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1 ive interactions of bacteria at the membrane-substrate level.
2 tracking is integral to the structure at the substrate level.
3 ense oligonucleotides in the presence of low substrate level.
4 reased enzyme activity and not to changes in substrate level.
5 the enhancement of the metabolic rate at the substrate level.
6  of gut microbial carbohydrate metabolism at substrate levels.
7 ells were correlated with >50% reductions in substrate levels.
8 nd contribution to the control of conjugated-substrate levels.
9 ovide a complete model for the enzyme at all substrate levels.
10 des expressions for response time and active substrate levels.
11  autophagy upregulation and lowers autophagy substrate levels.
12  relative to the enzyme turnover at ug L(-1) substrate levels.
13 t to alter both dynamic and steady-state ADO substrate levels.
14 c reactions, transporters, cofactors, enzyme substrate-level activation and inhibition relationships,
15                                         This substrate-level activation does not require autophosphor
16 doxin, which increases the efficiency of the substrate level and electron transport phosphorylations.
17 reference, adapting to the prevailing plasma substrate levels and hormonal milieu, but in type 1 diab
18 sm that allows SM to accommodate fluctuating substrate levels and may contribute to its widely report
19 mote interorgan signaling that alters muscle substrate levels and metabolism, thereby contributing to
20 n the KO background reverted both NUDT3 mRNA substrate levels and P-body counts to those of wild-type
21 rs to run with a constant speed at different substrate levels and, therefore, is a substantial criter
22 A (alpha-GalA) activities, glycosphingolipid substrate levels, and in vitro mutation expression were
23 y by acetylation and OAA accumulation at the substrate level are two strategies for the host to respo
24 than competitive inhibitors when the natural substrate levels are high.
25 tate production and a significant portion of substrate-level ATP produced anaerobically, were tested
26 romote anaerobic metabolism and thus sustain substrate-level ATP production.
27 rwise inaccessible parameters such as active substrate levels, b) accurate response-time predictions
28 ions and/or contributions from oxidative and substrate-level bioenergetics is unknown.
29 t mammalian antioxidant, is regulated at the substrate level by cysteine, which is synthesized from h
30                       Adenine nucleotides at substrate level concentrations inhibit the reaction of L
31                           We also reveal the substrate-level control of adenosine triphosphate (ATP)-
32 unded plants, but that the AOS hydroperoxide substrate levels, controlled by upstream enzymes (lipoxy
33 rometry-based enzyme functional analysis and substrate level-controlled enzyme kinetics consistently
34 tegy that allows acetic acid removal without substrate-level (de)phosphorylation may instead be emplo
35 the effects of metabolite concentrations and substrate-level enzyme regulation while identifying meta
36                              Yet, we provide substrate-level evidence for the functional role of thes
37 5Ac concentrations, thereby providing higher substrate levels for sialyltransferases.
38 ced oxidants, O(2) evolution, and metabolite substrates levels for glycogen synthesis in normal mediu
39 rial oxidative phosphorylation, increases in substrate level generation of ATP and reducing equivalen
40                           Plasma hormone and substrate levels, hepatic gluconeogenic gene expression,
41 relates with lowered pERK but unchanged pPKA substrate levels in D1 medium spiny neurons as well as i
42 ormation of synthetic prions and the role of substrate levels in their evolution.
43  associated negative PE occurred even at low substrate levels in this study could be attributed to li
44                          Interestingly, high substrate levels in vitro significantly reduce Cdc20 aut
45 tive interventions aiming at alleviating the substrate-level inhibition of key enzymes in order to en
46 idic operations, instrument portability, and substrate-level integration with other pre- and post-PCR
47  proteasome inhibition, and this increase in substrate level is consistent with the observed loss of
48 zation of genome-annotated, respiratory, and substrate-level lactate dehydrogenases (LDHs) from the o
49 erability of DA neurons and that enhancing G-substrate levels may be a neuroprotective strategy for t
50 e the complete inhibition of MOC, indicating substrate level phosphorylation and explicit anaerobic s
51 ondrial enzyme capable of ATP production via substrate level phosphorylation in the absence of oxygen
52 PHOS) with BDQ and simultaneously inhibiting substrate level phosphorylation via genetic disruption o
53 cations of oxygen consumption rate (OCR) and substrate level phosphorylation via glycolysis (i.e., vi
54 ion of acetate to methane that yields ATP by substrate level phosphorylation.
55 ee acids results in the formation of ATP via substrate level phosphorylation.
56 elding succinyl-CoA supporting mitochondrial substrate-level phosphorylation (mtSLP), releasing succi
57 robically generate ATP by intramitochondrial substrate-level phosphorylation and maintain DeltaPsi(m)
58                             Chemiosmosis and substrate-level phosphorylation are the 2 mechanisms emp
59              ATP is generated exclusively by substrate-level phosphorylation in hydrogenosomes, as op
60 ctions and is not fermentative, we find that substrate-level phosphorylation is its primary anaerobic
61 hate metabolism by linking acetyl CoA to the substrate-level phosphorylation of ADP.
62               In bloodstream-form organisms, substrate-level phosphorylation of glucose is sufficient
63 chanism is proposed for this unusual type of substrate-level phosphorylation reaction.
64 ed cells with Embden-Meyerhof glycolysis and substrate-level phosphorylation that lack the alpha-prot
65 oduce an acyl-CoA that is ultimately used in substrate-level phosphorylation to produce ATP.
66 tron acceptors, generates ATP primarily from substrate-level phosphorylation under anaerobic conditio
67                                        Since substrate-level phosphorylation via the Embden-Meyerhof
68 ive phosphorylation via the pmf, but also by substrate-level phosphorylation via the enzyme AckA.
69 te as the electron acceptor, consistent with substrate-level phosphorylation yielding a significant a
70 asses (e.g., fermentation pathways bypassing substrate-level phosphorylation), substrate channeling (
71 NAD(+)/NADH ratio, generate more ATP through substrate-level phosphorylation, and accumulate biomass
72 -derived polysaccharides that rely mostly on substrate-level phosphorylation, as they seem to lack mo
73 the central pathway does not gain net ATP by substrate-level phosphorylation, chemolithoautotrophic g
74 ding carbon fixation, the shikimate pathway, substrate-level phosphorylation, gluconeogenesis and gly
75           Oxidative pathways produce ATP via substrate-level phosphorylation, whereas reductive pathw
76 eased mitochondrial matrix-localized ATP via substrate-level phosphorylation.
77 n of hexokinase II and production of ATP via substrate-level phosphorylation.
78  hydrogenosomal-type pyruvate metabolism and substrate-level phosphorylation.
79 c acid cycle enzyme that conserves energy by substrate-level phosphorylation.
80 e ATP needed for cell growth is derived from substrate-level phosphorylation.
81 ounted for if ATP synthesis occurred only by substrate-level phosphorylation.
82           We investigated how mutant SPT and substrate levels regulate neurite growth.
83  is significantly higher than of disulfides, substrate level regulation favors the synthesis of H2S o
84      This suggests that OAP may be a form of substrate level regulation in PG biosynthesis.
85 ranscriptional and translational regulation, substrate-level regulation of enzyme activity, post-tran
86 se results reveal the critical importance of substrate-level regulation of spectrin cleavage for the
87  this balance between calpain activation and substrate-level regulation of spectrin cleavage is unkno
88 li74) core kinetic model for E. coli with 55 substrate-level regulations using the newly developed K-
89 457 model reactions, 337 metabolites and 295 substrate-level regulatory interactions.
90 differential effects of the two compounds on substrate levels that feed into starch synthesis and on
91 conditions of reduced mitogen or nutritional substrate levels, the serine/threonine kinase target of
92             PKA activity is regulated at the substrate level through interactions of PKA regulatory s
93 suggest that the early kinetic events at the substrate level ultimately govern successful chaperonin-
94 ne was adaptively regulated by extracellular substrate level via transcriptionally mediated mechanism
95           These structures provide the first substrate-level view of the local structural differences
96  enzyme); conversely, when the intracellular substrate level was reduced by methionine deprivation, t
97           IFG effects on GCase stability and substrate levels were evaluated in a mouse model (hG/4L/
98 ining other ESX systems, we found that ESX-1 substrate levels were increased in both the CF and OMM f