Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 4.1.2.4 extracted from

  • Chen, L.; Dumas, D.P.; Wong, C.H.
    Deoxyribose-5-phosphate aldolase as a catalyst in asymetric aldol condensation (1992), J. Am. Chem. Soc., 114, 741-748.
No PubMed abstract available

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
additional information
-
additional information
-
Escherichia coli
1.7
-
acetaldehyde
-
Escherichia coli

Organism

Organism UniProt Comment Textmining
Escherichia coli
-
-
-

Purification (Commentary)

Purification (Comment) Organism
-
Escherichia coli

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
189
-
-
Escherichia coli

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2-deoxy-D-ribose 5-phosphate
-
Escherichia coli D-glyceraldehyde 3-phosphate + acetaldehyde
-
?
D-(R)-3-Azido-2-hydroxypropanal + acetaldehyde
-
Escherichia coli 5-Azido-(2R)-methyl-2,5-dideoxy-D-ribo-furanose
-
?
D-(R)-3-Azido-2-hydroxypropanal + acetone
-
Escherichia coli 6-Azido-1,3,5-trideoxy-D-erythro-hexulose
-
?
D-(R)-3-Azido-2-hydroxypropanal + fluoroacetone
-
Escherichia coli 6-Azido-1-fluoro-1,3,5-trideoxy-D-erythro-hexulose
-
?
additional information a new stereogenic center with 3(S) configuration is formed when acetaldehyde, fluoroacetone, or acetone. With propanal, two stereogenic centers are formed with 2(R) and 3(S) configuration Escherichia coli ?
-
?