Ki Summary BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetComplement C1r subcomponent
LigandBDBM50063745
Substrate/Competitorn/a
Meas. Tech.ChEMBL_48026 (CHEMBL661599)
IC50 400±n/a nM
Citation Plummer, JSCai, CHays, SJGilmore, JLEmmerling, MRMichael, WNarasimhan, LSWatson, MDWang, KNath, REvans, LMJaen, JC Benzenesulfonamide derivatives of 2-substituted 4H-3,1-benzoxazin-4-ones and benzthiazin-4-ones as inhibitors of complement C1r protease. Bioorg Med Chem Lett9:815-20 (1999) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Complement C1r subcomponent
Name:Complement C1r subcomponent
Synonyms:C1R | C1R_HUMAN | Complement C1r | Complement C1r subcomponent
Type:Enzyme
Mol. Mass.:80113.65
Organism:Homo sapiens (Human)
Description:P00736
Residue:705
Sequence:
MWLLYLLVPALFCRAGGSIPIPQKLFGEVTSPLFPKPYPNNFETTTVITVPTGYRVKLVF
QQFDLEPSEGCFYDYVKISADKKSLGRFCGQLGSPLGNPPGKKEFMSQGNKMLLTFHTDF
SNEENGTIMFYKGFLAYYQAVDLDECASRSKSGEEDPQPQCQHLCHNYVGGYFCSCRPGY
ELQEDTHSCQAECSSELYTEASGYISSLEYPRSYPPDLRCNYSIRVERGLTLHLKFLEPF
DIDDHQQVHCPYDQLQIYANGKNIGEFCGKQRPPDLDTSSNAVDLLFFTDESGDSRGWKL
RYTTEIIKCPQPKTLDEFTIIQNLQPQYQFRDYFIATCKQGYQLIEGNQVLHSFTAVCQD
DGTWHRAMPRCKIKDCGQPRNLPNGDFRYTTTMGVNTYKARIQYYCHEPYYKMQTRAGSR
ESEQGVYTCTAQGIWKNEQKGEKIPRCLPVCGKPVNPVEQRQRIIGGQKAKMGNFPWQVF
TNIHGRGGGALLGDRWILTAAHTLYPKEHEAQSNASLDVFLGHTNVEELMKLGNHPIRRV
SVHPDYRQDESYNFEGDIALLELENSVTLGPNLLPICLPDNDTFYDLGLMGYVSGFGVME
EKIAHDLRFVRLPVANPQACENWLRGKNRMDVFSQNMFCAGHPSLKQDACQGDSGGVFAV
RDPNTDRWVATGIVSWGIGCSRGYGFYTKVLNYVDWIKKEMEEED
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50063745
n/a
NameBDBM50063745
Synonyms:2-(2-Iodo-phenylamino)-7-trifluoromethyl-benzo[d][1,3]oxazin-4-one | CHEMBL10312
TypeSmall organic molecule
Emp. Form.C15H8F3IN2O2
Mol. Mass.432.1359
SMILESFC(F)(F)c1ccc2c(c1)nc(Nc1ccccc1I)oc2=O
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: