Q96SN7 (ORAI2_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 84.
History...
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Protein orai-2 Alternative name(s): CAP-binding protein complex-interacting protein 2 Transmembrane protein 142B | ||||||
| Gene names |
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| Organism | Homo sapiens (Human) [Reference proteome] | ||||||
| Taxonomic identifier | 9606 [NCBI] | ||||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo![]() |
Protein attributes
| Sequence length | 254 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Function | Ca2+ release-activated Ca2+-like (CRAC-like) channel subunit which mediates Ca2+ influx and increase in Ca2+-selective current by synergy with the Ca2+ sensor, STIM1. Ref.6 Ref.8 |
| Subunit structure | Interacts with EFCAB4B/CRACR2A. Ref.9 |
| Subcellular location | Membrane; Multi-pass membrane protein By similarity. |
| Sequence similarities | Belongs to the Orai family. |
| Sequence caution | The sequence AAG23755.1 differs from that shown. Reason: Erroneous translation. Wrong choice of CDS. The sequence AAP22352.1 differs from that shown. Reason: Erroneous gene model prediction. The sequence CAG33568.1 differs from that shown. Reason: Erroneous translation. Wrong choice of CDS. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Membrane |
| Coding sequence diversity | Polymorphism |
| Domain | Transmembrane Transmembrane helix |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Cellular_component | integral to membrane Inferred from electronic annotation. Source: UniProtKB-KW |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 254 | 254 | Protein orai-2 | PRO_0000234391 | |||||
Regions | |||||||||
| Transmembrane | 66 – 83 | 18 | Helical; Potential | ||||||
| Transmembrane | 94 – 114 | 21 | Helical; Potential | ||||||
| Transmembrane | 148 – 168 | 21 | Helical; Potential | ||||||
| Transmembrane | 196 – 216 | 21 | Helical; Potential | ||||||
Natural variations | |||||||||
| Natural variant | 15 | 1 | A → P. Corresponds to variant rs34947403 [ dbSNP | Ensembl ]. | VAR_053543 | |||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Complete sequencing and characterization of 21,243 full-length human cDNAs." Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S. Sugano S.Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]. Tissue: Teratocarcinoma. |
| [2] | "The DNA sequence of human chromosome 7." Hillier L.W., Fulton R.S., Fulton L.A., Graves T.A., Pepin K.H., Wagner-McPherson C., Layman D., Maas J., Jaeger S., Walker R., Wylie K., Sekhon M., Becker M.C., O'Laughlin M.D., Schaller M.E., Fewell G.A., Delehaunty K.D., Miner T.L. Wilson R.K.Nature 424:157-164(2003) [PubMed] [Europe PMC] [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] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]. Tissue: Brain. |
| [4] | "Large-scale cDNA transfection screening for genes related to cancer development and progression." Wan D., Gong Y., Qin W., Zhang P., Li J., Wei L., Zhou X., Li H., Qiu X., Zhong F., He L., Yu J., Yao G., Jiang H., Qian L., Yu Y., Shu H., Chen X. Gu J.Proc. Natl. Acad. Sci. U.S.A. 101:15724-15729(2004) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 191-254. |
| [5] | "Cloning of human full open reading frames in Gateway(TM) system entry vector (pDONR201)." Ebert L., Schick M., Neubert P., Schatten R., Henze S., Korn B. Submitted (JUN-2004) to the EMBL/GenBank/DDBJ databases Cited for: PARTIAL NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]. |
| [6] | "Large store-operated calcium selective currents due to co-expression of Orai1 or Orai2 with the intracellular calcium sensor, Stim1." Mercer J.C., Dehaven W.I., Smyth J.T., Wedel B., Boyles R.R., Bird G.S., Putney J.W. Jr. J. Biol. Chem. 281:24979-24990(2006) [PubMed] [Europe PMC] [Abstract] Cited for: FUNCTION. |
| [7] | "A mutation in Orai1 causes immune deficiency by abrogating CRAC channel function." Feske S., Gwack Y., Prakriya M., Srikanth S., Puppel S.-H., Tanasa B., Hogan P.G., Lewis R.S., Daly M., Rao A. Nature 441:179-185(2006) [PubMed] [Europe PMC] [Abstract] Cited for: IDENTIFICATION. |
| [8] | "Calcium inhibition and calcium potentiation of orai1, orai2, and orai3 calcium release-activated calcium channels." Dehaven W.I., Smyth J.T., Boyles R.R., Putney J.W. Jr. J. Biol. Chem. 282:17548-17556(2007) [PubMed] [Europe PMC] [Abstract] Cited for: FUNCTION. |
| [9] | "A novel EF-hand protein, CRACR2A, is a cytosolic Ca2+ sensor that stabilizes CRAC channels in T cells." Srikanth S., Jung H.J., Kim K.D., Souda P., Whitelegge J., Gwack Y. Nat. Cell Biol. 12:436-446(2010) [PubMed] [Europe PMC] [Abstract] Cited for: INTERACTION WITH EFCAB4B. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AK027639 mRNA. Translation: BAB55256.1. AC093668 Genomic DNA. Translation: AAP22351.1. AC093668 Genomic DNA. Translation: AAP22352.1. Sequence problems. BC069270 mRNA. Translation: AAH69270.1. AF258552 mRNA. Translation: AAG23755.1. Sequence problems. CR457287 mRNA. Translation: CAG33568.1. Sequence problems. |
| IPI | IPI00045842. |
| RefSeq | NP_001119812.1. NM_001126340.2. NP_001258747.1. NM_001271818.1. NP_116220.1. NM_032831.3. |
| UniGene | Hs.363308. |
3D structure databases | |
| ProteinModelPortal | Q96SN7. |
| ModBase | Search... |
Protein-protein interaction databases | |
| DIP | DIP-48944N. |
| IntAct | Q96SN7. 7 interactions. |
| MINT | MINT-1373233. |
| STRING | 9606.ENSP00000348752. |
PTM databases | |
| PhosphoSite | Q96SN7. |
Polymorphism databases | |
| DMDM | 74732728. |
Proteomic databases | |
| PaxDb | Q96SN7. |
| PRIDE | Q96SN7. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000356387; ENSP00000348752; ENSG00000160991. ENST00000403646; ENSP00000385489; ENSG00000160991. ENST00000473939; ENSP00000417928; ENSG00000160991. ENST00000478730; ENSP00000418140; ENSG00000160991. |
| GeneID | 80228. |
| KEGG | hsa:80228. |
| UCSC | uc003uzj.2. human. |
Organism-specific databases | |
| CTD | 80228. |
| GeneCards | GC07P102074. |
| HGNC | HGNC:21667. ORAI2. |
| MIM | 610929. gene. |
| neXtProt | NX_Q96SN7. |
| PharmGKB | PA162398454. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG263788. |
| HOGENOM | HOG000246925. |
| HOVERGEN | HBG081343. |
| InParanoid | Q96SN7. |
| KO | K16057. |
| OMA | PACSEPG. |
| OrthoDB | EOG4DV5MR. |
Gene expression databases | |
| ArrayExpress | Q96SN7. |
| Bgee | Q96SN7. |
| CleanEx | HS_ORAI2. |
| Genevestigator | Q96SN7. |
| GermOnline | ENSG00000160991. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR012446. CRAC_channel. [Graphical view] |
| Pfam | PF07856. Orai-1. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| ChiTaRS | ORAI2. human. |
| GenomeRNAi | 80228. |
| NextBio | 70657. |
| SOURCE | Search... |
Entry information
| Entry name | ORAI2_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q96SN7 Secondary accession number(s): Q6IA68, Q8WY94, Q9H9Y3 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| Disclaimer | Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care. | ||||||||
Relevant documents
| Human chromosome 7 Human chromosome 7: 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
