Unreviewed,
UniProtKB/TrEMBL Q9NS88 (Q9NS88_HUMAN)
Last modified
January 19, 2010.
Version 56.
History...
Clusters with 100%,
90%,
50% identity |
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Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Sequences · References · Cross-references · Entry information
Names and origin
| Protein names | Submitted name: Alpha1A-voltage-dependent calcium channel EMBL BAA94766.2 | ||
| Gene names |
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| Organism | Homo sapiens (Human) EMBL BAA94766.2 | ||
| Taxonomic identifier | 9606 [NCBI] | ||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 2506 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level. |
General annotation (Comments)
| Subcellular location | Membrane; Multi-pass membrane protein By similarity RuleBase RU003808V0. |
| Sequence similarities | Belongs to the calcium channel alpha-1 subunit (TC 1.A.1.11) family. [View classification] |
Ontologies
Sequences
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References
| [1] | "Spinocerebellar ataxia type 6 mutation alters P-type calcium channel function." Toru S., Murakoshi T., Ishikawa K., Saegusa H., Fujigasaki H., Uchihara T., Nagayama S., Osanai M., Mizusawa H., Tanabe T. J. Biol. Chem. 275:10893-10898(2000) [PubMed: 10753886] [Abstract] Cited for: NUCLEOTIDE SEQUENCE. Strain: TMDN-CNT-001 EMBL BAA94766.2. Tissue: Cerebellum EMBL BAA94766.2. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AB035727 mRNA. Translation: BAA94766.2. |
| IPI | IPI00291347. |
| RefSeq | NP_001120694.1. |
| UniGene | Hs.501632 |
3D structure databases | |
| SMR | Q9NS88. Positions 1241-1317, 1558-1689. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | Q9NS88. |
Proteomic databases | |
| PRIDE | Q9NS88. |
Genome annotation databases | |
| Ensembl | ENST00000360228; ENSP00000353362; ENSG00000141837; Homo sapiens. [Genome view] |
| GeneID | 773. |
Organism-specific databases | |
| CTD | 773. |
| HGNC | HGNC:1388. CACNA1A. |
| GenAtlas | Search... |
Phylogenomic databases | |
| HOGENOM | HBG713873. |
| HOVERGEN | Q9NS88. |
Gene expression databases | |
| ArrayExpress | Q9NS88. |
| Bgee | Q9NS88. |
Family and domain databases | |
| InterPro | IPR005821. Ion_trans. IPR014873. VDCC_a1su_IQ. IPR005448. VDCC_P/Q_a1su. IPR002077. VDCCAlpha1. [Graphical view] |
| PANTHER | PTHR10037:SF59. PQVDCCAlpha1. 1 hit. |
| Pfam | PF08763. Ca_chan_IQ. 1 hit. PF00520. Ion_trans. 4 hits. [Graphical view] |
| PRINTS | PR00167. CACHANNEL. PR01632. PQVDCCALPHA1. |
| ProtoNet | Search... |
Entry information
| Entry name | Q9NS88_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9NS88 | ||||||||
| Entry history |
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| Entry status | Unreviewed (UniProtKB/TrEMBL) | ||||||||
| 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. | ||||||||

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