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1O8J

Pectate Lyase C from Erwinia Chrysanthemi at pH 4.5 with 30mM CA2+

1O8J の概要
エントリーDOI10.2210/pdb1o8j/pdb
関連するPDBエントリー1AIR 1O88 1O8D 1O8E 1O8F 1O8G 1O8H 1O8I 1O8K 1O8L 1O8M 1PLU 2PEC
分子名称PECTATE LYASE C, CALCIUM ION (3 entities in total)
機能のキーワードhydrolase, pectate lyase cleavage, calcium binding, parallel beta-helix
由来する生物種ERWINIA CHRYSANTHEMI
タンパク質・核酸の鎖数1
化学式量合計37773.68
構造登録者
Herron, S.R.,Jurnak, F.A. (登録日: 2002-11-27, 公開日: 2003-01-30, 最終更新日: 2023-12-13)
主引用文献Herron, S.R.,Scavetta, R.,Garrett, M.,Legner, M.,Jurnak, F.A.
Characterization and Implications of Ca2+ Binding to Pectate Lyase C
J.Biol.Chem., 278:12271-12277, 2003
Cited by
PubMed Abstract: Ca(2+) is essential for in vitro activity of Erwinia chrysanthemi pectate lyase C (PelC). Crystallographic analyses of 11 PelC-Ca(2+) complexes, formed at pH 4.5, 9.5, and 11.2 under varying Ca(2+) concentrations, have been solved and refined at a resolution of 2.2 A. The Ca(2+) site represents a new motif for Ca(2+), consisting primarily of beta-turns and beta-strands. The principal differences between PelC and the PelC-Ca(2+) structures at all pH values are the side-chain conformations of Asp-129 and Glu-166 as well as the occupancies of four water molecules. According to calculations of pK(a) values, the presence of Ca(2+) and associated structural changes lower the pK(a) of Arg-218, the amino acid responsible for proton abstraction during catalysis. The Ca(2+) affinity for PelC is weak, as the K(d) was estimated to be 0.132 (+/-0.004) mm at pH 9.5, 1.09 (+/-0.29) mm at pH 11.2, and 5.84 (+/-0.41) mm at pH 4.5 from x-ray diffraction studies and 0.133 (+/-0.045) mm at pH 9.5 from intrinsic tryptophan fluorescence measurements. Given the pH dependence of Ca(2+) affinity, PelC activity at pH 4.5 has been reexamined. At saturating Ca(2+) concentrations, PelC activity increases 10-fold at pH 4.5 but is less than 1% of maximal activity at pH 9.5. Taken together, the studies suggest that the primary Ca(2+) ion in PelC has multiple functions.
PubMed: 12540845
DOI: 10.1074/JBC.M209306200
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.2 Å)
構造検証レポート
Validation report summary of 1o8j
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2024-10-30に公開中

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