Unreviewed,
UniProtKB/TrEMBL Q59GD8 (Q59GD8_HUMAN)
Last modified
January 19, 2010.
Version 39.
History...
Clusters with 100%,
90%,
50% identity |
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Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information
Names and origin
| Protein names | Submitted name: Calcium channel, voltage-dependent, L type, alpha 1D subunit variant EMBL BAD92408.1 |
| Organism | Homo sapiens (Human) EMBL BAD92408.1 |
| Taxonomic identifier | 9606 [NCBI] |
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 1854 AA. |
| Sequence status | Fragment. |
| 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
| Keywords | |
|---|---|
| Biological process | Calcium transport Ion transport Transport |
| Cellular component | Membrane |
| Domain | Transmembrane RuleBase RU003378V0 |
| Ligand | Calcium |
| Molecular function | Calcium channel RuleBase RU003808V0 Ionic channel Voltage-gated channel RuleBase RU003808V0 |
| Gene Ontology (GO) | |
| Biological process | calcium ion transport Inferred from electronic annotation. Source: UniProtKB-KW transmembrane transportInferred from electronic annotation. Source: InterPro |
| Cellular component | voltage-gated calcium channel complex Inferred from electronic annotation. Source: InterPro |
| Molecular function | calcium ion binding Inferred from electronic annotation. Source: UniProtKB-KW voltage-gated calcium channel activityInferred from electronic annotation. Source: InterPro |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | |||
Experimental info | ||||||||
|---|---|---|---|---|---|---|---|---|
| Non-terminal residue | 1 | 1 | EMBL BAD92408.1 | |||||
Sequences
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References
| [1] | "Homo sapiens protein coding cDNA." Totoki Y., Toyoda A., Takeda T., Sakaki Y., Tanaka A., Yokoyama S., Ohara O., Nagase T., Kikuno R.F. Submitted (MAR-2005) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE. Tissue: Brain EMBL BAD92408.1. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AB209171 mRNA. Translation: BAD92408.1. |
| IPI | IPI00947531. |
| RefSeq | NP_000711.1. NP_001122312.1. |
| UniGene | Hs.476358 |
3D structure databases | |
| SMR | Q59GD8. Positions 574-656, 892-1161, 1293-1321. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | Q59GD8. |
Genome annotation databases | |
| Ensembl | ENST00000481478; ENSP00000418014; ENSG00000157388; Homo sapiens. [Genome view] |
| GeneID | 776. |
| KEGG | hsa:776. |
| UCSC | uc003dgw.2. human. |
Organism-specific databases | |
| CTD | 776. |
| HGNC | HGNC:1391. CACNA1D. |
Phylogenomic databases | |
| HOGENOM | HBG713873. |
| HOVERGEN | Q59GD8. |
Gene expression databases | |
| ArrayExpress | Q59GD8. |
| Bgee | Q59GD8. |
Family and domain databases | |
| InterPro | IPR005821. Ion_trans. IPR005452. LVDCC_a1dsu. IPR014873. VDCC_a1su_IQ. IPR002077. VDCCAlpha1. [Graphical view] |
| PANTHER | PTHR10037:SF48. LVDCCAlpha1D. 1 hit. |
| Pfam | PF08763. Ca_chan_IQ. 1 hit. PF00520. Ion_trans. 4 hits. [Graphical view] |
| PRINTS | PR00167. CACHANNEL. PR01636. LVDCCALPHA1D. |
| ProtoNet | Search... |
Entry information
| Entry name | Q59GD8_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q59GD8 | ||||||||
| 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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