日本語
 
Help Privacy Policy ポリシー/免責事項
  詳細検索ブラウズ

アイテム詳細

  Retaining Glycosyltransferase Mechanism Studied by QM/MM Methods: Lipopolysaccharyl-α-1,4-galactosyltransferase C Transfers α-Galactose via an Oxocarbenium Ion-like Transition State

Gomez, H., Polyak, I., Thiel, W., Lluch, J. M., & Masgrau, L. (2012). Retaining Glycosyltransferase Mechanism Studied by QM/MM Methods: Lipopolysaccharyl-α-1,4-galactosyltransferase C Transfers α-Galactose via an Oxocarbenium Ion-like Transition State. Journal of the American Chemical Society, 134(10), 4743-4752. doi:10.1021/ja210490f.

Item is

基本情報

表示: 非表示:
資料種別: 学術論文

ファイル

表示: ファイル

関連URL

表示:

作成者

表示:
非表示:
 作成者:
Gomez, Hansel1, 著者           
Polyak, Iakov1, 著者           
Thiel, W.1, 著者           
Lluch, Jose M.2, 著者
Masgrau, Laura2, 著者
所属:
1Research Department Thiel, Max-Planck-Institut für Kohlenforschung, Max Planck Society, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr, DE, ou_1445590              
2Univ Autonoma Barcelona, Inst Biotecnol & Biomed, E-08193 Barcelona, Spain, ou_persistent22              

内容説明

表示:
非表示:
キーワード: APPROXIMATE COULOMB POTENTIALS; ENZYMATIC GLYCOSYL TRANSFER; AUXILIARY BASIS-SETS; GAUSSIAN-BASIS SETS; NEISSERIA-MENINGITIDIS; GALACTOSYLTRANSFERASE LGTC; MOLECULAR-DYNAMICS; CORRELATION-ENERGY; COMPLEX MATERIALS; ZEOLITE STRUCTURE
 要旨: Glycosyltransferases (GTs) catalyze the highly specific biosynthesis of glycosidic bonds and, as such, are important both as drug targets and for biotechnological purposes. Despite their broad interest, fundamental questions about their reaction mechanism remain to be answered, especially for those GTs that transfer the sugar with net retention of the configuration at the anomeric carbon (retaining glycosyltransferases, ret-GTs). In the present work, we focus on the reaction catalyzed by lipopolysaccharyl-alpha-1,4-galactosyltransferase C (LgtC) from Neisseria meningitides. We study and compare the different proposed mechanisms (S(N)i, S(N)i-like, and double displacement mechanism via a covalent glycosyl-enzyme intermediate, CGE) by using density functional theory (DFT) and quantum mechanics/molecular mechanics (QM/MM) calculations on the full enzyme. We characterize a dissociative single-displacement (S(N)i) mechanism consistent with the experimental data, in which the acceptor substrate attacks on the side of the UDP leaving group that acts as a catalytic base. We identify several key interactions that help this front-side attack by stabilizing the transition state. Among them, Gln189, the putative nucleophile in a double displacement mechanism, is shown to favor the charge development at the anomeric center by about 2 kcal/mol, compatible with experimental mutagenesis data. We predict that using 3-deoxylactose as acceptor would result in a reduction of k(cat) to 0.6-3% of that for the unmodified substrates. The reactions of the Q189A and Q189E mutants have also been investigated. For Q189E, there is a change in mechanism since a CGE can be formed which, however, is not able to evolve to products. The current findings are discussed in the light of the available experimental data and compared with those for other ret-GTs.

資料詳細

表示:
非表示:
言語: eng - English
 日付: 2012-02-21
 出版の状態: 出版
 ページ: -
 出版情報: -
 目次: -
 査読: 査読あり
 識別子(DOI, ISBNなど): DOI: 10.1021/ja210490f
 学位: -

関連イベント

表示:

訴訟

表示:

Project information

表示:

出版物 1

表示:
非表示:
出版物名: Journal of the American Chemical Society
  その他 : J. Am. Chem. Soc.
種別: 学術雑誌
 著者・編者:
所属:
出版社, 出版地: American Chemical Society
ページ: - 巻号: 134 (10) 通巻号: - 開始・終了ページ: 4743 - 4752 識別子(ISBN, ISSN, DOIなど): ISSN: 0002-7863
CoNE: https://pure.mpg.de/cone/journals/resource/954925376870