Both domain 19 and domain 20 of factor H are involved in binding to complement C3b and C3d
- 31 May 2010
- journal article
- Published by Elsevier in Molecular Immunology
- Vol. 47 (9) , 1686-1691
- https://doi.org/10.1016/j.molimm.2010.03.007
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Mutations of Factor H Impair Regulation of Surface-bound C3b by Three Mechanisms in Atypical Hemolytic Uremic SyndromeJournal of Biological Chemistry, 2009
- The Binding of Factor H to a Complex of Physiological Polyanions and C3b on Cells Is Impaired in Atypical Hemolytic Uremic SyndromeThe Journal of Immunology, 2009
- Translational Mini-Review Series on Complement Factor H: Genetics and disease associations of human complement factor HClinical and Experimental Immunology, 2007
- Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domainsThe Journal of Experimental Medicine, 2007
- Structure of complement factor H carboxyl-terminus reveals molecular basis of atypical haemolytic uremic syndromeThe EMBO Journal, 2006
- REFMAC5 dictionary: organization of prior chemical knowledge and guidelines for its useActa Crystallographica Section D-Biological Crystallography, 2004
- Coot: model-building tools for molecular graphicsActa Crystallographica Section D-Biological Crystallography, 2004
- Electrostatics of nanosystems: Application to microtubules and the ribosomeProceedings of the National Academy of Sciences, 2001
- Each of the Three Binding Sites on Complement Factor H Interacts with a Distinct Site on C3bJournal of Biological Chemistry, 2000
- Refinement of Macromolecular Structures by the Maximum-Likelihood MethodActa Crystallographica Section D-Biological Crystallography, 1997