PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 21410432-4 2011 Here, we present crystal structures of the CARM1 catalytic domain in complex with cofactors [SAH (S-adenosyl-L-homocysteine) or SNF (sinefungin)] and indole or pyazole inhibitors. S-Adenosylhomocysteine 98-123 acyl-CoA synthetase medium chain family member 3 Homo sapiens 93-96 20864509-1 2010 S-adenosyl-(L)-homocysteine (SAH) riboswitches are regulatory elements found in bacterial mRNAs that up-regulate genes involved in the S-adenosyl-(L)-methionine (SAM) regeneration cycle. S-Adenosylhomocysteine 0-27 acyl-CoA synthetase medium chain family member 3 Homo sapiens 29-32 34783058-8 2022 S-adenosylmethionine//S-adenosylhomocysteine (SAM/SAH) levels were evaluated by enzyme-linked immunosorbent assay. S-Adenosylhomocysteine 22-44 acyl-CoA synthetase medium chain family member 3 Homo sapiens 46-53 17004132-1 2006 Homocysteine is a sulfur-containing, nonproteinogenic, neurotoxic amino acid biosynthesized during methyl cycles after demethylation of S-adenosylmethionine (SAM) to S-adenosylhomocysteine (SAH) and subsequent hydrolysis of SAH into homocysteine and adenosine. S-Adenosylhomocysteine 166-188 acyl-CoA synthetase medium chain family member 3 Homo sapiens 190-193 12859184-3 2003 Unlike most SAM-dependent methyltransferases, GNMT has a relatively high value and is weakly inhibited by the product S-adenosyl-l-homocysteine (SAH). S-Adenosylhomocysteine 118-143 acyl-CoA synthetase medium chain family member 3 Homo sapiens 145-148 33020707-4 2020 In the present study, molecular recognition between the two natural nucleoside analogs (S-adenosyl-L-homocysteine (SAH) and sinefungin (SFG)) and the SARS-CoV-2 nsp16/nsp10/m7GpppAC5 was studied using all-atom molecular dynamics simulations and free energy calculations based on MM/GBSA and WaterSwap approaches. S-Adenosylhomocysteine 88-113 acyl-CoA synthetase medium chain family member 3 Homo sapiens 115-118 33993848-7 2022 Our study uncovers a new axis of SAH-AHCYL1-PIK3C3, which senses the intracellular level of SAH to inhibit autophagy in an MTORC1-independent manner.Abbreviations: ADOX: adenosine dialdehyde; AHCY: adenosylhomocysteinase; AHCYL1: adenosylhomocysteinase like 1; cLEU: cycloleucine; PIK3C3: phosphatidylinositol 3-kinase catalytic subunit type 3; PtdIns3P: phosphatidylinositol-3-phosphate; SAH: S-adenosyl-l-homocysteine; SAM: S-adenosyl-l-methionine. S-Adenosylhomocysteine 394-419 acyl-CoA synthetase medium chain family member 3 Homo sapiens 33-36 33993848-7 2022 Our study uncovers a new axis of SAH-AHCYL1-PIK3C3, which senses the intracellular level of SAH to inhibit autophagy in an MTORC1-independent manner.Abbreviations: ADOX: adenosine dialdehyde; AHCY: adenosylhomocysteinase; AHCYL1: adenosylhomocysteinase like 1; cLEU: cycloleucine; PIK3C3: phosphatidylinositol 3-kinase catalytic subunit type 3; PtdIns3P: phosphatidylinositol-3-phosphate; SAH: S-adenosyl-l-homocysteine; SAM: S-adenosyl-l-methionine. S-Adenosylhomocysteine 394-419 acyl-CoA synthetase medium chain family member 3 Homo sapiens 92-95 33993848-7 2022 Our study uncovers a new axis of SAH-AHCYL1-PIK3C3, which senses the intracellular level of SAH to inhibit autophagy in an MTORC1-independent manner.Abbreviations: ADOX: adenosine dialdehyde; AHCY: adenosylhomocysteinase; AHCYL1: adenosylhomocysteinase like 1; cLEU: cycloleucine; PIK3C3: phosphatidylinositol 3-kinase catalytic subunit type 3; PtdIns3P: phosphatidylinositol-3-phosphate; SAH: S-adenosyl-l-homocysteine; SAM: S-adenosyl-l-methionine. S-Adenosylhomocysteine 394-419 acyl-CoA synthetase medium chain family member 3 Homo sapiens 92-95 6091559-3 1984 In the hydrolysis direction, the enzyme has a pH optimum of 7.5, a Km for S-adenosyl-L-homocysteine (SAH) of 6 microM, and a Vmax of 0.22 mumol min-1 mg-1. S-Adenosylhomocysteine 74-99 acyl-CoA synthetase medium chain family member 3 Homo sapiens 101-104 33993848-1 2022 S-adenosyl-l-homocysteine (SAH), an amino acid derivative, is a key intermediate metabolite in methionine metabolism, which is normally considered as a harmful by-product and hydrolyzed quickly once formed. S-Adenosylhomocysteine 0-25 acyl-CoA synthetase medium chain family member 3 Homo sapiens 27-30 27934872-6 2016 A structural analysis revealed that, despite the simultaneous presence of both substrate (sarcosine) and cofactor (S-adenosyl-L-homocysteine; SAH), the enzyme was likely crystallized in an inactive conformation, as additional structural changes are required to complete the active site assembly. S-Adenosylhomocysteine 115-140 acyl-CoA synthetase medium chain family member 3 Homo sapiens 142-145 29679079-2 2018 We employed molecular dynamics and Gaussian accelerated molecular dynamics techniques to investigate the structure of Zika NS5 protein with S-adenosyl-L-homocysteine (SAH) and an RNA analogue, namely 7-methylguanosine 5"-triphosphate (m7GTP). S-Adenosylhomocysteine 140-165 acyl-CoA synthetase medium chain family member 3 Homo sapiens 167-170