Structure of PDB 1kbq Chain C
Receptor sequence
>1kbqC (length=271) Species:
9606
(Homo sapiens) [
Search protein sequence
]
RRALIVLAHSERTSFNYAMKEAAAAALKKKGWEVVESDLYAMNFNPIISR
KDITGKLKDPANFQYPAESVLAYKEGHLSPDIVAEQKKLEAADLVIFQFP
LQWFGVPAILKGWFERVFIGEFAYTYAAMYDKGPFRSKKAVLSITTGGSG
SMYSLQGIHGDMNVILWPIQSGILHFCGFQVLEPQLTYSIGHTPADARIQ
ILEGWKKRLENIWDETPLYFAPSSLFDLNFQAGFLMKKEVQDEEKNKKFG
LSVGHHLGKSIPTDNQIKARK
3D structure
PDB
1kbq
Characterization of a mechanism-based inhibitor of NAD(P)H:quinone oxidoreductase 1 by biochemical, X-ray crystallographic, and mass spectrometric approaches.
Chain
C
Resolution
1.8 Å
3D
structure
Catalytic site residues are labeled in the structure
[
Spin on
]
[
Spin off
]
[
Reset orientation
]
[
High quality
]
[
Low quality
]
[
White background
]
[
Black background
]
[
Download
]
[
Download structure with residue number starting from 1
]
Enzymatic activity
Catalytic site (original residue number in PDB)
G149 Y155 H161
Catalytic site (residue number reindexed from 1)
G147 Y153 H159
Enzyme Commision number
1.6.5.2
: NAD(P)H dehydrogenase (quinone).
Interaction with ligand
Site
#
Ligand
Ligand
chain
Binding residues on receptor
(original residue number in PDB)
Binding residues on receptor
(residue number reindexed from 1)
Binding affinity
BS01
FAD
C
Q66 Y67 P68
Q64 Y65 P66
BS02
936
C
W105 G149 G150 M154
W103 G147 G148 M152
MOAD
: Ki=0.45uM
BindingDB: Ki=450nM
BS03
FAD
C
H11 S16 F17 N18 A20 P102 L103 Q104 W105 F106 T147 T148 G149 Y155 I192 R200
H9 S14 F15 N16 A18 P100 L101 Q102 W103 F104 T145 T146 G147 Y153 I190 R198
BS04
936
C
P68 Y126 Y128 F178 F232 F236
P66 Y124 Y126 F176 F230 F234
MOAD
: Ki=0.45uM
BindingDB: Ki=450nM
Gene Ontology
Molecular Function
GO:0003723
RNA binding
GO:0003955
NAD(P)H dehydrogenase (quinone) activity
GO:0004128
cytochrome-b5 reductase activity, acting on NAD(P)H
GO:0004784
superoxide dismutase activity
GO:0005515
protein binding
GO:0008753
NADPH dehydrogenase (quinone) activity
GO:0016491
oxidoreductase activity
GO:0042802
identical protein binding
GO:0050136
NADH:ubiquinone reductase (non-electrogenic) activity
Biological Process
GO:0000209
protein polyubiquitination
GO:0002931
response to ischemia
GO:0006116
NADH oxidation
GO:0006743
ubiquinone metabolic process
GO:0006801
superoxide metabolic process
GO:0006805
xenobiotic metabolic process
GO:0006809
nitric oxide biosynthetic process
GO:0006979
response to oxidative stress
GO:0007271
synaptic transmission, cholinergic
GO:0007584
response to nutrient
GO:0009410
response to xenobiotic stimulus
GO:0009636
response to toxic substance
GO:0009725
response to hormone
GO:0009743
response to carbohydrate
GO:0014070
response to organic cyclic compound
GO:0014075
response to amine
GO:0019430
removal of superoxide radicals
GO:0030163
protein catabolic process
GO:0032355
response to estradiol
GO:0032496
response to lipopolysaccharide
GO:0033574
response to testosterone
GO:0034599
cellular response to oxidative stress
GO:0042177
negative regulation of protein catabolic process
GO:0042360
vitamin E metabolic process
GO:0042373
vitamin K metabolic process
GO:0043066
negative regulation of apoptotic process
GO:0043279
response to alkaloid
GO:0043525
positive regulation of neuron apoptotic process
GO:0045087
innate immune response
GO:0045454
cell redox homeostasis
GO:0045471
response to ethanol
GO:0051602
response to electrical stimulus
GO:0070301
cellular response to hydrogen peroxide
GO:0070995
NADPH oxidation
GO:0071248
cellular response to metal ion
GO:0110076
negative regulation of ferroptosis
GO:1904772
response to tetrachloromethane
GO:1904844
response to L-glutamine
GO:1904880
response to hydrogen sulfide
GO:1905395
response to flavonoid
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0030425
dendrite
GO:0043025
neuronal cell body
GO:0045202
synapse
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1kbq
,
PDBe:1kbq
,
PDBj:1kbq
PDBsum
1kbq
PubMed
11735396
UniProt
P15559
|NQO1_HUMAN NAD(P)H dehydrogenase [quinone] 1 (Gene Name=NQO1)
[
Back to BioLiP
]