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TargetSalicyl-AMP ligase / salicyl-S-ArCP synthetase
LigandBDBM50412835
Substrate/Competitorn/a
Meas. Tech.ChEMBL_496141 (CHEMBL999364)
Ki 1.9±n/a nM
Citation Gupte, ABoshoff, HIWilson, DJNeres, JLabello, NPSomu, RVXing, CBarry, CEAldrich, CC Inhibition of siderophore biosynthesis by 2-triazole substituted analogues of 5'-O-[N-(salicyl)sulfamoyl]adenosine: antibacterial nucleosides effective against Mycobacterium tuberculosis. J Med Chem51:7495-507 (2009) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Salicyl-AMP ligase / salicyl-S-ArCP synthetase
Name:Salicyl-AMP ligase / salicyl-S-ArCP synthetase
Synonyms:2,3-dihydroxybenzoate-AMP ligase | MBTA_MYCTU | mbtA
Type:PROTEIN
Mol. Mass.:59275.32
Organism:Mycobacterium tuberculosis
Description:ChEMBL_423930
Residue:565
Sequence:
MPPKAADGRRPSPDGGLGGFVPFPADRAASYRAAGYWSGRTLDTVLSDAARRWPDRLAVA
DAGDRPGHGGLSYAELDQRADRAAAALHGLGITPGDRVLLQLPNGCQFAVALFALLRAGA
IPVMCLPGHRAAELGHFAAVSAATGLVVADVASGFDYRPMARELVADHPTLRHVIVDGDP
GPFVSWAQLCAQAGTGSPAPPADPGSPALLLVSGGTTGMPKLIPRTHDDYVFNATASAAL
CRLSADDVYLVVLAAGHNFPLACPGLLGAMTVGATAVFAPDPSPEAAFAAIERHGVTVTA
LVPALAKLWAQSCEWEPVTPKSLRLLQVGGSKLEPEDARRVRTALTPGLQQVFGMAEGLL
NFTRIGDPPEVVEHTQGRPLCPADELRIVNADGEPVGPGEEGELLVRGPYTLNGYFAAER
DNERCFDPDGFYRSGDLVRRRDDGNLVVTGRVKDVICRAGETIAASDLEEQLLSHPAIFS
AAAVGLPDQYLGEKICAAVVFAGAPITLAELNGYLDRRGVAAHTRPDQLVAMPALPTTPI
GKIDKRAIVRQLGIATGPVTTQRCH
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  Blast E-value cutoff:
BDBM50412835
n/a
NameBDBM50412835
Synonyms:CHEMBL612051
TypeSmall organic molecule
Emp. Form.C23H27N9O8S
Mol. Mass.589.581
SMILESCCCCc1cn(nn1)-c1nc(N)c2ncn(C3OC(COS(=O)(=O)NC(=O)c4ccccc4O)C(O)C3O)c2n1
Structure
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