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TargetS-adenosylmethionine synthase isoform type-2
LigandBDBM50452293
Substrate/Competitorn/a
Meas. Tech.ChEBML_105118
Ki 48000±n/a nM
Citation Kappler, FHai, TTCotter, RJHyver, KJHampton, A Isozyme-specific enzyme inhibitors. 11. L-homocysteine-ATP S-C5' covalent adducts as inhibitors of rat methionine adenosyltransferases. J Med Chem29:1030-8 (1986) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
S-adenosylmethionine synthase isoform type-2
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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  Blast E-value cutoff:
BDBM50452293
n/a
NameBDBM50452293
Synonyms:CHEMBL2092766
TypeSmall organic molecule
Emp. Form.C13H22N5O13P3
Mol. Mass.549.2608
SMILESCCC[C@]1(COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12 |r|
Structure
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