An improved understanding of TNFL/TNFR interactions using structure-based classifications

被引:32
作者
Magis, Cedrik [1 ]
van der Sloot, Almer M. [2 ]
Serrano, Luis [2 ,3 ]
Notredame, Cedric [1 ]
机构
[1] Ctr Genom Regulat CRG, Bioinformat & Genom Program, Barcelona, Spain
[2] UPF, Ctr Genom Regulat CRG, EMBL CRG Syst Biol Res Unit, Barcelona, Spain
[3] ICREA, Barcelona 08019, Spain
关键词
TNFL; TNFR; structure-based classification; MSA; evolution; MULTIPLE SEQUENCE ALIGNMENTS; PRELIGAND ASSEMBLY DOMAIN; CYSTEINE-RICH DOMAIN; CRYSTAL-STRUCTURE; TNF SUPERFAMILY; FUNCTIONAL-CHARACTERIZATION; T-COFFEE; RECEPTOR; LIGAND; FAMILY;
D O I
10.1016/j.tibs.2012.06.002
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
Tumor Necrosis Factor Ligand (TNFL)-Tumor Necrosis Factor Receptor (TNFR) interactions control key cellular processes; however, the molecular basis of the specificity of these interactions remains poorly understood. Using the T-RMSD (tree based on root mean square deviation), a newly developed structure-based sequence clustering method, we have re-analyzed the available structural data to re-interpret the interactions between TNFLs and TNFRs. This improves the classification of both TNFLs and TNFRs, such that the new groups defined here are in much stronger agreement with structural and functional features than existing schemes. Our clustering approach also identifies traces of a convergent evolutionary process for TNFLs and TNFRs, leading us to propose the co-evolution of TNFLs and the third cysteine rich domain (CRD) of large TNFRs.
引用
收藏
页码:353 / 363
页数:11
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