4.5 Article

Crystal structure of the LMAN1-CRD/MCFD2 transport receptor complex provides insight into combined deficiency of factor V and factor VIII

期刊

FEBS LETTERS
卷 584, 期 5, 页码 878-882

出版社

WILEY
DOI: 10.1016/j.febslet.2010.02.009

关键词

Glycoprotein transport; ER quality control; Protein complex; Crystal structure; ERGIC-53

资金

  1. Human Frontier Science Program and The Swedish Research Council
  2. The European Commission FP6 Marie Curie programme
  3. Medical Research Council [G0500367] Funding Source: researchfish
  4. MRC [G0500367] Funding Source: UKRI

向作者/读者索取更多资源

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. Structured summary: MINT-7557086: lman1 (uniprotkb:P49257) and mcfd2 (uniprotkb:Q8NI22) bind (MI:0407) by X-ray crystallography (MI: 0114) (C) 2010 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

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