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TargetPhosphomannomutase 2
LigandBDBM44382
Substrate/Competitorn/a
Meas. Tech.ChEMBL_747526 (CHEMBL1777060)
IC50 12900±n/a nM
Citation Dahl, RBravo, YSharma, VIchikawa, MDhanya, RPHedrick, MBrown, BRascon, JVicchiarelli, MMangravita-Novo, AYang, LStonich, DSu, YSmith, LHSergienko, EFreeze, HHCosford, ND Potent, selective, and orally available benzoisothiazolone phosphomannose isomerase inhibitors as probes for congenital disorder of glycosylation Ia. J Med Chem54:3661-8 (2011) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Phosphomannomutase 2
Name:Phosphomannomutase 2
Synonyms:PMM2 | PMM2_HUMAN
Type:Enzyme Catalytic Domain
Mol. Mass.:28082.33
Organism:Homo sapiens (Human)
Description:gi_4557839
Residue:246
Sequence:
MAAPGPALCLFDVDGTLTAPRQKITKEMDDFLQKLRQKIKIGVVGGSDFEKVQEQLGNDV
VEKYDYVFPENGLVAYKDGKLLCRQNIQSHLGEALIQDLINYCLSYIAKIKLPKKRGTFI
EFRNGMLNVSPIGRSCSQEERIEFYELDKKENIRQKFVADLRKEFAGKGLTFSIGGQISF
DVFPDGWDKRYCLRHVENDGYKTIYFFGDKTMPGGNDHEIFTDPRTMGYSVTAPEDTRRI
CELLFS
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM44382
n/a
NameBDBM44382
Synonyms:3-(2-Chloro-phenyl)-7-methyl-7H-pyrazolo[4,3-e][1,2,4]triazolo[4,3-c]pyrimidine | MLS000033568 | SMR000013322 | cid_646130
TypeSmall organic molecule
Emp. Form.C13H9ClN6
Mol. Mass.284.704
SMILESCn1ncc2c1ncn1c(nnc21)-c1ccccc1Cl
Structure
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