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MAT1A catalyzes the formation of S-adenosylmethionine from methionine and ATP. Methionine adenosyltransferase deficiency is caused by recessive and dominant mutations, the latter identified in autosomal dominant persistant hypermethioninemia.This gne encodes methionine adenosyltransferase I (alpha isoform), which catalyzes the formation of S-adenosylmethionine from methionine and ATP. Methionine adenosyltransferase deficiency is caused by recessive and dominant mutations, the latter identified in autosomal dominant persistant hypermethioninemia.
AdoMet; AdoMet synthase 1; adoMet synthetase 1; AI046368; Ams; Ams1; Cartilage matrix protein; CMP; CRTM; MAT; MAT 1; Mat1a; MATA1; MAT-I/III; MATN1; matrilin 1, cartilage matrix protein; Matrilin-1; Methionine adenosyltransferase 1; methionine adenosyltransferase 1A; methionine adenosyltransferase I, alpha; methionine adenosyltransferase I/III; S - adenosylmethionine synthetase; SADE; S-adenosylmethionine synthase; S-adenosylmethionine synthase isoform type-1; S-adenosylmethionine synthase isoform type-1; S-adenosylmethionine synthase; S-adenosylmethionine synthetase isoform type-1; SAMS; SAMS1; SAS; similar to S-adenosylmethionine synthetase alpha and beta forms (Methionine adenosyltransferase) (AdoMet synthetase) (MAT-I/III); wu:fi35e01; zgc:55442
100 µg
150 µL
100 µL
100 µL
100 µL
100 µL
100 µL
100 µg
150 µL
100 µL
100 µL
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