Structure of PDB 2fpz Chain D Binding Site BS01
Receptor Information
>2fpz Chain D (length=243) Species:
9606
(Homo sapiens) [
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IVGGQEAPRSKWPWQVSLRVHGPYWMHFCGGSLIHPQWVLTAAHCVGPDV
KDLAALRVQLREQHLYYQDQLLPVSRIIVHPQFYTAQIGADIALLELEEP
VKVSSHVHTVTLPPASETFPPGMPCWVTGWGDVDNDERLPPPFPLKQVKV
PIMENHICDAKYHLGAYTGDDVRIVRDDMLCAGNTRRDSCQGDSGGPLVC
KVNGTWLQAGVVSWGEGCAQPNRPGIYTRVTYYLDWIHHYVPK
Ligand information
Ligand ID
270
InChI
InChI=1S/C7H7N3/c8-7-9-5-3-1-2-4-6(5)10-7/h1-4,7H,8H2
InChIKey
DERVZEOWPBCBHO-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C1=CC2=NC(N=C2C=C1)N
ACDLabs 10.04
N1=C2C=CC=CC2=NC1N
CACTVS 3.341
NC1N=C2C=CC=CC2=N1
Formula
C7 H7 N3
Name
2H-BENZOIMIDAZOL-2-YLAMINE;
ZK-800270
ChEMBL
DrugBank
DB01665
ZINC
ZINC000034919930
PDB chain
2fpz Chain D Residue 1003 [
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Receptor-Ligand Complex Structure
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PDB
2fpz
Structure-guided design of Peptide-based tryptase inhibitors.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
D189 S190 C191 W215 G216 G219
Binding residue
(residue number reindexed from 1)
D188 S189 C190 W214 G215 G217
Annotation score
1
Binding affinity
MOAD
: Ki=110uM
Enzymatic activity
Catalytic site (original residue number in PDB)
H57 D102 Q192 G193 D194 S195 G196
Catalytic site (residue number reindexed from 1)
H44 D91 Q191 G192 D193 S194 G195
Enzyme Commision number
3.4.21.59
: tryptase.
Gene Ontology
Molecular Function
GO:0004252
serine-type endopeptidase activity
GO:0005515
protein binding
GO:0008236
serine-type peptidase activity
Biological Process
GO:0006508
proteolysis
Cellular Component
GO:0005576
extracellular region
GO:0005615
extracellular space
GO:0062023
collagen-containing extracellular matrix
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2fpz
,
PDBe:2fpz
,
PDBj:2fpz
PDBsum
2fpz
PubMed
16681368
UniProt
P20231
|TRYB2_HUMAN Tryptase beta-2 (Gene Name=TPSB2)
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