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4AY6

Human O-GlcNAc transferase (OGT) in complex with UDP-5SGlcNAc and substrate peptide

4AY6 の概要
エントリーDOI10.2210/pdb4ay6/pdb
関連するPDBエントリー1W3B 2J4O 2YDS 2YIY 4AY5
分子名称UDP-N-ACETYLGLUCOSAMINE--PEPTIDE N-ACETYLGLUCOSAMINYLTRANS FERASE 110 KDA SUBUNIT, TGF-BETA-ACTIVATED KINASE 1 AND MAP3K7-BINDING PROTEIN 1, SULFATE ION, ... (4 entities in total)
機能のキーワードtransferase, glycosyl transferase
由来する生物種HOMO SAPIENS (HUMAN)
詳細
細胞内の位置Isoform 2: Mitochondrion. Isoform 3: Cytoplasm. Isoform 4: Cytoplasm: O15294
タンパク質・核酸の鎖数8
化学式量合計332013.57
構造登録者
主引用文献Schimpl, M.,Zheng, X.,Borodkin, V.S.,Blair, D.E.,Ferenbach, A.T.,Schuettelkopf, A.W.,Navratilova, I.,Aristotelous, T.,Albarbarawi, O.,Robinson, D.A.,Macnaughtan, M.A.,Van Aalten, D.M.F.
O-Glcnac Transferase Invokes Nucleotide Sugar Pyrophosphate Participation in Catalysis
Nat.Chem.Biol., 8:969-, 2012
Cited by
PubMed Abstract: Protein O-GlcNAcylation is an essential post-translational modification on hundreds of intracellular proteins in metazoa, catalyzed by O-linked β-N-acetylglucosamine (O-GlcNAc) transferase (OGT) using unknown mechanisms of transfer and substrate recognition. Through crystallographic snapshots and mechanism-inspired chemical probes, we define how human OGT recognizes the sugar donor and acceptor peptide and uses a new catalytic mechanism of glycosyl transfer, involving the sugar donor α-phosphate as the catalytic base as well as an essential lysine. This mechanism seems to be a unique evolutionary solution to the spatial constraints imposed by a bulky protein acceptor substrate and explains the unexpected specificity of a recently reported metabolic OGT inhibitor.
PubMed: 23103942
DOI: 10.1038/NCHEMBIO.1108
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (3.3 Å)
構造検証レポート
Validation report summary of 4ay6
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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