Reaction Details |
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Target | Alpha-mannosidase 2C1 |
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Ligand | BDBM50016703 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_105324 |
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IC50 | 100000±n/a nM |
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Citation | Winkler, DA; Holan, G Design of potential anti-HIV agents. 1. Mannosidase inhibitors. J Med Chem32:2084-9 (1989) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Alpha-mannosidase 2C1 |
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Name: | Alpha-mannosidase 2C1 |
Synonyms: | MA2C1_RAT | Man2c1 |
Type: | PROTEIN |
Mol. Mass.: | 115965.84 |
Organism: | Rattus norvegicus |
Description: | ChEMBL_32499 |
Residue: | 1040 |
Sequence: | MAAAPFLKHWRTTFERVEKFVSPIYFTDCNLRGRLFGDSCPVTLSSFLTPERLPYEKAVQ
QNFSPAQVGDSFGPTWWTCWFRVELVIPEVWVGKEVHLCWESDGESLVWRDGEPVQGLTK
EGEKTSYVLSERLHAADPRSLTLYVEVACNGLLGAGKGSMIAAPDPEKMFQLSQAKLAVF
HRDVHNLLVDLELLLGVAKGLGEDNQRSFQALYTANQMVNICDPAQPETYPAAEALASKF
FGQRGGESQHTIHATGHCHIDTAWLWPFKETVRKCARSWSTAVKLMERNTEFTFACSQAQ
QLEWVKNQYPGLYAQLQEFACRGQFVPVGGTWVEMDGNLPSGEAMVRQFLQGQNFFLQEF
GKMCSEFWLPDTFGYSAQLPQIMQGCGIKRFLTQKLSWNLVNSFPHHTFFWEGLDGSQVL
VHFPPGDSYGMQGSVEEVLKTVTNNRDKGRTNHSGFLFGFGDGGGGPTQTMLDRLKRLGN
TDGQPRVQLSSPGQLFTALERDSGQLCTWVGELFLELHNGTYTTHAQLKKGNRECEQILH
DVELLSSLALARSAQFLYPAVQLQRLWRLLLLNQFHDVVTGSCIQLVAEDAMNYYEDIRS
HGNTLLSAAAAALCAGEPGPKGLRHYQHTALEAHRSVGTTQGLVGLTRLALVTVPSIGYA
PAPTPTSLQPLLPQQPVFVMQETDGSVTLDNGIIRVRLDPTGCLTSLVLVASGREAIAEG
ALGNQFVLFDDVPLYWDAWDVMDYHLETRKPVRGQAGTLAVGAEGGLRGSAWFLLQISPN
SRLSQEVVLDVGCPYVRFHTEVHWHETHKFLKVEFPARVRSPQATYEIQFGHLQEADPQQ
HSWDWARYEVWAHRWIDLSECDFGLALLNNCKYGTSVRGNVLSLSLLRAPKAPDVTADMG
RHEFTYALMPHKGSFQEAGVIQAAYNLNFPLLALPAPGPAPDTTWSAFSVSSPAVVLETI
KQAEKSHQHRTLVLRLYEAHGSHVDCWLHTSLPVQEATLCDLLEQRDPTGHLSLQDNRLK
LTFSPFQVRSLLLVLQPPAN
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BDBM50016703 |
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n/a |
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Name | BDBM50016703 |
Synonyms: | 2-Hydroxymethyl-pyrrolidine-3,4-diol | BDBM50031485 | CHEMBL80254 | Imino-D-Arabinitol |
Type | Small organic molecule |
Emp. Form. | C5H11NO3 |
Mol. Mass. | 133.1457 |
SMILES | OC[C@H]1NC[C@@H](O)[C@@H]1O |r| |
Structure |
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