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TargetS-adenosylmethionine synthase isoform type-1/type-2
LigandBDBM50226770
Substrate/Competitorn/a
Meas. Tech.ChEMBL_104956 (CHEMBL715638)
Ki 3000±n/a nM
Citation Vrudhula, VMKappler, FHampton, A Isozyme-specific enzyme inhibitors. 13. S-[5'(R)-[(N-triphosphoamino)methyl]adenosyl]-L-homocysteine, a potent inhibitor of rat methionine adenosyltransferases. J Med Chem30:888-94 (1987) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
S-adenosylmethionine synthase isoform type-1/type-2
Name:S-adenosylmethionine synthase isoform type-1/type-2
Synonyms:S-adenosylmethionine synthetase (MAT 1 and MAT 2)
Type:n/a
Mol. Mass.:n/a
Description:ASSAY_ID of ChEMBL is 104961
Components:This complex has 2 components.
Component 1
Name:S-adenosylmethionine synthase isoform type-1
Synonyms:AdoMet synthetase 1 | Ams1 | MAT 1 | MAT-I/III | METK1_RAT | Mat1a | Methionine adenosyltransferase 1 | Methionine adenosyltransferase I/III | S-adenosylmethionine synthetase (MAT 1 and MAT 2) | S-adenosylmethionine synthetase alpha and beta forms | S-adenosylmethionine synthetase isoform type-1
Type:PROTEIN
Mol. Mass.:43692.87
Organism:Rattus norvegicus
Description:ChEMBL_11027
Residue:397
Sequence:
MNGPVDGLCDHSLSEEGAFMFTSESVGEGHPDKICDQISDAVLDAHLKQDPNAKVACETV
CKTGMVLLCGEITSMAMIDYQRVVRDTIKHIGYDDSAKGFDFKTCNVLVALEQQSPDIAQ
CVHLDRNEEDVGAGDQGLMFGYATDETEECMPLTIVLAHKLNTRMADLRRSGVLPWLRPD
SKTQVTVQYVQDNGAVIPVRVHTIVISVQHNEDITLEAMREALKEQVIKAVVPAKYLDED
TIYHLQPSGRFVIGGPQGDAGVTGRKIIVDTYGGWGAHGGGAFSGKDYTKVDRSAAYAAR
WVAKSLVKAGLCRRVLVQVSYAIGVAEPLSISIFTYGTSKKTERDELLEVVNKNFDLRPG
VIVRDLDLKKPIYQKTACYGHFGRSEFPWEVPKKLVF
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Component 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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BDBM50226770
n/a
NameBDBM50226770
Synonyms:CHEMBL609078
TypeSmall organic molecule
Emp. Form.C15H26N7O14P3S
Mol. Mass.653.392
SMILES[H][C@@]1(OC([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)[C@H](CNP(O)(=O)OP(O)(=O)OP(O)(O)=O)SCCC(N)C(O)=O |r|
Structure
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