Turnover number of F1F0 ATP synthase when inactivating a percentage of the ATPase with DCCD (N,N-dicyclohexylcarbodiimide)
|
Bacteria Escherichia coli |
270 (±40) |
sec^-1 |
115178 |
Tomashek JJ, Glagoleva OB... |
Fraction of phosphorylation sites that may be nonfunctional
|
Eukaryotes |
≤65 |
% |
113381 |
Vlastaridis P et al.... |
Fraction of minimal theoretical ATP requirement consumed by translation
|
Unspecified |
>70 |
% |
111918 |
Pontes MH, Sevostyanova A... |
Turnover number of F1F0 ATP synthase in non-DCCD (N,N-dicyclohexylcarbodiimide)-treated membranes
|
Bacteria Escherichia coli |
ATP synthesis 82: ATP hydrolysis 425 |
sec^-1 |
115179 |
Tomashek JJ, Glagoleva OB... |
Fraction of intracellular ATP that may be utilized by protein kinases for phosphorylating their numerous targets
|
Yeast |
≤23 |
% |
113380 |
Vlastaridis P et al.... |
Fraction of total ATP turnover that is ATP consumption to maintain protein levels in the absence of growth in vitro
|
Mammals |
in isolated rabbit reticulocytes 50%: in cultured mice ascites tumour cells 36% |
% |
113243 |
Brown GC. Total cell... |
Decrease in conductance of voltage-dependent anion channel 1 (VDAC1) in the presence of ATP
|
Mitochondria |
42 |
% |
116637 |
Choudhary OP, Paz A,... |
Rate of ATP passage in voltage-dependent anion channel 1 (VDAC1) in the absence of a membrane potential in vitro
|
Mitochondria |
millions (of) |
ATP/sec |
116550 |
Choudhary OP, Paz A,... |
Diffusion coefficient of ATP in voltage-dependent anion channel (VDAC)
|
Mitochondria |
16 - 33 |
µm^2/sec |
116638 |
Rostovtseva TK, Bezrukov... |
Rate of ATP passage in voltage-dependent anion channel 1 (VDAC1) under physiological conditions
|
Mitochondria |
≤100000 |
ATP/sec |
116548 |
Choudhary OP, Paz A,... |
ATP flux through VDAC1 (voltage-dependent anion channel 1) in high ATP concentrations
|
Bread mold Neurospora crassa |
50000 |
ATP/sec |
116877 |
Choudhary OP, Paz A,... |
Cost of degradation of a single protein with proteasome
|
Eukaryotes |
100 - 200 |
~P (ATP) |
112155 |
Michael Lynch and Georgi... |
Cost of opening an origin of replication [ORI]
|
Unspecified |
≤20 |
~P (ATP) |
112151 |
Michael Lynch and Georgi... |
Number of NADH produced per ATP produced
|
Bacteria Escherichia coli |
in acetate fermentation 1 to 1: in respiration 2.5 to 1 |
NADH per ATP |
114728 |
Szenk M, Dill KA, de... |
Cost of assembly of the sliding clamp associated with the polymerase in DNA replication
|
Microbes |
2 - 4 |
~P (ATP)/event |
112152 |
Michael Lynch and Georgi... |
Cost of amino-acid export from lysosome back to cytoplasm
|
Metazoa animals |
~1 |
~P (ATP)/3-4 amino acids |
112156 |
Michael Lynch and Georgi... |
Maximum percentage of ATP that is utilized out of that produced in substrate cycles
|
Sunflower Helianthus annuus |
20 |
% |
108772 |
Alonso AP, Goffman FD... |
Energy required to reduce carbon in the Calvin‐Benson cycle
|
Chloroplast |
590 |
kJ/mol |
116863 |
Kranz SA, Young JN, Hopkinson... |
Percentage of ATP produced that is used for biomass production
|
Sunflower Helianthus annuus |
~11 |
% |
108773 |
Alonso AP, Goffman FD... |
ATP that could be produced via mitochondrial respiration
|
Sunflower Helianthus annuus |
3708 |
nmol ATP/h/embryo |
108769 |
Alonso AP, Goffman FD... |