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1U30

In situ extension as an approach for identifying novel alpha-amylase inhibitors, structure containing maltosyl-alpha (1,4)-D-gluconhydroximo-1,5-lactam

1U30 の概要
エントリーDOI10.2210/pdb1u30/pdb
関連するPDBエントリー1U2Y 1U33
分子名称Alpha-amylase, pancreatic, 2-acetamido-2-deoxy-beta-D-glucopyranose, MALTOSYL-ALPHA (1,4)-(Z,3S,4S,5R,6R)-3,4,5-TRIHYDROXY-6-HYDROXYMETHYL-PIPERIDIN-2-ONE OXIME, ... (7 entities in total)
機能のキーワードglycosidase, human pancreatic alpha-amylase, acarbose, inhibitor, glucosidase, enzyme mechanism, hydrolase
由来する生物種Homo sapiens (human)
タンパク質・核酸の鎖数1
化学式量合計56936.67
構造登録者
Numao, S.,Li, C.,Damager, I.,Wrodnigg, T.M.,Begum, A.,Overall, C.M.,Brayer, G.D.,Withers, S.G. (登録日: 2004-07-20, 公開日: 2004-09-07, 最終更新日: 2020-11-11)
主引用文献Numao, S.,Damager, I.,Li, C.,Wrodnigg, T.M.,Begum, A.,Overall, C.M.,Brayer, G.D.,Withers, S.G.
In Situ Extension as an Approach for Identifying Novel alpha-Amylase Inhibitors.
J.Biol.Chem., 279:48282-48291, 2004
Cited by
PubMed: 15304511
DOI: 10.1074/jbc.M406804200
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.9 Å)
構造検証レポート
Validation report summary of 1u30
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2024-04-24に公開中

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