COMMD1

Protein-coding gene in humans
COMMD1
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

2H2M

Identifiers
AliasesCOMMD1, C2orf5, MURR1, copper metabolism domain containing 1
External IDsOMIM: 607238; MGI: 109474; HomoloGene: 17604; GeneCards: COMMD1; OMA:COMMD1 - orthologs
Gene location (Human)
Chromosome 2 (human)
Chr.Chromosome 2 (human)[1]
Chromosome 2 (human)
Genomic location for COMMD1
Genomic location for COMMD1
Band2p15Start61,888,724 bp[1]
End62,147,247 bp[1]
Gene location (Mouse)
Chromosome 11 (mouse)
Chr.Chromosome 11 (mouse)[2]
Chromosome 11 (mouse)
Genomic location for COMMD1
Genomic location for COMMD1
Band11 A3.2|11 14.22 cMStart22,846,136 bp[2]
End22,932,382 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • myocardium of left ventricle

  • tibialis anterior muscle

  • cardiac muscle tissue of right atrium

  • right ventricle

  • deltoid muscle

  • Skeletal muscle tissue of biceps brachii

  • right auricle

  • vena cava

  • skin of arm

  • mucosa of ileum
Top expressed in
  • embryo

  • embryo

  • spermatocyte

  • right kidney

  • ventricular zone

  • external carotid artery

  • intercostal muscle

  • epiblast

  • medullary collecting duct

  • internal carotid artery
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
  • protein homodimerization activity
  • phosphatidylinositol-3,5-bisphosphate binding
  • metal ion binding
  • phosphatidylinositol-3,4-bisphosphate binding
  • phosphatidic acid binding
  • protein binding
  • identical protein binding
  • phosphatidylinositol-4,5-bisphosphate binding
  • copper ion binding
  • phosphatidylinositol-3,4,5-trisphosphate binding
  • lipid binding
Cellular component
  • cytoplasm
  • recycling endosome
  • endosome
  • membrane
  • Cul2-RING ubiquitin ligase complex
  • early endosome
  • endosome membrane
  • cytoplasmic vesicle
  • nucleus
  • nucleoplasm
  • cytosol
Biological process
  • negative regulation of sodium ion transmembrane transport
  • regulation of transcription, DNA-templated
  • transcription, DNA-templated
  • negative regulation of protein localization to cell surface
  • plasma membrane to endosome transport
  • regulation of proteasomal ubiquitin-dependent protein catabolic process
  • protein transport
  • negative regulation of NF-kappaB transcription factor activity
  • positive regulation of protein ubiquitination
  • Golgi to plasma membrane transport
  • post-translational protein modification
  • copper ion homeostasis
  • protein ubiquitination
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

150684

17846

Ensembl

ENSG00000173163

ENSMUSG00000051355

UniProt

Q8N668

Q8K4M5

RefSeq (mRNA)

NM_152516
NM_001321781
NM_001321782
NM_001371765

NM_144514
NM_001361661

RefSeq (protein)

NP_001308710
NP_001308711
NP_689729
NP_001358694

NP_653097
NP_001348590

Location (UCSC)Chr 2: 61.89 – 62.15 MbChr 11: 22.85 – 22.93 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

COMM domain-containing protein 1 is a protein that is encoded by the COMMD1 gene in humans. It was originally regarded as Murr1 before being differentiated and renamed by Dr. Ezra Burstein's Lab[5][6][7]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000173163 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000051355 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Nabetani A, Hatada I, Morisaki H, Oshimura M, Mukai T (Feb 1997). "Mouse U2af1-rs1 is a neomorphic imprinted gene". Mol Cell Biol. 17 (2): 789–98. doi:10.1128/mcb.17.2.789. PMC 231805. PMID 9001233.
  6. ^ van De Sluis B, Rothuizen J, Pearson PL, van Oost BA, Wijmenga C (Jan 2002). "Identification of a new copper metabolism gene by positional cloning in a purebred dog population". Hum Mol Genet. 11 (2): 165–73. doi:10.1093/hmg/11.2.165. PMID 11809725.
  7. ^ "Entrez Gene: COMMD1 copper metabolism (Murr1) domain containing 1".

External links

Further reading

  • Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
  • Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
  • Harrington JJ, Sherf B, Rundlett S, et al. (2001). "Creation of genome-wide protein expression libraries using random activation of gene expression". Nat. Biotechnol. 19 (5): 440–5. doi:10.1038/88107. PMID 11329013. S2CID 25064683.
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
  • Müller T, van de Sluis B, Zhernakova A, et al. (2003). "The canine copper toxicosis gene MURR1 does not cause non-Wilsonian hepatic copper toxicosis". J. Hepatol. 38 (2): 164–8. doi:10.1016/S0168-8278(02)00356-2. PMID 12547404.
  • Tao TY, Liu F, Klomp L, et al. (2004). "The copper toxicosis gene product Murr1 directly interacts with the Wilson disease protein". J. Biol. Chem. 278 (43): 41593–6. doi:10.1074/jbc.C300391200. PMID 12968035.
  • Klomp AE, van de Sluis B, Klomp LW, Wijmenga C (2004). "The ubiquitously expressed MURR1 protein is absent in canine copper toxicosis". J. Hepatol. 39 (5): 703–9. doi:10.1016/S0168-8278(03)00380-5. PMID 14568250.
  • Biasio W, Chang T, McIntosh CJ, McDonald FJ (2004). "Identification of Murr1 as a regulator of the human delta epithelial sodium channel". J. Biol. Chem. 279 (7): 5429–34. doi:10.1074/jbc.M311155200. PMID 14645214.
  • Ganesh L, Burstein E, Guha-Niyogi A, et al. (2004). "The gene product Murr1 restricts HIV-1 replication in resting CD4+ lymphocytes". Nature. 426 (6968): 853–7. doi:10.1038/nature02171 (inactive 2024-04-25). hdl:2027.42/62709. PMID 14685242. S2CID 4344050.{{cite journal}}: CS1 maint: DOI inactive as of April 2024 (link)
  • Burstein E, Ganesh L, Dick RD, et al. (2004). "A novel role for XIAP in copper homeostasis through regulation of MURR1". EMBO J. 23 (1): 244–54. doi:10.1038/sj.emboj.7600031. PMC 1271669. PMID 14685266.
  • Stuehler B, Reichert J, Stremmel W, Schaefer M (2005). "Analysis of the human homologue of the canine copper toxicosis gene MURR1 in Wilson disease patients". J. Mol. Med. 82 (9): 629–34. doi:10.1007/s00109-004-0557-9. PMID 15205742. S2CID 8184776.
  • Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
  • Burstein E, Hoberg JE, Wilkinson AS, et al. (2005). "COMMD proteins, a novel family of structural and functional homologs of MURR1". J. Biol. Chem. 280 (23): 22222–32. doi:10.1074/jbc.M501928200. PMID 15799966.
  • Coronado VA, Bonneville JA, Nazer H, et al. (2006). "COMMD1 (MURR1) as a candidate in patients with copper storage disease of undefined etiology". Clin. Genet. 68 (6): 548–51. doi:10.1111/j.1399-0004.2005.00524.x. PMID 16283886. S2CID 27815621.
  • Zhang Z, Joh K, Yatsuki H, et al. (2006). "Comparative analyses of genomic imprinting and CpG island-methylation in mouse Murr1 and human MURR1 loci revealed a putative imprinting control region in mice". Gene. 366 (1): 77–86. doi:10.1016/j.gene.2005.08.020. PMID 16305817.
  • de Bie P, van de Sluis B, Burstein E, et al. (2006). "Characterization of COMMD protein-protein interactions in NF-kappaB signalling". Biochem. J. 398 (1): 63–71. doi:10.1042/BJ20051664. PMC 1525016. PMID 16573520.
  • Sommerhalter M, Zhang Y, Rosenzweig AC (2007). "Solution structure of the COMMD1 N-terminal domain". J. Mol. Biol. 365 (3): 715–21. doi:10.1016/j.jmb.2006.10.030. PMC 2706016. PMID 17097678.
  • Maine GN, Mao X, Komarck CM, Burstein E (2007). "COMMD1 promotes the ubiquitination of NF-kappaB subunits through a cullin-containing ubiquitin ligase". EMBO J. 26 (2): 436–47. doi:10.1038/sj.emboj.7601489. PMC 1783443. PMID 17183367.
  • v
  • t
  • e
  • 2h2m: Solution Structure of the N-terminal domain of COMMD1 (Murr1)
    2h2m: Solution Structure of the N-terminal domain of COMMD1 (Murr1)


Stub icon

This article on a gene on human chromosome 2 is a stub. You can help Wikipedia by expanding it.

  • v
  • t
  • e