Structure of PDB 3uqd Chain A Binding Site BS01
Receptor Information
>3uqd Chain A (length=309) Species:
83333
(Escherichia coli K-12) [
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MVRIYTLTLAPSLDSATITPQIYPEGKLRCTAPVFEPGGGGINVARAIAH
LGGSATAIFPAGGATGEHLVSLLADENVPVATVEAKDWTRQNLHVHVEAS
GEQYRFVMPGAALNEDEFRQLEEQVLEIESGAILVISGSLPPGVKLEKLT
QLISAAQKQGIRCIVDSSGEALSAALAIGNIELVKPNQKELSALVNRELT
QPDDVRKAAQEIVNSGKAKRVVVSLGPQGALGVDSENCIQVVPPPVKSQS
TVGAGDSMVGAMTLKLAENASLEEMVRFGVAAGSAATLNQGTRLCSHDDT
QKIYAYLSR
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
3uqd Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
3uqd
Studying the phosphoryl transfer mechanism of theE. coliphosphofructokinase-2: from X-ray structure to quantum mechanics/molecular mechanics simulations.
Resolution
2.14 Å
Binding residue
(original residue number in PDB)
K185 S224 G226 P227 G229 T251 G255 M258 V280 G283 S284 T287
Binding residue
(residue number reindexed from 1)
K185 S224 G226 P227 G229 T251 G255 M258 V280 G283 S284 T287
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
G253 A254 G255 D256
Catalytic site (residue number reindexed from 1)
G253 A254 G255 D256
Enzyme Commision number
2.7.1.11
: 6-phosphofructokinase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003872
6-phosphofructokinase activity
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0009024
tagatose-6-phosphate kinase activity
GO:0016301
kinase activity
GO:0016772
transferase activity, transferring phosphorus-containing groups
GO:0016773
phosphotransferase activity, alcohol group as acceptor
GO:0042802
identical protein binding
GO:0042803
protein homodimerization activity
GO:0046872
metal ion binding
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0006096
glycolytic process
GO:0006974
DNA damage response
GO:0016310
phosphorylation
GO:0061615
glycolytic process through fructose-6-phosphate
Cellular Component
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3uqd
,
PDBe:3uqd
,
PDBj:3uqd
PDBsum
3uqd
PubMed
30996866
UniProt
P06999
|PFKB_ECOLI ATP-dependent 6-phosphofructokinase isozyme 2 (Gene Name=pfkB)
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