Structure of PDB 4gj8 Chain B Binding Site BS01
Receptor Information
>4gj8 Chain B (length=335) Species:
9606
(Homo sapiens) [
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LTLGNTTSSVILTNYMDTQYYGEIGIGTPPQTFKVVFDTGSSNVWVPSSK
CSTACVYHKLFDASDSSSYKHNGTELTLRYSTGTVSGFLSQDIITVGGIT
VTQMFGEVTEMPALPFMLAEFDGVVGMGFIEQAIGRVTPIFDNIISQGVL
KEDVFSFYYNRDSSQSLGGQIVLGGSDPQHYEGNFHYINLIKTGVWQIQM
KGVSVGSSTLLCEDGCLALVDTGASYISGSTSSIEKLMEALGAKKRLFDY
VVKCNEGPTLPDISFHLGGKEYTLTSADYVFQESYSSKKLCTLAIHAMDI
PPPTGPTWALGATFIRKFYTEFDRRNNRIGFALAR
Ligand information
Ligand ID
0LW
InChI
InChI=1S/C20H23NOS/c22-15(14-21-11-5-6-12-21)13-18-16-7-1-3-9-19(16)23-20-10-4-2-8-17(18)20/h1-4,7-10,15,18,22H,5-6,11-14H2/t15-/m1/s1
InChIKey
SJCVUEZFZDNDKT-OAHLLOKOSA-N
SMILES
Software
SMILES
CACTVS 3.370
O[CH](C[CH]1c2ccccc2Sc3ccccc13)CN4CCCC4
ACDLabs 12.01
OC(CN1CCCC1)CC3c4c(Sc2c3cccc2)cccc4
CACTVS 3.370
O[C@H](C[C@H]1c2ccccc2Sc3ccccc13)CN4CCCC4
OpenEye OEToolkits 1.7.6
c1ccc2c(c1)C(c3ccccc3S2)CC(CN4CCCC4)O
OpenEye OEToolkits 1.7.6
c1ccc2c(c1)C(c3ccccc3S2)C[C@H](CN4CCCC4)O
Formula
C20 H23 N O S
Name
(2R)-1-(pyrrolidin-1-yl)-3-(9H-thioxanthen-9-yl)propan-2-ol
ChEMBL
DrugBank
ZINC
ZINC000095580771
PDB chain
4gj8 Chain B Residue 1001 [
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Receptor-Ligand Complex Structure
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PDB
4gj8
A novel class of oral direct Renin inhibitors: highly potent 3,5-disubstituted piperidines bearing a tricyclic p3-p1 pharmacophore.
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
S76 P111 A115 F117 G217
Binding residue
(residue number reindexed from 1)
S81 P115 A119 F121 G223
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D32 S35 N37 W39 Y75 D215 A218
Catalytic site (residue number reindexed from 1)
D38 S41 N43 W45 Y80 D221 A224
Enzyme Commision number
3.4.23.15
: renin.
Gene Ontology
Molecular Function
GO:0004190
aspartic-type endopeptidase activity
Biological Process
GO:0006508
proteolysis
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Molecular Function
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Biological Process
External links
PDB
RCSB:4gj8
,
PDBe:4gj8
,
PDBj:4gj8
PDBsum
4gj8
PubMed
23360239
UniProt
P00797
|RENI_HUMAN Renin (Gene Name=REN)
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