Structure of PDB 1gi7 Chain B Binding Site BS02
Receptor Information
>1gi7 Chain B (length=245) Species:
9606
(Homo sapiens) [
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IIGGEFTTIENQPWFAAIYRRHRGGSVTYVCGGSLMSPCWVISATHCFID
YPKKEDYIVYLGRSRLNSNTQGEMKFEVENLILHKDYSADTLAHHNDIAL
LKIRSKEGRCAQPSRTIQTICLPSMYNDPQFGTSCEITGFGKEASTDYLY
PEQLKMTVVKLISHRECQQPHYYGSEVTTKMLCAADPQWKTDSCQGDSGG
PLVCSLQGRMTLTGIVSWGRGCALKDKPGVYTRVSHFLPWIRSHT
Ligand information
Ligand ID
120
InChI
InChI=1S/C13H11N5O/c14-11(15)7-3-4-9-10(6-7)18-12(17-9)8-2-1-5-16-13(8)19/h1-6H,(H3,14,15)(H,16,19)(H,17,18)/p+1
InChIKey
PUOKYJMONGPAIM-UHFFFAOYSA-O
SMILES
Software
SMILES
CACTVS 3.341
NC(=[NH2+])c1ccc2[nH]c(nc2c1)C3=CC=CNC3=O
OpenEye OEToolkits 1.5.0
c1cc2c(cc1C(=[NH2+])N)nc([nH]2)C3=CC=CNC3=O
ACDLabs 10.04
O=C3NC=CC=C3c2nc1cc(ccc1n2)\C(=[NH2+])N
Formula
C13 H12 N5 O
Name
2-(2-OXO-1,2-DIHYDRO-PYRIDIN-3-YL)-1H-BENZOIMIDAZOLE-5-CARBOXAMIDINE
ChEMBL
DrugBank
DB04442
ZINC
PDB chain
1gi7 Chain B Residue 246 [
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Receptor-Ligand Complex Structure
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PDB
1gi7
A novel serine protease inhibition motif involving a multi-centered short hydrogen bonding network at the active site.
Resolution
1.79 Å
Binding residue
(original residue number in PDB)
D189 S190 C191 Q192 G219
Binding residue
(residue number reindexed from 1)
D192 S193 C194 Q195 G221
Annotation score
1
Binding affinity
MOAD
: Ki=31uM
PDBbind-CN
: -logKd/Ki=4.51,Ki=31uM
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:1gi7
,
PDBe:1gi7
,
PDBj:1gi7
PDBsum
1gi7
PubMed
11292354
UniProt
P00749
|UROK_HUMAN Urokinase-type plasminogen activator (Gene Name=PLAU)
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