MAT2A - methionine adenosyltransferase 2A Gene

Also Known as MATA2; MATII; SAMS2

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 4144

About MAT2A

Cytogenetic location: 2p11.2 Genomic coordinates (GRCh38): 2:85,539,168-85,545,281 (from NCBI)

This gene has 6 transcripts (splice variants), 292 orthologues, 1 paralogue and is associated with 1 phenotype. Ubiquitous expression in thyroid (RPKM 234.0), adrenal (RPKM 141.3) and 25 other tissues.

Summary

The protein encoded by this gene catalyzes the production of S-adenosylmethionine (AdoMet) from methionine and ATP. AdoMet is the key methyl donor in cellular processes. [provided by RefSeq, Jun 2011]

MAT2A Products (1)

mRNA Protein Name
NM_005911.6 NP_005902.1 S-adenosylmethionine synthase isoform type-2
Molecular Function GO Annotation Evidence References Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
enables methionine adenosyltransferase activity IDA
IDA: Inferred from direct assay
7665609 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
10644686 GOA
enables small molecule binding EXP
EXP: Inferred from Experiment
26858410 GOA
Biological Process GO Annotation Evidence References Source
involved in S-adenosylmethionine biosynthetic process IDA
IDA: Inferred from direct assay
10644686 GOA
involved in cellular response to methionine IDA
IDA: Inferred from direct assay
38006878 GOA
involved in positive regulation of TORC1 signaling IDA
IDA: Inferred from direct assay
38006878 GOA
involved in protein heterooligomerization IDA
IDA: Inferred from direct assay
25075345 GOA
involved in protein hexamerization IDA
IDA: Inferred from direct assay
25075345 GOA
Cellular Component GO Annotation Evidence References Source
part of methionine adenosyltransferase complex IDA
IDA: Inferred from direct assay
10644686 GOA
part of methionine adenosyltransferase complex IPI
IPI: Inferred from physical interaction
25075345 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

MAT2A Protein Structure

S-AdoMet_synt_N

S-AdoMet_synt_N: S-adenosylmethionine synthetase, N-terminal domain (17 - 115)

S-AdoMet_synt_M

S-AdoMet_synt_M: S-adenosylmethionine synthetase, central domain (129 - 250)

S-AdoMet_synt_C

S-AdoMet_synt_C: S-adenosylmethionine synthetase, C-terminal domain (252 - 388)

  • 0
  • 100
  • 200
  • 300
  • 395 a.a.
Protein Preferred Names Protein Names

S-adenosylmethionine synthase isoform type-2

  • MAT 2

MAT2A Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
MAT2A P31153 MAT2B Homo sapiens Q9NZL9 25416956
Intra
MAT2A P31153 MAT2B Homo sapiens Q9NZL9 25416956
Intra
MAT2A P31153 MAT2B Homo sapiens Q9NZL9 33961781
Intra
MAT2A P31153 MAT2B Homo sapiens Q9NZL9 25416956
Intra
MAT2A P31153 MAT1A Homo sapiens Q00266 32296183
Intra
MAT2A P31153 MAT2A Homo sapiens P31153 32296183
Intra
MAT2A P31153 MAT2A Homo sapiens P31153 32296183
Intra
MAT2A P31153 MAT1A Homo sapiens Q00266 32296183
Intra
MAT2A P31153 MAT1A Homo sapiens Q00266 32296183
Intra
MAT2A P31153 MAT2A Homo sapiens P31153 32296183
Intra
MAT2A P31153 MAT2A Homo sapiens P31153 25416956
Intra
MAT2A P31153 IFI35 Homo sapiens P80217-2 32814053
Intra
MAT2A P31153 IFI35 Homo sapiens P80217-2 32814053
Intra
MAT2A P31153 IFI35 Homo sapiens P80217-2 32814053
Intra
MAT2A P31153 ZMYM6 Homo sapiens O95789-4 32814053
Intra
MAT2A P31153 ZMYM6 Homo sapiens O95789-4 32814053
Intra
MAT2A P31153 ZMYM6 Homo sapiens O95789-4 32814053
Intra
MAT2A P31153 KLF15 Homo sapiens Q9UIH9 32814053
Intra
MAT2A P31153 KLF15 Homo sapiens Q9UIH9 32814053
Intra
MAT2A P31153 KLF15 Homo sapiens Q9UIH9 32814053
Intra
MAT2A P31153 FAM117B Homo sapiens Q6P1L5 32814053
Intra
MAT2A P31153 FAM117B Homo sapiens Q6P1L5 32814053
Intra
MAT2A P31153 FAM117B Homo sapiens Q6P1L5 32814053
Intra
MAT2A P31153 CAMK1G Homo sapiens Q96NX5 32814053
Intra
MAT2A P31153 CAMK1G Homo sapiens Q96NX5 32814053
Intra
MAT2A P31153 CAMK1G Homo sapiens Q96NX5 32814053
Intra
MAT2A P31153 CCDC141 Homo sapiens Q6ZP82-1 32814053
Intra
MAT2A P31153 CCDC141 Homo sapiens Q6ZP82-1 32814053
Intra
MAT2A P31153 CCDC141 Homo sapiens Q6ZP82-1 32814053
Intra
MAT2A P31153 SNW1 Homo sapiens Q13573 32814053
Intra
MAT2A P31153 SNW1 Homo sapiens Q13573 32814053
Intra
MAT2A P31153 SNW1 Homo sapiens Q13573 32814053
Intra
MAT2A P31153 PRC1 Homo sapiens O43663 32296183
Intra
MAT2A P31153 PRC1 Homo sapiens O43663 32296183
Intra
MAT2A P31153 RBM11 Homo sapiens P57052 32814053
Intra
MAT2A P31153 RBM11 Homo sapiens P57052 32814053
Intra
MAT2A P31153 RBM11 Homo sapiens P57052 32814053
Intra
MAT2A P31153 GATA1 Homo sapiens P15976-2 32814053
Intra
MAT2A P31153 GATA1 Homo sapiens P15976-2 32814053
Intra
MAT2A P31153 GATA1 Homo sapiens P15976-2 32814053
Intra
MAT2A P31153 MT2A Homo sapiens P02795 32814053
Intra
MAT2A P31153 MT2A Homo sapiens P02795 32814053
Intra
MAT2A P31153 MT2A Homo sapiens P02795 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

MAT2A Antibodies

Cat. No. Product Name Application Reactivity
HY-P83181 MAT2A Antibody (YA2926) WB, ICC/IF Human, Mouse, Rat

Related Diseases

Diseases Alias
Glycine N-Methyltransferase Deficiency
  • GNMT DEFICIENCY

  • Hypermethioninemia Due To Glycine N-Methyltransferase Deficiency

  • Hypermethioninemia Due To Gnmt Deficiency

  • Hypermethioninemia

  • Hepatic Methionine Adenosyltransferase Deficiency

Aortic Aneurysm, Familial Thoracic 1
  • Thoracic Aortic Aneurysm

  • Annuloaortic Ectasia

  • Familial Thoracic Aortic Aneurysm And Aortic Dissection

  • Familial Aortic Dissection

  • Familial Taad

  • Familial Thoracic Aortic Aneurysm

  • Congenital Aneurysm Of Ascending Aorta

  • Familial Aortic Aneurysm

  • Familial Thoracic Aortic Aneurysm And Dissection

  • Aortic Aneurysm, Thoracic

  • AAT1

  • Faa1

  • Aortic Dissection, Familial

  • Aortic Aneurysm, Familial Thoracic

  • Aneurysm, Thoracic Aortic

  • Faa

  • Ftaad

  • Taa

  • Taad

  • Cystic Medial Necrosis Of Aorta

  • Familial Non-Syndromic Thoracic Aortic Aneurysm And Aortic Dissection

  • Aortic Aneurysm Thoracic

  • Familial Aortic Aneurysms

  • Aneurysm, Aortic, Thoracic, Familial, Type 1

  • Aneurysm Of Thoracic Aorta

  • Intrathoracic Aneurysm

  • Thoracic Aorta Aneurysm

  • Thoracic Aortic Aneurysm Without Rupture

  • Thoracic Aneurysm

  • Thorax Arterial Aneurysm

  • Thoracic Artery Aneurysm

  • Thoracic Arterial Aneurysm

  • Thorax Aneurysm

  • Thorax Aortic Aneurysm

  • Dissection Of Thoracic Aorta

Hypermethioninemia
  • Hepatic Methionine Adenosyltransferase Deficiency

  • Deficiency Of Methionine Adenosyltransferase

  • Glycine N-Methyltransferase Deficiency

  • Met

  • S-Adenosylhomocysteine Hydrolase Deficiency

  • Gnmt Deficiency

  • Mat Deficiency

  • Methionine Adenosyltransferase Deficiency

  • Methioninemia

  • Deficiency Of Acetyl-Coa Acetyltransferase

Aortic Valve Disease 1
  • Aortic Valve Disease

  • Bicuspid Aortic Valve

  • Aortic Valve Disorder

  • AOVD1

  • Bav

  • Bicuspid Aortic Valve Disease

  • Familial Bicuspid Aortic Valve

  • Aortic Valve Calcification

  • Aovd

  • Aortic Valve, Bicuspid

  • Aortic Valve, Calcification Of

  • Aortic Stenosis, Calcific

  • Familial Bav

  • Calcific Aortic Stenosis

  • Calcification Of Aortic Valve

  • Abnormality Of The Aortic Valve

  • Aortic Valve Disease, Type 1

  • Aortic Valve Disease 2

  • Bicommissural Aortic Valve

Hepatocellular Carcinoma
  • Liver Cancer

  • Primary Liver Cancer

  • HCC

  • Hepatoma

  • Malignant Neoplasm Of Liver

  • Liver Neoplasms

  • Cancer, Hepatocellular

  • Liver Cell Carcinoma

  • Lcc

  • Hepatoblastoma, Somatic

  • Hepatic Cancer

  • Primary Malignant Neoplasm Of Liver

  • Rare Tumor Of Liver And Intrahepatic Biliary Tract

  • Hepatocellular Carcinoma, Somatic

  • Hepatocellular Carcinoma, Childhood Type, Somatic

  • Hepatocellular Cancer, Somatic

  • Ca Liver - Primary

  • Hepatic Neoplasm

  • Malignant Hepato-Biliary Neoplasm

  • Malignant Neoplasm Of Liver, Not Specified As Primary Or Secondary

  • Malignant Neoplasm Of Liver, Primary

  • Malignant Tumor Of Liver

  • Neoplasm Of Liver

  • Non-Resectable Primary Hepatic Malignant Neoplasm

  • Resectable Malignant Neoplasm Of Liver

  • Resectable Malignant Neoplasm Of The Liver

  • Primary Liver Carcinoma

  • Primary Malignant Liver Neoplasm

  • Primary Cancer Of Liver

  • Primary Tumor Of The Liver

  • Rare Tumor Of Liver And Ibt

  • Hepatocellular Cancer

  • Neoplasm Of The Liver

  • Carcinoma, Hepatocellular

  • Hepatomas

  • Liver Neoplasm

  • Liver Carcinoma

  • Liver And Intrahepatic Biliary Tract Carcinoma

  • Malignant Hepatobiliary Neoplasm

  • Adult Primary Hepatocellular Carcinoma

  • Hepatoblastoma

  • Carcinoma Of Liver

  • Malignant Liver Tumour

  • Malignant Hepatic Tumour

Loeys-Dietz Syndrome
  • Loeys-Dietz Aortic Aneurysm Syndrome

  • Lds

  • Aortic Aneurysm Syndrome Due To Tgf-Beta Receptors Anomalies

  • Furlong Syndrome

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus MAT2A VGNC VGNC:50214
Canis familiaris MAT2A VGNC VGNC:49922
Felis catus MAT2A VGNC VGNC:68193
Rattus norvegicus MAT2A RGD RGD:619985
Mus musculus MAT2A MGD MGI:2443731
Macaca mulatta MAT2A VGNC VGNC:74664
Others MAT2A NCBI