Sequence of C71DI_MENGR
EC Number:1.14.14.51
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
Reaction
(S)-limonene + [reduced NADPH-hemoprotein reductase] + O2 = (-)-trans-carveol + [oxidized NADPH-hemoprotein reductase] + H2O
Other sequences found for EC No. 1.14.14.51
General information:
Sequence
0 MELDLLSAII ILVATYIVSL LINQWRKSKS QQNLPPSPPK LPVIGHLHFL WGGLPQHVFR
60 SIAQKYGPVA HVQLGEVYSV VLSSAEAAKQ AMKVLDPNFA DRFDGIGSRT MWYDKDDIIF
120 SPYNDHWRQM RRICVTELLS PKNVRSFGYI RQEEIERLIR LLGSSGGAPV DVTEEVSKMS
180 CVVVCRAAFG SVLKDQGSLA ELVKESLALA SGFELADLYP SSWLLNLLSL NKYRLQRMRR
240 RLDHILDGFL EEHREKKSGE FGGEDIVDVL FRMQKGSDIK IPITSNCIKG FIFDTFSAGA
300 ETSSTTISWA LSELMRNPAK MAKVQAEVRE ALKGKTVVDL SEVQELKYLR SVLKETLRLH
360 PPFPLIPRQS REECEVNGYT IPAKTRIFIN VWAIGRDPQY WEDPDTFRPE RFDEVSRDFM
420 GNDFEFIPFG AGRRICPGLH FGLANVEIPL AQLLYHFDWK LPQGMTDADL DMTETPGLSG
480 PKKKNVCLVP TLYKSP
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Sequence related references
Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
139847
Bertea C.,Schalk M.,Mau C.J.D.,Karp F.,Wildung M.R.,Croteau R.
Molecular evaluation of a spearmint mutant altered in the expression of limonene hydroxylases that direct essential oil monoterpene biosynthesis.
Phytochemistry
64
1203-1211
2003
139848
Wuest M.,Little D.B.,Schalk M.,Croteau R.
Hydroxylation of limonene enantiomers and analogs by recombinant (-)-limonene 3- and 6-hydroxylases from mint (Mentha) species: evidence for catalysis within sterically constrained active sites.
Arch. Biochem. Biophys.
387
125-136
2001