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8K0F

Human collagen prolyl processing enzyme complex, P3H1/CRTAP/PPIB heterotrimer, in its apo state

Summary for 8K0F
Entry DOI10.2210/pdb8k0f/pdb
EMDB information36763
DescriptorProlyl 3-hydroxylase 1, Cartilage-associated protein, Peptidyl-prolyl cis-trans isomerase B, ... (5 entities in total)
Functional Keywordscomplex, hydroxylase, collagen, er protein, cytosolic protein
Biological sourceHomo sapiens (human)
More
Total number of polymer chains3
Total formula weight163845.19
Authors
Li, W.,Peng, J.,Yao, D.,Rao, B.,Xia, Y.,Wang, Q.,Li, S.,Cao, M.,Shen, Y.,Ma, P.,Liao, R.,Qin, A.,Zhao, J.,Cao, Y. (deposition date: 2023-07-08, release date: 2024-09-18, Last modification date: 2024-10-23)
Primary citationLi, W.,Peng, J.,Yao, D.,Rao, B.,Xia, Y.,Wang, Q.,Li, S.,Cao, M.,Shen, Y.,Ma, P.,Liao, R.,Qin, A.,Zhao, J.,Cao, Y.
The structural basis for the collagen processing by human P3H1/CRTAP/PPIB ternary complex.
Nat Commun, 15:7844-7844, 2024
Cited by
PubMed Abstract: Collagen posttranslational processing is crucial for its proper assembly and function. Disruption of collagen processing leads to tissue development and structure disorders like osteogenesis imperfecta (OI). OI-related collagen processing machinery includes prolyl 3-hydroxylase 1 (P3H1), peptidyl-prolyl cis-trans isomerase B (PPIB), and cartilage-associated protein (CRTAP), with their structural organization and mechanism unclear. We determine cryo-EM structures of the P3H1/CRTAP/PPIB complex. The active sites of P3H1 and PPIB form a face-to-face bifunctional reaction center, indicating a coupled modification mechanism. The structure of the P3H1/CRTAP/PPIB/collagen peptide complex reveals multiple binding sites, suggesting a substrate interacting zone. Unexpectedly, a dual-ternary complex is observed, and the balance between ternary and dual-ternary states can be altered by mutations in the P3H1/PPIB active site and the addition of PPIB inhibitors. These findings provide insights into the structural basis of collagen processing by P3H1/CRTAP/PPIB and the molecular pathology of collagen-related disorders.
PubMed: 39245686
DOI: 10.1038/s41467-024-52321-6
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.37 Å)
Structure validation

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数据于2025-06-18公开中

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