Structure and function of the SPRY/B30.2 domain proteins involved in innate immunity

被引:109
作者
D'Cruz, Akshay A. [1 ,2 ]
Babon, Jeffrey J. [2 ]
Norton, Raymond S. [3 ]
Nicola, Nicos A. [2 ]
Nicholson, Sandra E. [2 ]
机构
[1] Walter & Eliza Hall Inst Med Res, Inflammat Div, Parkville, Vic 3052, Australia
[2] Univ Melbourne, Dept Med Biol, Parkville, Vic 3052, Australia
[3] Monash Univ, Monash Inst Pharmaceut Sci, Parkville, Vic, Australia
基金
澳大利亚研究理事会; 澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
SPRY domain; PRY; B30; 2; domain; TRIM; BTN; SPSB; SOCS box; IgG; innate immunity; structure; function; FAMILIAL MEDITERRANEAN FEVER; NF-KAPPA-B; SINGLE AMINO-ACID; SPRY DOMAIN; TRIPARTITE-MOTIF; UBIQUITIN LIGASE; SOCS BOX; B30.2; DOMAIN; TRIM5-ALPHA RESTRICTION; MULTIGENIC FAMILIES;
D O I
10.1002/pro.2185
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The SPRY domain is a protein interaction module found in 77 murine and 100 human proteins, and is implicated in important biological pathways, including those that regulate innate and adaptive immunity. The current definition of the SPRY domain is based on a sequence repeat discovered in the splA kinase and ryanodine receptors. The greater SPRY family is divided into the B30.2 (which contains a PRY extension at the N-terminus) and SPRY-only sub-families. In this brief review, we examine the current structural and biochemical literature on SPRY/B30.2 domain involvement in key immune processes and highlight a PRY-like 60 amino acid region in the N-terminus of SPRY-only proteins. Phylogenetic, structural, and functional analyses suggest that this N-terminal region is related to the PRY region of B30.2 and should be characterized as part of an extended SPRY domain. Greater understanding of the functional importance of the N-terminal region in SPRY only proteins will enhance our ability to interrogate SPRY interactions with their respective binding partners.
引用
收藏
页码:1 / 10
页数:10
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