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5WZT

Crystal structure of human secreted phospholipase A2 group IIE with Compound 14

Summary for 5WZT
Entry DOI10.2210/pdb5wzt/pdb
Related5WZM 5WZO 5WZS 5WZU 5WZV 5WZW
DescriptorGroup IIE secretory phospholipase A2, CALCIUM ION, GLYCEROL, ... (6 entities in total)
Functional Keywordsphospholipase a2, hydrolase-inhibitor complex, hydrolase/inhibitor
Biological sourceHomo sapiens (Human)
Cellular locationSecreted: Q9NZK7
Total number of polymer chains1
Total formula weight14641.70
Authors
Hou, S.,Xu, J.,Xu, T.,Liu, J. (deposition date: 2017-01-18, release date: 2018-01-24, Last modification date: 2024-10-23)
Primary citationHou, 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
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.4 Å)
Structure validation

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