1.14.18.3: methane monooxygenase (particulate)
This is an abbreviated version!
For detailed information about methane monooxygenase (particulate), go to the full flat file.
Word Map on EC 1.14.18.3
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1.14.18.3
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pmmos
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methanotrophs
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methylococcus
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capsulatus
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bath
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methylocystis
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methylosinus
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ch4
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trichosporium
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pmocab
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methylomicrobium
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duroquinol
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environmental protection
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analysis
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trinuclear
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nadh:quinone
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monocopper
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diiron
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ammonia-oxidizing
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energy production
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degradation
- 1.14.18.3
-
pmmos
- methanotrophs
- methylococcus
- capsulatus
- bath
- methylocystis
- methylosinus
- ch4
- trichosporium
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pmocab
- methylomicrobium
- duroquinol
- environmental protection
- analysis
-
trinuclear
-
nadh:quinone
-
monocopper
-
diiron
-
ammonia-oxidizing
- energy production
- degradation
Reaction
Synonyms
copper-containing membrane monooxygenase, copper-containing membrane-bound monooxygenase, CuMMO, membrane-associated methane monooxygenase, membrane-bound methane monooxygenase, membrane-embedded methane monooxygenase, methane hydroxylase, mMMO, MMO, particulate methane mono-oxygenase, particulate methane monooxygenas, particulate methane monooxygenase, particulate methane monooxygenase A, particulate methane-oxidizing complex, particulate MMO, PMH, pMMO, pMMO hydroxylase, pMMO-H, pMMO1, pMMO2, PmoA, PmoB, sMMO, soluble methane monooxygenase, spmoB
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Specific Activity
Specific Activity on EC 1.14.18.3 - methane monooxygenase (particulate)
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0.003
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using propylene as substrate, pH and temperature not specified in the publication
0.0053
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using propylene as substrate, pH and temperature not specified in the publication
0.011
0.012
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purified enzyme, using propylene as substrate, in 25 mM MOPS buffer (pH 7.0), at 30°C
0.016
using propylene as substrate, pH and temperature not specified in the publication
0.1037
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at 45°C and pH 7.0, with NADH as cosubstrate, in the presence of bacteriohemerythrin
0.1228
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at 45°C and pH 7.0, with duroquinol as cosubstrate, in the presence of bacteriohemerythrin
additional information
0.011
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crude extract, using propylene as substrate, in 25 mM MOPS buffer (pH 7.0), at 30°C
additional information
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optimization of a coupled assay method with propylene as substrate and a duroquinol-based NADH regeneration system