Structure of PDB 4h82 Chain D Binding Site BS02
Receptor Information
>4h82 Chain D (length=160) Species:
9606
(Homo sapiens) [
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FEGDLKWHHHNITYWIQNYSEDLPRAVIDDAFARAFALWSAVTPLTFTRV
YSRDADIVIQFGVAEHGDGYPFDGKDGLLAHAFPPGPGIQGDAHFDDDEL
WSLGKGQGYSLFLVAAHQFGHALGLDHSSVPEALMYPMYRFTEGPPLHKD
DVNGIRHLYG
Ligand information
Ligand ID
L29
InChI
InChI=1S/C46H52N6O10S2/c1-31(2)41(45(55)49-57)51(63(59,60)39-22-18-35(19-23-39)33-12-7-5-8-13-33)28-26-47-43(53)37-16-11-17-38(30-37)44(54)48-27-29-52(42(32(3)4)46(56)50-58)64(61,62)40-24-20-36(21-25-40)34-14-9-6-10-15-34/h5-25,30-32,41-42,57-58H,26-29H2,1-4H3,(H,47,53)(H,48,54)(H,49,55)(H,50,56)/t41-,42-/m1/s1
InChIKey
JPMXJRBHCOULJI-NCRNUEESSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=S(=O)(N(C(C(=O)NO)C(C)C)CCNC(=O)c3cccc(C(=O)NCCN(C(C(=O)NO)C(C)C)S(=O)(=O)c2ccc(c1ccccc1)cc2)c3)c5ccc(c4ccccc4)cc5
CACTVS 3.370
CC(C)[CH](N(CCNC(=O)c1cccc(c1)C(=O)NCCN([CH](C(C)C)C(=O)NO)[S](=O)(=O)c2ccc(cc2)c3ccccc3)[S](=O)(=O)c4ccc(cc4)c5ccccc5)C(=O)NO
OpenEye OEToolkits 1.7.6
CC(C)C(C(=O)NO)N(CCNC(=O)c1cccc(c1)C(=O)NCCN(C(C(C)C)C(=O)NO)S(=O)(=O)c2ccc(cc2)c3ccccc3)S(=O)(=O)c4ccc(cc4)c5ccccc5
OpenEye OEToolkits 1.7.6
CC(C)[C@H](C(=O)NO)N(CCNC(=O)c1cccc(c1)C(=O)NCCN([C@H](C(C)C)C(=O)NO)S(=O)(=O)c2ccc(cc2)c3ccccc3)S(=O)(=O)c4ccc(cc4)c5ccccc5
CACTVS 3.370
CC(C)[C@@H](N(CCNC(=O)c1cccc(c1)C(=O)NCCN([C@H](C(C)C)C(=O)NO)[S](=O)(=O)c2ccc(cc2)c3ccccc3)[S](=O)(=O)c4ccc(cc4)c5ccccc5)C(=O)NO
Formula
C46 H52 N6 O10 S2
Name
N,N'-bis(2-{(biphenyl-4-ylsulfonyl)[(2R)-1-(hydroxyamino)-3-methyl-1-oxobutan-2-yl]amino}ethyl)benzene-1,3-dicarboxamide (non-preferred name)
ChEMBL
CHEMBL3891386
DrugBank
ZINC
ZINC000150344349
PDB chain
4h82 Chain D Residue 303 [
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Receptor-Ligand Complex Structure
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PDB
4h82
Crystallization of bi-functional ligand protein complexes.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
L187 L188 A189 L222 V223 H226 Q227 H230 H236 Y245 P246 Y248
Binding residue
(residue number reindexed from 1)
L78 L79 A80 L113 V114 H117 Q118 H121 H127 Y136 P137 Y139
Annotation score
1
Binding affinity
BindingDB: IC50=5.5nM
Enzymatic activity
Catalytic site (original residue number in PDB)
H226 Q227 H230 H236
Catalytic site (residue number reindexed from 1)
H117 Q118 H121 H127
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:4h82
,
PDBe:4h82
,
PDBj:4h82
PDBsum
4h82
PubMed
23567804
UniProt
P14780
|MMP9_HUMAN Matrix metalloproteinase-9 (Gene Name=MMP9)
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