Structure of PDB 4fwn Chain A Binding Site BS01
Receptor Information
>4fwn Chain A (length=394) Species:
99287
(Salmonella enterica subsp. enterica serovar Typhimurium str. LT2) [
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FPVVLVINCGSSSIKFSVLDVATCDVLMAGIADGMNTENAFLSINGDKPI
NLAHSNYEDALKAIAFELEKRDLTDSVALIGHRIAHGGELFTQSVIITDE
IIDNIRRVSPLAPLHNYANLSGIDAARHLFPAVRQVAVFDTSFHQTLAPE
AYLYGLPWEYFSSLGVRRYGFHGTSHRYVSRRAYELLDLDEKDSGLIVAH
LGNGASICAVRNGQSVDTSMGMTPLEGLMMGTRSGDVDFGAMAWIAKETG
QTLSDLERVVNKESGLLGISGLSSDLRVLEKAWHEGHERARLAIKTFVHR
IARHIAGHAASLHRLDGIIFTGGIGENSVLIRQLVIEHLGVLGLTLDVEM
NKQPNSHGERIISANPSQVICAVIPTNEEKMIALDAIHLGNVKA
Ligand information
Ligand ID
AQP
InChI
InChI=1S/C10H17N5O16P4/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(28-10)1-27-33(21,22)30-35(25,26)31-34(23,24)29-32(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H,23,24)(H,25,26)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
WWMWAMFHUSTZTA-KQYNXXCUSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P@](O)(=O)O[P@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
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)O[P@@](=O)(O)OP(=O)(O)O)O)O)N
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=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[P](O)(O)=O)[CH](O)[CH]3O
Formula
C10 H17 N5 O16 P4
Name
ADENOSINE-5'-TETRAPHOSPHATE
ChEMBL
CHEMBL490984
DrugBank
ZINC
ZINC000008551576
PDB chain
4fwn Chain A Residue 503 [
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Receptor-Ligand Complex Structure
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PDB
4fwn
Mechanistic features of Salmonella typhimurium propionate kinase (TdcD): insights from kinetic and crystallographic studies.
Resolution
3.0 Å
Binding residue
(original residue number in PDB)
H175 H203 N206 G207 D278 L279 R280 G326 I327 N330
Binding residue
(residue number reindexed from 1)
H172 H200 N203 G204 D275 L276 R277 G323 I324 N327
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
N11 R86 H175 R236 E381
Catalytic site (residue number reindexed from 1)
N8 R83 H172 R233 E378
Enzyme Commision number
2.7.2.15
: propionate kinase.
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0008776
acetate kinase activity
GO:0008980
propionate kinase activity
GO:0016301
kinase activity
GO:0016774
phosphotransferase activity, carboxyl group as acceptor
GO:0046872
metal ion binding
Biological Process
GO:0006082
organic acid metabolic process
GO:0006083
acetate metabolic process
GO:0016310
phosphorylation
GO:0070689
L-threonine catabolic process to propionate
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:4fwn
,
PDBe:4fwn
,
PDBj:4fwn
PDBsum
4fwn
PubMed
23747922
UniProt
O06961
|TDCD_SALTY Propionate kinase (Gene Name=tdcD)
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