Sequence of C71C1_MAIZE
EC Number:1.14.14.109
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
Reaction
3-hydroxyindolin-2-one + [reduced NADPH-hemoprotein reductase] + O2 = 2-hydroxy-2H-1,4-benzoxazin-3(4H)-one + [oxidized NADPH-hemoprotein reductase] + H2O
Other sequences found for EC No. 1.14.14.109
General information:
Sequence
0 MALEAGYDYL HVAVVQCTPT QAAAVLGVLL LLAIRLAAAA RSSSATSPKW KQHRLPPTPP
60 GKLPIIGHLH LIGSHPHVSF RDLHAKYGHN GLMLVQVGAV PTIVVSTPQA AEAVLRTHDH
120 VLASRPRNPV ADIIRYNSTD VAFAPYGVYW RTARKVVNTH LLSAKMVFSK RREREEEVRL
180 VVARIRDAAE ASPGTALDMT ELLGGYASDF VCRAVLGESH RKQGRNKLFR ELTETSAALL
240 GGFNVEDYFP KLADVDLFLR IICAKAKSVS KRWDSLFNEL LSEYALSGGK QGDHNSEDFV
300 HLLLSLQKDY GLTTDNIKGI LVNMFEAAIE TSFLVLEYSM SELMNNRHVL AKLQKEVRTA
360 TPDGRMVMEE DLSRMPYLKA TIKESMRIHP PAPFLLPHFS THDCEINGYT IPAGTRVIVN
420 AWALARDPTC WDKAEEFFPE RFLEQGRDAE VDMYGKDIRF VPFGAGRRIC AGATFAIATV
480 EIMLANLIYH FDWEMPAEME RTGAKVDMSD QFGMTLRRTQ KLYLVPRIPK CVSSS
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Sequence related references
Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
521832
Frey M.,Kliem R.,Saedler H.,Gierl A.
Expression of a cytochrome P450 gene family in maize.
Mol. Gen. Genet.
246
100-109
1995
521833
Frey M.,Chomet P.,Glawischnig E.,Stettner C.,Grun S.,Winklmair A.,Eisenreich W.,Bacher A.,Meeley R.B.,Briggs S.P.,Simcox K.,Gierl A.
Analysis of a chemical plant defense mechanism in grasses.
Science
277
696-699
1997
521834
Spiteller P.,Glawischnig E.,Gierl A.,Steglich W.
Studies on the biosynthesis of 2-hydroxy-1,4-benzoxazin-3-one (HBOA) from 3-hydroxyindolin-2-one in Zea mays.
Phytochemistry
57
373-376
2001