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TargetEpstein-Barr nuclear antigen 1
LigandBDBM62493
Substrate/Competitorn/a
Meas. Tech.Fluorescence polarization-based biochemical high throughput dose response assay for inhibitors of the Epstein-Barr virus nuclear antigen 1 (EBNA-1)
IC50 6649±n/a nM
Citation PubChem, PC Fluorescence polarization-based biochemical high throughput dose response assay for inhibitors of the Epstein-Barr virus nuclear antigen 1 (EBNA-1) PubChem Bioassay(2010)[AID]
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
Epstein-Barr nuclear antigen 1
Name:Epstein-Barr nuclear antigen 1
Synonyms:EBNA-1 protein | EBNA1 | EBNA1_EBVB9 | Epstein-Barr virus protease (EBV Pr)
Type:Enzyme Catalytic Domain
Mol. Mass.:56444.81
Organism:Human herpesvirus 4
Description:gi_23893623
Residue:641
Sequence:
MSDEGPGTGPGNGLGEKGDTSGPEGSGGSGPQRRGGDNHGRGRGRGRGRGGGRPGAPGGS
GSGPRHRDGVRRPQKRPSCIGCKGTHGGTGAGAGAGGAGAGGAGAGGGAGAGGGAGGAGG
AGGAGAGGGAGAGGGAGGAGGAGAGGGAGAGGGAGGAGAGGGAGGAGGAGAGGGAGAGGG
AGGAGAGGGAGGAGGAGAGGGAGAGGAGGAGGAGAGGAGAGGGAGGAGGAGAGGAGAGGA
GAGGAGAGGAGGAGAGGAGGAGAGGAGGAGAGGGAGGAGAGGGAGGAGAGGAGGAGAGGA
GGAGAGGAGGAGAGGGAGAGGAGAGGGGRGRGGSGGRGRGGSGGRGRGGSGGRRGRGRER
ARGGSRERARGRGRGRGEKRPRSPSSQSSSSGSPPRRPPPGRRPFFHPVGEADYFEYHQE
GGPDGEPDVPPGAIEQGPADDPGEGPSTGPRGQGDGGRRKKGGWFGKHRGQGGSNPKFEN
IAEGLRALLARSHVERTTDEGTWVAGVFVYGGSKTSLYNLRRGTALAIPQCRLTPLSRLP
FGMAPGPGPQPGPLRESIVCYFMVFLQTHIFAEVLKDAIKDLVMTKPAPTCNIRVTVCSF
DDGVDLPPWFPPMVEGAAAEGDDGDDGDEGGDGDEGEEGQE
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  Blast E-value cutoff:
BDBM62493
n/a
NameBDBM62493
Synonyms:MLS001163282 | N-[3-[(4-bromobenzoyl)amino]phenyl]thiophene-2-carboxamide | N-[3-[(4-bromophenyl)carbonylamino]phenyl]thiophene-2-carboxamide | N-[3-[[(4-bromophenyl)-oxomethyl]amino]phenyl]-2-thiophenecarboxamide | N-{3-[(4-bromobenzoyl)amino]phenyl}-2-thiophenecarboxamide | SMR000497184 | cid_1273132
TypeSmall organic molecule
Emp. Form.C18H13BrN2O2S
Mol. Mass.401.277
SMILESBrc1ccc(cc1)C(=O)Nc1cccc(NC(=O)c2cccs2)c1
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: