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TargetTelomere resolvase ResT
LigandBDBM50335558
Substrate/Competitorn/a
Meas. Tech.ChEMBL_713937 (CHEMBL1660353)
IC50 3160±n/a nM
Citation Lefas, GChaconas, G High-throughput screening identifies three inhibitor classes of the telomere resolvase from the lyme disease spirochete. Antimicrob Agents Chemother53:4441-9 (2009) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Telomere resolvase ResT
Name:Telomere resolvase ResT
Synonyms:REST_BORBU | resT
Type:PROTEIN
Mol. Mass.:54325.70
Organism:Borrelia burgdorferi
Description:ChEMBL_713937
Residue:449
Sequence:
MPPKVKIKNDFEIFRKELEILYKKYLNNELSYLKLKEKLKILAENHKAILFRKDKFTNRS
IILNLSKTRKIIKEYINLSVIERIRRDNTFLFFWKSRRIKELKNIGIKDRKKIEELIFSN
QMNDEKSYFQYFIDLFVTPKWLNDYAHKYKIEKINSYRKEQIFVKINLNTYIEIIKLLLN
QSRDIRLKFYGVLMAIGRRPVEVMKLSQFYIADKNHIRMEFIAKKRENNIVNEVVFPVFA
DPELIINSIKEIRYMEQTENLTKEIISSNLAYSYNRLFRQIFNNIFAPEESVYFCRAIYC
KFSYLAFAPKNMEMNYWITKVLGHEPNDITTAFHYNRYVLDNLDDKADNSLLTLLNQRIY
TYVRRKATYSTLTMDRLESLIKEHHIFDDNYIKTLIVIKNLMLKDNLETLAMVRGLNVKI
RKAFKATYGYNYNYIKLTEYLSIIFNYKL
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  Blast E-value cutoff:
BDBM50335558
n/a
NameBDBM50335558
Synonyms:2-(4-(6-(6-carboxy-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)-1H-benzo[d]imidazol-2-yl)phenyl)-1,3-dioxo-2,3-dihydro-1H-benzo[de]isoquinoline-6-carboxylic acid | CHEMBL1649740
TypeSmall organic molecule
Emp. Form.C39H20N4O8
Mol. Mass.672.5981
SMILESOC(=O)c1ccc2C(=O)N(C(=O)c3cccc1c23)c1ccc(cc1)-c1nc2ccc(cc2[nH]1)N1C(=O)c2cccc3c(ccc(C1=O)c23)C(O)=O
Structure
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