4M7Y

Staphylococcus aureus Type II pantothenate kinase in complex with a pantothenate analog

4M7Y の概要

• エントリーDOI: 10.2210/pdb4m7y/pdb
• 関連するPDBエントリー: 4M7X
• 分子名称: Type II pantothenate kinase, N~3~-[(2R)-2-hydroxy-3,3-dimethyl-4-(phosphonooxy)butanoyl]-N-pentyl-beta-alaninamide, ADENOSINE-5'-DIPHOSPHATE, ... (6 entities in total)
• 機能のキーワード: pantothenate kinase, inhibitor, antibacterial, structural genomics, structural genomics consortium, sgc, transferase-transferase inhibitor complex, transferase/transferase inhibitor
• 由来する生物種: Staphylococcus aureus subsp. aureus
• 細胞内の位置: Cytoplasm : Q8NVG0
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 62167.56

構造登録者

Mottaghi, K.,Hong, B.,Tempel, W.,Park, H.,Structural Genomics Consortium (SGC) (登録日: 2013-08-12, 公開日: 2014-09-03, 最終更新日: 2023-09-20)

主引用文献

Hughes, S.J.,Barnard, L.,Mottaghi, K.,Tempel, W.,Antoshchenko, T.,Hong, B.S.,Allali-Hassani, A.,Smil, D.,Vedadi, M.,Strauss, E.,Park, H.W.
Discovery of Potent Pantothenamide Inhibitors of Staphylococcus aureus Pantothenate Kinase through a Minimal SAR Study: Inhibition Is Due to Trapping of the Product.
ACS Infect Dis, 2:627-641, 2016

PubMed Abstract: The potent antistaphylococcal activity of N-substituted pantothenamides (PanAms) has been shown to at least partially be due to the inhibition of Staphylococcus aureus's atypical type II pantothenate kinase (SaPanK), the first enzyme of coenzyme A biosynthesis. This mechanism of action follows from SaPanK having a binding mode for PanAms that is distinct from those of other PanKs. To dissect the molecular interactions responsible for PanAm inhibitory activity, we conducted a mini SAR study in tandem with the cocrystallization of SaPanK with two classic PanAms (N5-Pan and N7-Pan), culminating in the synthesis and characterization of two new PanAms, N-Pip-PanAm and MeO-N5-PanAm. The cocrystal structures showed that all of the PanAms are phosphorylated by SaPanK but remain bound at the active site; this occurs primarily through interactions with Tyr240' and Thr172'. Kinetic analysis showed a strong correlation between k (slow PanAm turnover) and IC (inhibition of pantothenate phosphorylation) values, suggesting that SaPanK inhibition occurs via a delay in product release. In-depth analysis of the PanAm-bound structures showed that the capacity for accepting a hydrogen bond from the amide of Thr172' was a stronger determinant for PanAm potency than the capacity to π-stack with Tyr240'. The two new PanAms, N-Pip-PanAm and MeO-N5-PanAm, effectively combine both hydrogen bonding and hydrophobic interactions, resulting in the most potent SaPanK inhibition described to date. Taken together, our results are consistent with an inhibition mechanism wherein PanAms act as SaPanK substrates that remain bound upon phosphorylation. The phospho-PanAm-SaPanK interactions described herein may help future antistaphylococcal drug development.

PubMed: 27759386
DOI: 10.1021/acsinfecdis.6b00090

実験手法

X-RAY DIFFRACTION (1.8 Å)