Reaction Details |
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Target | S-adenosylmethionine synthase isoform type-2 |
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Ligand | BDBM50367301 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_105120 (CHEMBL713238) |
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Ki | 48000±n/a nM |
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Citation | Kappler, F; Hai, TT; Hampton, A Isozyme-specific enzyme inhibitors. 10. Adenosine 5'-triphosphate derivatives as substrates or inhibitors of methionine adenosyltransferases of rat normal and hepatoma tissues. J Med Chem29:318-22 (1986) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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S-adenosylmethionine synthase isoform type-2 |
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Name: | S-adenosylmethionine synthase isoform type-2 |
Synonyms: | AdoMet synthetase 2 | Ams2 | MAT 2 | MAT-II | METK2_RAT | Mat2a | Methionine adenosyltransferase 2 | Methionine adenosyltransferase II | S-Adenosylmethionine Synthase (AdoMet) | S-adenosylmethionine synthetase (MAT 1 and MAT 2) | S-adenosylmethionine synthetase gamma form | S-adenosylmethionine synthetase isoform type-2 |
Type: | PROTEIN |
Mol. Mass.: | 43713.68 |
Organism: | Rattus norvegicus |
Description: | ChEMBL_105118 |
Residue: | 395 |
Sequence: | MNGQLNGFHEAFIEEGTFLFTSESVGEGHPDKICDQINDAVLDAHLQQDPDAKVACETVA
KTGMILLAGEITSRAAIDYQKVVREAIKHIGYDDSSKGFDYKTCNVLVALEQQSPDIAQG
VHLDRNEEDIGAGDQGLMFGYATDETEECMPLTIVLAHKLNAKLAELRRNGTLPWLRPDS
KTQVTVQYMQDRGAVIPIRVHTIVISVQHDEEVCLDEMRDALKEKLIKAVVPAKYLDEDT
IYHLQPSGRFVIGGPQGDAGLTGRKIIVDTYGGWGAHGGGAFSGKDYTKVDRSAAYAARW
VAKSLVKGGLCRRVLVQVSYAIGVSHPLSISIFHYGTSQKSERELLEIVKNNFDLRPGVI
VRDLDLKKPIYQRTAAYGHFGRDSFPWEVPKKLKY
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BDBM50367301 |
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n/a |
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Name | BDBM50367301 |
Synonyms: | CHEMBL1791432 |
Type | Small organic molecule |
Emp. Form. | C13H22N5O13P3 |
Mol. Mass. | 549.2608 |
SMILES | CCCC(OP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12 |r| |
Structure |
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