8K0E
Human collagen prolyl processing enzyme complex, P3H1/CRTAP heterodimer
Summary for 8K0E
Entry DOI | 10.2210/pdb8k0e/pdb |
EMDB information | 36762 |
Descriptor | Prolyl 3-hydroxylase 1, Cartilage-associated protein, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (4 entities in total) |
Functional Keywords | complex, hydroxylase, collagen, er protein, cytosolic protein |
Biological source | Homo sapiens (human) More |
Total number of polymer chains | 2 |
Total formula weight | 135988.36 |
Authors | |
Primary citation | 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. 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: 39245686DOI: 10.1038/s41467-024-52321-6 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (3.65 Å) |
Structure validation
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