7YWP
Closed conformation of Oligopeptidase B from Serratia proteomaculans with covalently bound TCK
7YWP の概要
| エントリーDOI | 10.2210/pdb7ywp/pdb |
| 分子名称 | Oligopeptidase B, N-[(1S)-5-amino-1-(chloroacetyl)pentyl]-4-methylbenzenesulfonamide (3 entities in total) |
| 機能のキーワード | hydrolase |
| 由来する生物種 | Serratia proteamaculans |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 78593.49 |
| 構造登録者 | Petrenko, D.E.,Boyko, K.M.,Nikolaeva, A.Y.,Vlaskina, A.V.,Mikhailova, A.G.,Timofeev, V.I.,Rakitina, T.V. (登録日: 2022-02-14, 公開日: 2023-02-22, 最終更新日: 2024-11-13) |
| 主引用文献 | Petrenko, D.E.,Karlinsky, D.M.,Gordeeva, V.D.,Arapidi, G.P.,Britikova, E.V.,Britikov, V.V.,Nikolaeva, A.Y.,Boyko, K.M.,Timofeev, V.I.,Kuranova, I.P.,Mikhailova, A.G.,Bocharov, E.V.,Rakitina, T.V. Crystal Structure of Inhibitor-Bound Bacterial Oligopeptidase B in the Closed State: Similarity and Difference between Protozoan and Bacterial Enzymes. Int J Mol Sci, 24:-, 2023 Cited by PubMed Abstract: The crystal structure of bacterial oligopeptidase B from (SpOpB) in complex with a chloromethyl ketone inhibitor was determined at 2.2 Å resolution. SpOpB was crystallized in a closed (catalytically active) conformation. A single inhibitor molecule bound simultaneously to the catalytic residues S532 and H652 mimicked a tetrahedral intermediate of the catalytic reaction. A comparative analysis of the obtained structure and the structure of OpB from (TbOpB) in a closed conformation showed that in both enzymes, the stabilization of the D-loop (carrying the catalytic D) in a position favorable for the formation of a tetrahedral complex occurs due to interaction with the neighboring loop from the β-propeller. However, the modes of interdomain interactions were significantly different for bacterial and protozoan OpBs. Instead of a salt bridge (as in TbOpB), in SpOpB, a pair of polar residues following the catalytic D617 and a pair of neighboring arginine residues from the β-propeller domain formed complementary oppositely charged surfaces. Bioinformatics analysis and structural modeling show that all bacterial OpBs can be divided into two large groups according to these two modes of D-loop stabilization in closed conformations. PubMed: 36768612DOI: 10.3390/ijms24032286 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.2 Å) |
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