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Q86X83 (COMD2_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 69. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (4) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
COMM domain-containing protein 2
Gene names
Name:COMMD2
ORF Names:HSPC042, My004
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length199 AA.
Sequence statusComplete.
Protein existenceEvidence at protein level

General annotation (Comments)

Function

May down-regulate activation of NF-kappa-B. Ref.1

Subunit structure

Interacts (via COMM domain) with COMMD1 (via COMM domain). Ref.1

Tissue specificity

Ubiquitous. Ref.1

Sequence similarities

Contains 1 COMM domain.

Sequence caution

The sequence AAD39913.1 differs from that shown. Reason: Frameshift at positions 111, 160, 174 and 188.

Ontologies

Keywords
   Coding sequence diversityPolymorphism
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Molecular functionprotein binding

Inferred from physical interaction Ref.1. Source: UniProtKB

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 199199COMM domain-containing protein 2
PRO_0000077386

Regions

Domain123 – 19068COMM

Natural variations

Natural variant1131I → L. Ref.1 Ref.3 Ref.4
Corresponds to variant rs9843784 [ dbSNP | Ensembl ].
VAR_028010
Natural variant1771Q → H.
Corresponds to variant rs1546732 [ dbSNP | Ensembl ].
VAR_028011

Experimental info

Sequence conflict1991K → Q in AAD39913. Ref.3

Sequences

Sequence LengthMass (Da)Tools
Q86X83 [UniParc].

Last modified October 17, 2006. Version 2.
Checksum: ECB4B7C26FCEA0F2

FASTA19922,745
        10         20         30         40         50         60 
MLLELSEEHK EHLAFLPQVD SAVVAEFGRI AVEFLRRGAN PKIYEGAARK LNVSSDTVQH 

        70         80         90        100        110        120 
GVEGLTYLLT ESSKLMISEL DFQDSVFVLG FSEELNKLLL QLYLDNRKEI RTILSELAPS 

       130        140        150        160        170        180 
LPSYHNLEWR LDVQLASRSL RQQIKPAVTI KLHLNQNGDH NTKVLQTDPA TLLHLVQQLE 

       190 
QALEEMKTNH CRRVVRNIK 

« Hide

References

« Hide 'large scale' references
[1]"COMMD proteins, a novel family of structural and functional homologs of MURR1."
Burstein E., Hoberg J.E., Wilkinson A.S., Rumble J.M., Csomos R.A., Komarck C.M., Maine G.N., Wilkinson J.C., Mayo M.W., Duckett C.S.
J. Biol. Chem. 280:22222-22232(2005) [PubMed: 15799966] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA], FUNCTION, INTERACTION WITH COMMD1, TISSUE SPECIFICITY, VARIANT LEU-113.
[2]Mao Y.M., Xie Y., Zhou Z.X.
Submitted (APR-1998) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
Tissue: Fetal brain.
[3]"Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells."
Zhang Q.-H., Ye M., Wu X.-Y., Ren S.-X., Zhao M., Zhao C.-J., Fu G., Shen Y., Fan H.-Y., Lu G., Zhong M., Xu X.-R., Han Z.-G., Zhang J.-W., Tao J., Huang Q.-H., Zhou J., Hu G.-X. expand/collapse author list , Gu J., Chen S.-J., Chen Z.
Genome Res. 10:1546-1560(2000) [PubMed: 11042152] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT LEU-113.
Tissue: Umbilical cord blood.
[4]"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res. 14:2121-2127(2004) [PubMed: 15489334] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT LEU-113.
Tissue: Liver.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AY542158 mRNA. Translation: AAS22240.1.
AF059618 mRNA. Translation: AAG43117.1.
AF125096 mRNA. Translation: AAD39913.1. Frameshift.
BC046131 mRNA. Translation: AAH46131.1.
IPIIPI00456048.
RefSeqNP_057178.2. NM_016094.3.
UniGeneHs.432729.
Hs.730365.

3D structure databases

ProteinModelPortalQ86X83.
ModBaseSearch...

Protein-protein interaction databases

IntActQ86X83. 5 interactions.
STRINGQ86X83.

Polymorphism databases

DMDM116241310.

Proteomic databases

PeptideAtlasQ86X83.
PRIDEQ86X83.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000473414; ENSP00000419475; ENSG00000114744.
GeneID51122.
KEGGhsa:51122.
UCSCuc003exk.1. human.

Organism-specific databases

CTD51122.
GeneCardsGC03M149448.
H-InvDBHIX0200475.
HGNCHGNC:24993. COMMD2.
HPAHPA044190.
neXtProtNX_Q86X83.
PharmGKBPA134923363.
GenAtlasSearch...

Phylogenomic databases

GeneTreeENSGT00390000008489.
HOGENOMHBG716304.
HOVERGENHBG060564.
InParanoidQ86X83.
OMAKLLLQLY.
OrthoDBEOG4B8JF3.
PhylomeDBQ86X83.

Gene expression databases

ArrayExpressQ86X83.
BgeeQ86X83.
CleanExHS_COMMD2.
GenevestigatorQ86X83.
GermOnlineENSG00000114744. Homo sapiens.

Family and domain databases

InterProIPR017920. COMM.
IPR009886. HCaRG.
[Graphical view]
PfamPF07258. HCaRG. 1 hit.
[Graphical view]
PROSITEPS51269. COMM. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

NextBio53905.

Entry information

Entry nameCOMD2_HUMAN
AccessionPrimary (citable) accession number: Q86X83
Secondary accession number(s): Q9H3L5, Q9Y5V1
Entry history
Integrated into UniProtKB/Swiss-Prot: August 16, 2004
Last sequence update: October 17, 2006
Last modified: January 25, 2012
This is version 69 of the entry and version 2 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care.

Relevant documents

Human chromosome 3

Human chromosome 3: entries, gene names and cross-references to MIM

Human entries with polymorphisms or disease mutations

List of human entries with polymorphisms or disease mutations

Human polymorphisms and disease mutations

Index of human polymorphisms and disease mutations

SIMILARITY comments

Index of protein domains and families