crystal structure of CTX-M-14 in complex with Ixazomib
7Q11 の概要
エントリーDOI | 10.2210/pdb7q11/pdb |
関連するPDBエントリー | 7Q0Y 7Q0Z |
分子名称 | Beta-lactamase, DIMETHYL SULFOXIDE, [(1~{R})-1-[2-[[2,5-bis(chloranyl)phenyl]carbonylamino]ethanoylamino]-3-methyl-butyl]boronic acid, ... (6 entities in total) |
機能のキーワード | lactamase, antibiotic, resistence, 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 | 29173.76 |
構造登録者 | Werner, N.,Perbandt, M.,Hinrichs, W.,Prester, A.,Rohde, H.,Aepfelbacher, M.,Betzel, C. (登録日: 2021-10-17, 公開日: 2022-04-13, 最終更新日: 2024-11-06) |
主引用文献 | Perbandt, M.,Werner, N.,Prester, A.,Rohde, H.,Aepfelbacher, M.,Hinrichs, W.,Betzel, C. Structural basis to repurpose boron-based proteasome inhibitors Bortezomib and Ixazomib as beta-lactamase inhibitors. Sci Rep, 12:5510-5510, 2022 Cited by PubMed Abstract: β-lactamases are a major cause of rapidly emerging and spreading antibiotic resistance. Currently β-lactamase inhibitors (BLIs) in clinical use act only on Ambler Class A, C and some class D lactamases. The urgent need to identify new BLIs recently lead to FDA approval of boron-based compounds BLIs, e.g. Vaborbactam. The boron-based proteasome inhibitors Bortezomib and Ixazomib are used in cancer therapy as multiple myeloma drugs but they also bind to Ser-/Thr- proteases. In this study we show the crystal structures of the β-lactamase CTX-M-14 with covalently bound Bortezomib and Ixazomib at high resolutions of 1.3 and 1.1 Å, respectively. Ixazomib is well defined in electron density whereas Bortezomib show some disorder which corresponds to weaker inhibition efficiency observed for Ixazomib. Both inhibitors mimic the deacylation transition state of β-lactam hydrolysis, because they replace the deacylating water molecule. We further investigate differences in binding of Bortezomib/Ixazomib to CTX-M-14 and its target proteases as well as known β-lactamase drugs. Our findings can help to use Bortezomib/Ixazomib as lead compounds for development of new BLIs. PubMed: 35365689DOI: 10.1038/s41598-022-09392-6 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.14 Å) |
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