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1 nd 14 extension modules, and merE encoding a cytochrome P450 monooxygenase.
2 sequence with predicted protein homology to cytochrome P450 monooxygenases.
3 one or more oxidation reactions catalyzed by cytochrome P450 monooxygenases.
4 ion of genes encoding diterpenoid synthases, cytochrome P450 monooxygenases, 2-oxoglutarate-dependent
6 The P450 enzymes (mixed function oxidases, cytochrome P450 monooxygenases), a diverse class of enzy
7 nthetic pathway, including a multifunctional cytochrome P450 monooxygenase, a hydroxylating nonheme-i
9 O-methyltransferases and dihydroxylation by cytochrome P450 monooxygenases, although the precise seq
10 lants and chemical analyses, we identified a cytochrome P450 monooxygenase and two isomerases which h
11 extremely large repertoire of genes encoding cytochrome P450 monooxygenases and glutathione S-transfe
13 erentially expressed genes (DEGs), including cytochrome P450 monooxygenases and UDP-glycosyltransfera
14 om the predicted proteome, we also annotated cytochrome P450 monooxygenases, and transporters, these
15 rrently, lipoxygenases, cyclooxygenases, and cytochrome P450 monooxygenases are considered the primar
16 Cinnamate 4-hydroxylase (C4H; CYP73A) is a cytochrome P450 monooxygenase associated externally with
17 atetraenoic acid (12[R]-HETE) is formed by a cytochrome P450 monooxygenase; both give rise to the pot
19 ses (Cop1 to Cop6) and two terpene-oxidizing cytochrome P450 monooxygenases (Cox1 and Cox2) from Copr
20 noic acid-derived lipids of lipoxygenase and cytochrome P450 monooxygenase (CYP) (e.g., 17-HDHA, 18-H
21 use a combination of in vivo measurements of cytochrome P450 monooxygenase (CYP) biotransformation po
23 Cytochrome P450 Engineering Database, CYPED; cytochrome P450 monooxygenase, CYP; Hidden Markov Model,
26 vestigated whether stromal expression of the cytochrome P450 monooxygenase CYP26 modulates BTZ sensit
27 on is catalyzed by the Brassicaceae-specific cytochrome P450 monooxygenase CYP705A1 and is transientl
28 pathway, amorphadiene synthase, and a novel cytochrome P450 monooxygenase (CYP71AV1) from A. annua t
29 eport the genomics-enabled discovery of five cytochrome P450 monooxygenases (CYP71Z25-CYP71Z29) that
31 iochemical function of a rice (Oryza sativa) cytochrome P450 monooxygenase, CYP76M7, which seems to a
32 ation of the ovule primordium; O40 encodes a cytochrome P450 monooxygenase (CYP78A2) that is pollen t
34 share the same epoxide substrate made by the cytochrome P450 monooxygenase CYP88A154, but generate tw
38 talyzed by both microsomal and mitochondrial cytochrome P450 monooxygenases (CYPs), are strongly impl
39 howing high sequence similarity to bacterial cytochrome P450 monooxygenases (CYPs), from the Plm bios
40 own inhibitors of the important enzyme class cytochrome P450 monooxygenases (CYPs), thereby influenci
45 the most rapid hole hopping escape routes in cytochrome P450 monooxygenase, cytochrome c peroxidase,
47 ur results suggest that a single enzyme, the cytochrome P450 monooxygenase encoded by sare1259, catal
48 bition of cyclooxygenase, lipooxygenase, and cytochrome P450 monooxygenase enzymes prior to exposure
49 bolized by cyclooxygenase, lipoxygenase, and cytochrome P450 monooxygenase enzymes to biologically ac
50 ron-containing enzymatic catalyst-based on a cytochrome P450 monooxygenase-for the highly enantiosele
51 ncoded in the biosynthetic gene cluster, the cytochrome P450 monooxygenase Fr9R, was assigned as a 4-
52 fied a gene, designated CYP716Y1, encoding a cytochrome P450 monooxygenase from Bupleurum falcatum th
59 biosynthetic gene cluster implicated SgvP, a cytochrome P450 monooxygenase, in late-stage installatio
60 ally, knockout of the tropD gene, encoding a cytochrome P450 monooxygenase, indicated its place as th
62 hts into the cuticle composition of congenic cytochrome P450 monooxygenase insecticide resistant and
63 ydroxylation reactions catalyzed by class II cytochrome P450 monooxygenases involved in the synthesis
64 Direct epoxidation of aromatic nuclei by cytochrome P450 monooxygenases is one of the major metab
66 ss this question, we cloned cDNAs encoding a cytochrome P450 monooxygenase (LsM88) and a caffeate O-m
67 , we demonstrate that CYP82G1 (At3g25180), a cytochrome P450 monooxygenase of the Arabidopsis CYP82 f
71 nce that maize CYP72A27-Zm gene represents a cytochrome P450 monooxygenase (P450) gene recently captu
72 at a rate (V(max) of 10.02 pmol/min/pmol of cytochrome P450 monooxygenase (P450)) significantly high
74 s controlling the expression and activity of cytochrome P450 monooxygenase (P450s) detoxificative enz
82 idered to be the primary mechanisms by which cytochrome P450 monooxygenases (P450s) have radiated int
86 as not yet been defined, each of the encoded cytochrome P450 monooxygenases (P450s) metabolizes an ar
87 ere, we show that y-terpinene is oxidized by cytochrome P450 monooxygenases (P450s) of the CYP71D sub
89 howed that more than half (51.2%) of the CBP cytochrome P450 monooxygenases (P450s) that are up-regul
90 tion and screening of soybean cDNAs encoding cytochrome P450 monooxygenases (P450s) was used in an at
91 s of genes encoding metabolic enzymes, i.e., cytochrome P450 monooxygenases (P450s), esterases, and g
92 enobiotic metabolism by inducing the phase I cytochrome P450 monooxygenases, phase II conjugating tra
95 roaromatic amines (ArNH(2)) are activated by cytochrome P450 monooxygenases, primarily CYP1A2, into r
96 hidonic acid metabolism by lipoxygenases and cytochrome P450 monooxygenases produces regioisomeric hy
97 nts because they contain an abundance of the cytochrome P450 monooxygenases required for generation o
98 The predicted PAD3 protein appears to be a cytochrome P450 monooxygenase, similar to those from mai
99 sis (Arabidopsis thaliana) CYP86A and CYP94B cytochrome P450 monooxygenase subfamilies, which share s
102 s coopted the ancient CB5D, forming a modern cytochrome P450 monooxygenase system for aromatic ring m
103 f this study, we believe the presence of the cytochrome P450 monooxygenase system in glial cells of t
104 e rat glioma C6 cell line contains an active cytochrome P450 monooxygenase system that can be induced
106 nvolves a remarkably versatile and iterative cytochrome P450 monooxygenase (TamI) and a flavin adenin
109 ntified the CYP78A5 gene encoding a putative cytochrome P450 monooxygenase that is the first member o
110 rt a multiparametric fitness landscape for a cytochrome P450 monooxygenase that was engineered for th
111 e four of these enzymes are characterized as cytochrome P450 monooxygenases, the nature of a fifth ox
113 M on large Arabidopsis gene families such as cytochrome P450 monooxygenases to group the members func
115 ones but also alter the product profile of a cytochrome P450 monooxygenase via preference for the ald
117 cloning, and functional characterization of cytochrome P450 monooxygenases, we established that tran
118 gested that the catalytic mechanisms of both cytochrome P450 monooxygenases were similar to the other
119 quence analysis revealed that DWF4 encodes a cytochrome P450 monooxygenase with 43% identity to the p
120 uced by ZmTPS9 are further oxidized by three cytochrome P450 monooxygenases, ZmCYP71Z16, ZmCYP71Z18,