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Volumn 16, Issue 8, 2002, Pages 1881-1892
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Chimeras of the rat and human FSH receptors (FSHRs) identify residues that permit or suppress transmembrane 6 mutation-induced constitutive activation of the FSHR via rearrangements of hydrophobic interactions between helices 6 and 7
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Author keywords
[No Author keywords available]
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Indexed keywords
FOLLITROPIN RECEPTOR;
G PROTEIN COUPLED RECEPTOR;
LUTEINIZING HORMONE RECEPTOR;
HYBRID PROTEIN;
ANIMAL CELL;
ARTICLE;
CHIMERA;
COMPUTER MODEL;
GENE MUTATION;
HORMONE RECEPTOR INTERACTION;
HUMAN;
HUMAN CELL;
HYDROPHOBICITY;
NONHUMAN;
POINT MUTATION;
PRIORITY JOURNAL;
RAT;
AMINO ACID SEQUENCE;
AMINO ACID SUBSTITUTION;
ANIMAL;
CELL LINE;
CHEMICAL STRUCTURE;
CHEMISTRY;
COMPARATIVE STUDY;
COMPUTER SIMULATION;
GENETICS;
METABOLISM;
MOLECULAR GENETICS;
PROTEIN CONFORMATION;
PROTEIN SECONDARY STRUCTURE;
SPECIES DIFFERENCE;
AMINO ACID SEQUENCE;
AMINO ACID SUBSTITUTION;
ANIMAL;
CELL LINE;
CHIMERIC PROTEINS;
COMPARATIVE STUDY;
COMPUTER SIMULATION;
HUMAN;
HYDROPHOBICITY;
MODELS, MOLECULAR;
MOLECULAR SEQUENCE DATA;
POINT MUTATION;
PROTEIN CONFORMATION;
PROTEIN STRUCTURE, SECONDARY;
RATS;
RECEPTORS, FSH;
SPECIES SPECIFICITY;
SUPPORT, NON-U.S. GOV'T;
SUPPORT, U.S. GOV'T, P.H.S.;
ANIMALS;
HUMANS;
RECOMBINANT FUSION PROTEINS;
ANIMALIA;
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EID: 0036020508
PISSN: 08888809
EISSN: None
Source Type: Journal
DOI: 10.1210/me.2001-0199 Document Type: Article |
Times cited : (24)
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References (32)
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