Structure of PDB 2a87 Chain B Binding Site BS02
Receptor Information
>2a87 Chain B (length=304) Species:
1773
(Mycobacterium tuberculosis) [
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RDVIVIGSGPAGYTAALYAARAQLAPLVFEGTSFGGALMTTTDVENYPGF
RNGITGPELMDEMREQALRFGADLRMEDVESVSLHGPLKSVVTADGQTHR
ARAVILAMGAAARYLQVPGEQELLGRGVSSCATCDGFFFRDQDIAVIGGG
DSAMEEATFLTRFARSVTLVHRRDEFRASKIMLDRARNNDKIRFLTNHTV
VAVDGDTTVTGLRVRDTNTGAETTLPVTGVFVAIGHEPRSGLVREAIDVD
PDGYVLVQGRTTSTSLPGVFAAGDLVDRTYRQAVTAAGSGCAAAIDAERW
LAEH
Ligand information
Ligand ID
NAP
InChI
InChI=1S/C21H28N7O17P3/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/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
XJLXINKUBYWONI-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
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)C(=O)N
CACTVS 3.341
NC(=O)c1ccc[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
CACTVS 3.341
NC(=O)c1ccc[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
OpenEye OEToolkits 1.5.0
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)C(=O)N
Formula
C21 H28 N7 O17 P3
Name
NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE;
2'-MONOPHOSPHOADENOSINE 5'-DIPHOSPHORIBOSE
ChEMBL
CHEMBL295069
DrugBank
DB03461
ZINC
PDB chain
2a87 Chain B Residue 481 [
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Receptor-Ligand Complex Structure
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PDB
2a87
Conformational flexibility of Mycobacterium tuberculosis thioredoxin reductase: crystal structure and normal-mode analysis.
Resolution
3.0 Å
Binding residue
(original residue number in PDB)
G162 G164 D165 S166 H185 R186 R191 I248 G249 Y268 R292 R295
Binding residue
(residue number reindexed from 1)
G148 G150 D151 S152 H171 R172 R177 I234 G235 Y254 R278 R281
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
F48 L52 D57 C145 C148 D149
Catalytic site (residue number reindexed from 1)
F34 L38 D43 C131 C134 D135
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:0015035
protein-disulfide reductase activity
GO:0016491
oxidoreductase activity
GO:0050660
flavin adenine dinucleotide binding
GO:0070402
NADPH binding
Biological Process
GO:0001666
response to hypoxia
GO:0019430
removal of superoxide radicals
GO:0045454
cell redox homeostasis
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:2a87
,
PDBe:2a87
,
PDBj:2a87
PDBsum
2a87
PubMed
16301794
UniProt
P9WHH1
|TRXB_MYCTU Thioredoxin reductase (Gene Name=trxB)
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