Title : ER stress-induced upregulation of NNMT contributes to alcohol-related fatty liver development.

Pub. Date : 2020 Oct

PMID : 32389809






4 Functional Relationships(s)
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Protein Name
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1 BACKGROUND & AIM: Abundantly expressed in the metabolically active cells including hepatocytes, N-nicotinamide methyltransferase (NNMT) catalyzes S-adenosylmethionine (SAM)-dependent methylation/degradation of nicotinamide, the predominant precursor for intracellular nicotinamide adenine dinucleotide (NAD+) regeneration via the salvage pathway. S-Adenosylmethionine nicotinamide N-methyltransferase Mus musculus
2 BACKGROUND & AIM: Abundantly expressed in the metabolically active cells including hepatocytes, N-nicotinamide methyltransferase (NNMT) catalyzes S-adenosylmethionine (SAM)-dependent methylation/degradation of nicotinamide, the predominant precursor for intracellular nicotinamide adenine dinucleotide (NAD+) regeneration via the salvage pathway. S-Adenosylmethionine nicotinamide N-methyltransferase Mus musculus
3 BACKGROUND & AIM: Abundantly expressed in the metabolically active cells including hepatocytes, N-nicotinamide methyltransferase (NNMT) catalyzes S-adenosylmethionine (SAM)-dependent methylation/degradation of nicotinamide, the predominant precursor for intracellular nicotinamide adenine dinucleotide (NAD+) regeneration via the salvage pathway. S-Adenosylmethionine nicotinamide N-methyltransferase Mus musculus
4 BACKGROUND & AIM: Abundantly expressed in the metabolically active cells including hepatocytes, N-nicotinamide methyltransferase (NNMT) catalyzes S-adenosylmethionine (SAM)-dependent methylation/degradation of nicotinamide, the predominant precursor for intracellular nicotinamide adenine dinucleotide (NAD+) regeneration via the salvage pathway. S-Adenosylmethionine nicotinamide N-methyltransferase Mus musculus