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4E0U

Crystal structure of CdpNPT in complex with thiolodiphosphate and (S)-benzodiazependione

4E0U の概要
エントリーDOI10.2210/pdb4e0u/pdb
関連するPDBエントリー4E0T
分子名称Cyclic dipeptide N-prenyltransferase, (3S)-3-(1H-indol-3-ylmethyl)-3,4-dihydro-1H-1,4-benzodiazepine-2,5-dione, TRIHYDROGEN THIODIPHOSPHATE, ... (7 entities in total)
機能のキーワードpt-fold, c(3)b-prenyltransferase, transferase
由来する生物種Aspergillus fumigatus
タンパク質・核酸の鎖数2
化学式量合計98927.45
構造登録者
Schuller, J.M.,Zocher, G.,Stehle, T. (登録日: 2012-03-05, 公開日: 2012-05-30, 最終更新日: 2023-09-13)
主引用文献Schuller, J.M.,Zocher, G.,Liebhold, M.,Xie, X.,Stahl, M.,Li, S.M.,Stehle, T.
Structure and catalytic mechanism of a cyclic dipeptide prenyltransferase with broad substrate promiscuity.
J.Mol.Biol., 422:87-99, 2012
Cited by
PubMed Abstract: Fungal indole prenyltransferases (PTs) typically act on specific substrates, and they are able to prenylate their target compounds with remarkably high regio- and stereoselectivity. Similar to several indole PTs characterized to date, the cyclic dipeptide N-prenyltransferase (CdpNPT) is able to prenylate a range of diverse substrates, thus exhibiting an unusually broad substrate promiscuity. To define the structural basis for this promiscuity, we have determined crystal structures of unliganded CdpNPT and of a ternary complex of CdpNPT bound to (S)-benzodiazepinedione and thiolodiphosphate. Analysis of the structures reveals a limited number of specific interactions with (S)-benzodiazepinedione, which projects into a largely hydrophobic surface. This surface can also accommodate other substrates, explaining the ability of the enzyme to prenylate a range of compounds. The location of the bound substrates suggests a likely reaction mechanism for the conversion of (S)-benzodiazepinedione. Structure-guided mutagenesis experiments confirm that, in addition to (S)-benzodiazepinedione, CdpNPT can also act on (R)-benzodiazepinedione and several cyclic dipeptides, albeit with relaxed specificity. Finally, nuclear magnetic resonance spectroscopy demonstrates that CdpNPT is a C-3 reverse PT that catalyzes the formation of C-3β prenylated indolines from diketopiperazines of tryptophan-containing cyclic dipeptides.
PubMed: 22683356
DOI: 10.1016/j.jmb.2012.05.033
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.6 Å)
構造検証レポート
Validation report summary of 4e0u
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-01-28に公開中

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