Structure of PDB 4k6f Chain D Binding Site BS01
Receptor Information
>4k6f Chain D (length=245) Species:
216591
(Burkholderia cenocepacia J2315) [
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KRIAVVTGGMGGLGEAVSIRLNDAGHRVVVTYSPNNTGADRWLTEMHAAG
REFHAYPVDVADHDSCQQCIEKIVRDVGPVDILVNNAGITRDMTLRKLDK
VNWDAVIRTNLDSVFNMTKPVCDGMVERGWGRIVNISSVNGSKGSVGQTN
YAAAKAGMHGFTKSLALEIARKGVTVNTVSPGYLATKMVTAIPQDILDTK
ILPQIPAGRLGKPEEVAALVAYLCSEEAGFVTGSNIAINGGQHMH
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
4k6f Chain D Residue 300 [
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Receptor-Ligand Complex Structure
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PDB
4k6f
X-ray crystal structure of a putative Acetoacetyl-CoA reductase from Burkholderia cenocepacia bound to the co-factor NADP
Resolution
1.5 Å
Binding residue
(original residue number in PDB)
G10 G13 G14 L15 Y34 S35 N38 V60 D61 V62 N88 A89 G90 I91 Y153 K157 P183 L186 T188
Binding residue
(residue number reindexed from 1)
G8 G11 G12 L13 Y32 S33 N36 V58 D59 V60 N86 A87 G88 I89 Y151 K155 P181 L184 T186
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
G14 N104 S140 Y153 K157
Catalytic site (residue number reindexed from 1)
G12 N102 S138 Y151 K155
Enzyme Commision number
1.1.1.36
: acetoacetyl-CoA reductase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0016491
oxidoreductase activity
GO:0018454
acetoacetyl-CoA reductase activity
Biological Process
GO:0042619
poly-hydroxybutyrate biosynthetic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4k6f
,
PDBe:4k6f
,
PDBj:4k6f
PDBsum
4k6f
PubMed
UniProt
B4EAU4
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