Structure of PDB 1gi8 Chain B Binding Site BS02
Receptor Information
>1gi8 Chain B (length=245) Species:
9606
(Homo sapiens) [
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IIGGEFTTIENQPWFAAIYRRHRGGSVTYVCGGSLMSPCWVISATHCFID
YPKKEDYIVYLGRSRLNSNTQGEMKFEVENLILHKDYSADTLAHHNDIAL
LKIRSKEGRCAQPSRTIQTICLPSMYNDPQFGTSCEITGFGKEASTDYLY
PEQLKMTVVKLISHRECQQPHYYGSEVTTKMLCAADPQWKTDSCQGDSGG
PLVCSLQGRMTLTGIVSWGRGCALKDKPGVYTRVSHFLPWIRSHT
Ligand information
Ligand ID
BMZ
InChI
InChI=1S/C14H12N4O/c15-13(16)8-5-6-10-11(7-8)18-14(17-10)9-3-1-2-4-12(9)19/h1-7,19H,(H3,15,16)(H,17,18)/p+1
InChIKey
URJKRCBBKTXOHS-UHFFFAOYSA-O
SMILES
Software
SMILES
ACDLabs 10.04
Oc3ccccc3c2nc1cc(ccc1n2)\C(=[NH2+])N
OpenEye OEToolkits 1.5.0
c1ccc(c(c1)c2[nH]c3ccc(cc3n2)C(=[NH2+])N)O
CACTVS 3.341
NC(=[NH2+])c1ccc2[nH]c(nc2c1)c3ccccc3O
Formula
C14 H13 N4 O
Name
2-(2-HYDROXY-PHENYL)-1H-BENZOIMIDAZOLE-5-CARBOXAMIDINE
ChEMBL
DrugBank
DB02287
ZINC
PDB chain
1gi8 Chain B Residue 246 [
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Receptor-Ligand Complex Structure
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PDB
1gi8
A novel serine protease inhibition motif involving a multi-centered short hydrogen bonding network at the active site.
Resolution
1.75 Å
Binding residue
(original residue number in PDB)
H57 S190 C191 Q192 S195 V213 W215 G216
Binding residue
(residue number reindexed from 1)
H46 S193 C194 Q195 S198 V216 W218 G219
Annotation score
1
Binding affinity
PDBbind-CN
: -logKd/Ki=5.05,Ki=8.9uM
Enzymatic activity
Catalytic site (original residue number in PDB)
H57 D102 Q192 G193 D194 S195 G196
Catalytic site (residue number reindexed from 1)
H46 D97 Q195 G196 D197 S198 G199
Enzyme Commision number
3.4.21.73
: u-plasminogen activator.
Gene Ontology
Molecular Function
GO:0004252
serine-type endopeptidase activity
Biological Process
GO:0006508
proteolysis
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Molecular Function
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Biological Process
External links
PDB
RCSB:1gi8
,
PDBe:1gi8
,
PDBj:1gi8
PDBsum
1gi8
PubMed
11292354
UniProt
P00749
|UROK_HUMAN Urokinase-type plasminogen activator (Gene Name=PLAU)
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