Structure of PDB 3a14 Chain A Binding Site BS02
Receptor Information
>3a14 Chain A (length=362) Species:
2336
(Thermotoga maritima) [
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ERTLVILGATGSIGTQTLDVLKKVKGIRLIGISFHSNLELAFKIVKEFNV
KNVAITGDVEFEDSSINVWKGSHSIEEMLEALKPDITMVAVSGFSGLRAV
LASLEHSKRVCLANKESLVCGGFLVKKKLKEKGTELIPVDSEHSAIFQVM
EPEVEKVVLTASGGALRDWKISKIDRARPEDVLARITVDSATMVNKAFEV
LEAMELFELPFEKIEVKIHREGLVHGAVVLPDGNVKMVVSPPDMRIPISY
ALFYPRRVALEPFFLRTISLSFEDPDPEKYPAFFLLKEIKDSYALRTAFN
AADEVAVEAFLKGRIRFGGIHRVIEKTLEEFQGYPQPRTLDDVERIHFEA
IKKAERVTEWLS
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
3a14 Chain A Residue 3001 [
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Receptor-Ligand Complex Structure
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PDB
3a14
Crystal structure of 1-deoxy-d-xylulose 5-phosphate reductoisomerase from the hyperthermophile Thermotoga maritima for insights into the coordination of conformational changes and an inhibitor binding.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
G10 T12 G13 S14 I15 H37 S38 N39 T58 A92 V93 S94 S97 A115 K117 D142 I196
Binding residue
(residue number reindexed from 1)
G8 T10 G11 S12 I13 H35 S36 N37 T56 A90 V91 S92 S95 A113 K115 D140 I186
Annotation score
4
Enzymatic activity
Enzyme Commision number
1.1.1.267
: 1-deoxy-D-xylulose-5-phosphate reductoisomerase.
Gene Ontology
Molecular Function
GO:0016491
oxidoreductase activity
GO:0030145
manganese ion binding
GO:0030604
1-deoxy-D-xylulose-5-phosphate reductoisomerase activity
GO:0046872
metal ion binding
GO:0070402
NADPH binding
Biological Process
GO:0008299
isoprenoid biosynthetic process
GO:0019288
isopentenyl diphosphate biosynthetic process, methylerythritol 4-phosphate pathway
GO:0051484
isopentenyl diphosphate biosynthetic process, methylerythritol 4-phosphate pathway involved in terpenoid biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3a14
,
PDBe:3a14
,
PDBj:3a14
PDBsum
3a14
PubMed
20353826
UniProt
Q9WZZ1
|DXR_THEMA 1-deoxy-D-xylulose 5-phosphate reductoisomerase (Gene Name=dxr)
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