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1X84

IPP isomerase (wt) reacted with (S)-bromohydrine of IPP

1X84 の概要
エントリーDOI10.2210/pdb1x84/pdb
関連するPDBエントリー1PPV 1X83
分子名称Isopentenyl-diphosphate delta-isomerase, MANGANESE (II) ION, MAGNESIUM ION, ... (5 entities in total)
機能のキーワードisomerase, complex
由来する生物種Escherichia coli
細胞内の位置Cytoplasm: Q46822
タンパク質・核酸の鎖数2
化学式量合計43791.03
構造登録者
Wouters, J.,Oldfield, E. (登録日: 2004-08-17, 公開日: 2005-01-25, 最終更新日: 2024-12-25)
主引用文献Wouters, J.,Yin, F.,Song, Y.,Zhang, Y.,Oudjama, Y.,Stalon, V.,Droogmans, L.,Morita, C.T.,Oldfield, E.
A Crystallographic Investigation of Phosphoantigen Binding to Isopentenyl Pyrophosphate/Dimethylallyl Pyrophosphate Isomerase
J.Am.Chem.Soc., 127:536-537, 2005
Cited by
PubMed Abstract: We report the crystallographic structures of the potent phosphoantigens Phosphostim (the bromohydrin of isopentenyl pyrophosphate) and E-4-hydroxy-3-methyl-but-2-enyl pyrophosphate bound to the mevalonate pathway enzyme isopentenyl pyrophosphate/dimethylallyl pyrophosphate isomerase (IPPI). Racemic Phosphostim forms covalent complexes with IPPI: a 4-thioether with C67 and a 4-ester with E116. Only the E116 ester forms with the chiral species, S-Phosphostim, with the w.t. enzyme, while the C67 thioether forms with a mutant Y104F IPPI. The potent phosphoantigen HMBPP also binds to IPPI, but is only a weak ( approximately 50 muM) inhibitor. These results strongly support an SN2 reaction for inhibition of IPPI by Phosphostim, in contrast to the SN1 or concerted type of reaction found with epoxide inhibitors, which react at C-3, and are of general interest in the context of the development of novel mevalonate pathway inhibitors. They also provide clues as to the nature of the binding site of synthetic phosphoantigens in gammadelta T cell activation. In particular, both bromohydrin and epoxy phosphoantigens are potent, irreversible inhibitors of IPPI while HMBPP is only a weak inhibitor, ruling out an IPPI or IPPI-like target for HMBPP in gammadelta T cell activation.
PubMed: 15643873
DOI: 10.1021/ja040207i
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.78 Å)
構造検証レポート
Validation report summary of 1x84
検証レポート(詳細版)ダウンロードをダウンロード

246905

件を2025-12-31に公開中

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