信号通路： Glycolysis / Gluconeogenesis;Cysteine and methionine metabolism;Pyruvate metabolism;Propanoate metabolism;
功能： catalytic activity:(S)-lactate + NAD(+) = pyruvate + NADH.,disease:Defects in LDHB are a cause of hereditary LDHB deficiency [MIM:150100]. LDHB deficiency is usually asymptomatic.,online information:Lactate dehydrogenase entry,pathway:Fermentation; pyruvate fermentation to lactate; (S)-lactate from pyruvate: step 1/1.,similarity:Belongs to the LDH/MDH superfamily.,similarity:Belongs to the LDH/MDH superfamily. LDH family.,subunit:Homotetramer.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Cytoplasm. Mitochondrion inner membrane ; Peripheral membrane protein .
组织表达： Predominantly expressed in aerobic tissues such as cardiac muscle.
信号通路： Glycolysis / Gluconeogenesis;Cysteine and methionine metabolism;Pyruvate metabolism;Propanoate metabolism;
功能： catalytic activity:(S)-lactate + NAD(+) = pyruvate + NADH.,disease:Defects in LDHB are a cause of hereditary LDHB deficiency [MIM:150100]. LDHB deficiency is usually asymptomatic.,online information:Lactate dehydrogenase entry,pathway:Fermentation; pyruvate fermentation to lactate; (S)-lactate from pyruvate: step 1/1.,similarity:Belongs to the LDH/MDH superfamily.,similarity:Belongs to the LDH/MDH superfamily. LDH family.,subunit:Homotetramer.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Cytoplasm. Mitochondrion inner membrane ; Peripheral membrane protein .
组织表达： Predominantly expressed in aerobic tissues such as cardiac muscle.
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