Reviewed,
UniProtKB/Swiss-Prot Q9NZQ8 (TRPM5_HUMAN)
Last modified
June 16, 2009.
Version 42.
History...
Clusters with 100%,
90%,
50% identity |
Documents (5) |
Third-party data |
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Names and origin
| Protein names | Recommended name: Transient receptor potential cation channel subfamily M member 5 Alternative name(s): Long transient receptor potential channel 5 Short name=LTrpC5 MLSN1- and TRP-related gene 1 protein | ||||
| Gene names |
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| Organism | Homo sapiens (Human) | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 1165 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is not processed. |
| Protein existence | Evidence at protein level. |
General annotation (Comments)
| Function | Voltage-modulated Ca2+-activated, monovalent cation channel (VCAM) that mediates a transient membrane depolarization and plays a central role in taste transduction. Monovalent-specific, non-selective cation channel that mediates the transport of Na+, K+ and Cs+ ions equally well. Activated directly by increases in intracellular Ca2+, but is impermeable to it. Gating is voltage-dependent and displays rapid activation and deactivation kinetics upon channel stimulation even during sustained elevations in Ca2+. Also activated by a fast intracellular Ca2+ increase in response to inositol 1,4,5-triphosphate-producing receptor agonists. The channel is blocked by extracellular acidification. External acidification has 2 effects, a fast reversible block of the current and a slower irreversible enhancement of current inactivation. Is a highly temperature-sensitive, heat activated channel showing a steep increase of inward currents at temperatures between 15 and 35 degrees Celsius. Heat activation is due to a shift of the voltage-dependent activation curve to negative potentials. Activated by arachidonic acid in vitro. May be involved in perception of bitter, sweet and umami tastes. May also be involved in sensing semiochemicals. Ref.5 UniProtKB Q9JJH7 |
| Subcellular location | Cell membrane; Multi-pass membrane protein Potential. |
| Tissue specificity | Strongly expressed in fetal brain, liver and kidney, and in adult prostate, testis, ovary, colon and peripheral blood leukocytes. Also expressed in a large proportion of Wilms' tumors and rhabdomyosarcomas. In monochromosomal cell lines shows exclusive paternal expression. Ref.1 |
| Sequence similarities | Belongs to the transient receptor family. LTrpC subfamily. Ref.5 |
Ontologies
| Keywords | |
|---|---|
| Biological process | Ion transport Transport |
| Cellular component | Cell membrane Membrane |
| Coding sequence diversity | Alternative splicing Polymorphism |
| Domain | Coiled coil Transmembrane |
| Molecular function | Ionic channel Receptor Voltage-gated channel |
| PTM | Phosphoprotein |
| Gene Ontology (GO) | |
| Biological process | ion transport Inferred from electronic annotation. Source: UniProtKB-KW |
| Cellular component | integral to membrane Ref.1 Traceable author statement. Source: ProtInc plasma membraneInferred from electronic annotation. Source: UniProtKB-SubCell |
| Molecular function | receptor activity Inferred from electronic annotation. Source: UniProtKB-KW voltage-gated ion channel activityInferred from electronic annotation. Source: UniProtKB-KW |
| Complete GO annotation... | |
Alternative products
| This entry describes 3 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 Ref.1 Ref.3 Ref.2 (identifier: Q9NZQ8-1) This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry. | ||||||
| Isoform 2 Ref.4 (identifier: Q9NZQ8-2) The sequence of this isoform differs from the canonical sequence as follows: 155-155: Q → QVH | ||||||
| Isoform 3 Ref.1 (identifier: Q9NZQ8-3) The sequence of this isoform differs from the canonical sequence as follows: 870-872: MKD → KPV 873-1165: Missing. | ||||||
| Note: No experimental confirmation available. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 1165 | 1165 | Transient receptor potential cation channel subfamily M member 5 | PRO_0000328933 | |||||
Regions | |||||||||
| Topological domain | 1 – 646 | 646 | Cytoplasmic Potential | ||||||
| Transmembrane | 647 – 667 | 21 | Potential | ||||||
| Topological domain | 668 – 733 | 66 | Extracellular Potential | ||||||
| Transmembrane | 734 – 754 | 21 | Potential | ||||||
| Topological domain | 755 – 811 | 57 | Cytoplasmic Potential | ||||||
| Transmembrane | 812 – 832 | 21 | Potential | ||||||
| Topological domain | 833 – 835 | 3 | Extracellular Potential | ||||||
| Transmembrane | 836 – 856 | 21 | Potential | ||||||
| Topological domain | 857 – 872 | 16 | Cytoplasmic Potential | ||||||
| Transmembrane | 873 – 893 | 21 | Potential | ||||||
| Topological domain | 894 – 954 | 61 | Extracellular Potential | ||||||
| Transmembrane | 955 – 975 | 21 | Potential | ||||||
| Topological domain | 976 – 1165 | 190 | Cytoplasmic Potential | ||||||
| Coiled coil | 553 – 581 | 29 | Potential | ||||||
Amino acid modifications | |||||||||
| Modified residue | 419 | 1 | Phosphotyrosine Ref.6 | ||||||
Natural variations | |||||||||
| Alternative sequence | 155 | 1 | Q → QVH in isoform 2. Ref.4 | VSP_052741 | |||||
| Alternative sequence | 870 – 872 | 3 | MKD → KPV in isoform 3. Ref.1 | VSP_052742 | |||||
| Alternative sequence | 873 – 1165 | 293 | Missing in isoform 3. Ref.1 | VSP_052743 | |||||
| Natural variant | 235 | 1 | N → S: dbSNP rs886277. | VAR_052377 | |||||
| Natural variant | 254 | 1 | V → A: dbSNP rs3986599. Ref.3 | VAR_042578 | |||||
| Natural variant | 335 | 1 | V → L: dbSNP rs34350821. | VAR_052378 | |||||
| Natural variant | 456 | 1 | A → T: dbSNP rs34551253. | VAR_052379 | |||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression." Prawitt D., Enklaar T., Klemm G., Gaertner B., Spangenberg C., Winterpacht A., Higgins M., Pelletier J., Zabel B. Hum. Mol. Genet. 9:203-216(2000) [PubMed: 10607831] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1), ALTERNATIVE SPLICING (ISOFORM 3), TISSUE SPECIFICITY. |
| [2] | "Human chromosome 11 DNA sequence and analysis including novel gene identification." Taylor T.D., Noguchi H., Totoki Y., Toyoda A., Kuroki Y., Dewar K., Lloyd C., Itoh T., Takeda T., Kim D.-W., She X., Barlow K.F., Bloom T., Bruford E., Chang J.L., Cuomo C.A., Eichler E., FitzGerald M.G. Sakaki Y.Nature 440:497-500(2006) [PubMed: 16554811] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [3] | "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)." The MGC Project Team Genome Res. 14:2121-2127(2004) [PubMed: 15489334] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1), VARIANT ALA-254. |
| [4] | "Comparative sequence analysis and characterization of the imprinting cluster on the human chromosome 11p15.5 and distal mouse chromosome 7." Paulsen M., El-Maarri O., Engemann S., Franck O., Stroedicke M., Davies K.R., Bowden L.M., Reinhardt R., Reik W., Harteneck C., Walter J. Submitted (JAN-2000) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 9-1165 (ISOFORM 2). |
| [5] | "TRPM5 is a transient Ca2+-activated cation channel responding to rapid changes in [Ca2+]i." Prawitt D., Monteilh-Zoller M.K., Brixel L., Spangenberg C., Zabel B., Fleig A., Penner R. Proc. Natl. Acad. Sci. U.S.A. 100:15166-15171(2003) [PubMed: 14634208] [Abstract] Cited for: FUNCTION. |
| [6] | "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks." Olsen J.V., Blagoev B., Gnad F., Macek B., Kumar C., Mortensen P., Mann M. Cell 127:635-648(2006) [PubMed: 17081983] [Abstract] Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT TYR-419, MASS SPECTROMETRY. Tissue: Epithelium. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| AF177473 mRNA. Translation: AAF26288.1. AC124057 Genomic DNA. No translation available. BC093787 mRNA. Translation: AAH93787.1. BC093789 mRNA. Translation: AAH93789.1. AJ270996 mRNA. Translation: CAB66342.1. | |
| IPI | IPI00329503. IPI00889724. IPI00889744. |
| RefSeq | NP_055370.1. |
| UniGene | Hs.272287 |
3D structure databases | |
| ModBase | Search... |
Protein family/group databases | |
| TCDB | 1.A.4.5.3. transient receptor potential Ca2+ channel (TRP-CC) family. |
Proteomic databases | |
| PRIDE | Q9NZQ8. |
Genome annotation databases | |
| Ensembl | ENSG00000070985. Homo sapiens. [Contig view] |
| GeneID | 29850. |
| KEGG | hsa:29850. |
Organism-specific databases | |
| GeneCards | GC11M002382. |
| HGNC | HGNC:14323. TRPM5. |
| MIM | 604600. gene. |
| PharmGKB | PA37869. |
| GenAtlas | Search... |
Phylogenomic databases | |
| HOVERGEN | Q9NZQ8. |
| OMA | Q9NZQ8. LVKACKS. |
Gene expression databases | |
| ArrayExpress | Q9NZQ8. |
| Bgee | Q9NZQ8. |
| CleanEx | HS_TRPM5. |
Family and domain databases | |
| InterPro | IPR005821. Ion_trans. [Graphical view] |
| Pfam | PF00520. Ion_trans. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other Resources | |
| NextBio | 52387. |
| SOURCE | Search... |
Entry information
| Entry name | TRPM5_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9NZQ8 Secondary accession number(s): A6NHS0, Q52LU2, Q9NY34 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation project | HPI (Human Proteome Initiative) | ||||||||
Relevant documents
| Human chromosome 11 Human chromosome 11: entries, gene names and cross-references to MIM |
| Human entries with polymorphisms or disease mutations List of human entries with polymorphisms or disease mutations |
| Human polymorphisms and disease mutations Index of human polymorphisms and disease mutations |
| MIM cross-references Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot |
| SIMILARITY comments Index of protein domains and families |

Clusters with


