Homo sapiens Protein: AURKC | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-385547.4 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | AURKC | ||||||||||||||||||
Protein Name | aurora kinase C | ||||||||||||||||||
Synonyms | AIE2; AIK3; ARK3; AurC; aurora-C; SPGF5; STK13; | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000407162 | ||||||||||||||||||
InnateDB Gene | IDBG-71872 (AURKC) | ||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||
Function | Serine/threonine-protein kinase component of the chromosomal passenger complex (CPC), a complex that acts as a key regulator of mitosis. The CPC complex has essential functions at the centromere in ensuring correct chromosome alignment and segregation and is required for chromatin-induced microtubule stabilization and spindle assembly. Plays also a role in meiosis and more particularly in spermatogenesis. Has redundant cellular functions with AURKB and can rescue an AURKB knockdown. Like AURKB, AURKC phosphorylates histone H3 at 'Ser-10' and 'Ser-28'. Phosphorylates TACC1, another protein involved in cell division, at 'Ser-228'. {ECO:0000269PubMed:15316025, ECO:0000269PubMed:15499654, ECO:0000269PubMed:15670791, ECO:0000269PubMed:15938719, ECO:0000269PubMed:21493633, ECO:0000269PubMed:21531210}. | ||||||||||||||||||
Subcellular Localization | Nucleus. Chromosome. Chromosome, centromere. Cytoplasm, cytoskeleton, spindle. Note=Distributes in the condensed chromosomes during prophase to metaphase. After entering anaphase, there is a dissociation from separated chromosomes and a redistribution to midzone microtubules, and finally remains in the midbody during cytokinesis. | ||||||||||||||||||
Disease Associations | Spermatogenic failure 5 (SPGF5) [MIM:243060]: An infertility disorder caused by spermatogenesis defects. Semen from affected men show close to 100% morphologically abnormal multiflagellar spermatozoa with low motility, oversized irregular heads, and abnormal midpiece and acrosome. {ECO:0000269PubMed:17435757, ECO:0000269PubMed:21733974}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||
Tissue Specificity | Isoform 1 and isoform 2 are expressed in testis. Elevated expression levels were seen only in a subset of cancer cell lines such as Hep-G2, Huh-7 and HeLa. Expression is maximum at M phase. {ECO:0000269PubMed:15670791}. | ||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 17 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||
PDB ID | |||||||||||||||||||
InterPro |
IPR000719
Protein kinase domain IPR001245 Serine-threonine/tyrosine-protein kinase catalytic domain IPR002290 Serine/threonine/dual specificity protein kinase, catalytic domain IPR011009 Protein kinase-like domain IPR020635 Tyrosine-protein kinase, catalytic domain |
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PFAM |
PF00069
PF07714 |
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PRINTS |
PR00109
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PIRSF | |||||||||||||||||||
SMART |
SM00220
SM00219 |
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q9UQB9 | ||||||||||||||||||
PhosphoSite | PhosphoSite-Q9UQB9 | ||||||||||||||||||
TrEMBL | |||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 6795 | ||||||||||||||||||
UniGene | Hs.98338 | ||||||||||||||||||
RefSeq | NP_001015879 | ||||||||||||||||||
HUGO | HGNC:11391 | ||||||||||||||||||
OMIM | 603495 | ||||||||||||||||||
CCDS | CCDS46205 | ||||||||||||||||||
HPRD | 04605 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AB017332 AC005261 AF054621 AF059681 AY661554 BC075064 CH471135 | ||||||||||||||||||
GenPept | AAC25955 AAC77369 AAH75064 AAT64422 BAA76292 EAW72485 | ||||||||||||||||||