Reaction Details |
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Target | Beta-hexosaminidase subunit beta |
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Ligand | BDBM40765 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Inhibition Assay |
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Ki | 5000±0.0 nM |
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Citation | Liu, J; Shikhman, AR; Lotz, MK; Wong, CH Hexosaminidase inhibitors as new drug candidates for the therapy of osteoarthritis. Chem Biol8:701-11 (2001) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Beta-hexosaminidase subunit beta |
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Name: | Beta-hexosaminidase subunit beta |
Synonyms: | Beta-N-acetylhexosaminidase subunit beta | Beta-hexosaminidase subunit beta | Beta-hexosaminidase subunit beta (Hex B) | HEXB | HEXB_HUMAN | Hexosaminidase subunit B |
Type: | Enzyme |
Mol. Mass.: | 63112.58 |
Organism: | Homo sapiens (Human) |
Description: | P07686 |
Residue: | 556 |
Sequence: | MELCGLGLPRPPMLLALLLATLLAAMLALLTQVALVVQVAEAARAPSVSAKPGPALWPLP
LSVKMTPNLLHLAPENFYISHSPNSTAGPSCTLLEEAFRRYHGYIFGFYKWHHEPAEFQA
KTQVQQLLVSITLQSECDAFPNISSDESYTLLVKEPVAVLKANRVWGALRGLETFSQLVY
QDSYGTFTINESTIIDSPRFSHRGILIDTSRHYLPVKIILKTLDAMAFNKFNVLHWHIVD
DQSFPYQSITFPELSNKGSYSLSHVYTPNDVRMVIEYARLRGIRVLPEFDTPGHTLSWGK
GQKDLLTPCYSRQNKLDSFGPINPTLNTTYSFLTTFFKEISEVFPDQFIHLGGDEVEFKC
WESNPKIQDFMRQKGFGTDFKKLESFYIQKVLDIIATINKGSIVWQEVFDDKAKLAPGTI
VEVWKDSAYPEELSRVTASGFPVILSAPWYLDLISYGQDWRKYYKVEPLDFGGTQKQKQL
FIGGEACLWGEYVDATNLTPRLWPRASAVGERLWSSKDVRDMDDAYDRLTRHRCRMVERG
IAAQPLYAGYCNHENM
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BDBM40765 |
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n/a |
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Name | BDBM40765 |
Synonyms: | Iminocyclitol, 8 |
Type | Small organic molecule |
Emp. Form. | C7H13N2O7S |
Mol. Mass. | 269.253 |
SMILES | CN1[C@H](NC(C)=O)[C@@H](O)[C@H](O)[C@H]1OS([O-])(=O)=O |r| |
Structure |
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