UNC45A

General Information

Full gene name:unc-45 homolog A (C. elegans)
Entrez Gene ID:55898
Location:15q26.1
Synonyms:SMAP1, GCUNC-45, GCUNC45, GC-UNC45, IRO039700, SMAP-1
Type:protein-coding

User SNPs

SNPs given by the user that are near or inside this gene:

SNP Distance (bp) Direction
rs8042680 24014 downstream

NCBI Summary

UNC45A plays a role in cell proliferation and myoblast fusion, binds progesterone receptor (PGR; MIM 607311) and HSP90 (HSPCA; MIM 140571), and acts as a regulator of the progesterone receptor chaperoning pathway (Price et al., 2002 [PubMed 12356907]; Chadli et al., 2006 [PubMed 16478993]).[supplied by OMIM, Mar 2008]

OMIM

OMIM ID:`OMIM ID 611219 `_

NCBI Phenotypes

No phenotypes found linked to this gene.

Gene Ontology

  • chaperone-mediated protein folding
  • muscle organ development
  • Hsp90 protein binding
  • nucleus
  • perinuclear region of cytoplasm
  • cell differentiation

KEGG Pathways

No pathways found linked to this gene.

GeneRIFs

  • GCUNC45 is required for the normal cellular distribution of Hsp90beta, but not Hsp90alpha. [PMID 18285346]
  • elevated GC UNC-45 protein expression in ovarian carcinoma proliferation and metastasis. [PMID 17872978]
  • Affinity Capture-MS [PMID 19615732]
  • Affinity Capture-MS [PMID 20562859]
  • Affinity Capture-MS [PMID 21906983]
  • The authors found that UNC-45A is alternatively expressed at the mRNA and protein levels as two isoforms and that the two isoforms differ only by a proline-rich 15-amino-acid sequence near the amino-terminus. [PMID 21802425]
  • GCUNC-45 is a novel modulator of progesterone receptor chaperoning by hsp90. [PMID 16478993]

PubMed Articles

Recent articles:

  • Kim W et al. “Systematic and quantitative assessment of the ubiquitin-modified proteome.” Mol Cell. 2011 Oct 21;44(2):325-40. PMID 21906983
  • Wagner SA et al. “A proteome-wide, quantitative survey of in vivo ubiquitylation sites reveals widespread regulatory roles.” Mol Cell Proteomics. 2011 Oct;10(10):M111.013284. PMID 21890473
  • Guo W et al. “Differential turnover of myosin chaperone UNC-45A isoforms increases in metastatic human breast cancer.” J Mol Biol. 2011 Sep 23;412(3):365-78. PMID 21802425
  • Danielsen JM et al. “Mass spectrometric analysis of lysine ubiquitylation reveals promiscuity at site level.” Mol Cell Proteomics. 2011 Mar;10(3):M110.003590. PMID 21139048
  • Behrends C et al. “Network organization of the human autophagy system.” Nature. 2010 Jul 1;466(7302):68-76. PMID 20562859
  • Sowa ME et al. “Defining the human deubiquitinating enzyme interaction landscape.” Cell. 2009 Jul 23;138(2):389-403. PMID 19615732
  • Chadli A et al. “GCUNC45 is the first Hsp90 co-chaperone to show alpha/beta isoform specificity.” J Biol Chem. 2008 Apr 11;283(15):9509-12. PMID 18285346
  • Bazzaro M et al. “Myosin II co-chaperone general cell UNC-45 overexpression is associated with ovarian cancer, rapid proliferation, and motility.” Am J Pathol. 2007 Nov;171(5):1640-9. PMID 17872978
  • Ewing RM et al. “Large-scale mapping of human protein-protein interactions by mass spectrometry.” Mol Syst Biol. 2007;3:89. PMID 17353931
  • Olsen JV et al. “Global, in vivo, and site-specific phosphorylation dynamics in signaling networks.” Cell. 2006 Nov 3;127(3):635-48. PMID 17081983

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