Mutation C176A in TSHR Human

MutationC176A  >>View Structure<<
RegionLRR5
General number GPCRDB / Ballesteros-Extended0
5069
ReceptorTSHR HumanSwiss-Prot
Crossreferences at GPCRDB
PhenotypeConstitutivity (compared to WT): Unknown
Cell-surface expression (%WT): 78
Binding affinity of native hormone: Unknown
Additional commentsThis mutation was investigated to study its involvement in ectodomain multimer formation. It seems not to play a role according to Latif et al.
DownloadDownload the flat text file of this mutant (more info here)
Reference #1 A tyrosine residue on the TSH receptor stabilizes multimer formation.
Latif R, Michalek K, Morshed SA, Davies TF
PLoS One. 2010 Feb 26;5(2):e9449.
Pubmed


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