2V77

Crystal Structure of Human Carboxypeptidase A1

2V77 の概要

• エントリーDOI: 10.2210/pdb2v77/pdb
• 分子名称: CARBOXYPEPTIDASE A1, OCTANE-1,3,5,7-TETRACARBOXYLIC ACID, ZINC ION, ... (5 entities in total)
• 機能のキーワード: metal-binding, metalloprotease, carboxypeptidase, protein degradation, zinc, zymogen, protease, secreted, hydrolase
• 由来する生物種: HOMO SAPIENS (HUMAN)
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 70835.95

構造登録者

Pallares, I.,Fernandez, D.,Comellas-Bigler, M.,Fernandez-Recio, J.,Ventura, S.,Aviles, F.X.,Vendrell, J. (登録日: 2007-07-27, 公開日: 2008-07-01, 最終更新日: 2024-10-16)

主引用文献

Pallares, I.,Fernandez, D.,Comellas-Bigler, M.,Fernandez-Recio, J.,Ventura, S.,Aviles, F.X.,Bode, W.,Vendrell, J.
Direct interaction between a human digestive protease and the mucoadhesive poly(acrylic acid).
Acta Crystallogr. D Biol. Crystallogr., D64:784-791, 2008

PubMed Abstract: Carboxypeptidase A1 has been the subject of extensive research in the last 30 y and is one of the most widely studied zinc metalloenzymes. However, the three-dimensional structure of the human form of the enzyme is not yet available. This report describes the three-dimensional structure of human carboxypeptidase A1 (hCPA1) derived from crystals that belong to the tetragonal space group P4(3)2(1)2 and diffract to 1.6 angstroms resolution. A description of the ternary complex hCPA1-Zn2+-poly(acrylic acid) is included as a model of the interaction of mucoadhesive polymers with proteases in the gastrointestinal tract. The direct mode of interaction between poly(acrylic acid) and the active site of the target protease was confirmed by in vitro inhibition assays. The structure was further analyzed in silico through the optimal docking-area method. The characterization of binding sites on the surface of hCPA1 and a comparison with other available carboxypeptidase structures provided further insights into the formation of multiprotein complexes and the activation mechanisms of carboxypeptidase zymogens. The high-resolution structure of hCPA1 provides an excellent template for the modelling of physiologically relevant carboxypeptidases and could also contribute to the design of specific agents for biomedical purposes.

PubMed: 18566513
DOI: 10.1107/S0907444908013474

実験手法

X-RAY DIFFRACTION (1.603 Å)