Reaction Details |
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Target | Adenosylhomocysteinase |
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Ligand | BDBM50369379 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_196552 (CHEMBL801947) |
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Ki | 3900±n/a nM |
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Citation | Wnuk, SF; Mao, Y; Yuan, CS; Borchardt, RT; Andrei, G; Balzarini, J; De Clercq, E; Robins, MJ Discovery of type II (covalent) inactivation of S-adenosyl-L-homocysteine hydrolase involving its"hydrolytic activity": synthesis and evaluation of dihalohomovinyl nucleoside analogues derived from adenosine. J Med Chem41:3078-83 (1998) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Adenosylhomocysteinase |
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Name: | Adenosylhomocysteinase |
Synonyms: | AHCY | Adenosylhomocysteinase | SAHH | SAHH_HUMAN |
Type: | PROTEIN |
Mol. Mass.: | 47714.06 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1507791 |
Residue: | 432 |
Sequence: | MSDKLPYKVADIGLAAWGRKALDIAENEMPGLMRMRERYSASKPLKGARIAGCLHMTVET
AVLIETLVTLGAEVQWSSCNIFSTQDHAAAAIAKAGIPVYAWKGETDEEYLWCIEQTLYF
KDGPLNMILDDGGDLTNLIHTKYPQLLPGIRGISEETTTGVHNLYKMMANGILKVPAINV
NDSVTKSKFDNLYGCRESLIDGIKRATDVMIAGKVAVVAGYGDVGKGCAQALRGFGARVI
ITEIDPINALQAAMEGYEVTTMDEACQEGNIFVTTTGCIDIILGRHFEQMKDDAIVCNIG
HFDVEIDVKWLNENAVEKVNIKPQVDRYRLKNGRRIILLAEGRLVNLGCAMGHPSFVMSN
SFTNQVMAQIELWTHPDKYPVGVHFLPKKLDEAVAEAHLGKLNVKLTKLTEKQAQYLGMS
CDGPFKPDHYRY
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BDBM50369379 |
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n/a |
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Name | BDBM50369379 |
Synonyms: | CHEMBL607755 |
Type | Small organic molecule |
Emp. Form. | C11H11BrFN5O3 |
Mol. Mass. | 360.139 |
SMILES | Nc1ncnc2n(cnc12)C1O[C@H](\C=C(\F)Br)[C@@H](O)[C@H]1O |r| |
Structure |
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