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6JLI

Crystal structure of CTLD7 domain of human PLA2R

Summary for 6JLI
Entry DOI10.2210/pdb6jli/pdb
DescriptorSecretory phospholipase A2 receptor, 2-acetamido-2-deoxy-beta-D-glucopyranose (3 entities in total)
Functional Keywordsimn, epitope, pla2r, ctld7, immune system
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight15540.28
Authors
Yu, B.,Hu, Z.,Kong, D.,Cheng, C.,He, Y. (deposition date: 2019-03-06, release date: 2019-07-17, Last modification date: 2024-10-16)
Primary citationYu, B.,Hu, Z.,Kong, D.,Cheng, C.,He, Y.
Crystal structure of the CTLD7 domain of human M-type phospholipase A2 receptor.
J.Struct.Biol., 207:295-300, 2019
Cited by
PubMed Abstract: M-type phospholipase A2 receptor (PLA2R) is a member of the mannose receptor family. Recent evidence shows that PLA2R is a major autoantigen causing idiopathic membranous nephropathy (IMN), which is an autoimmune disease and one of the most common causes for nephrotic syndrome in adults. The epitope mapping data suggest that the major epitopes of PLA2R locate at the CysR, CTLD1 and CTLD7 domains. However, due to the lack of the high-resolution structural information, it is unclear how the autoantibodies interact with PLA2R. Here we determine the crystal structure of the CTLD7 domain of PLA2R at 1.8 Å, showing that it adopts a typical CTLD fold, and the structural alignments also provide hints for the potential antibody binding regions. In addition, the high-resolution structural information of CTLD7 could be applied to identify the epitopes for autoantibodies, which would facilitate the therapeutic strategies against IMN.
PubMed: 31271865
DOI: 10.1016/j.jsb.2019.06.007
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.778 Å)
Structure validation

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