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1 aker responses to farnesyl pyrophosphate and geranylgeranyl diphosphate.
2 e formation of both farnesyl diphosphate and geranylgeranyl diphosphate.
3 e bond of the universal diterpene precursor, geranylgeranyl diphosphate.
4 in the cytosol that synthesizes omega,E,E,E-geranylgeranyl diphosphate.
5 e blocked by geranylgeraniol, a precursor of geranylgeranyl diphosphate.
6 de novo synthesis of phytyl-diphosphate from geranylgeranyl-diphosphate.
8 complex cyclization-rearrangement of (E,E,E)-geranylgeranyl diphosphate (8, GGPP) to a mixture of abi
9 hway-intermediates, farnesyl diphosphate and geranylgeranyl diphosphate, also reduced endometrial cel
10 etic evaluation of abietadiene synthase with geranylgeranyl diphosphate and (+)-copalyl diphosphate p
11 l, mechanistically distinct cyclizations, of geranylgeranyl diphosphate and of copalyl diphosphate, i
12 sidues deleted from the preprotein converted geranylgeranyl diphosphate and the intermediate (+)-copa
14 nant Escherichia coli-expressed protein used geranylgeranyl diphosphate as substrate and catalyzed th
18 for renal function, identifying dysregulated geranylgeranyl diphosphate biosynthesis as a potential d
20 iphosphate, which is made from the all-trans geranylgeranyl diphosphate by copal-8-ol diphosphate syn
21 the enzymatic product generated from [10-2H1]geranylgeranyl diphosphate confirmed the intramolecular
22 ps from the universal diterpenoid progenitor geranylgeranyl diphosphate derived by the plastidial met
23 ays use [(3)H]farnesyl diphosphate and [(3)H]geranylgeranyl diphosphate, electrophoretic mobility shi
24 se (FPS) into synthases capable of producing geranylgeranyl diphosphate (F112A), geranylfarnesyl (C25
26 r for protein geranylgeranylation reactions, geranylgeranyl diphosphate (GGDP), is the product of the
27 ilic substitution reaction between the C(20) geranylgeranyl diphosphate (GGPP) and a protein-derived
28 of approximately 55 carbons in length using geranylgeranyl diphosphate (GGPP) and isopentenyl diphos
30 diphosphates farnesyl diphosphate (FPP) and geranylgeranyl diphosphate (GGPP) are intermediates in t
31 In plants, farnesyl diphosphate (FPP) and geranylgeranyl diphosphate (GGPP) are precursors to many
32 hypothesis, the current study identifies C20 geranylgeranyl diphosphate (GGPP) as a precursor for lyc
33 alized) metabolism via cycloisomerization of geranylgeranyl diphosphate (GGPP) by diterpene synthases
34 (MpGPS.SSU) on production of monoterpene and geranylgeranyl diphosphate (GGPP) diversities, and plant
35 LSU produced GPP, farnesyl diphosphate, and geranylgeranyl diphosphate (GGPP) from dimethylallyl dip
36 PS2) of specialized metabolism that converts geranylgeranyl diphosphate (GGPP) into labda-7,13E-dieny
38 logues suggests that the C-10 locus of bound geranylgeranyl diphosphate (GGPP) is in close proximity
39 es a bifunctional farnesyl diphosphate (FPP)/geranylgeranyl diphosphate (GGPP) synthase (TgFPPS) that
40 uced elsewhere in the plant cell derive from geranylgeranyl diphosphate (GGPP) synthesized by GGPP sy
41 clization of the linear isoprenoid substrate geranylgeranyl diphosphate (GGPP) to form taxa-4(5),11(1
42 talyzes the condensation of two molecules of geranylgeranyl diphosphate (GGPP) to give prephytoene di
43 lation of (S)-glyceryl phosphate [(S)-GP] by geranylgeranyl diphosphate (GGPP) to produce (S)-geranyl
44 ynthase catalyzes the cyclization of (E,E,E)-geranylgeranyl diphosphate (GGPP) to taxa-4(5),11(12)-di
45 bon farnesyl diphosphate (FPP), or 20-carbon geranylgeranyl diphosphate (GGPP) via a dioxygenase- or
47 ynthase catalyzes the synthesis of all-trans-geranylgeranyl diphosphate (GGPP), an isoprenoid used fo
48 te synthase (CPS), whose substrate, (E,E,E,)-geranylgeranyl diphosphate (GGPP), is also a direct prec
49 nthesis, is composed of a chlorin ring and a geranylgeranyl diphosphate (GGPP)-derived isoprenoid, wh
52 ne synthase-catalyzed cyclization of (E,E,E)-geranylgeranyl diphosphate (GGPP, 7) to taxadiene (5) is
53 e presence of either farnesyl diphosphate or geranylgeranyl diphosphate, GST-lHDAg was preferentially
54 ne of the expressed proteins was active with geranylgeranyl diphosphate; however, one truncated prote
55 ct derived by enzymatic cyclization of [1-3H]geranylgeranyl diphosphate in 2H2O indicated little inco
56 tional class I diTPS PxaTPS8, which converts geranylgeranyl diphosphate into a previously unknown 5,7
57 In M. tuberculosis, however, omega,E,E,E-geranylgeranyl diphosphate is not utilized for the synth
58 decaprenyl diphosphate, and the omega,E,E,E-geranylgeranyl diphosphate is utilized by a membrane-ass
59 fold), and in planta geranyl diphosphate and geranylgeranyl diphosphate levels (4- to 8-fold) were si
61 hosphate synthase, shown here to produce the geranylgeranyl diphosphate precursor, providing a critic
62 oding isoprenoid isopentenyl diphosphate and geranylgeranyl diphosphate-producing enzymes, DXS3, DXR,
63 hesis and forces reevaluation of the role of geranylgeranyl diphosphate reductase in tocopherol biosy
64 ich is produced from the substrate all-trans geranylgeranyl diphosphate, represents a so far unidenti
65 f lipid groups from farnesyl diphosphate and geranylgeranyl diphosphate, respectively, to a cysteine
66 of modifying the chain length specificity of geranylgeranyl diphosphate synthase (but not, apparently
67 rotein that could be identified as the mouse geranylgeranyl diphosphate synthase (GGPP synthase) base
68 h-rescue" and enzyme-inhibition experiments, geranylgeranyl diphosphate synthase (GGPPS) is shown to
69 large subunit, which may be either an active geranylgeranyl diphosphate synthase (GGPPS) or an inacti
70 of farnesyl diphosphate synthase (FPPS) and geranylgeranyl diphosphate synthase (GGPPS), the two enz
71 report the inhibition of a human recombinant geranylgeranyl diphosphate synthase (GGPPSase) by 23 bis
72 way by generating combinatorial mutations in geranylgeranyl diphosphate synthase and levopimaradiene
73 ave expressed in Escerichia coli the enzymes geranylgeranyl diphosphate synthase and phytoene synthas
74 tional spruce IDS, a geranyl diphosphate and geranylgeranyl diphosphate synthase in white spruce (Pic
75 acts with a catalytic large subunit, such as geranylgeranyl diphosphate synthase, and determines its
76 e known to serve as inhibitors of the enzyme geranylgeranyl diphosphate synthase, and their activity
77 In contrast, a strain of E. coli carrying geranylgeranyl diphosphate synthase, phytoene desaturase
78 including farnesyl diphosphate synthase and geranylgeranyl diphosphate synthase, that catalyzes the
79 Unlike farnesyl diphosphate synthase and geranylgeranyl diphosphate synthase, which are homodimer
81 the first bifunctional farnesyl-diphosphate/geranylgeranyl-diphosphate synthase identified in eukary
82 o enzymes, farnesyl-diphosphate synthase and geranylgeranyl-diphosphate synthase, required for the pr
84 -erythritol-4-phosphate (MEP) pathway genes, geranylgeranyl diphosphate synthases 3 (GGPPS3) and GGPP
85 ound in polyprenyl synthases including FPPS, geranylgeranyl diphosphate synthases and hexaprenyl diph
86 ll subunit with the phylogenetically distant geranylgeranyl diphosphate synthases from Taxus canadens
87 f amino acid sequence identity (56-75%) with geranylgeranyl diphosphate synthases of plant origin.
88 eam pathways for isopentenyl diphosphate and geranylgeranyl diphosphate synthesis and the downstream
89 This study suggests that, in osteoclasts, geranylgeranyl diphosphate, the substrate for prenylatio
90 tive sites, the first for the cyclization of geranylgeranyl diphosphate to (+)-copalyl diphosphate an
91 se residues in catalyzing the cyclization of geranylgeranyl diphosphate to (+)-copalyl diphosphate.
92 andis), is synthesized by the cyclization of geranylgeranyl diphosphate to (-)-abieta-7(8),13(14)-die
93 that was catalytically active in converting geranylgeranyl diphosphate to a diterpene olefin that wa
94 y distinct cyclizations in the conversion of geranylgeranyl diphosphate to a mixture of abietadiene d
95 eaction involving the initial cyclization of geranylgeranyl diphosphate to a transient verticillyl ca
97 g diterpene cyclases that together transform geranylgeranyl diphosphate to ent-kaurene, the olefin pr
98 converts the universal diterpenoid precursor geranylgeranyl diphosphate to syn-CPP catalyzes the comm
99 ynthesis of Taxol involve the cyclization of geranylgeranyl diphosphate to taxa-4(5),11(12)-diene fol
100 has been shown to involve the cyclization of geranylgeranyl diphosphate to taxa-4(5),11(12)-diene.
101 atalyzes the transfer of a prenyl group from geranylgeranyl diphosphate to the carboxy-terminal cyste
102 oth the protonation-initiated cyclization of geranylgeranyl diphosphate to the intermediate (+)-copal
103 rming the ubiquitous isoprenoid intermediate geranylgeranyl diphosphate to the parent olefin with a t
104 hase) for conversion of the acyclic, achiral geranylgeranyl diphosphate to the polycyclic, chiral abi
105 , converts the universal diterpene precursor geranylgeranyl diphosphate to the stable bicyclic interm
107 ranyl diphosphate, farnesyl diphosphate, and geranylgeranyl diphosphate, to the parent structures of
109 ate from the universal diterpenoid precursor geranylgeranyl diphosphate was also mapped to this same
110 ubation of Ypt1p with PGGTase-II, Msi4p, and geranylgeranyl diphosphate was digested with trypsin.
112 ega,E,Z-farnesyl diphosphate, or omega,E,E,E-geranylgeranyl diphosphate, with Km values for the allyl
113 or 5',6' bond positions of lycopene but not geranylgeranyl diphosphate, zeta-carotene, or phytoene.
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