Structure of PDB 1aog Chain B Binding Site BS01
Receptor Information
>1aog Chain B (length=483) Species:
5693
(Trypanosoma cruzi) [
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IFDLVVIGAGSGGLEAAWNAATLYKKRVAVIDVQMVHGPPFFSALGGTCV
NVGCVPKKLMVTGAQYMEHLRESAGFGWEFDRTTLRAEWKNLIAVKDEAV
LNINKSYDEMFRDTEGLEFFLGWGSLESKNVVNVRESADPASAVKERLET
EHILLASGSWPHMPNIPGIEHCISSNEAFYLPEPPRRVLTVGGGFISVEF
AGIFNAYKPKDGQVTLCYRGEMILRGFDHTLREELTKQLTANGIQILTKE
NPAKVELNADGSKSVTFESGKKMDFDLVMMAIGRSPRTKDLQLQNAGVMI
KNGGVQVDEYSRTNVSNIYAIGDVTNRVMLTPVAINEAAALVDTVFGTTP
RKTDHTRVASAVFSIPPIGTCGLIEEVASKRYEVVAVYLSSFTPLMHKVS
GSKYKTFVAKIITNHSDGTVLGVHLLGDNAPEIIQGIGICLKLNAKISDF
YNTIGVHPTSAEELCSMRTPSYYYVKGEKMEKP
Ligand information
Ligand ID
FAD
InChI
InChI=1S/C27H33N9O15P2/c1-10-3-12-13(4-11(10)2)35(24-18(32-12)25(42)34-27(43)33-24)5-14(37)19(39)15(38)6-48-52(44,45)51-53(46,47)49-7-16-20(40)21(41)26(50-16)36-9-31-17-22(28)29-8-30-23(17)36/h3-4,8-9,14-16,19-21,26,37-41H,5-7H2,1-2H3,(H,44,45)(H,46,47)(H2,28,29,30)(H,34,42,43)/t14-,15+,16+,19-,20+,21+,26+/m0/s1
InChIKey
VWWQXMAJTJZDQX-UYBVJOGSSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)CO[P@](O)(=O)O[P@@](O)(=O)OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)n5cnc6c(N)ncnc56)c2cc1C
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)n5cnc6c5ncnc6N)O)O)O)O)O
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@@H](CO[P@@](=O)(O)O[P@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5ncnc6N)O)O)O)O)O
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[CH](O)[CH](O)[CH](O)CO[P](O)(=O)O[P](O)(=O)OC[CH]4O[CH]([CH](O)[CH]4O)n5cnc6c(N)ncnc56)c2cc1C
ACDLabs 10.04
O=C2C3=Nc1cc(c(cc1N(C3=NC(=O)N2)CC(O)C(O)C(O)COP(=O)(O)OP(=O)(O)OCC6OC(n5cnc4c(ncnc45)N)C(O)C6O)C)C
Formula
C27 H33 N9 O15 P2
Name
FLAVIN-ADENINE DINUCLEOTIDE
ChEMBL
CHEMBL1232653
DrugBank
DB03147
ZINC
ZINC000008215434
PDB chain
1aog Chain B Residue 492 [
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Receptor-Ligand Complex Structure
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PDB
1aog
The crystal structure of trypanothione reductase from the human pathogen Trypanosoma cruzi at 2.3 A resolution.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
I11 G12 G14 S15 G16 D36 V37 S47 G51 T52 C53 V56 G57 C58 K61 W127 G128 A160 S161 G162 F199 R288 R291 G326 D327 M333 L334 T335
Binding residue
(residue number reindexed from 1)
I7 G8 G10 S11 G12 D32 V33 S43 G47 T48 C49 V52 G53 C54 K57 W123 G124 A156 S157 G158 F195 R284 R287 G322 D323 M329 L330 T331
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
S15 L49 C53 C58 K61 R86 T87 F199 E203 I339 G459 H461 E466 E485 K486
Catalytic site (residue number reindexed from 1)
S11 L45 C49 C54 K57 R82 T83 F195 E199 I335 G455 H457 E462 E481 K482
Enzyme Commision number
1.8.1.12
: trypanothione-disulfide reductase.
Gene Ontology
Molecular Function
GO:0004362
glutathione-disulfide reductase (NADPH) activity
GO:0015036
disulfide oxidoreductase activity
GO:0015042
trypanothione-disulfide reductase (NADPH) activity
GO:0016491
oxidoreductase activity
GO:0016668
oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor
GO:0050660
flavin adenine dinucleotide binding
Biological Process
GO:0006749
glutathione metabolic process
GO:0034599
cellular response to oxidative stress
GO:0045454
cell redox homeostasis
GO:0098869
cellular oxidant detoxification
Cellular Component
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1aog
,
PDBe:1aog
,
PDBj:1aog
PDBsum
1aog
PubMed
8771196
UniProt
P28593
|TYTR_TRYCR Trypanothione reductase (Gene Name=TPR)
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