Structure of PDB 1f6m Chain E Binding Site BS02
Receptor Information
>1f6m Chain E (length=320) Species:
562
(Escherichia coli) [
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GTTKHSKLLILGSGPAGYTAAVYAARANLQPVLITGMEKGGQLTTTTEVE
NWPGDPNDLTGPLLMERMHEHATKFETEIIFDHINKVDLQNRPFRLNGDN
GEYTCDALIIATGASARYLGLPSEEAFKGRGVSASATCDGFFYRNQKVAV
IGGGNTAVEEALYLSNIASEVHLIHRRDGFRAEKILIKRLMDKVENGNII
LHTNRTLEEVTGDQMGVTGVRLRDTQNSDNIESLDVAGLFVAIGHSPNTA
IFEGQLELENGYIKVQSGIHGNATQTSIPGVFAAGDVMDHIYRQAITSAG
TGCMAALDAERYLDGLADAK
Ligand information
Ligand ID
3AA
InChI
InChI=1S/C20H28N7O16P3/c21-9-2-1-3-26(4-9)19-15(30)13(28)10(40-19)5-38-45(34,35)43-46(36,37)39-6-11-14(29)16(42-44(31,32)33)20(41-11)27-8-25-12-17(22)23-7-24-18(12)27/h1-4,7-8,10-11,13-16,19-20,28-30H,5-6,21H2,(H5-,22,23,24,31,32,33,34,35,36,37)/p+1/t10-,11-,13-,14-,15-,16-,19-,20-/m1/s1
InChIKey
JRGQEVHOKKZPIX-HISDBWNOSA-O
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.5
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)(O)OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)OP(=O)(O)O)O)O)O)N
CACTVS 3.385
Nc1ccc[n+](c1)[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
OpenEye OEToolkits 1.7.5
c1cc(c[n+](c1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)(O)O[P@](=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)OP(=O)(O)O)O)O)O)N
CACTVS 3.385
Nc1ccc[n+](c1)[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
Formula
C20 H29 N7 O16 P3
Name
3-AMINOPYRIDINE-ADENINE DINUCLEOTIDE PHOSPHATE;
ADENOSINE 5'-(TRIHYDROGEN DIPHOSPHATE) 2'-(DIHYDROGEN PHOSPHATE)ESTER WITH 3-(AMINO)-1-BETA-D-RIBOFURANOSYLPYRIDINIUM INNER SALT
ChEMBL
DrugBank
ZINC
ZINC000058638392
PDB chain
1f6m Chain E Residue 3501 [
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Receptor-Ligand Complex Structure
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PDB
1f6m
Twists in catalysis: alternating conformations of Escherichia coli thioredoxin reductase.
Resolution
2.95 Å
Binding residue
(original residue number in PDB)
L119 G153 G154 N155 T156 E159 H175 R176 R177 R181 I243 G244 H245 R293 Q294
Binding residue
(residue number reindexed from 1)
L119 G153 G154 N155 T156 E159 H175 R176 R177 R181 I243 G244 H245 R293 Q294
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
S135 C138 D139
Catalytic site (residue number reindexed from 1)
S135 C138 D139
Enzyme Commision number
1.8.1.9
: thioredoxin-disulfide reductase.
Gene Ontology
Molecular Function
GO:0004791
thioredoxin-disulfide reductase (NADPH) activity
GO:0005515
protein binding
GO:0016491
oxidoreductase activity
GO:0050660
flavin adenine dinucleotide binding
Biological Process
GO:0019430
removal of superoxide radicals
GO:0045454
cell redox homeostasis
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:1902515
thioredoxin-disulfide reductase complex
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1f6m
,
PDBe:1f6m
,
PDBj:1f6m
PDBsum
1f6m
PubMed
10947986
UniProt
P0A9P4
|TRXB_ECOLI Thioredoxin reductase (Gene Name=trxB)
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