Structure of PDB 3fhy Chain B Binding Site BS01
Receptor Information
>3fhy Chain B (length=305) Species:
9606
(Homo sapiens) [
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ECRVLSIQSHVIRGYVGNRAATFPLQVLGFEIDAVNSVQFSNHTGYAHWK
GQVLNSDELQELYEGLRLNNMNKYDYVLTGYTRDKSFLAMVVDIVQELKQ
QNPRLVYVCDPVLGDKWDGEGSMYVPEDLLPVYKEKVVPLADIITPNQFE
AELLSGRKIHSQEEALRVMDMLHSMGPDTVVITSSDLPSPQGSNYLIVLG
SQRRRNPAGSVVMERIRMDIRKVDAVFVGTGNLFAAMLLAWTHKHPNNLK
VACEKTVSTLHHVLQRTIQCAKAQARPSPMQLELRMVQSKRDIEDPEIVV
QATVL
Ligand information
Ligand ID
ATP
InChI
InChI=1S/C10H16N5O13P3/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(26-10)1-25-30(21,22)28-31(23,24)27-29(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H,23,24)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
ZKHQWZAMYRWXGA-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
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)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@](O)(=O)O[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
Formula
C10 H16 N5 O13 P3
Name
ADENOSINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL14249
DrugBank
DB00171
ZINC
ZINC000004261765
PDB chain
3fhy Chain B Residue 407 [
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Receptor-Ligand Complex Structure
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PDB
3fhy
Kinetic and structural studies of the role of the active site residue Asp235 of human pyridoxal kinase.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
D118 N150 E153 T186 S187 V226 T233 L267
Binding residue
(residue number reindexed from 1)
D115 N147 E150 T183 S184 V223 T230 L264
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.7.1.35
: pyridoxal kinase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0005524
ATP binding
GO:0008270
zinc ion binding
GO:0008478
pyridoxal kinase activity
GO:0016301
kinase activity
GO:0016773
phosphotransferase activity, alcohol group as acceptor
GO:0030170
pyridoxal phosphate binding
GO:0030955
potassium ion binding
GO:0031402
sodium ion binding
GO:0031403
lithium ion binding
GO:0042803
protein homodimerization activity
GO:0046872
metal ion binding
Biological Process
GO:0009443
pyridoxal 5'-phosphate salvage
GO:0016310
phosphorylation
GO:0042816
vitamin B6 metabolic process
GO:0042817
pyridoxal metabolic process
GO:0042818
pyridoxamine metabolic process
GO:0042822
pyridoxal phosphate metabolic process
Cellular Component
GO:0005576
extracellular region
GO:0005634
nucleus
GO:0005654
nucleoplasm
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0034774
secretory granule lumen
GO:0035580
specific granule lumen
GO:0070062
extracellular exosome
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3fhy
,
PDBe:3fhy
,
PDBj:3fhy
PDBsum
3fhy
PubMed
19351586
UniProt
O00764
|PDXK_HUMAN Pyridoxal kinase (Gene Name=PDXK)
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