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1 hiolate of C221 and the keto carbon of the 2-oxoacid.
2 teracts with the C4-methyl of 4(S)-hydroxy-2-oxoacids.
3 fatty acid hydroperoxides into aldehydes and oxoacids.
4 s the alpha-amino group of l-Lys to acceptor oxoacids.
5                   Biotransformation of gamma-oxoacid 5, in the culture of Beauveria bassiana AM278 an
6 ow concentrations of sulfuric acid or iodine oxoacids above 10(5) cm(-3), reaching rates around 30 cm
7 that is required for aerobic metabolism of 2-oxoacids and for C(1) metabolism.
8 echanisms involving organics, amines, iodine oxoacids and HNO(3) probably dominate NPF in most region
9 ocess is almost exclusively driven by iodine oxoacids and iodine oxide vapours, with average oxygen-t
10                                       Iodine oxoacids and iodine oxides are observed in newly formed
11 in exocytosis for glucose and branched-chain oxoacids as secretagogues (it does so partially for fatt
12 te and multiple independent innovations of 2-oxoacid-binding basic residues among these superfamilies
13 cted to enable the binding of 4(R)-hydroxy-2-oxoacids by relieving the steric hindrance between the 5
14 tivated receptor-alpha (decreased by 51%), 3-oxoacid CoA transferase (decreased by 67%), and acetyl-C
15  of the key ketolytic enzyme, succinyl-CoA:3-oxoacid CoA transferase (SCOT; encoded by Oxct1), as wel
16 drial enzyme CoA transferase (succinyl-CoA:3-oxoacid CoA transferase, SCOT, encoded by nuclear Oxct1)
17 fied with partial sequence as succinyl-CoA:3-oxoacid CoA-transferase (SCOT; EC ).
18 ses the catalytic activity of succinyl-CoA:3-oxoacid CoA-transferase, and induces aggregation of mito
19 pression of the gene encoding succinyl-CoA:3-oxoacid-CoA transferase, the rate-limiting enzyme for my
20 arate dehydrogenase (OGDH), branched-chain 2-oxoacid dehydrogenase (BCKDH), and pyruvate dehydrogenas
21 enase complex (PDC-E2), the branched chain 2-oxoacid dehydrogenase complex E (BCOADC-E2), and the 2-o
22 is mechanism could be a general feature of 2-oxoacid dehydrogenase complexes because such interfacial
23 her NAD(P)H/NAD(P)(+) ratios, although the 2-oxoacid dehydrogenase complexes produced superoxide/H2O2
24 ase activity data indicate that all of the 2-oxoacid dehydrogenase components are present.
25  catalyzed by the E1 and E2 enzymes of the 2-oxoacid dehydrogenase multienzyme complexes by a previou
26 e for anti-M2 antibodies reacting with the 2-oxoacid-dehydrogenase complex (ODC) also antibodies to t
27 substrates as well as lipoic acid from two 2-oxoacid dehydrogenases and an isolated lipoylated lipoyl
28 hed cofactor essential for the activity of 2-oxoacid dehydrogenases and the glycine cleavage system.
29 e lipoyl domains of the E2 subunits of the 2-oxoacid dehydrogenases of aerobic metabolism.
30  for octanoylation of the E2 components of 2-oxoacid dehydrogenases to provide the substrates of LipA
31   Lipoamidase-mediated inactivation of the 2-oxoacid dehydrogenases was observed both in vivo and in
32 egrity, thus modulating lipoate-containing 2-oxoacid dehydrogenases with consequent control over glyc
33 poic acid in the reaction mechanism of the 2-oxoacid dehydrogenases, the identity of the lipoamidase
34 ich are generally the E2 components of the 2-oxoacid dehydrogenases.
35 ate salvage, shows no interaction with the 2-oxoacid dehydrogenases.
36 a-helix type structures of the Fe(II)- and 2-oxoacid-dependent dioxygenases, such as collagen prolyl
37 berate, completing three iterations of the 2-oxoacid elongation pathway.
38 aldococcus jannaschii uses three different 2-oxoacid elongation pathways, which extend the chain leng
39                  Like other members of the 2-oxoacid:ferredoxin oxidoreductase family, OOR contains t
40 (4) is frequently found together with iodine oxoacids [HIO(x), i.e., iodic acid (HIO(3)) and iodous a
41 substrate substitutes reveals that certain 2-oxoacids, including naturally present metabolites, manif
42 ly bonded dimers and trimers of the starting oxoacids, many of which are multi-tailed lipids.
43 ) modulation of IDH1/2 variant activity by 2-oxoacid natural products, including some present in comm
44 y, based on microbial lactonization of gamma-oxoacids, naturally occurring opposite isomers of whisky
45 e, and several other amino acids to generate oxoacids or derived products in vitro.
46 ogenic active site AspH variants by use of 2-oxoacids, or 2-oxoacid precursors, other than 2OG.
47  (i) IDH1/2 variant-catalyzed reduction of 2-oxoacids other than 2OG in cells, (ii) modulation of IDH
48        Our measurements indicate that iodine oxoacid particle formation can compete with sulfuric aci
49 ite AspH variants by use of 2-oxoacids, or 2-oxoacid precursors, other than 2OG.
50 t acetone; this simple procedure affords the oxoacid salt in 94% yield.
51 e now available to create chiral 4-hydroxy-2-oxoacid skeletons as synthons for organic reactions.
52 h rates only when oxidizing their specific 2-oxoacid substrates and not in the reverse reaction from
53                   The 3,3,3-trisubstituted 2-oxoacids thus produced were converted into 2-oxolactones
54 es the aldol addition of 3,3-disubstituted 2-oxoacids to aldehydes catalyzed by metal dependent 3-met
55 s demonstrating differential expression of 3-oxoacid transferase, the key enzyme for ketolytic energy
56 tate aminotransferase [Got2] and hydroxyacid-oxoacid transhydrogenase [Adhfe1]).
57                                    The alkyl oxoacids under study here can undergo a Norrish Type II
58  of HIF-1 hydroxylation by glucose-derived 2-oxoacids underlies the prominent basal HIF-1 activity co
59  variants are able to synthesize 4-hydroxy-2-oxoacids up to eight carbons in length, which were the o
60  carbon-carbon bond formation of 4-hydroxy-2-oxoacids up to eight carbons in length.
61  proteolysis and sequencing, but the bound 2-oxoacid was released during the protocol.
62              OOR also oxidizes a few other 2-oxoacids (which do not induce OOR) also without any requ