Source:http://linkedlifedata.com/resource/pubmed/id/16147994
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
45
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pubmed:dateCreated |
2005-11-7
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pubmed:abstractText |
The Ca(2+)-sensing receptor (CaSR) belongs to the class III G-protein-coupled receptors (GPCRs), which include receptors for pheromones, amino acids, sweeteners, and the neurotransmitters glutamate and gamma-aminobutyric acid (GABA). These receptors are characterized by a long extracellular amino-terminal domain called a Venus flytrap module (VFTM) containing the ligand binding pocket. To elucidate the molecular determinants implicated in Ca(2+) recognition by the CaSR VFTM, we developed a homology model of the human CaSR VFTM from the x-ray structure of the metabotropic glutamate receptor type 1 (mGluR1), and a phylogenetic analysis of 14 class III GPCR VFTMs. We identified critical amino acids delineating a Ca(2+) binding pocket predicted to be adjacent to, but distinct from, a cavity reminiscent of the binding site described for amino acids in mGluRs, GABA-B receptor, and GPRC6a. Most interestingly, these Ca(2+)-contacting residues are well conserved within class III GPCR VFTMs. Our model was validated by mutational and functional analysis, including the characterization of activating and inactivating mutations affecting a single amino acid, Glu-297, located within the proposed Ca(2+) binding pocket of the CaSR and associated with autosomal dominant hypocalcemia and familial hypocalciuric hypercalcemia, respectively, genetic diseases characterized by perturbations in Ca(2+) homeostasis. Altogether, these data define a Ca(2+) binding pocket within the CaSR VFTM that may be conserved in several other class III GPCRs, thereby providing a molecular basis for extracellular Ca(2+) sensing by these receptors.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
11
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pubmed:volume |
280
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
37917-23
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16147994-Amino Acid Sequence,
pubmed-meshheading:16147994-Animals,
pubmed-meshheading:16147994-Base Sequence,
pubmed-meshheading:16147994-Binding Sites,
pubmed-meshheading:16147994-Calcium,
pubmed-meshheading:16147994-Female,
pubmed-meshheading:16147994-Humans,
pubmed-meshheading:16147994-Male,
pubmed-meshheading:16147994-Mutation,
pubmed-meshheading:16147994-Pedigree,
pubmed-meshheading:16147994-Phylogeny,
pubmed-meshheading:16147994-Rats,
pubmed-meshheading:16147994-Receptors, AMPA,
pubmed-meshheading:16147994-Receptors, Calcium-Sensing
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pubmed:year |
2005
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pubmed:articleTitle |
Delineating a Ca2+ binding pocket within the venus flytrap module of the human calcium-sensing receptor.
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pubmed:affiliation |
INSERM, U426, Faculté deMédecine Xavier Bichat and IFR02, Paris, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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