| Literature DB >> 20138881 |
Edvard Wigren1, Jean-Marie Bourhis, Inari Kursula, Jodie E Guy, Ylva Lindqvist.
Abstract
LMAN1 is a glycoprotein receptor, mediating transfer from the ER to the ER-Golgi intermediate compartment. Together with the co-receptor MCFD2, it transports coagulation factors V and VIII. Mutations in LMAN1 and MCFD2 can cause combined deficiency of factors V and VIII (F5F8D). We present the crystal structure of the LMAN1/MCFD2 complex and relate it to patient mutations. Circular dichroism data show that the majority of the substitution mutations give rise to a disordered or severely destabilized MCFD2 protein. The few stable mutation variants are found in the binding surface of the complex leading to impaired LMAN1 binding and F5F8D. Copyright (c) 2010 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.Entities:
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Year: 2010 PMID: 20138881 DOI: 10.1016/j.febslet.2010.02.009
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124