6RYO
Bacterial membrane enzyme structure by the in meso method at 1.9 A resolution
6RYO の概要
エントリーDOI | 10.2210/pdb6ryo/pdb |
分子名称 | Lipoprotein signal peptidase, Globomycin, (2R)-2,3-dihydroxypropyl (9Z)-octadec-9-enoate, ... (7 entities in total) |
機能のキーワード | in meso, lipid cubic phases, lipoprotein signal peptidase, globomycin, hydrolase |
由来する生物種 | Staphylococcus aureus 詳細 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 27670.57 |
構造登録者 | Huang, C.Y.,Olatunji, S.,Bailey, J.,Yu, X.,Olieric, V.,Wang, M.,Caffrey, M. (登録日: 2019-06-11, 公開日: 2020-01-15, 最終更新日: 2024-11-13) |
主引用文献 | Olatunji, S.,Yu, X.,Bailey, J.,Huang, C.Y.,Zapotoczna, M.,Bowen, K.,Remskar, M.,Muller, R.,Scanlan, E.M.,Geoghegan, J.A.,Olieric, V.,Caffrey, M. Structures of lipoprotein signal peptidase II from Staphylococcus aureus complexed with antibiotics globomycin and myxovirescin. Nat Commun, 11:140-140, 2020 Cited by PubMed Abstract: Antimicrobial resistance is a major global threat that calls for new antibiotics. Globomycin and myxovirescin are two natural antibiotics that target the lipoprotein-processing enzyme, LspA, thereby compromising the integrity of the bacterial cell envelope. As part of a project aimed at understanding their mechanism of action and for drug development, we provide high-resolution crystal structures of the enzyme from the human pathogen methicillin-resistant Staphylococcus aureus (MRSA) complexed with globomycin and with myxovirescin. Our results reveal an instance of convergent evolution. The two antibiotics possess different molecular structures. Yet, they appear to inhibit identically as non-cleavable tetrahedral intermediate analogs. Remarkably, the two antibiotics superpose along nineteen contiguous atoms that interact similarly with LspA. This 19-atom motif recapitulates a part of the substrate lipoprotein in its proposed binding mode. Incorporating this motif into a scaffold with suitable pharmacokinetic properties should enable the development of effective antibiotics with built-in resistance hardiness. PubMed: 31919415DOI: 10.1038/s41467-019-13724-y 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.924 Å) |
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