Structure of PDB 1zh8 Chain B Binding Site BS01
Receptor Information
>1zh8 Chain B (length=324) Species:
243274
(Thermotoga maritima MSB8) [
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RKIRLGIVGCGIAARELHLPALKNLSHLFEITAVTSRTRSHAEEFAKMVG
NPAVFDSYEELLESGLVDAVDLTLPVELNLPFIEKALRKGVHVICEKPIS
TDVETGKKVVELSEKSEKTVYIAENFRHVPAFWKAKELVESGAIGDPVFM
NWQIWVGMDENNKYVHTDWRKKPKHVGGFLSDGGVHHAAAMRLILGEIEW
ISAVAKDLSPLLGGMDFLSSIFEFENGTVGNYTISYSLKGNERFEITGTK
GKISISWDKIVLNEEEMKVPQENSYQKEFEDFYQVVAEGKPNDLGSPVQA
LKDLAFIEACVRSAGNKVFVSSLL
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
1zh8 Chain B Residue 400 [
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Receptor-Ligand Complex Structure
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PDB
1zh8
Crystal structure of Oxidoreductase (TM0312) from Thermotoga maritima at 2.50 A resolution
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
G13 C14 G15 I16 A17 S40 R41 T42 H45 T77 L78 P79 L82 E100 K101 N129 Y168 T171 W173 R174 H190 Y279
Binding residue
(residue number reindexed from 1)
G9 C10 G11 I12 A13 S36 R37 T38 H41 T73 L74 P75 L78 E96 K97 N125 Y164 T167 W169 R170 H186 Y275
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
K101 H190
Catalytic site (residue number reindexed from 1)
K97 H186
Enzyme Commision number
1.1.1.-
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0016491
oxidoreductase activity
Biological Process
GO:0006740
NADPH regeneration
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Molecular Function
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Biological Process
External links
PDB
RCSB:1zh8
,
PDBe:1zh8
,
PDBj:1zh8
PDBsum
1zh8
PubMed
UniProt
Q9WYE8
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