Structure of PDB 2pjt Chain B Binding Site BS05
Receptor Information
>2pjt Chain B (length=164) Species:
9606
(Homo sapiens) [
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YNVFPTLKWSKMNLTYRIVNYTPDMTHSEVEKAFKKAFKVWSDVTPLNFT
RLHDGIADIMISFGIKEHGDFYPFDGPSGLLAHAFPPGPNYGGDAHFDDD
ETWTSSSKGYNLFLVAAHEFGHSLGLDHSKDPGALMFPIYTYTGKSHFML
PDDDVQGIQSLYGP
Ligand information
Ligand ID
347
InChI
InChI=1S/C22H31N3O6S/c1-5-6-13-23-17-7-9-18(10-8-17)32(29,30)16-22(19(26)24-28)11-14-25(15-12-22)20(27)31-21(2,3)4/h7-10,23,28H,11-16H2,1-4H3,(H,24,26)
InChIKey
RXFCFGLSOUOCEA-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC#CCNc1ccc(cc1)S(=O)(=O)CC2(CCN(CC2)C(=O)OC(C)(C)C)C(=O)NO
CACTVS 3.341
CC#CCNc1ccc(cc1)[S](=O)(=O)CC2(CCN(CC2)C(=O)OC(C)(C)C)C(=O)NO
ACDLabs 10.04
O=S(=O)(c1ccc(NCC#CC)cc1)CC2(C(=O)NO)CCN(C(=O)OC(C)(C)C)CC2
Formula
C22 H31 N3 O6 S
Name
TERT-BUTYL 4-({[4-(BUT-2-YN-1-YLAMINO)PHENYL]SULFONYL}METHYL)-4-[(HYDROXYAMINO)CARBONYL]PIPERIDINE-1-CARBOXYLATE
ChEMBL
CHEMBL236573
DrugBank
DB07013
ZINC
ZINC000028861972
PDB chain
2pjt Chain B Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
2pjt
Structure-based design of TACE selective inhibitors: manipulations in the S1'-S3' pocket.
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
L160 A161 L193 V194 H197 E198 H201 H207 L214 P217 Y219
Binding residue
(residue number reindexed from 1)
L81 A82 L114 V115 H118 E119 H122 H128 L135 P138 Y140
Annotation score
1
Binding affinity
BindingDB: IC50=860nM
Enzymatic activity
Catalytic site (original residue number in PDB)
H197 E198 H201 H207
Catalytic site (residue number reindexed from 1)
H118 E119 H122 H128
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:2pjt
,
PDBe:2pjt
,
PDBj:2pjt
PDBsum
2pjt
PubMed
17606376
UniProt
P45452
|MMP13_HUMAN Collagenase 3 (Gene Name=MMP13)
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