MTA2
Metastasis-associated protein MTA2
Also known as: MTA1-L1, MTA1L1, MTA2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O94776
- Gene
- MTA2
- Ensembl
- ENSG00000149480
- Chromosome
- 11
- Canonical length
- 668 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
This gene encodes a protein that has been identified as a component of NuRD, a nucleosome remodeling deacetylase complex identified in the nucleus of human cells. It shows a very broad expression pattern and is strongly expressed in many tissues. It may represent one member of a small gene family that encode different but related proteins involved either directly or indirectly in transcriptional regulation. Their indirect effects on transcriptional regulation may include chromatin remodeling. It is closely related to another member of this family, a protein that has been correlated with the metastatic potential of certain carcinomas. These two proteins are so closely related that they share the same types of domains. These domains include two DNA binding domains, a dimerization domain, and a domain commonly found in proteins that methylate DNA. One of the proteins known to be a target protein for this gene product is p53. Deacetylation of p53 is correlated with a loss of growth inhibition in transformed cells supporting a connection between these gene family members and metastasis. [provided by RefSeq, May 2011]
Canonical amino-acid sequenceUniProt
668 residues, UniProt reviewed canonical sequence.
>O94776|MTA2
1 MAANMYRVGD YVYFENSSSN PYLVRRIEEL NKTANGNVEA KVVCLFRRRD ISSSLNSLAD
61 SNAREFEEES KQPGVSEQQR HQLKHRELFL SRQFESLPAT HIRGKCSVTL LNETDILSQY
121 LEKEDCFFYS LVFDPVQKTL LADQGEIRVG CKYQAEIPDR LVEGESDNRN QQKMEMKVWD
181 PDNPLTDRQI DQFLVVARAV GTFARALDCS SSIRQPSLHM SAAAASRDIT LFHAMDTLQR
241 NGYDLAKAMS TLVPQGGPVL CRDEMEEWSA SEAMLFEEAL EKYGKDFNDI RQDFLPWKSL
301 ASIVQFYYMW KTTDRYIQQK RLKAAEADSK LKQVYIPTYT KPNPNQIISV GSKPGMNGAG
361 FQKGLTCESC HTTQSAQWYA WGPPNMQCRL CASCWIYWKK YGGLKTPTQL EGATRGTTEP
421 HSRGHLSRPE AQSLSPYTTS ANRAKLLAKN RQTFLLQTTK LTRLARRMCR DLLQPRRAAR
481 RPYAPINANA IKAECSIRLP KAAKTPLKIH PLVRLPLATI VKDLVAQAPL KPKTPRGTKT
541 PINRNQLSQN RGLGGIMVKR AYETMAGAGV PFSANGRPLA SGIRSSSQPA AKRQKLNPAD
601 APNPVVFVAT KDTRALRKAL THLEMRRAAR RPNLPLKVKP TLIAVRPPVP LPAPSHPAST
661 NEPIVLEDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MTA2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.47
- Highest tissue expression
- 111 nTPM
Expression across tissuesHPA
Tissue
- retina: 111 nTPM
- tonsil: 86 nTPM
- thymus: 84 nTPM
- esophagus: 77 nTPM
- skin: 71 nTPM
- lymph node: 66 nTPM
Single-cell type
- rod photoreceptor cells: 51 nCPM
- megakaryocyte progenitors: 29 nCPM
- cone photoreceptor cells: 27 nCPM
- erythrocyte progenitors: 24 nCPM
- ocular epithelial cells: 23 nCPM
- monocyte progenitors: 22 nCPM
Immune cell
- gdT-cell: 19 nTPM
- non-classical monocyte: 17 nTPM
- MAIT T-cell: 16 nTPM
- memory CD4 T-cell: 15 nTPM
- naive CD8 T-cell: 14 nTPM
- naive CD4 T-cell: 14 nTPM
Brain region
- white matter: 53 nTPM
- medulla oblongata: 47 nTPM
- pons: 41 nTPM
- basal ganglia: 41 nTPM
- spinal cord: 41 nTPM
- midbrain: 40 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about MTA2.
Disease | ImmuneIEDB
Conditions an epitope on MTA2 was assayed in.
- stomach cancer T cell
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.36
- gnomAD pLI
- 0.74
- gnomAD missense Z
- 3.13
- DepMap mean gene effect
- -0.22
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- chromatin organization
- chromatin remodeling
- genomic imprinting
- negative regulation of DNA-templated transcription
- negative regulation of transcription by RNA polymerase II
- positive regulation of DNA-templated transcription
- positive regulation of transcription by RNA polymerase II
- regulation of cell fate specification
- regulation of fibroblast migration
- regulation of stem cell differentiation
Molecular functions
- chromatin binding
- histone deacetylase activity
- histone deacetylase binding
- RNA polymerase II-specific DNA-binding transcription factor binding
- sequence-specific DNA binding
- transcription coactivator activity
- transcription corepressor activity
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Zinc finger, GATA-type
- ELM2 domain
- SANT/Myb domain
- Bromo adjacent homology (BAH) domain
- Homedomain-like superfamily
- SANT domain
- Metastasis-associated protein MTA1, R1 domain
- Mesoderm induction early response protein/metastasis-associated protein
- Bromo adjacent homology (BAH) domain superfamily
- Myb-like DNA-binding domain
- GATA zinc finger
- BAH domain
- ELM2 domain
- MTA R1 domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MTA2 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MTA2 as an antibody target. Whether an autoantibody or antibody against MTA2 could matter depends on whether native MTA2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MTA2 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label MTA2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...