Homo sapiens Protein: MAT1A
Summary
InnateDB Protein IDBP-80411.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MAT1A
Protein Name methionine adenosyltransferase I, alpha
Synonyms MAT; MATA1; SAMS; SAMS1;
Species Homo sapiens
Ensembl Protein ENSP00000361287
InnateDB Gene IDBG-80409 (MAT1A)
Protein Structure
UniProt Annotation
Function Catalyzes the formation of S-adenosylmethionine from methionine and ATP.
Subcellular Localization
Disease Associations Methionine adenosyltransferase deficiency (MATD) [MIM:250850]: An inborn error of metabolism resulting in isolated hypermethioninemia. Most patients have no clinical abnormalities, although some neurologic symptoms may be present in rare cases with severe loss of methionine adenosyltransferase activity. {ECO:0000269PubMed:10677294, ECO:0000269PubMed:7560086, ECO:0000269PubMed:8770875, ECO:0000269PubMed:9042912}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Expressed in liver.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 5 experimentally validated interaction(s) in this database.
They are also associated with 2 interaction(s) predicted by orthology.
Experimentally validated
Total 5 [view]
Protein-Protein 4 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 2 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004478 methionine adenosyltransferase activity
GO:0005524 ATP binding
GO:0046872 metal ion binding
Biological Process
GO:0000096 sulfur amino acid metabolic process
GO:0006520 cellular amino acid metabolic process
GO:0006556 S-adenosylmethionine biosynthetic process
GO:0006730 one-carbon metabolic process
GO:0006805 xenobiotic metabolic process
GO:0032259 methylation
GO:0034641 cellular nitrogen compound metabolic process
GO:0044281 small molecule metabolic process
Cellular Component
GO:0005829 cytosol
Protein Structure and Domains
PDB ID
InterPro IPR002133 S-adenosylmethionine synthetase
IPR022628 S-adenosylmethionine synthetase, N-terminal
IPR022629 S-adenosylmethionine synthetase, central domain
IPR022630 S-adenosylmethionine synthetase, C-terminal
IPR022636 S-adenosylmethionine synthetase superfamily
PFAM PF00438
PF02772
PF02773
PRINTS
PIRSF PIRSF000497
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q00266
PhosphoSite PhosphoSite-Q00266
TrEMBL
UniProt Splice Variant
Entrez Gene 4143
UniGene Hs.282670
RefSeq NP_000420
HUGO HGNC:6903
OMIM 610550
CCDS CCDS7365
HPRD 02013
IMGT
EMBL AL359195 BC018359 CH471142 D49357 X69078
GenPept AAH18359 BAA08355 CAA48822 CAI13695 EAW80396 EAW80397