Reaction Details |
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Target | Beta-glucosidase |
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Ligand | BDBM18351 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1366789 (CHEMBL3297224) |
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Ki | 12000±n/a nM |
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Citation | Zoidl, M; Müller, B; Torvisco, A; Tysoe, C; Benazza, M; Siriwardena, A; Withers, SG; Wrodnigg, TM Concise synthesis of C-1-cyano-iminosugars via a new Staudinger/aza Wittig/Strecker multicomponent reaction strategy. Bioorg Med Chem Lett24:2777-80 (2014) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Beta-glucosidase |
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Name: | Beta-glucosidase |
Synonyms: | BGLS_RHIRD | cbg-1 |
Type: | PROTEIN |
Mol. Mass.: | 88266.88 |
Organism: | Agrobacterium tumefaciens |
Description: | ChEMBL_1366789 |
Residue: | 818 |
Sequence: | MIDDILDKMTLEEQVSLLSGADFWTTVAIERLGVPKIKVTDGPNGARGGGSLVGGVKSAC
FPVAIALGATWDPELIERAGVALGGQAKSKGASVLLAPTVNIHRSGLNGRNFECYSEDPA
LTAACAVAYINGVQSQGVAATIKHFVANESEIERQTMSSDVDERTLREIYLPPFEEAVKK
AGVKAVMSSYNKLNGTYTSENPWLLTKVLREEWGFDGVVMSDWFGSHSTAETINAGLDLE
MPGPWRDRGEKLVAAVREGKVKAETVRASARRILLLLERVGAFEKAPDLAEHALDLPEDR
ALIRQLGAEGAVLLKNDGVLPLAKSSFDQIAVIGPNAASARVMGGGSARIAAHYTVSPLE
GIRAALSNANSLRHAVGCNNNRLIDVFSGEMTVEYFKGRGFESRPVHVETVEKGEFFWFD
LPSGDLDLADFSARMTATFVPQETGEHIFGMTNAGLARLFVDGELVVDGYDGWTKGENFF
GTANSEQRRAVTLGAARRYRVVVEYEAPKASLDGINICALRFGVEKPLGDAGIAEAVETA
RKSDIVLLLVGREGEWDTEGLDLPDMRLPGRQEELIEAVAETNPNVVVVLQTGGPIEMPW
LGKVRAVLQMWYPGQELGNALADVLFGDVEPAGRLPQTFPKALTDNSAITDDPSIYPGQD
GHVRYAEGIFVGYRHHDTREIEPLFPFGFGLGYTRFTWGAPQLSGTEMGADGLTVTVDVT
NIGDRAGSDVVQLYVHSPNARVERPFKELRAFAKLKLAPGATGTAVLKIAPRDLAYFDVE
AGRFRADAGKYELIVAASAIDIRASVSIHLPVDHVMEP
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BDBM18351 |
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n/a |
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Name | BDBM18351 |
Synonyms: | (2R,3R,4R,5S)-2-(Hydroxymethyl)piperidine-3,4,5-triol, 10 | (2R,3R,4R,5S)-2-(hydroxymethyl)piperidine-3,4,5-triol | 1-Deoxynojirimycin | 1-deoxynojirimycin (DNJ) | CHEMBL307429 | US20230339856, Compound DNJ | US9181184, 1 | dNM |
Type | natural product |
Emp. Form. | C6H13NO4 |
Mol. Mass. | 163.1717 |
SMILES | OC[C@H]1NC[C@H](O)[C@@H](O)[C@@H]1O |
Structure |
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