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TargetComplement C1r subcomponent
LigandBDBM50075992
Substrate/Competitorn/a
Meas. Tech.ChEBML_48023
IC50 1500±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:
BDBM50075992
n/a
NameBDBM50075992
Synonyms:4-Guanidino-N-methyl-N-(4-oxo-4H-benzo[d][1,3]oxazin-2-yl)-benzenesulfonamide | CHEMBL167523
TypeSmall organic molecule
Emp. Form.C16H15N5O4S
Mol. Mass.373.386
SMILES[#6]-[#7](-c1nc2ccccc2c(=O)o1)S(=O)(=O)c1ccc(cc1)\[#7]=[#6](/[#7])-[#7]
Structure
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