Structure of PDB 4fgk Chain B Binding Site BS02
Receptor Information
>4fgk Chain B (length=230) Species:
9606
(Homo sapiens) [
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AGKKVLIVYAHQEPKSFNGSLKNVAVDELSRQGCTVTVSDLYAMNFEPRA
TDKDITGTLSNPEVFNYGVETHEAYKQRSLASDITDEQKKVREADLVIFQ
FPLYWFSVPAILKGWMDRVLCQGFAFDIPGFYDSGLLQGKLALLSVTTGG
TAEMYTKTGVNGDSRYFLWPLQHGTLHFCGFKVLAPQISFAPEIASEEER
KGMVAAWSQRLQTIWKEEPIPCTAHWHFGQ
Ligand information
Ligand ID
0TX
InChI
InChI=1S/C18H26ClN3/c1-4-22(5-2)12-6-7-14(3)21-17-10-11-20-18-13-15(19)8-9-16(17)18/h8-11,13-14H,4-7,12H2,1-3H3,(H,20,21)/t14-/m0/s1
InChIKey
WHTVZRBIWZFKQO-AWEZNQCLSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
CCN(CC)CCC[C@H](C)Nc1ccnc2c1ccc(c2)Cl
CACTVS 3.370
CCN(CC)CCC[C@H](C)Nc1ccnc2cc(Cl)ccc12
OpenEye OEToolkits 1.7.6
CCN(CC)CCCC(C)Nc1ccnc2c1ccc(c2)Cl
CACTVS 3.370
CCN(CC)CCC[CH](C)Nc1ccnc2cc(Cl)ccc12
ACDLabs 12.01
Clc1cc2nccc(c2cc1)NC(C)CCCN(CC)CC
Formula
C18 H26 Cl N3
Name
(4S)-N~4~-(7-chloroquinolin-4-yl)-N~1~,N~1~-diethylpentane-1,4-diamine
ChEMBL
CHEMBL250447
DrugBank
ZINC
ZINC000019144231
PDB chain
4fgk Chain A Residue 304 [
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Receptor-Ligand Complex Structure
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PDB
4fgk
Crystal structures of quinone reductase 2 bound to antimalarial drugs reveal conformational change upon reduction
Resolution
1.401 Å
Binding residue
(original residue number in PDB)
V69 F178
Binding residue
(residue number reindexed from 1)
V69 F178
Annotation score
1
Binding affinity
BindingDB: IC50=1500nM
Enzymatic activity
Catalytic site (original residue number in PDB)
G149 Y155 N161
Catalytic site (residue number reindexed from 1)
G149 Y155 N161
Enzyme Commision number
1.10.5.1
: ribosyldihydronicotinamide dehydrogenase (quinone).
Gene Ontology
Molecular Function
GO:0001512
dihydronicotinamide riboside quinone reductase activity
GO:0003955
NAD(P)H dehydrogenase (quinone) activity
GO:0005515
protein binding
GO:0008270
zinc ion binding
GO:0009055
electron transfer activity
GO:0016491
oxidoreductase activity
GO:0016661
oxidoreductase activity, acting on other nitrogenous compounds as donors
GO:0031404
chloride ion binding
GO:0042803
protein homodimerization activity
GO:0046872
metal ion binding
GO:0071949
FAD binding
GO:1904408
melatonin binding
GO:1905594
resveratrol binding
Biological Process
GO:1901662
quinone catabolic process
Cellular Component
GO:0005654
nucleoplasm
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0070062
extracellular exosome
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4fgk
,
PDBe:4fgk
,
PDBj:4fgk
PDBsum
4fgk
PubMed
UniProt
P16083
|NQO2_HUMAN Ribosyldihydronicotinamide dehydrogenase [quinone] (Gene Name=NQO2)
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