Results
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| Property | Organism | Value | Units | ID | Details |
|---|---|---|---|---|---|
| Inorganic reactions as energy sources for bacterial growth | bacteria | Table - link | N/A | 105831 | Harold, F. M. The Vital... |
| Oxidant range of reactivity-A range of 11 orders of magnitude for the second-order rate constants in the reaction of various oxidants with methionine (at neutral pH, in water) | Unspecified | Table - link | M^-1×sec^-1 | 114091 | Sies H et al., Oxidative... |
| Changes of Gibbs free energies under standard conditions in hydrogen-consuming reactions involved in interspecies hydrogen transfer | Generic | Table - link | N/A | 108746 | Stanley Falkow, Eugene... |
| Most prominent redox reactions in landfill leachate plumes | Biosphere | Table - link | N/A | 104565 | Christensen et al, B... |
| Changes of Gibbs free energies under standard conditions in hydrogen-releasing and hydrogen-consuming reactions and corresponding redox potentials | Generic | Table - link | N/A | 104423 | Schink B. Energetics... |
| Extracellular H2O2 (hydrogen peroxide) concentration required to activate the OxyR regulon | Bacteria Escherichia coli | 1 | μM | 112949 | Imlay JA. The molecular... |
| Typical range of kcat/Km (rate constants) for reactions between H2O2 (hydrogen peroxide) and the dehydratases and mononuclear enzymes and half-time for enzyme inactivation by H2O2 | Bacteria Escherichia coli | kcat/Km 10^3 to 10^4M^−1×s^−1: half-time for enzyme inactivation 20min | N/A | 112945 | Imlay JA. The molecular... |
| Intracellular H2O2 (hydrogen peroxide) levels result in (and see comments section): | Bacteria Escherichia coli | OxyR system is calibrated when H2O2 reaches ~200nM: growth defects become evident at 400nM | nM | 112947 | Imlay JA. The molecular... |
| Number of ATP produced in glycolysis | Generic | 2 | ATPs/glucose molecule | 110681 | Fan J, Kamphorst JJ, Mathew R... |
| Number of ATP produced in oxidative phosphorylation | Generic | on average 2.5 ATPs per NADH oxidation and 1.5 ATP per FADH2 oxidation | N/A | 110682 | Fan J, Kamphorst JJ, Mathew R... |
| Rate constant (kcat/Km) for inactivation of dehydratases and mononuclear enzymes by O2− (superoxide) and half-time for enzyme inactivation by O2- | Bacteria Escherichia coli | kcat/Km >10^6M^−1×s^−1: half-time for enzyme inactivation 20min | N/A | 112950 | Imlay JA. The molecular... |
| The rate constant for Fe–S cluster damage by O2− (superoxide) in dehydratase and O2- concentration in wildtype | Bacteria Escherichia coli | kcat/Km ≤5×10^6M^−1×s^−1: O2− concentration in wildtype cell 10^−10M | N/A | 112963 | Imlay JA. The molecular... |
| Titre and rate constant (kcat/Km) of superoxide dismutases (SODs) and steady state O2− (superoxide) concentration | Bacteria Escherichia coli | SOD titre 20μM: SOD kcat/Km 10^9M^−1×s^−1: O2− steady-state concentration ~0.2nM | N/A | 112948 | Imlay JA. The molecular... |
| Evolution of oxygenic photosynthesis by cyanobacteria | Biosphere | ~2.8 | Billion years ago | 114975 | Kihara S, Hartzler DA... |
| Theoretical and observed carbon fixation for Thiobacillus species | Bacteria Thiobacillus | Table - link | N/A | 103644 | Donovan P. Kelly, Th... |
| Half-time for repair of dehydratase clusters | Bacteria Escherichia coli | ~5 | min | 112946 | Imlay JA. The molecular... |
| Circulating concentration of acetate | Human Homo sapiens | 0.17 | mM | 111963 | Philip W. Wertz, The... |
| Redox potential of (H2PO2)-/P | Generic | -922 | mV | 104420 | Schink B, Friedrich M.... |
| Redox potential of P/Phosphine | Generic | -525 | mV | 104421 | Schink B, Friedrich M.... |
| Redox potential of (HPO4)2-/(HPO3)2- | Generic | -690 | mV | 104418 | Schink B, Friedrich M.... |