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Rhodopsin-like receptors

(Redirected from Rhodopsin-like receptor)

Rhodopsin-like receptors are a family of proteins that comprise the largest group of G protein-coupled receptors.[2]

Rhodopsin-like receptors
Structure of rhodopsin: A G protein-coupled receptor.[1]
Identifiers
Symbol7tm_1
PfamPF00001
Pfam clanGPCR_A
InterProIPR000276
PROSITEPDOC00211
SCOP21f88 / SCOPe / SUPFAM
OPM superfamily6
OPM protein1gzm
CDDcd00637
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary
PDB1U19 2R4R 2R4S 2RH1 1f88, 1hzx, 1l9h, 2g87, 2hpy, 2i35, 2i36, 2i37, 2j4y, 2ped

Scope

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G-protein-coupled receptors, GPCRs, constitute a vast protein family that encompasses a wide range of functions (including various autocrine, paracrine, and endocrine processes). They show considerable diversity at the sequence level, on the basis of which they can be separated into distinct groups. GPCRs are usually described as "superfamily" because they embrace a group of families for which there are indications of evolutionary relationship, but between which there is no statistically significant similarity in sequence.[2] The currently known superfamily members include the rhodopsin-like GPCRs (this family), the secretin-like GPCRs, the cAMP receptors, the fungal mating pheromone receptors, and the metabotropic glutamate receptor family. There is a specialised database for GPCRs.[3]

Function

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The rhodopsin-like GPCRs themselves represent a widespread protein family that includes hormone, neuropeptide, neurotransmitter, and light receptors, all of which transduce extracellular signals through interaction with guanine nucleotide-binding (G) proteins. Although their activating ligands vary widely in structure and character, the amino acid sequences of the receptors are very similar and are believed to adopt a common structural framework comprising 7 transmembrane (TM) helices.[4][5][6]

Classes

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Rhodopsin-like GPCRs have been classified into the following 19 subgroups (A1-A19) based on a phylogenetic analysis.[7]

Subfamily A1

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Subfamily A2

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Subfamily A3

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Subfamily A4

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Subfamily A5

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Subfamily A6

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Subfamily A7

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Subfamily A8

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Subfamily A9

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Subfamily A10

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Subfamily A11

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Subfamily A12

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Subfamily A13

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Subfamily A14

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Subfamily A15

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Subfamily A16

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Subfamily A17

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Subfamily A18

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Subfamily A19

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Unclassified

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References

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  1. ^ Palczewski K, Kumasaka T, Hori T, et al. (August 2000). "Crystal structure of rhodopsin: A G protein-coupled receptor". Science. 289 (5480): 739–45. Bibcode:2000Sci...289..739P. doi:10.1126/science.289.5480.739. PMID 10926528.
  2. ^ a b Attwood TK, Findlay JB (1994). "Fingerprinting G-protein-coupled receptors". Protein Eng. 7 (2): 195–203. doi:10.1093/protein/7.2.195. PMID 8170923.
  3. ^ "Information system for G protein-coupled receptors". GPCRDB. www.gpcr.org. Archived from the original on 2009-04-22. Retrieved 2008-12-05.
  4. ^ Birnbaumer L (1990). "G proteins in signal transduction". Annu. Rev. Pharmacol. Toxicol. 30: 675–705. doi:10.1146/annurev.pa.30.040190.003331. PMID 2111655.
  5. ^ Gilman AG, Casey PJ (1988). "G protein involvement in receptor-effector coupling". J. Biol. Chem. 263 (6): 2577–2580. doi:10.1016/S0021-9258(18)69103-3. PMID 2830256.
  6. ^ Attwood TK, Findlay JB (1993). "Design of a discriminating fingerprint for G-protein-coupled receptors". Protein Eng. 6 (2): 167–176. doi:10.1093/protein/6.2.167. PMID 8386361.
  7. ^ Joost P, Methner A (2002). "Phylogenetic analysis of 277 human G-protein-coupled receptors as a tool for the prediction of orphan receptor ligands". Genome Biol. 3 (11): research0063.1–0063.16. doi:10.1186/gb-2002-3-11-research0063. PMC 133447. PMID 12429062.
  8. ^ Terakita A (2005). "The opsins". Genome Biol. 6 (3): 213. doi:10.1186/gb-2005-6-3-213. PMC 1088937. PMID 15774036.
  9. ^ a b Nordström KJ, Sällman Almén M, Edstam MM, Fredriksson R, Schiöth HB (September 2011). "Independent HHsearch, Needleman—Wunsch-based, and motif analyses reveal the overall hierarchy for most of the G protein-coupled receptor families". Molecular Biology and Evolution. 28 (9): 2471–80. doi:10.1093/molbev/msr061. PMID 21402729.
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