1JYW
E. COLI (lacZ) BETA-GALACTOSIDASE (E537Q) IN COMPLEX WITH PNPG
1JYW の概要
エントリーDOI | 10.2210/pdb1jyw/pdb |
関連するPDBエントリー | 1DP0 1F49 1JYN 1JYV 1JYX 1JYY 1JYZ 1JZ0 1JZ1 1JZ2 1JZ3 1JZ4 1JZ5 1JZ6 1JZ7 1JZ8 |
分子名称 | Beta-Galactosidase, 4-nitrophenyl beta-D-galactopyranoside, MAGNESIUM ION, ... (6 entities in total) |
機能のキーワード | tim barrel (alpha/beta barrel), jelly-roll barrel, immunoglobulin, beta supersandwich, hydrolase |
由来する生物種 | Escherichia coli |
タンパク質・核酸の鎖数 | 4 |
化学式量合計 | 476475.03 |
構造登録者 | |
主引用文献 | Juers, D.H.,Heightman, T.D.,Vasella, A.,McCarter, J.D.,Mackenzie, L.,Withers, S.G.,Matthews, B.W. A Structural View of the Action of Escherichia Coli (Lacz) Beta-Galactosidase Biochemistry, 40:14781-14794, 2001 Cited by PubMed Abstract: The structures of a series of complexes designed to mimic intermediates along the reaction coordinate for beta-galactosidase are presented. These complexes clarify and enhance previous proposals regarding the catalytic mechanism. The nucleophile, Glu537, is seen to covalently bind to the galactosyl moiety. Of the two potential acids, Mg(2+) and Glu461, the latter is in better position to directly assist in leaving group departure, suggesting that the metal ion acts in a secondary role. A sodium ion plays a part in substrate binding by directly ligating the galactosyl 6-hydroxyl. The proposed reaction coordinate involves the movement of the galactosyl moiety deep into the active site pocket. For those ligands that do bind deeply there is an associated conformational change in which residues within loop 794-804 move up to 10 A closer to the site of binding. In some cases this can be inhibited by the binding of additional ligands. The resulting restricted access to the intermediate helps to explain why allolactose, the natural inducer for the lac operon, is the preferred product of transglycosylation. PubMed: 11732897DOI: 10.1021/bi011727i 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.55 Å) |
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