P0C862 (C1T9A_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 31.
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: Complement C1q and tumor necrosis factor-related protein 9A Alternative name(s): Complement C1q and tumor necrosis factor-related protein 9 | ||||||
| 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 | 333 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is further processed into a mature form. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Function | Probable adipokine. Activates AMPK, AKT, and p44/42 MAPK signaling pathways By similarity. |
| Subunit structure | Multimers (predominantly trimers). Interacts with ADIPOQ via the C1q domain to form a heterotrimeric complex By similarity. Interacts with CTRP9B. Forms heterotrimers and heterooligomeric complexes with CTRP9B. Ref.1 |
| Subcellular location | |
| Tissue specificity | Expressed predominantly in adipose tissue. Ref.1 |
| Sequence similarities | Contains 1 C1q domain. Contains 3 collagen-like domains. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Secreted |
| Coding sequence diversity | Polymorphism |
| Domain | Collagen Repeat Signal |
| Molecular function | Hormone |
| PTM | Glycoprotein Hydroxylation |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Cellular component | collagen Inferred from electronic annotation. Source: UniProtKB-KW |
| Molecular function | hormone activity 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 | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Signal peptide | 1 – 19 | 19 | Potential | ||||||
| Chain | 20 – 333 | 314 | Complement C1q and tumor necrosis factor-related protein 9A | PRO_0000291751 | |||||
Regions | |||||||||
| Domain | 24 – 82 | 59 | Collagen-like 1 | ||||||
| Domain | 95 – 154 | 60 | Collagen-like 2 | ||||||
| Domain | 155 – 191 | 37 | Collagen-like 3 | ||||||
| Domain | 197 – 333 | 137 | C1q | ||||||
Amino acid modifications | |||||||||
| Modified residue | 31 | 1 | 4-hydroxyproline By similarity | ||||||
| Modified residue | 34 | 1 | 4-hydroxyproline By similarity | ||||||
| Modified residue | 40 | 1 | 4-hydroxyproline By similarity | ||||||
| Modified residue | 58 | 1 | 4-hydroxyproline By similarity | ||||||
| Modified residue | 61 | 1 | 4-hydroxyproline By similarity | ||||||
| Modified residue | 64 | 1 | 4-hydroxyproline By similarity | ||||||
| Modified residue | 73 | 1 | 5-hydroxylysine By similarity | ||||||
| Modified residue | 127 | 1 | 5-hydroxylysine By similarity | ||||||
| Modified residue | 151 | 1 | 4-hydroxyproline By similarity | ||||||
| Modified residue | 160 | 1 | 4-hydroxyproline By similarity | ||||||
| Modified residue | 175 | 1 | 4-hydroxyproline By similarity | ||||||
| Glycosylation | 73 | 1 | O-linked (Gal...) By similarity | ||||||
| Glycosylation | 127 | 1 | O-linked (Gal...) By similarity | ||||||
Natural variations | |||||||||
| Natural variant | 6 | 1 | L → F. Corresponds to variant rs1974332 [ dbSNP | Ensembl ]. | VAR_059148 | |||||
| Natural variant | 219 | 1 | M → V. Ref.2 Ref.3 Ref.4 Corresponds to variant rs3751357 [ dbSNP | Ensembl ]. | VAR_032840 | |||||
| Natural variant | 301 | 1 | V → M. Ref.3 Corresponds to variant rs4589405 [ dbSNP | Ensembl ]. | VAR_032841 | |||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "CTRP8 and CTRP9B are novel proteins that hetero-oligomerize with C1q/TNF family members." Peterson J.M., Wei Z., Wong G.W. Biochem. Biophys. Res. Commun. 388:360-365(2009) [PubMed: 19666007] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA], SUBCELLULAR LOCATION, INTERACTION WITH C1QL1, TISSUE SPECIFICITY. Tissue: Hippocampus. |
| [2] | "The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment." Clark H.F., Gurney A.L., Abaya E., Baker K., Baldwin D.T., Brush J., Chen J., Chow B., Chui C., Crowley C., Currell B., Deuel B., Dowd P., Eaton D., Foster J.S., Grimaldi C., Gu Q., Hass P.E. Gray A.M.Genome Res. 13:2265-2270(2003) [PubMed: 12975309] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT VAL-219. |
| [3] | "The DNA sequence and analysis of human chromosome 13." Dunham A., Matthews L.H., Burton J., Ashurst J.L., Howe K.L., Ashcroft K.J., Beare D.M., Burford D.C., Hunt S.E., Griffiths-Jones S., Jones M.C., Keenan S.J., Oliver K., Scott C.E., Ainscough R., Almeida J.P., Ambrose K.D., Andrews D.T. Ross M.T.Nature 428:522-528(2004) [PubMed: 15057823] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA], VARIANTS VAL-219 AND MET-301. |
| [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: 15489334] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT VAL-219. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AY358145 mRNA. Translation: AAQ88512.1. AL359736 Genomic DNA. Translation: CAH72292.1. AL359736 Genomic DNA. Translation: CAH72293.1. BC040438 mRNA. Translation: AAH40438.1. |
| IPI | IPI00552240. |
| RefSeq | NP_848635.2. NM_178540.3. |
| UniGene | Hs.362854. |
3D structure databases | |
| ProteinModelPortal | P0C862. |
| SMR | P0C862. Positions 28-109, 197-332. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | P0C862. |
Polymorphism databases | |
| DMDM | 205686199. |
Proteomic databases | |
| PRIDE | P0C862. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000332018; ENSP00000333737; ENSG00000240654. ENST00000382071; ENSP00000371503; ENSG00000240654. |
| GeneID | 338872. |
| KEGG | hsa:338872. |
Organism-specific databases | |
| CTD | 338872. |
| GeneCards | GC13P024881. |
| HGNC | HGNC:28732. C1QTNF9. |
| MIM | 614285. gene. |
| neXtProt | NX_P0C862. |
| PharmGKB | PA145008937. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | prNOG05639. |
| GeneTree | ENSGT00590000082736. |
| HOVERGEN | HBG108220. |
| InParanoid | P0C862. |
| OMA | GMRGWKG. |
| OrthoDB | EOG4D7Z64. |
Gene expression databases | |
| ArrayExpress | P0C862. |
| Bgee | P0C862. |
| CleanEx | HS_C1QTNF9. |
| Genevestigator | P0C862. |
Family and domain databases | |
| InterPro | IPR001073. C1q. IPR008160. Collagen. IPR008983. Tumour_necrosis_fac-like. [Graphical view] |
| Gene3D | G3DSA:2.60.120.40. Tumour_necrosis_fac-like. 1 hit. |
| Pfam | PF00386. C1q. 1 hit. PF01391. Collagen. 3 hits. [Graphical view] |
| PRINTS | PR00007. COMPLEMNTC1Q. |
| SMART | SM00110. C1Q. 1 hit. [Graphical view] |
| SUPFAM | SSF49842. TNF_like. 1 hit. |
| PROSITE | PS50871. C1Q. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| SOURCE | Search... |
Entry information
| Entry name | C1T9A_HUMAN | ||||||||
| Accession | Primary (citable) accession number: P0C862 Secondary accession number(s): A2A3T6 Q8IUU4 | ||||||||
| 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 13 Human chromosome 13: 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