Ki Summary BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetMetallo-beta-lactamase type 2
LigandBDBM531027
Substrate/Competitorn/a
Meas. Tech.Enzyme Activity: Determination of IC50
IC50 0.610±n/a nM
Citation Pasternak, ADong, SScott, JDTang, HZhao, ZYang, DGu, XJiang, JXiao, L Metallo-beta-lactamase inhibitors and methods of use thereof US Patent US11207312 Publication Date 12/28/2021
More Info.:Get all data from this article,  Assay Method
 
Metallo-beta-lactamase type 2
Name:Metallo-beta-lactamase type 2
Synonyms:B2 metallo-beta-lactamase | BLAN1_KLEPN | Beta-lactamase NDM-1 | Beta-lactamase type II | Metallo-beta-lactamase NDM-1 | Metallo-beta-lactamase type 2 | Metallo-beta-lactamase type II | NDM-1 | New Delhi metallo-beta-lactamase-1 | blaNDM-1
Type:PROTEIN
Mol. Mass.:28498.15
Organism:Klebsiella pneumoniae
Description:ChEMBL_103887
Residue:270
Sequence:
MELPNIMHPVAKLSTALAAALMLSGCMPGEIRPTIGQQMETGDQRFGDLVFRQLAPNVWQ
HTSYLDMPGFGAVASNGLIVRDGGRVLVVDTAWTDDQTAQILNWIKQEINLPVALAVVTH
AHQDKMGGMDALHAAGIATYANALSNQLAPQEGMVAAQHSLTFAANGWVEPATAPNFGPL
KVFYPGPGHTSDNITVGIDGTDIAFGGCLIKDSKAKSLGNLGDADTEHYAASARAFGAAF
PKASMIVMSHSAPDSRAAITHTARMADKLR
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM531027
n/a
NameBDBM531027
Synonyms:4-(4-hydroxy-2-oxopiperidin-1- yl)-N1-((R)-pyrrolidin-3-yl)-3- (2H-tetrazol-5-yl)benzene-1,2- disulfonamide | US11207312, Example 159
TypeSmall organic molecule
Emp. Form.C16H22N8O6S2
Mol. Mass.486.526
SMILESNS(=O)(=O)c1c(ccc(N2CCC(O)CC2=O)c1-c1nn[nH]n1)S(=O)(=O)N[C@@H]1CCNC1 |r|
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: