Q06432 (CCG1_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 107.
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: Voltage-dependent calcium channel gamma-1 subunit Alternative name(s): Dihydropyridine-sensitive L-type, skeletal muscle calcium channel subunit gamma | ||||
| Gene names |
| ||||
| 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 | 222 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Function | This protein is a subunit of the dihydropyridine (DHP) sensitive calcium channel. Plays a role in excitation-contraction coupling. The skeletal muscle DHP-sensitive Ca2+ channel may function only as a multiple subunit complex. |
| Subunit structure | The L-type calcium channel is composed of five subunits: alpha-1, alpha-2/delta, beta and gamma. |
| Subcellular location | |
| Tissue specificity | Skeletal muscle. |
| Sequence similarities | Belongs to the PMP-22/EMP/MP20 family. CACNG subfamily. |
Ontologies
| Keywords | |
|---|---|
| Biological process | Calcium transport Ion transport Transport |
| Cellular component | Membrane |
| Coding sequence diversity | Polymorphism |
| Domain | Transmembrane Transmembrane helix |
| Ligand | Calcium |
| Molecular function | Calcium channel Ion channel Voltage-gated channel |
| PTM | Glycoprotein |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological_process | muscle contraction Traceable author statement Ref.1. Source: ProtInc |
| Cellular_component | voltage-gated calcium channel complex Traceable author statement Ref.1. Source: ProtInc |
| Molecular_function | voltage-gated calcium channel activity Traceable author statement Ref.1. Source: ProtInc |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 222 | 222 | Voltage-dependent calcium channel gamma-1 subunit | PRO_0000164669 | |||||
Regions | |||||||||
| Transmembrane | 11 – 29 | 19 | Helical; Potential | ||||||
| Transmembrane | 105 – 129 | 25 | Helical; Potential | ||||||
| Transmembrane | 140 – 155 | 16 | Helical; Potential | ||||||
| Transmembrane | 180 – 204 | 25 | Helical; Potential | ||||||
Amino acid modifications | |||||||||
| Glycosylation | 43 | 1 | N-linked (GlcNAc...) Potential | ||||||
| Glycosylation | 79 | 1 | N-linked (GlcNAc...) Potential | ||||||
Natural variations | |||||||||
| Natural variant | 196 | 1 | G → S. Corresponds to variant rs1799938 [ dbSNP | Ensembl ]. | VAR_012063 | |||||
Sequences
| ||||||||||||||||||
References
| « Hide 'large scale' references | |
| [1] | "Molecular characterization of the gene encoding the gamma subunit of the human skeletal muscle 1,4-dihydropyridine-sensitive Ca2+ channel (CACNLG), cDNA sequence, gene structure, and chromosomal location." Powers P.A., Liu S., Hogan K., Gregg R.G. J. Biol. Chem. 268:9275-9279(1993) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA]. Tissue: Fetal skeletal muscle. |
| [2] | "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: Skeletal muscle. |
| [3] | Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M., Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J., Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S., Turner R. Venter J.C.Submitted (JUL-2005) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [4] | "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]. |
| [5] | "Localization of the gamma-subunit of the skeletal muscle L-type voltage-dependent calcium channel gene (CACNLG) to human chromosome band 17q24 by in situ hybridization and identification of a polymorphic repetitive DNA sequence at the gene locus." Iles D.E., Segers B., Weghuis D.O., Suikerbuijk R., Wieringa B. Cytogenet. Cell Genet. 64:227-230(1993) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 102-147 AND 174-222. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | L07738 mRNA. Translation: AAA51904.1. AK313852 mRNA. Translation: BAG36580.1. CH471099 Genomic DNA. Translation: EAW89022.1. BC069493 mRNA. Translation: AAH69493.1. BC113486 mRNA. Translation: AAI13487.1. BC113492 mRNA. Translation: AAI13493.1. Z19603 Genomic DNA. Translation: CAA79671.1. Z19587 Genomic DNA. Translation: CAB62573.1. Sequence problems. |
| IPI | IPI00030935. |
| PIR | A46658. |
| RefSeq | NP_000718.1. NM_000727.3. |
| UniGene | Hs.147989. |
3D structure databases | |
| ProteinModelPortal | Q06432. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | 9606.ENSP00000226021. |
Protein family/group databases | |
| TCDB | 8.A.16.1.1. Ca+ channel auxiliary subunit gamma1-gamma8 (CCAgamma) family. |
Polymorphism databases | |
| DMDM | 1168946. |
Proteomic databases | |
| PaxDb | Q06432. |
| PRIDE | Q06432. |
Protocols and materials databases | |
| DNASU | 786. |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000226021; ENSP00000226021; ENSG00000108878. |
| GeneID | 786. |
| KEGG | hsa:786. |
| UCSC | uc002jfu.3. human. |
Organism-specific databases | |
| CTD | 786. |
| GeneCards | GC17P065040. |
| HGNC | HGNC:1405. CACNG1. |
| MIM | 114209. gene. |
| neXtProt | NX_Q06432. |
| PharmGKB | PA26015. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG47450. |
| HOGENOM | HOG000293219. |
| HOVERGEN | HBG003868. |
| InParanoid | Q06432. |
| KO | K04866. |
| OMA | WAVLSPH. |
| OrthoDB | EOG49PB0K. |
| PhylomeDB | Q06432. |
Gene expression databases | |
| Bgee | Q06432. |
| CleanEx | HS_CACNG1. |
| Genevestigator | Q06432. |
| GermOnline | ENSG00000108878. Homo sapiens. |
Family and domain databases | |
| InterPro | IPR005421. VDCC_g1su. IPR008368. VDCC_gsu. [Graphical view] |
| PRINTS | PR01792. VDCCGAMMA. PR01601. VDCCGAMMA1. |
| ProtoNet | Search... |
Other | |
| BindingDB | Q06432. |
| DrugBank | DB00381. Amlodipine. DB00343. Diltiazem. DB00308. Ibutilide. DB00528. Lercanidipine. DB00653. Magnesium Sulfate. DB00393. Nimodipine. DB01054. Nitrendipine. DB00661. Verapamil. |
| GenomeRNAi | 786. |
| NextBio | 3202. |
| SOURCE | Search... |
Entry information
| Entry name | CCG1_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q06432 Secondary accession number(s): B2R9N3, Q14D59 | ||||||||
| Entry history |
| ||||||||
| 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 17 Human chromosome 17: 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
