Homo sapiens Protein: PCM1
Summary
InnateDB Protein IDBP-8870.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PCM1
Protein Name pericentriolar material 1
Synonyms PTC4;
Species Homo sapiens
Ensembl Protein ENSP00000327077
InnateDB Gene IDBG-8866 (PCM1)
Protein Structure
UniProt Annotation
Function Required for centrosome assembly and function. Essential for the correct localization of several centrosomal proteins including CEP250, CETN3, PCNT and NEK2. Required to anchor microtubules to the centrosome. Involved in the biogenesis of cilia. {ECO:0000269PubMed:12403812, ECO:0000269PubMed:15659651, ECO:0000269PubMed:16943179, ECO:0000269PubMed:20551181, ECO:0000269PubMed:24121310}.
Subcellular Localization Cytoplasm, cytoskeleton. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome. Cytoplasmic granule. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome, centriolar satellite. Cytoplasm, cytoskeleton, cilium basal body. Note=Recruitement to the centrosome requires microtubules and dynein. The majority of the protein dissociates from the centrosome during metaphase and subsequently localizes to the cleavage site in telophase. Displaced from centriolar satellites and centrosome in response to cellular stress, such as ultraviolet light (UV) radiation or heat shock, in a process that requires p38 MAP kinase signaling.
Disease Associations Thyroid papillary carcinoma (TPC) [MIM:188550]: A common tumor of the thyroid that typically arises as an irregular, solid or cystic mass from otherwise normal thyroid tissue. Papillary carcinomas are malignant neoplasm characterized by the formation of numerous, irregular, finger-like projections of fibrous stroma that is covered with a surface layer of neoplastic epithelial cells. Note=The disease is caused by mutations affecting the gene represented in this entry. A chromosomal aberration involving PCM1 is found in thyroid papillary carcinomas. Translocation t(8;10)(p21.3;q11.2) with RET links the protein kinase domain of RET to the major portion of PCM1.Note=A chromosomal aberration involving PCM1 is found in a variety of hematological malignancies including atypical chronic myeloid leukemia (atypical CML) and T-cell lymphoma. Translocation t(8;9)(p22;p24) with JAK2 links the protein kinase domain of JAK2 to the major portion of PCM1.
Tissue Specificity Expressed in blood, bone marrow, breast, lymph node, ovary and thyroid. {ECO:0000269PubMed:10980597, ECO:0000269PubMed:15184884, ECO:0000269PubMed:16270321, ECO:0000269PubMed:16424865}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 60 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 60 [view]
Protein-Protein 56 [view]
Protein-DNA 4 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0042802 identical protein binding
Biological Process
GO:0000086 G2/M transition of mitotic cell cycle
GO:0000278 mitotic cell cycle
GO:0022027 interkinetic nuclear migration
GO:0031122 cytoplasmic microtubule organization
GO:0034453 microtubule anchoring
GO:0034454 microtubule anchoring at centrosome
GO:0035735 intraciliary transport involved in cilium morphogenesis
GO:0042384 cilium assembly
GO:0050768 negative regulation of neurogenesis
GO:0051297 centrosome organization
GO:0071539 protein localization to centrosome
GO:0090316 positive regulation of intracellular protein transport
GO:0097150 neuronal stem cell maintenance
Cellular Component
GO:0000242 pericentriolar material
GO:0005737 cytoplasm
GO:0005813 centrosome
GO:0005829 cytosol
GO:0016020 membrane
GO:0031965 nuclear membrane
GO:0034451 centriolar satellite
GO:0036064 ciliary basal body
GO:0043234 protein complex
Protein Structure and Domains
PDB ID
InterPro
PFAM
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q15154
PhosphoSite PhosphoSite-Q15154
TrEMBL E5RGQ4
UniProt Splice Variant
Entrez Gene 5108
UniGene Hs.491148
RefSeq NP_006188
HUGO HGNC:8727
OMIM 600299
CCDS CCDS47812
HPRD 02624
IMGT
EMBL AC087273 AC087625 AJ297349 AK091406 BC000453 BC027477 BC065022 L27841
GenPept AAA60120 AAH00453 AAH27477 AAH65022 BAC03656 CAC14882