Structure of PDB 3kry Chain B Binding Site BS05
Receptor Information
>3kry Chain B (length=164) Species:
9606
(Homo sapiens) [
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YNVFPRTLKWSKMNLTYRIVNYTPDMTHSEVEKAFKKAFKVWSDVTPLNF
TRLHDGIADIMISFGIKEHGDFYPFDGPSGLLAHAFPPGPNYGGDAHFDD
DETWTSSSKGYNLFLVAAHEFGHSLGLDHSKDPGALMFPIYTYTGKSHFM
LPDDDVQGIQSLYG
Ligand information
Ligand ID
3KR
InChI
InChI=1S/C22H23F3N2O7S/c1-32-15-14-27-12-10-21(11-13-27,20(28)26-29)35(30,31)19-8-6-17(7-9-19)33-16-2-4-18(5-3-16)34-22(23,24)25/h2-9H,10-15H2,1H3
InChIKey
JMZMOQBVAXNXIQ-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
COCCN1CCC(CC1)(C(=O)N=O)S(=O)(=O)c2ccc(cc2)Oc3ccc(cc3)OC(F)(F)F
CACTVS 3.352
COCCN1CCC(CC1)(C(=O)N=O)[S](=O)(=O)c2ccc(Oc3ccc(OC(F)(F)F)cc3)cc2
Formula
C22 H23 F3 N2 O7 S
Name
1-(2-methoxyethyl)-N-oxo-4-({4-[4-(trifluoromethoxy)phenoxy]phenyl}sulfonyl)piperidine-4-carboxamide
ChEMBL
DrugBank
ZINC
ZINC000058655562
PDB chain
3kry Chain B Residue 2800 [
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Receptor-Ligand Complex Structure
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PDB
3kry
Orally-active MMP-1 sparing alpha-tetrahydropyranyl and alpha-piperidinyl sulfone matrix metalloproteinase (MMP) inhibitors with efficacy in cancer, arthritis, and cardiovascular disease
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
L184 L185 A186 H222 E223 H226 H232 L239 F241 P242 I243 T245
Binding residue
(residue number reindexed from 1)
L81 L82 A83 H119 E120 H123 H129 L136 F138 P139 I140 T142
Annotation score
1
Binding affinity
MOAD
: ic50=0.1nM
Enzymatic activity
Catalytic site (original residue number in PDB)
H222 E223 H226 H232
Catalytic site (residue number reindexed from 1)
H119 E120 H123 H129
Enzyme Commision number
3.4.24.-
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:3kry
,
PDBe:3kry
,
PDBj:3kry
PDBsum
3kry
PubMed
20726512
UniProt
P45452
|MMP13_HUMAN Collagenase 3 (Gene Name=MMP13)
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