Structure of PDB 5thk Chain E Binding Site BS01
Receptor Information
>5thk Chain E (length=256) Species:
216591
(Burkholderia cenocepacia J2315) [
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ATHTLADKVVLIAGGAKNLGGLIARDLAGHGAKAVAIHYNSAASQAQAEE
TAAAVRAAGAEAATFQADLTTAAAVEKLFDDAKQRFGKIDIAINTVGKVL
KKPFTEISEAEYDEMFAVNSKSAFFFIKEAGRHLEDHGKLVTLVTSLLGA
FTPFYAAYEGSKAPVEHFTRAASKEYGARGISVTAVGPGPMDTPFFYPAE
GADAVAYHKTAAALSPFSKTGLTDIEDVVPFIRHLVTDGWWITGQTILIN
GGYTTK
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
5thk Chain E Residue 300 [
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Receptor-Ligand Complex Structure
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PDB
5thk
Crystal Structure of a Putative Dehydrogenase from Burkholderia cenocepacia with bound NADP
Resolution
1.4 Å
Binding residue
(original residue number in PDB)
K18 N19 L20 H39 N41 S42 S45 D69 L70 T96 V97 G98 Y159 K163 G190 M192 T194 F196
Binding residue
(residue number reindexed from 1)
K17 N18 L19 H38 N40 S41 S44 D68 L69 T95 V96 G97 Y158 K162 G189 M191 T193 F195
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
T146 Y156 Y159 K163 D204
Catalytic site (residue number reindexed from 1)
T145 Y155 Y158 K162 D203
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0016491
oxidoreductase activity
GO:0016614
oxidoreductase activity, acting on CH-OH group of donors
GO:0046872
metal ion binding
View graph for
Molecular Function
External links
PDB
RCSB:5thk
,
PDBe:5thk
,
PDBj:5thk
PDBsum
5thk
PubMed
UniProt
B4E8W7
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