Structure of PDB 1c5y Chain B Binding Site BS02
Receptor Information
>1c5y Chain B (length=248) Species:
9606
(Homo sapiens) [
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IIGGEFTTIENQPWFAAIYRRHRGGSVTYVCGGSLMSPCWVISATHCFID
YPKKEDYIVYLGRSRLNSNTQGEMKFEVENLILHKDYSADTLAHHNDIAL
LKIRSKEGRCAQPSRTIQTICLPSMYNDPQFGTSCEITGFGKEASTDYLY
PEQLKMTVVKLISHRECQQPHYYGSEVTTKMLCAADPQWKTDSCQGDSGG
PLVCSLQGRMTLTGIVSWGRGCALKDKPGVYTRVSHFLPWIRSHTKEE
Ligand information
Ligand ID
ESP
InChI
InChI=1S/C8H7N3S/c9-7(10)6-4-5-2-1-3-11-8(5)12-6/h1-4H,(H3,9,10)/p+1
InChIKey
GZEJMYFXZMUAEC-UHFFFAOYSA-O
SMILES
Software
SMILES
CACTVS 3.341
NC(=[NH2+])c1sc2ncccc2c1
ACDLabs 10.04
n1cccc2c1sc(c2)\C(=[NH2+])N
OpenEye OEToolkits 1.5.0
c1cc2cc(sc2nc1)C(=[NH2+])N
Formula
C8 H8 N3 S
Name
THIENO[2,3-B]PYRIDINE-2-CARBOXAMIDINE
ChEMBL
DrugBank
DB03876
ZINC
PDB chain
1c5y Chain B Residue 251 [
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Receptor-Ligand Complex Structure
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PDB
1c5y
Structural basis for selectivity of a small molecule, S1-binding, submicromolar inhibitor of urokinase-type plasminogen activator.
Resolution
1.65 Å
Binding residue
(original residue number in PDB)
D189 S190 Q192 S195 W215 G216 G219 C220
Binding residue
(residue number reindexed from 1)
D192 S193 Q195 S198 W218 G219 G221 C222
Annotation score
1
Binding affinity
MOAD
: Ki=63uM
PDBbind-CN
: -logKd/Ki=4.20,Ki=63uM
BindingDB: Ki=63000nM
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:1c5y
,
PDBe:1c5y
,
PDBj:1c5y
PDBsum
1c5y
PubMed
10779411
UniProt
P00749
|UROK_HUMAN Urokinase-type plasminogen activator (Gene Name=PLAU)
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