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1.13.12.8: Watasenia-luciferin 2-monooxygenase

This is an abbreviated version!
For detailed information about Watasenia-luciferin 2-monooxygenase, go to the full flat file.

Reaction

Watasenia luciferin
+
O2
=
Oxidized Watasenia luciferin
+
CO2
+
hnu

Synonyms

alkanal monooxygenase (FMN-linked), bacterial luciferase, luciferase, luciferase (Photobacterium leiognathi), LuxAB, Photorhabdus luminescens luciferase, Vibrio fischeri luuciferase, Watasenia-type luciferase

ECTree

     1 Oxidoreductases
         1.13 Acting on single donors with incorporation of molecular oxygen (oxygenases)
             1.13.12 With incorporation of one atom of oxygen (internal monooxygenases or internal mixed-function oxidases)
                1.13.12.8 Watasenia-luciferin 2-monooxygenase

General Information

General Information on EC 1.13.12.8 - Watasenia-luciferin 2-monooxygenase

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GENERAL INFORMATION
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
evolution
physiological function
-
the organism produces flashes of blue light via a series of complicated luciferin-luciferase reactions involving ATP, Mg2+, and molecular oxygen. The enzyme catalyzes the two key steps. They are the addition of molecular oxygen to luciferin and the formation of light emitter. The oxygenation reaction occurs with a single electron-transfer (SET) mechanism, and the light emitter is produced via the mechanism of gradually reversible charge-transfer-induced luminescence (GRCTIL). Biolumiscence key steps are oxygenation of luciferin and thermolysis of the peroxide intermediate to produce light emitter
additional information
-
protein microcrystals in the arm photophores catalyse the bioluminescent reaction using ATP and the substrate coelenterazine disulfate. The crystals contain a major 63 kDa protein and a minor 81 kDa protein, in a mass ratio of about 8 to 1. Three homologous proteins comprise the luminescent arm tip microcrystals, i.e. proteins wsluc1-3, wsluc1-3 form a complex that crystallises inside the squid photophores. Analysis of the proteins from the protein crystal extraction identified by MALDI TOF/TOF mass spectrometry analysis, overview