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Literature summary for 3.5.1.4 extracted from

  • Andrade, J.; Karmali, A.; Carrondo, M.A.; Frazao, C.
    Crystallization, diffraction data collection and preliminary crystallographic analysis of hexagonal crystals of Pseudomonas aeruginosa amidase (2007), Acta Crystallogr. Sect. F, 63, 214-216.
    View publication on PubMedView publication on EuropePMC

Crystallization (Commentary)

Crystallization (Comment) Organism
purified wild-type enzyme, 25 mg/ml protein in 50 mM Tris-HCl, pH 7.2, containing 5 mM DTT and 1 mM EDTA, hexagonal crystals, X-ray diffraction structure determination and analysis at 1.25-1.4 A resolution Pseudomonas aeruginosa

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
38000
-
6 * 38000, SDS-PAGE Pseudomonas aeruginosa

Organism

Organism UniProt Comment Textmining
Pseudomonas aeruginosa
-
gene amiE, inducible enzyme
-

Purification (Commentary)

Purification (Comment) Organism
wild-type enzyme by acetamide affinity chromatography and gel filtration Pseudomonas aeruginosa

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information the enzyme catalyses the hydrolysis of small aliphatic amides Pseudomonas aeruginosa ?
-
?

Subunits

Subunits Comment Organism
hexamer 6 * 38000, SDS-PAGE Pseudomonas aeruginosa

Temperature Optimum [°C]

Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
25
-
assay at Pseudomonas aeruginosa

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
7.2
-
assay at Pseudomonas aeruginosa