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5WZM

Crystal structure of human secreted phospholipase A2 group IIE

5WZM の概要
エントリーDOI10.2210/pdb5wzm/pdb
関連するPDBエントリー5WZO 5WZS 5WZT 5WZU 5WZV 5WZW
分子名称Group IIE secretory phospholipase A2, CHLORIDE ION, CALCIUM ION, ... (5 entities in total)
機能のキーワードinhibitor, hydrolase-inhibitor complex, hydrolase/inhibitor
由来する生物種Homo sapiens (Human)
細胞内の位置Secreted: Q9NZK7
タンパク質・核酸の鎖数1
化学式量合計14366.94
構造登録者
Hou, S.,Xu, J.,Xu, T.,Liu, J. (登録日: 2017-01-18, 公開日: 2018-01-24, 最終更新日: 2024-11-13)
主引用文献Hou, S.,Xu, T.,Xu, J.,Qu, L.,Xu, Y.,Chen, L.,Liu, J.
Structural basis for functional selectivity and ligand recognition revealed by crystal structures of human secreted phospholipase A2 group IIE
Sci Rep, 7:10815-10815, 2017
Cited by
PubMed Abstract: Secreted phospholipases As (sPLAs) are involved in various pathological conditions such as rheumatoid arthritis and cardiovascular disease. Many inhibitors were developed and studied in clinical trials, but none have reached the market yet. This failure may be attributed to the lack of subtype selectivity for these inhibitors. Therefore, more structural information for subtype sPLA is needed to guide the selective inhibitor development. In this study, the crystal structure of human sPLA Group IIE (hGIIE), coupled with mutagenesis experiments, proved that the flexible second calcium binding site and residue Asn21 in hGIIE are essential to its enzymatic activity. Five inhibitor bound hGIIE complex structures revealed the key residues (Asn21 and Gly6) of hGIIE that are responsible for interacting with inhibitors, and illustrated the difference in the inhibitor binding pocket with other sPLAs. This will facilitate the structure-based design of sPLA's selective inhibitors.
PubMed: 28883454
DOI: 10.1038/s41598-017-11219-8
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2 Å)
構造検証レポート
Validation report summary of 5wzm
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2024-11-20に公開中

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