Loading
PDBj
メニューPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

2RDL

Hamster Chymase 2

2RDL の概要
エントリーDOI10.2210/pdb2rdl/pdb
関連するBIRD辞書のPRD_IDPRD_000402
分子名称Chymase 2, METHOXYSUCCINYL-ALA-ALA-PRO-ALA-CHLOROMETHYLKETONE INHIBITOR, SULFATE ION, ... (4 entities in total)
機能のキーワードchymase 2, serine protease, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
由来する生物種Mesocricetus auratus (golden hamster)
タンパク質・核酸の鎖数4
化学式量合計52047.10
構造登録者
Spurlino, J.,Abad, M.,Kervinen, J. (登録日: 2007-09-24, 公開日: 2007-10-30, 最終更新日: 2024-11-20)
主引用文献Kervinen, J.,Abad, M.,Crysler, C.,Kolpak, M.,Mahan, A.D.,Masucci, J.A.,Bayoumy, S.,Cummings, M.D.,Yao, X.,Olson, M.,de Garavilla, L.,Kuo, L.,Deckman, I.,Spurlino, J.
Structural basis for elastolytic substrate specificity in rodent alpha-chymases.
J.Biol.Chem., 283:427-436, 2008
Cited by
PubMed Abstract: Divergence of substrate specificity within the context of a common structural framework represents an important mechanism by which new enzyme activity naturally evolves. We present enzymological and x-ray structural data for hamster chymase-2 (HAM2) that provides a detailed explanation for the unusual hydrolytic specificity of this rodent alpha-chymase. In enzymatic characterization, hamster chymase-1 (HAM1) showed typical chymase proteolytic activity. In contrast, HAM2 exhibited atypical substrate specificity, cleaving on the carboxyl side of the P1 substrate residues Ala and Val, characteristic of elastolytic rather than chymotryptic specificity. The 2.5-A resolution crystal structure of HAM2 complexed to the peptidyl inhibitor MeOSuc-Ala-Ala-Pro-Ala-chloromethylketone revealed a narrow and shallow S1 substrate binding pocket that accommodated only a small hydrophobic residue (e.g. Ala or Val). The different substrate specificities of HAM2 and HAM1 are explained by changes in four S1 substrate site residues (positions 189, 190, 216, and 226). Of these, Asn(189), Val(190), and Val(216) form an easily identifiable triplet in all known rodent alpha-chymases that can be used to predict elastolytic specificity for novel chymase-like sequences. Phylogenetic comparison defines guinea pig and rabbit chymases as the closest orthologs to rodent alpha-chymases.
PubMed: 17981788
DOI: 10.1074/jbc.M707157200
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.5 Å)
構造検証レポート
Validation report summary of 2rdl
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

PDB statisticsPDBj update infoContact PDBjnumon