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High-level intrinsic disorder explains the universality of CLIP binding to diverse MHC class II variants
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作者 Vladimir N Uversky Yaping N Tu +3 位作者 onyekachi nwogu Shanitra N Butler Michael Ramsamooj George Blanck 《Cellular & Molecular Immunology》 SCIE CAS CSCD 2018年第1期76-78,共3页
MHC class I and II molecules bind peptides that are either recognized as self or as foreign to the immune system via interaction with T-cell receptors.The T-cell receptor makes molecular contacts with the peptide and ... MHC class I and II molecules bind peptides that are either recognized as self or as foreign to the immune system via interaction with T-cell receptors.The T-cell receptor makes molecular contacts with the peptide and the MHC molecule in the region of the MHC peptide binding cleft.The MHC class I and II molecules are highly polymorphic,which presumably allows for great diversity of antigen-binding sites over the population,leading to a species that is relatively fit to withstand foreign pathogens.In MHC class I molecules,this allelic variation predicts extensive variation in the sequence of peptides able to bind MHC class I molecules,and this is indeed the case. 展开更多
关键词 EXPLAIN class INTRINSIC
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