1.14.13.130: pyrrole-2-carboxylate monooxygenase

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For detailed information about pyrrole-2-carboxylate monooxygenase, go to the full flat file.

Reaction

ECTree

1 Oxidoreductases

1.14 Acting on paired donors, with incorporation or reduction of molecular oxygen

1.14.13 With NADH or NADPH as one donor, and incorporation of one atom of oxygen into the other donor

1.14.13.130 pyrrole-2-carboxylate monooxygenase

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Results	in table
2	AA Sequence
4	Cofactor
2	Expression
3	General Information
1	General Stability
8	Inhibitors
3	KM Value [mM]
3	Metals/Ions
4	Molecular Weight [Da]
3	Natural Substrates/ Products (Substrates)
3	Organism
2	pH Optimum
1	pH Range
1	pI Value
2	Purification (Commentary)
1	Reaction
3	Reference
3	Source Tissue
1	Specific Activity [micromol/min/mg]
1	Storage Stability
7	Substrates and Products (Substrate)
3	Subunits
1	Systematic Name
1	Temperature Optimum [°C]

Substrates Products

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Substrates Products on EC 1.14.13.130 - pyrrole-2-carboxylate monooxygenase

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pyrrole-2-carboxylate + NADH + H+ + O2

5-hydroxypyrrole-2-carboxylate + NAD+ + H2O

6 entries

additional information

Rhodococcus sp.

no enzymatic activity is detected with the analogous aromatic heterocyclic compounds furan-2-carboxylate and furan-3-carboxylate, and thiophene-2-carboxylate and thiophene-3-carboxylate (0.25 mM). Pyrrole, proline, indole, and indole-2-carboxylate (each 0.25 mM) do not serve as a substrate or effector of NADH oxidation for pyrrole-2-carboxylate monooxygenase. Chlorinated phenols and 4-hydroxyphenylacetate, which are substrates for the structurally related two-component flavin aromatic monooxygenases isolated from different sources, do not affect NADH oxidation or oxygen consumption catalyzed by pyrrole-2-carboxylate monooxygenase

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