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Literature summary for 3.5.1.88 extracted from

  • Lee, S.J.; Lee, S.J.; Lee, S.K.; Yoon, H.J.; Lee, H.H.; Kim, K.K.; Lee, B.J.; Lee, B.I.; Suh, S.W.
    Structures of Staphylococcus aureus peptide deformylase in complex with two classes of new inhibitors (2012), Acta Crystallogr. Sect. D, 68, 784-793.
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
recombinant overexpression of C-terminally His6-tagged enzyme in Escherichia coli strain C41 (DE3) Staphylococcus aureus

Crystallization (Commentary)

Crystallization (Comment) Organism
purified recombinant His6-tagged enzyme in complex with four hydroxamate inhibitors, hanging drop vapour-diffusion method, mixing of 30 mg/ml protein in 20 mM Tris-HCl, pH 7.5, and 120 mM NaCl, with reservoir solution consisting of 23% w/v PEG 4000, 50 mM Tris-HCl pH 8.5, 15% v/v glycerol, 100 mM MgCl2, 20mM CaCl2, X-ray diffraction structure determination and analysis at resolutions of 1.90-2.30 A Staphylococcus aureus

Inhibitors

Inhibitors Comment Organism Structure
(2R)-N-[(2S)-1-{4-[(2H-1,3-benzodioxol-5-yl)methyl]piperazin-1-yl}-3,3-dimethyl-1-oxobutan-2-yl]-2-(cyclopentylmethyl)-3-[formyl(hydroxy)amino]propanamide
-
Staphylococcus aureus
actinonin
-
Staphylococcus aureus
additional information effects of inhibitors on the enzyme structure, overview Staphylococcus aureus
N-(5-fluoro-1-hydroxypyridin-1-ium-2-yl)-1-[(2R)-2-[[formyl(hydroxy)amino]methyl]hexanoyl]prolinamide
-
Staphylococcus aureus
N-[(2-methoxyphenyl)carbamoyl]-3-methyl-L-valyl-N2-(cyclopentylmethyl)-N-hydroxyglycinamide binding structure, overview Staphylococcus aureus
N-[(2R,4S)-2-butyl-4-[[(2-fluorophenyl)carbamoyl]amino]-5-methyl-3-oxohexyl]-N-hydroxyformamide binding structure, overview Staphylococcus aureus
N-[(2R,4S)-2-butyl-5-methyl-4-[[(5-methylpyridin-2-yl)carbamoyl]amino]-3-oxohexyl]-N-hydroxyformamide binding structure, overview Staphylococcus aureus
N-[(3,5-difluorophenyl)carbamoyl]-3-methyl-L-valyl-N2-(cyclopentylmethyl)-N-hydroxyglycinamide binding structure, overview Staphylococcus aureus

Metals/Ions

Metals/Ions Comment Organism Structure
Zn2+ a zinc-metalloenzyme Staphylococcus aureus

Organism

Organism UniProt Comment Textmining
Staphylococcus aureus
-
-
-
Staphylococcus aureus ATCC 6538p
-
-
-

Purification (Commentary)

Purification (Comment) Organism
recombinant C-terminally His6-tagged enzyme from Escherichia coli strain C41 (DE3) by nickel affinity chromatography, gel filtration, and ultrafiltration Staphylococcus aureus

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
formyl-Met-Ala-Ser + H2O
-
Staphylococcus aureus formate + Met-Ala-Ser
-
?
formyl-Met-Ala-Ser + H2O
-
Staphylococcus aureus ATCC 6538p formate + Met-Ala-Ser
-
?

Synonyms

Synonyms Comment Organism
PDF
-
Staphylococcus aureus

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
9.5
-
assay at Staphylococcus aureus

Ki Value [mM]

Ki Value [mM] Ki Value maximum [mM] Inhibitor Comment Organism Structure
0.0000112
-
N-[(2R,4S)-2-butyl-5-methyl-4-[[(5-methylpyridin-2-yl)carbamoyl]amino]-3-oxohexyl]-N-hydroxyformamide pH 7.0, temperature not specified in the publication Staphylococcus aureus
0.0000351
-
N-[(2R,4S)-2-butyl-4-[[(2-fluorophenyl)carbamoyl]amino]-5-methyl-3-oxohexyl]-N-hydroxyformamide pH 7.0, temperature not specified in the publication Staphylococcus aureus
0.0000524
-
N-[(3,5-difluorophenyl)carbamoyl]-3-methyl-L-valyl-N2-(cyclopentylmethyl)-N-hydroxyglycinamide pH 7.0, temperature not specified in the publication Staphylococcus aureus
0.0000849
-
N-[(2-methoxyphenyl)carbamoyl]-3-methyl-L-valyl-N2-(cyclopentylmethyl)-N-hydroxyglycinamide pH 7.0, temperature not specified in the publication Staphylococcus aureus

General Information

General Information Comment Organism
physiological function peptide deformylase catalyzes the removal of the formyl group from the N-terminal methionine residue in newly synthesized polypeptides, which is an essential process in bacteria Staphylococcus aureus