MTA1
Metastasis-associated protein MTA1
Also known as: MTA1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q13330
- Gene
- MTA1
- Ensembl
- ENSG00000182979
- Chromosome
- 14
- Canonical length
- 715 aa
- Protein class
- Cancer-related genes, Disease related genes, Plasma proteins, Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
This gene encodes a protein that was identified in a screen for genes expressed in metastatic cells, specifically, mammary adenocarcinoma cell lines. Expression of this gene has been correlated with the metastatic potential of at least two types of carcinomas although it is also expressed in many normal tissues. The role it plays in metastasis is unclear. It was initially thought to be the 70kD component of a nucleosome remodeling deacetylase complex, NuRD, but it is more likely that this component is a different but very similar protein. These two proteins are so closely related, though, 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. The profile and activity of this gene product suggest that it is involved in regulating transcription and that this may be accomplished by chromatin remodeling. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011]
Canonical amino-acid sequenceUniProt
715 residues, UniProt reviewed canonical sequence.
>Q13330|MTA1
1 MAANMYRVGD YVYFENSSSN PYLIRRIEEL NKTANGNVEA KVVCFYRRRD ISSTLIALAD
61 KHATLSVCYK AGPGADNGEE GEIEEEMENP EMVDLPEKLK HQLRHRELFL SRQLESLPAT
121 HIRGKCSVTL LNETESLKSY LEREDFFFYS LVYDPQQKTL LADKGEIRVG NRYQADITDL
181 LKEGEEDGRD QSRLETQVWE AHNPLTDKQI DQFLVVARSV GTFARALDCS SSVRQPSLHM
241 SAAAASRDIT LFHAMDTLHK NIYDISKAIS ALVPQGGPVL CRDEMEEWSA SEANLFEEAL
301 EKYGKDFTDI QQDFLPWKSL TSIIEYYYMW KTTDRYVQQK RLKAAEAESK LKQVYIPNYN
361 KPNPNQISVN NVKAGVVNGT GAPGQSPGAG RACESCYTTQ SYQWYSWGPP NMQCRLCASC
421 WTYWKKYGGL KMPTRLDGER PGPNRSNMSP HGLPARSSGS PKFAMKTRQA FYLHTTKLTR
481 IARRLCREIL RPWHAARHPY LPINSAAIKA ECTARLPEAS QSPLVLKQAV RKPLEAVLRY
541 LETHPRPPKP DPVKSVSSVL SSLTPAKVAP VINNGSPTIL GKRSYEQHNG VDGNMKKRLL
601 MPSRGLANHG QARHMGPSRN LLLNGKSYPT KVRLIRGGSL PPVKRRRMNW IDAPDDVFYM
661 ATEETRKIRK LLSSSETKRA ARRPYKPIAL RQSQALPPRP PPPAPVNDEP IVIEDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MTA1 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
- 46 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 46 nTPM
- heart muscle: 37 nTPM
- ovary: 37 nTPM
- pituitary gland: 36 nTPM
- testis: 36 nTPM
- prostate: 30 nTPM
Single-cell type
- epididymal principal cells: 370 nCPM
- breast lactating cells: 243 nCPM
- esophageal apical cells: 114 nCPM
- bergmann glia: 74 nCPM
- breast secretory cells: 65 nCPM
- fallopian tube ciliated cells: 60 nCPM
Immune cell
- plasmacytoid DC: 0.9 nTPM
- eosinophil: 0.8 nTPM
- naive CD8 T-cell: 0.4 nTPM
- NK-cell: 0.4 nTPM
- gdT-cell: 0.3 nTPM
- MAIT T-cell: 0.3 nTPM
Brain region
- cerebral cortex: 45 nTPM
- amygdala: 45 nTPM
- hippocampal formation: 45 nTPM
- cerebellum: 44 nTPM
- thalamus: 42 nTPM
- basal ganglia: 42 nTPM
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)
- 0.11
- gnomAD pLI
- 1
- gnomAD missense Z
- 3.5
- DepMap mean gene effect
- -0.02
- 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 remodeling
- circadian regulation of gene expression
- double-strand break repair
- entrainment of circadian clock by photoperiod
- locomotor rhythm
- negative regulation of DNA-templated transcription
- negative regulation of gene expression, epigenetic
- negative regulation of transcription by RNA polymerase II
- positive regulation of DNA-templated transcription
- positive regulation of protein autoubiquitination
- proteasome-mediated ubiquitin-dependent protein catabolic process
- regulation of cell fate specification
- regulation of stem cell differentiation
- response to ionizing radiation
- signal transduction
Molecular functions
- chromatin binding
- histone deacetylase binding
- RNA polymerase II cis-regulatory region sequence-specific DNA binding
- RNA polymerase II-specific DNA-binding transcription factor 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 MTA1 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 MTA1 as an antibody target. Whether an autoantibody or antibody against MTA1 could matter depends on whether native MTA1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MTA1 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 MTA1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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