Structure of PDB 5ue3 Chain B Binding Site BS03
Receptor Information
>5ue3 Chain B (length=221) Species:
9606
(Homo sapiens) [
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DRQLAEEYLYRYGYTRVAEGPALLLLQKQLSLPETGELDSATLKAMRTPR
CGVPDLGRFQTFEGDLKWHHHNITYWIQNYSEDLPRAVIDDAFARAFALW
SAVTPLTFTRVYSRDADIVIQFGVAEHGDGYPFDGKDGLLAHAFPPGPGI
QGDAHFDDDELWSLGKGQGYSLFLVAAHEFGHALGLDHSSVPEALMYPMY
RFTEGPPLHKDDVNGIRHLYG
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
5ue3 Chain B Residue 303 [
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Receptor-Ligand Complex Structure
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PDB
5ue3
Discovery of a highly selective chemical inhibitor of matrix metalloproteinase-9 (MMP-9) that allosterically inhibits zymogen activation.
Resolution
1.599 Å
Binding residue
(original residue number in PDB)
D182 G183 D185 L187 D205 E208
Binding residue
(residue number reindexed from 1)
D134 G135 D137 L139 D157 E160
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
H226 E227 H230 H236
Catalytic site (residue number reindexed from 1)
H178 E179 H182 H188
Enzyme Commision number
3.4.24.35
: gelatinase B.
Gene Ontology
Molecular Function
GO:0004222
metalloendopeptidase activity
GO:0008237
metallopeptidase activity
GO:0008270
zinc ion binding
Biological Process
GO:0006508
proteolysis
Cellular Component
GO:0031012
extracellular matrix
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5ue3
,
PDBe:5ue3
,
PDBj:5ue3
PDBsum
5ue3
PubMed
28860188
UniProt
P14780
|MMP9_HUMAN Matrix metalloproteinase-9 (Gene Name=MMP9)
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