Structure of PDB 3f5m Chain B Binding Site BS01
Receptor Information
>3f5m Chain B (length=462) Species:
5691
(Trypanosoma brucei) [
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RVTSKLVKAHRAMLNSVTQEDLKVDRLPGADYPNPSKKDKTDYIMYNPRP
RDSSENPVSVSPLLCELAAARSRIHFNPTETTIGIVTCGGICPGLNDVIR
SITLTGINVYNVKRVIGFRFGYWGLSKKGSQTAIELHRGRVTNIHHYGGT
ILGSSRGPQDPKEMVDTLERLGVNILFTVGGDGTQRGALVISQEAKRRGV
DISVFGVPKTIDNDLSFSHRTFGFQTAVEKAVQAIRAAYAEAVSANYGVG
VVKLMGRDSGFIAAQAAVASAQANICLVPENPISEQEVMSLLERRFCHSR
SCVIIVAEGFGQDWGRYDASGNKKLIDIGVILTEKVKAFLKANKSRYPDS
TVKYIDPSYMIRACPPSANDALFCATLATLAVHEAMAGATGCIIAMRHNN
YILVPIKVATSVRRVLDLRGQLWRQVREITVDLGSDVRLARKLEIRRELE
AINRNRDRLHEE
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
3f5m Chain B Residue 1001 [
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Receptor-Ligand Complex Structure
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PDB
3f5m
The crystal structure of ATP-bound phosphofructokinase from Trypanosoma brucei reveals conformational transitions different from those of other phosphofructokinases.
Resolution
2.7 Å
Binding residue
(original residue number in PDB)
Y139 R173 G174 P175 G198 G200 T201 R203 G204 S341 N343
Binding residue
(residue number reindexed from 1)
Y122 R156 G157 P158 G181 G183 T184 R186 G187 S320 N322
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
G107 R173 G174 D199 G200 K226 T227 D229 D231 R274
Catalytic site (residue number reindexed from 1)
G90 R156 G157 D182 G183 K209 T210 D212 D214 R257
Enzyme Commision number
2.7.1.11
: 6-phosphofructokinase.
Gene Ontology
Molecular Function
GO:0003872
6-phosphofructokinase activity
GO:0005524
ATP binding
GO:0016301
kinase activity
GO:0042301
phosphate ion binding
GO:0046872
metal ion binding
Biological Process
GO:0006002
fructose 6-phosphate metabolic process
GO:0006096
glycolytic process
GO:0016310
phosphorylation
GO:0061615
glycolytic process through fructose-6-phosphate
Cellular Component
GO:0005737
cytoplasm
GO:0020015
glycosome
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3f5m
,
PDBe:3f5m
,
PDBj:3f5m
PDBsum
3f5m
PubMed
19084537
UniProt
O15648
|PFKA_TRYBB ATP-dependent 6-phosphofructokinase (Gene Name=pfk)
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