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Literature summary for 3.5.2.10 extracted from

  • Beuth, B.; Niefind, K.; Schomburg, D.
    Crystallization and preliminary crystallographic analysis of creatininase from Pseudomonas putida (2002), Acta Crystallogr. Sect. D, 58, 1356-1358.
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
expressed in Escherichia coli Pseudomonas putida

Crystallization (Commentary)

Crystallization (Comment) Organism
sitting drop vapour diffusion method with 22% ethanol, 20% PEG 8000, and 0.1 M MOPS pH 7.5 Pseudomonas putida

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
28399
-
6 * 28399, calculated from amino acid sequence Pseudomonas putida
28400
-
6 * 28400, MALDI-TOF mass spectrometry Pseudomonas putida
170400
-
SDS-PAGE Pseudomonas putida
173000
-
dynamic light scattering Pseudomonas putida

Organism

Organism UniProt Comment Textmining
Pseudomonas putida
-
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
creatinine + H2O
-
Pseudomonas putida creatine
-
?

Subunits

Subunits Comment Organism
homohexamer 6 * 28399, calculated from amino acid sequence Pseudomonas putida
homohexamer 6 * 28400, MALDI-TOF mass spectrometry Pseudomonas putida

Synonyms

Synonyms Comment Organism
CrnA
-
Pseudomonas putida

pH Stability

pH Stability pH Stability Maximum Comment Organism
6 9 the enzyme tends to precipitate at pH values of under 6.0 and over 9.0 corresponding to the stability range of the enzyme Pseudomonas putida