2c0l
From Proteopedia
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TPR DOMAIN OF HUMAN PEX5P IN COMPLEX WITH HUMAN MSCP2
Contents |
Overview
Peroxisomes require the translocation of folded and functional target, proteins of various sizes across the peroxisomal membrane. We have, investigated the structure and function of the principal import receptor, Pex5p, which recognizes targets bearing a C-terminal peroxisomal targeting, signal type 1. Crystal structures of the receptor in the presence and, absence of a peroxisomal target, sterol carrier protein 2, reveal major, structural changes from an open, snail-like conformation into a closed, circular conformation. These changes are caused by a long loop C terminal, to the 7-fold tetratricopeptide repeat segments. Mutations in residues of, this loop lead to defects in peroxisomal import in human fibroblasts. The, structure of the receptor/cargo complex demonstrates that the primary, receptor-binding site of the cargo is structurally and topologically, autonomous, enabling the cargo to retain its native structure and, function.
Disease
Known diseases associated with this structure: Adrenoleukodystrophy, neonatal OMIM:[600414], Zellweger syndrome OMIM:[600414]
About this Structure
2C0L is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Recognition of a functional peroxisome type 1 target by the dynamic import receptor pex5p., Stanley WA, Filipp FV, Kursula P, Schuller N, Erdmann R, Schliebs W, Sattler M, Wilmanns M, Mol Cell. 2006 Dec 8;24(5):653-63. PMID:17157249
Page seeded by OCA on Fri Feb 15 17:17:40 2008
Categories: Homo sapiens | Protein complex | Kursula, P. | Stanley, W.A. | Wilmanns, M. | Alternative initiation | Disease mutation | Import receptor complex | Lipid transport | Lipid-binding | Mitochondrion | Peroxisome | Protein transport | Tpr repeat | Transit peptide | Transport | Transport protein/receptor complex | Zellweger syndrome