Structure of PDB 1mu8 Chain B Binding Site BS02
Receptor Information
>1mu8 Chain B (length=250) Species:
9606
(Homo sapiens) [
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IVEGSDAEIGMSPWQVMLFRKSPQELLCGASLISDRWVLTAAHCLLYPPW
DKNFTENDLLVRIGKHSRTRYERNIEKISMLEKIYIHPRYNWRENLDRDI
ALMKLKKPVAFSDYIHPVCLPDRETAASLLQAGYKGRVTGWGNLKEGQPS
VLQVVNLPIVERPVCKDSTRIRITDNMFCAGYKPDEGKRGDACEGDSGGP
FVMKSPFNNRWYQMGIVSWGEGCDRDGKYGFYTHVFRLKKWIQKVIDQFG
Ligand information
>1mu8 Chain C (length=11) Species:
6421
(Hirudo medicinalis) [
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DFEEIPEEYLQ
Receptor-Ligand Complex Structure
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PDB
1mu8
Metabolism-directed optimization of 3-aminopyrazinone acetamide thrombin inhibitors. Development of an orally bioavailable series containing P1 and P3 pyridines.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
F34 Q38 L40 T74 R75 Y76 K81 I82
Binding residue
(residue number reindexed from 1)
F19 Q24 L26 T69 R70 Y71 K77 I78
Enzymatic activity
Catalytic site (original residue number in PDB)
H57 D102 E192 G193 D194 S195 G196
Catalytic site (residue number reindexed from 1)
H43 D99 E194 G195 D196 S197 G198
Enzyme Commision number
3.4.21.5
: thrombin.
Gene Ontology
Molecular Function
GO:0004252
serine-type endopeptidase activity
GO:0005509
calcium ion binding
Biological Process
GO:0006508
proteolysis
GO:0007596
blood coagulation
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Molecular Function
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Biological Process
External links
PDB
RCSB:1mu8
,
PDBe:1mu8
,
PDBj:1mu8
PDBsum
1mu8
PubMed
12570369
UniProt
P00734
|THRB_HUMAN Prothrombin (Gene Name=F2)
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