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Literature summary for 4.2.1.11 extracted from

  • Gao, X.; Zheng, C.; Liu, X.
    Expression, purification, and biological characterization of Anaplasma phagocytophilum enolase (2018), Biosci. Trends, 11, 651-657 .
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
expression in Escherichia coli Anaplasma phagocytophilum

KM Value [mM]

KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
6.053
-
2-phospho-D-glycerate pH 7.0, 30°C Anaplasma phagocytophilum

Organism

Organism UniProt Comment Textmining
Anaplasma phagocytophilum Q2GK24
-
-
Anaplasma phagocytophilum HZ Q2GK24
-
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2-phospho-D-glycerate
-
Anaplasma phagocytophilum phosphoenolpyruvate + H2O
-
?
2-phospho-D-glycerate
-
Anaplasma phagocytophilum HZ phosphoenolpyruvate + H2O
-
?

Subunits

Subunits Comment Organism
? x * 72000, SDS-PAGE, recombinant protein with GST-tag Anaplasma phagocytophilum

Temperature Optimum [°C]

Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
50
-
-
Anaplasma phagocytophilum

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
8
-
-
Anaplasma phagocytophilum

General Information

General Information Comment Organism
physiological function recombinant enolase retains its enzymatic activity and binds to human plasminogen. Binding can be significantly reduced in the presence of epsilon-aminocaproic acid. Eno promotes plasminogen to plasmin conversion in the presence of plasminogen activator Anaplasma phagocytophilum