Structure of PDB 1h6v Chain F Binding Site BS02
Receptor Information
>1h6v Chain F (length=490) Species:
10116
(Rattus norvegicus) [
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SYDFDLIIIGGGSGGLAAAKEAAKFDKKVMVLDFVTPTPLGTNWGLGGTC
VNVGCIPKKLMHQAALLGQALKDSRNYGWKLEDTVKHDWEKMTESVQNHI
GSLNWGYRVALREKKVVYENAYGKFIGPHKIMATNNKGKEKVYSAERFLI
ATGERPRYLGIPGDKEYCISSDDLFSLPYCPGKTLVVGASYVALECAGFL
AGIGLDVTVMVRSILLRGFDQDMANKIGEHMEEHGIKFIRQFVPTKIEQI
EAGTPGRLKVTAKSTNSEETIEDEFNTVLLAVGRDSCTRTIGLETVGVKI
NEKTGKIPVTDEEQTNVPYIYAIGDILEGKLELTPVAIQAGRLLAQRLYG
GSTVKCDYDNVPTTVFTPLEYGCCGLSEEKAVEKFGEENIEVYHSFFWPL
EWTVPSRDNNKCYAKVICNLKDNERVVGFHVLGPNAGEVTQGFAAALKCG
LTKQQLDSTIGIHPVCAEIFTTLSVTKRSGGDILQSGCCG
Ligand information
Ligand ID
NDP
InChI
InChI=1S/C21H30N7O17P3/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32/h1,3-4,7-8,10-11,13-16,20-21,29-31H,2,5-6H2,(H2,23,32)(H,36,37)(H,38,39)(H2,22,24,25)(H2,33,34,35)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
ACFIXJIJDZMPPO-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)N5C=CCC(=C5)C(=O)N)O)O)O)OP(=O)(O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[CH]2O[CH](CO[P](O)(=O)O[P](O)(=O)OC[CH]3O[CH]([CH](O[P](O)(O)=O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[C@@H]2O[C@H](CO[P@@](O)(=O)O[P@](O)(=O)OC[C@H]3O[C@H]([C@H](O[P](O)(O)=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)N5C=CCC(=C5)C(=O)N)O)O)O)OP(=O)(O)O)N
Formula
C21 H30 N7 O17 P3
Name
NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE
ChEMBL
CHEMBL407009
DrugBank
DB02338
ZINC
ZINC000008215411
PDB chain
1h6v Chain F Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
1h6v
Three-Dimensional Structure of a Mammalian Thioredoxin Reductase: Implication for Mechanism and Evolution of a Selenocysteine Dependent Enzyme
Resolution
3.0 Å
Binding residue
(original residue number in PDB)
R166 L168 A198 S199 R221 S222 R226 V291 G292
Binding residue
(residue number reindexed from 1)
R157 L159 A189 S190 R212 S213 R217 V282 G283
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
L55 C59 C64 K67 Y200 E204 G470 H472 E477 G496 C497
Catalytic site (residue number reindexed from 1)
L46 C50 C55 K58 Y191 E195 G461 H463 E468 G487 C488
Enzyme Commision number
1.11.1.2
: NADPH peroxidase.
1.8.1.9
: thioredoxin-disulfide reductase.
Gene Ontology
Molecular Function
GO:0004791
thioredoxin-disulfide reductase (NADPH) activity
GO:0016174
NAD(P)H oxidase H2O2-forming activity
GO:0016491
oxidoreductase activity
GO:0016668
oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor
GO:0033797
selenate reductase activity
GO:0042802
identical protein binding
GO:0045340
mercury ion binding
GO:0050137
NADPH peroxidase activity
GO:0050660
flavin adenine dinucleotide binding
GO:0071949
FAD binding
Biological Process
GO:0001707
mesoderm formation
GO:0006979
response to oxidative stress
GO:0007369
gastrulation
GO:0008283
cell population proliferation
GO:0009410
response to xenobiotic stimulus
GO:0010269
response to selenium ion
GO:0016259
selenocysteine metabolic process
GO:0042537
benzene-containing compound metabolic process
GO:0042744
hydrogen peroxide catabolic process
GO:0043065
positive regulation of apoptotic process
GO:0045454
cell redox homeostasis
GO:0048678
response to axon injury
GO:0055093
response to hyperoxia
GO:0070276
halogen metabolic process
GO:0070995
NADPH oxidation
GO:0071280
cellular response to copper ion
GO:0071455
cellular response to hyperoxia
GO:0098869
cellular oxidant detoxification
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005829
cytosol
GO:0043025
neuronal cell body
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1h6v
,
PDBe:1h6v
,
PDBj:1h6v
PDBsum
1h6v
PubMed
11481439
UniProt
O89049
|TRXR1_RAT Thioredoxin reductase 1, cytoplasmic (Gene Name=Txnrd1)
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