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1 tive product 2,5-dihydroxyphenylacetic acid (homogentisate).
2  of vitamin E is initiated by prenylation of homogentisate.
3 hat results in aromatic hydroxylated product homogentisate.
4                                              Homogentisate 1,2-dioxygenase (HGDO) uses a mononuclear
5 one can reduce HGA production in humans with homogentisate 1,2-dioxygenase deficiency, the long-term
6 utations in the HGD gene and a deficiency of homogentisate 1,2-dioxygenase, is characterized by accum
7 utations in the HGO gene and a deficiency of homogentisate 1,2-dioxygenase, results in an accumulatio
8     Due to an insertion in hmgA that encodes homogentisate 1,2-dioxygenase, the mutant secreted incre
9 Remarkably, two O(2)-dependent dioxygenases, homogentisate-1,2-dioxygenase (HmgA) and 4-hydroxyphenyl
10 and Phe by producing maleylacetoacetate from homogentisate (2,5-dihydroxyphenylacetate).
11 ully produced p-hydroxymandelate, along with homogentisate and an unknown compound.
12 me, it converts p-hydroxyphenylpyruvate into homogentisate and is part of the superfamily of alpha-ke
13 ersion of (4-hydroxyphenyl)pyruvate (HPP) to homogentisate as part of the tyrosine catabolism pathway
14 ncomitant with the formation of the product, homogentisate, based on rapid quench and pre-steady-stat
15                                              Homogentisate binds as a monodentate ligand to Fe(2+), a
16                         We show that reduced homogentisate catabolism in a soybean HGO mutant is an e
17 ch catalyzes the committed enzymatic step in homogentisate catabolism.
18 s the condensation of phytyl-diphosphate and homogentisate, derived from the methylerythritol phospha
19                             GmHGO1 encodes a homogentisate dioxygenase (HGO), which catalyzes the com
20 dy known to be involved in its biosynthesis (homogentisate dioxygenase and hydroxyphenylpyruvate diox
21 We further demonstrated that coexpression of homogentisate geranylgeranyl transferase (HGGT), stacked
22 l synthesis is initiated in monocot seeds by homogentisate geranylgeranyl transferase (HGGT).
23 the same substrates as HMS but forms instead homogentisate (HG).
24 n into 4-hydroxyphenylpyruvate (HPP) to form homogentisate (HG).
25 ersion of (4-hydroxyphenyl)pyruvate (HPP) to homogentisate (HG).
26 ersion of (4-hydroxyphenyl)pyruvate (HPP) to homogentisate (HG).
27 manol ring and a 15-carbon tail derived from homogentisate (HGA) and phytyl diphosphate, respectively
28 cid quench reactions and product analysis of homogentisate indicate that HPPD as isolated is fully ac
29                                   Binding of homogentisate is driven by enthalpy and is entropically
30  course of one turnover the concentration of homogentisate is stoichiometric with enzyme concentratio
31 bicides that target pathways associated with homogentisate metabolism.
32 ynthetic intermediate, whereas vte2 disrupts homogentisate phytyl transferase activity and does not a
33                                              Homogentisate phytyltransferase (HPT) is a key enzyme li
34                                              Homogentisate phytyltransferase (HPT) performs the first
35                    This enzyme is related to homogentisate phytyltransferase (HPT), which catalyzes t
36 hosphate (PDP) catalyzed by a membrane-bound homogentisate phytyltransferase (HPT).
37 we (i) confirmed previous results suggesting homogentisate phytyltransferase as the limiting enzymati
38 ptimized and codon-optimized versions of the homogentisate phytyltransferase vitamin E2 (VTE2) from S
39 a series of single-gene constructs (encoding homogentisate phytyltransferase, tocopherol cyclase, and
40 zyme in tocopherol (vitamin E) biosynthesis, homogentisate phytyltransferase.
41  resolved in a crystal grown anoxically with homogentisate, which was subsequently incubated with dio

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