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Structure, function and molecular genetics of human and murine C1r.

Authors :
Arlaud GJ
Gaboriaud C
Garnier G
Circolo A
Thielens NM
Budayova-Spano M
Fontecilla-Camps JC
Volanakis JE
Source :
Immunobiology [Immunobiology] 2002 Sep; Vol. 205 (4-5), pp. 365-82.
Publication Year :
2002

Abstract

C1r, the enzyme responsible for intrinsic activation of the C1 complex of complement, is a modular serine protease featuring an overall structural organization homologous to those of C1s and the mannan-binding lectin-associated serine proteases (MASPs). This review will initially summarize current information on the structure and function of C1r, with particular emphasis on the three-dimensional structure of its catalytic domain, which provides new insights into the activation mechanism of C1. The second part of this review will focus on recent discoveries dealing with a truncated, C1r-related protein, and the occurrence in the mouse of two isoforms, C1rA and C1rB, exhibiting tissue-specific expression patterns.

Details

Language :
English
ISSN :
0171-2985
Volume :
205
Issue :
4-5
Database :
MEDLINE
Journal :
Immunobiology
Publication Type :
Academic Journal
Accession number :
12396000
Full Text :
https://doi.org/10.1078/0171-2985-00139