Ki Summary BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
Targetalpha-1,2-Mannosidase
LigandBDBM50169002
Substrate/Competitorn/a
Meas. Tech.ChEMBL_305169 (CHEMBL832759)
IC50 110000±n/a nM
Citation Fiaux, HPopowycz, FFavre, SSchütz, CVogel, PGerber-Lemaire, SJuillerat-Jeanneret, L Functionalized pyrrolidines inhibit alpha-mannosidase activity and growth of human glioblastoma and melanoma cells. J Med Chem48:4237-46 (2005) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
alpha-1,2-Mannosidase
Name:alpha-1,2-Mannosidase
Synonyms:Alpha-mannosidase
Type:PROTEIN
Mol. Mass.:65344.50
Organism:Glycine max
Description:ChEMBL_32380
Residue:578
Sequence:
MARGSRSVGSSSSKWRYCNPSYYLKRPKRLALLFIVFVCVSFVFWDRQTLVREHQVEISE
LQKEVTDLKNLVDDLNNKQGGTSGKTDLGRKATKSSKDVLDDPIDIERREKVKEAMLHAW
GSYEKYAWGQDELQPQSKNGVNSFGGLGATLIDSLDTLYIMGLNEQFQKAREWVANSLDF
NKDYEASVFETTIRVVGGLLSAYDLSGDKVFLDKAIEIADRLLPAWNTPTGIPYNIINLS
HGRAHNPSWTGGESILADSGTEQLEFIVLSQRTGDLKYQQKVENVIAQLNKTFPDDGLLP
IYINPHSGAAGYSPITFGAMGDSFYEYLLKVWIQGNKTSSIKHYRDMWEKSMKGLSSLIR
RSTPSSFTYICEKNGGSLTDKMDELACFAPGMIALGSFGYSAADDSQKFLSLAEELAWTC
YNFYQSTPTKLAGENYFFHSGQDMSVGTSWNILRPETVESLFYLWRLTGNKTYQEWGWNI
FQAFEKNSRIESGYVGLKDVNSGVKDNMMQSFFLAETLKYFYLLFSPSSVISLDEWVFNT
EAHPLRIVTRHEEGLVKNLNEKQKPFSRIGGRKEGRSG
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50169002
n/a
NameBDBM50169002
Synonyms:(2R,3R,4S)-2-[((S)-Phenyl-1-(R)-2-hydroxy-2-phenyl-ethylamino)-methyl]-pyrrolidine-3,4-diol | CHEMBL188227
TypeSmall organic molecule
Emp. Form.C19H24N2O3
Mol. Mass.328.4055
SMILESO[C@H]([C@H](NC[C@H]1NC[C@H](O)[C@@H]1O)c1ccccc1)c1ccccc1
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: