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{{Underlinked|date=May 2016}}
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{{Infobox_gene}}
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'''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<ref name="pmid9001233">{{cite journal | vauthors = Nabetani A, Hatada I, Morisaki H, Oshimura M, Mukai T | title = Mouse U2af1-rs1 is a neomorphic imprinted gene | journal = Mol Cell Biol | volume = 17 | issue = 2 | pages = 789–98 |date=Feb 1997 | pmid = 9001233 | pmc = 231805 | doi =  }}</ref><ref name="pmid11809725">{{cite journal | vauthors = van De Sluis B, Rothuizen J, Pearson PL, van Oost BA, Wijmenga C | title = Identification of a new copper metabolism gene by positional cloning in a purebred dog population | journal = Hum Mol Genet | volume = 11 | issue = 2 | pages = 165–73 |date=Jan 2002 | pmid = 11809725 | pmc =  | doi =10.1093/hmg/11.2.165  }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: COMMD1 copper metabolism (Murr1) domain containing 1| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=150684| accessdate = }}</ref>
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{{GNF_Protein_box
| image = PBB_Protein_COMMD1_image.jpg
| image_source = [[Protein_Data_Bank|PDB]] rendering based on 2h2m.
  | PDB = {{PDB2|2h2m}}
| Name = Copper metabolism (Murr1) domain containing 1
| HGNCid = 23024
| Symbol = COMMD1
| AltSymbols =; C2orf5; MGC27155; MURR1
| OMIM = 607238
| ECnumber =
| Homologene = 17604
| MGIid = 109474
| GeneAtlas_image1 = PBB_GE_COMMD1_gnf1h07930_at_tn.png
| Function =  
  | Component =
| Process =
| Orthologs = {{GNF_Ortholog_box
    | Hs_EntrezGene = 150684
    | Hs_Ensembl = ENSG00000173163
    | Hs_RefseqProtein = NP_689729
    | Hs_RefseqmRNA = NM_152516
    | Hs_GenLoc_db = 
    | Hs_GenLoc_chr = 2
    | Hs_GenLoc_start = 61986292
    | Hs_GenLoc_end = 62216698
    | Hs_Uniprot = Q8N668
    | Mm_EntrezGene = 17846
    | Mm_Ensembl = ENSMUSG00000051355
    | Mm_RefseqmRNA = NM_144514
    | Mm_RefseqProtein = NP_653097
    | Mm_GenLoc_db =   
    | Mm_GenLoc_chr = 11
    | Mm_GenLoc_start = 22799728
    | Mm_GenLoc_end = 22882284
    | Mm_Uniprot = Q3UGT3
  }}
}}
'''Copper metabolism (Murr1) domain containing 1''', also known as '''COMMD1''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: COMMD1 copper metabolism (Murr1) domain containing 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=150684| accessdate = }}</ref>


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==References==
==References==
{{reflist|2}}
{{reflist}}
 
==External links==
* {{UCSC gene info|COMMD1}}
 
==Further reading==
==Further reading==
{{refbegin | 2}}
{{refbegin | 2}}
{{PBB_Further_reading  
{{PBB_Further_reading  
| citations =  
| citations =  
*{{cite journal  | author=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1-2 |pages= 171-4 |year= 1994 |pmid= 8125298 |doi=  }}
*{{cite journal  | vauthors=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1–2 |pages= 171–4 |year= 1994 |pmid= 8125298 |doi=10.1016/0378-1119(94)90802-8 }}
*{{cite journal  | author=Nabetani A, Hatada I, Morisaki H, ''et al.'' |title=Mouse U2af1-rs1 is a neomorphic imprinted gene. |journal=Mol. Cell. Biol. |volume=17 |issue= 2 |pages= 789-98 |year= 1997 |pmid= 9001233 |doi=  }}
*{{cite journal  | vauthors=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. |journal=Gene |volume=200 |issue= 1–2 |pages= 149–56 |year= 1997 |pmid= 9373149 |doi=10.1016/S0378-1119(97)00411-3 |display-authors=etal}}
*{{cite journal  | author=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, ''et al.'' |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. |journal=Gene |volume=200 |issue= 1-2 |pages= 149-56 |year= 1997 |pmid= 9373149 |doi= }}
*{{cite journal  | vauthors=Harrington JJ, Sherf B, Rundlett S |title=Creation of genome-wide protein expression libraries using random activation of gene expression. |journal=Nat. Biotechnol. |volume=19 |issue= 5 |pages= 440–5 |year= 2001 |pmid= 11329013 |doi= 10.1038/88107 |display-authors=etal}}
*{{cite journal  | author=Harrington JJ, Sherf B, Rundlett S, ''et al.'' |title=Creation of genome-wide protein expression libraries using random activation of gene expression. |journal=Nat. Biotechnol. |volume=19 |issue= 5 |pages= 440-5 |year= 2001 |pmid= 11329013 |doi= 10.1038/88107 }}
*{{cite journal  | vauthors=Strausberg RL, Feingold EA, Grouse LH |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899  | pmc=139241 |display-authors=etal}}
*{{cite journal  | author=van De Sluis B, Rothuizen J, Pearson PL, ''et al.'' |title=Identification of a new copper metabolism gene by positional cloning in a purebred dog population. |journal=Hum. Mol. Genet. |volume=11 |issue= 2 |pages= 165-73 |year= 2002 |pmid= 11809725 |doi=  }}
*{{cite journal  | vauthors=Müller T, van de Sluis B, Zhernakova A |title=The canine copper toxicosis gene MURR1 does not cause non-Wilsonian hepatic copper toxicosis. |journal=J. Hepatol. |volume=38 |issue= 2 |pages= 164–8 |year= 2003 |pmid= 12547404 |doi=10.1016/S0168-8278(02)00356-2 |display-authors=etal}}
*{{cite journal  | author=Strausberg RL, Feingold EA, Grouse LH, ''et al.'' |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899-903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 }}
*{{cite journal  | vauthors=Tao TY, Liu F, Klomp L |title=The copper toxicosis gene product Murr1 directly interacts with the Wilson disease protein. |journal=J. Biol. Chem. |volume=278 |issue= 43 |pages= 41593–6 |year= 2004 |pmid= 12968035 |doi= 10.1074/jbc.C300391200 |display-authors=etal}}
*{{cite journal  | author=Müller T, van de Sluis B, Zhernakova A, ''et al.'' |title=The canine copper toxicosis gene MURR1 does not cause non-Wilsonian hepatic copper toxicosis. |journal=J. Hepatol. |volume=38 |issue= 2 |pages= 164-8 |year= 2003 |pmid= 12547404 |doi= }}
*{{cite journal  | vauthors=Klomp AE, van de Sluis B, Klomp LW, Wijmenga C |title=The ubiquitously expressed MURR1 protein is absent in canine copper toxicosis. |journal=J. Hepatol. |volume=39 |issue= 5 |pages= 703–9 |year= 2004 |pmid= 14568250 |doi=10.1016/S0168-8278(03)00380-5  }}
*{{cite journal  | author=Tao TY, Liu F, Klomp L, ''et al.'' |title=The copper toxicosis gene product Murr1 directly interacts with the Wilson disease protein. |journal=J. Biol. Chem. |volume=278 |issue= 43 |pages= 41593-6 |year= 2004 |pmid= 12968035 |doi= 10.1074/jbc.C300391200 }}
*{{cite journal  | vauthors=Biasio W, Chang T, McIntosh CJ, McDonald FJ |title=Identification of Murr1 as a regulator of the human delta epithelial sodium channel. |journal=J. Biol. Chem. |volume=279 |issue= 7 |pages= 5429–34 |year= 2004 |pmid= 14645214 |doi= 10.1074/jbc.M311155200 }}
*{{cite journal  | author=Klomp AE, van de Sluis B, Klomp LW, Wijmenga C |title=The ubiquitously expressed MURR1 protein is absent in canine copper toxicosis. |journal=J. Hepatol. |volume=39 |issue= 5 |pages= 703-9 |year= 2004 |pmid= 14568250 |doi= }}
*{{cite journal  | vauthors=Ganesh L, Burstein E, Guha-Niyogi A |title=The gene product Murr1 restricts HIV-1 replication in resting CD4+ lymphocytes. |journal=Nature |volume=426 |issue= 6968 |pages= 853–7 |year= 2004 |pmid= 14685242 |doi= 10.1038/nature02171 |display-authors=etal}}
*{{cite journal  | author=Biasio W, Chang T, McIntosh CJ, McDonald FJ |title=Identification of Murr1 as a regulator of the human delta epithelial sodium channel. |journal=J. Biol. Chem. |volume=279 |issue= 7 |pages= 5429-34 |year= 2004 |pmid= 14645214 |doi= 10.1074/jbc.M311155200 }}
*{{cite journal  | vauthors=Burstein E, Ganesh L, Dick RD |title=A novel role for XIAP in copper homeostasis through regulation of MURR1. |journal=EMBO J. |volume=23 |issue= 1 |pages= 244–54 |year= 2004 |pmid= 14685266 |doi= 10.1038/sj.emboj.7600031  | pmc=1271669 |display-authors=etal}}
*{{cite journal  | author=Ganesh L, Burstein E, Guha-Niyogi A, ''et al.'' |title=The gene product Murr1 restricts HIV-1 replication in resting CD4+ lymphocytes. |journal=Nature |volume=426 |issue= 6968 |pages= 853-7 |year= 2004 |pmid= 14685242 |doi= 10.1038/nature02171 }}
*{{cite journal  | vauthors=Stuehler B, Reichert J, Stremmel W, Schaefer M |title=Analysis of the human homologue of the canine copper toxicosis gene MURR1 in Wilson disease patients. |journal=J. Mol. Med. |volume=82 |issue= 9 |pages= 629–34 |year= 2005 |pmid= 15205742 |doi= 10.1007/s00109-004-0557-9 }}
*{{cite journal  | author=Burstein E, Ganesh L, Dick RD, ''et al.'' |title=A novel role for XIAP in copper homeostasis through regulation of MURR1. |journal=EMBO J. |volume=23 |issue= 1 |pages= 244-54 |year= 2004 |pmid= 14685266 |doi= 10.1038/sj.emboj.7600031 }}
*{{cite journal  | vauthors=Gerhard DS, Wagner L, Feingold EA |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504  | pmc=528928 |display-authors=etal}}
*{{cite journal  | author=Stuehler B, Reichert J, Stremmel W, Schaefer M |title=Analysis of the human homologue of the canine copper toxicosis gene MURR1 in Wilson disease patients. |journal=J. Mol. Med. |volume=82 |issue= 9 |pages= 629-34 |year= 2005 |pmid= 15205742 |doi= 10.1007/s00109-004-0557-9 }}
*{{cite journal  | vauthors=Burstein E, Hoberg JE, Wilkinson AS |title=COMMD proteins, a novel family of structural and functional homologs of MURR1. |journal=J. Biol. Chem. |volume=280 |issue= 23 |pages= 22222–32 |year= 2005 |pmid= 15799966 |doi= 10.1074/jbc.M501928200 |display-authors=etal}}
*{{cite journal  | author=Gerhard DS, Wagner L, Feingold EA, ''et al.'' |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121-7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 }}
*{{cite journal  | vauthors=Coronado VA, Bonneville JA, Nazer H |title=COMMD1 (MURR1) as a candidate in patients with copper storage disease of undefined etiology. |journal=Clin. Genet. |volume=68 |issue= 6 |pages= 548–51 |year= 2006 |pmid= 16283886 |doi= 10.1111/j.1399-0004.2005.00524.x |display-authors=etal}}
*{{cite journal  | author=Burstein E, Hoberg JE, Wilkinson AS, ''et al.'' |title=COMMD proteins, a novel family of structural and functional homologs of MURR1. |journal=J. Biol. Chem. |volume=280 |issue= 23 |pages= 22222-32 |year= 2005 |pmid= 15799966 |doi= 10.1074/jbc.M501928200 }}
*{{cite journal  | vauthors=Zhang Z, Joh K, Yatsuki H |title=Comparative analyses of genomic imprinting and CpG island-methylation in mouse Murr1 and human MURR1 loci revealed a putative imprinting control region in mice. |journal=Gene |volume=366 |issue= 1 |pages= 77–86 |year= 2006 |pmid= 16305817 |doi= 10.1016/j.gene.2005.08.020 |display-authors=etal}}
*{{cite journal  | author=Coronado VA, Bonneville JA, Nazer H, ''et al.'' |title=COMMD1 (MURR1) as a candidate in patients with copper storage disease of undefined etiology. |journal=Clin. Genet. |volume=68 |issue= 6 |pages= 548-51 |year= 2006 |pmid= 16283886 |doi= 10.1111/j.1399-0004.2005.00524.x }}
*{{cite journal  | vauthors=de Bie P, van de Sluis B, Burstein E |title=Characterization of COMMD protein-protein interactions in NF-kappaB signalling. |journal=Biochem. J. |volume=398 |issue= 1 |pages= 63–71 |year= 2006 |pmid= 16573520 |doi= 10.1042/BJ20051664  | pmc=1525016 |display-authors=etal}}
*{{cite journal  | author=Zhang Z, Joh K, Yatsuki H, ''et al.'' |title=Comparative analyses of genomic imprinting and CpG island-methylation in mouse Murr1 and human MURR1 loci revealed a putative imprinting control region in mice. |journal=Gene |volume=366 |issue= 1 |pages= 77-86 |year= 2006 |pmid= 16305817 |doi= 10.1016/j.gene.2005.08.020 }}
*{{cite journal  | vauthors=Sommerhalter M, Zhang Y, Rosenzweig AC |title=Solution structure of the COMMD1 N-terminal domain. |journal=J. Mol. Biol. |volume=365 |issue= 3 |pages= 715–21 |year= 2007 |pmid= 17097678 |doi= 10.1016/j.jmb.2006.10.030  | pmc=2706016 }}
*{{cite journal  | author=de Bie P, van de Sluis B, Burstein E, ''et al.'' |title=Characterization of COMMD protein-protein interactions in NF-kappaB signalling. |journal=Biochem. J. |volume=398 |issue= 1 |pages= 63-71 |year= 2006 |pmid= 16573520 |doi= 10.1042/BJ20051664 }}
*{{cite journal  | vauthors=Maine GN, Mao X, Komarck CM, Burstein E |title=COMMD1 promotes the ubiquitination of NF-kappaB subunits through a cullin-containing ubiquitin ligase. |journal=EMBO J. |volume=26 |issue= 2 |pages= 436–47 |year= 2007 |pmid= 17183367 |doi= 10.1038/sj.emboj.7601489 | pmc=1783443 }}
*{{cite journal | author=Sommerhalter M, Zhang Y, Rosenzweig AC |title=Solution structure of the COMMD1 N-terminal domain. |journal=J. Mol. Biol. |volume=365 |issue= 3 |pages= 715-21 |year= 2007 |pmid= 17097678 |doi= 10.1016/j.jmb.2006.10.030 }}
*{{cite journal  | author=Maine GN, Mao X, Komarck CM, Burstein E |title=COMMD1 promotes the ubiquitination of NF-kappaB subunits through a cullin-containing ubiquitin ligase. |journal=EMBO J. |volume=26 |issue= 2 |pages= 436-47 |year= 2007 |pmid= 17183367 |doi= 10.1038/sj.emboj.7601489 }}
}}
}}
{{refend}}
{{refend}}
{{PDB Gallery|geneid=150684}}
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Latest revision as of 09:54, 30 August 2017

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez

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Ensembl

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UniProt

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RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

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[1][2][3]


References

  1. ↑ 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. PMC 231805. PMID 9001233.
  2. ↑ 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.
  3. ↑ "Entrez Gene: COMMD1 copper metabolism (Murr1) domain containing 1".

External links

Further reading



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