EC Number | Cloned (Comment) | Organism |
---|---|---|
7.1.2.2 | gene atpZ, encoded in the atp operon, sequence comparison, overview | Alkalihalophilus pseudofirmus |
7.1.2.2 | sequence comparison, overview | Bacillus sp. (in: Bacteria) |
7.1.2.2 | sequence comparison, overview | Bacillus licheniformis |
7.1.2.2 | sequence comparison, overview | Halalkalibacterium halodurans |
7.1.2.2 | sequence comparison, overview | Alkalihalobacillus clausii |
7.1.2.2 | sequence comparison, overview | Oceanobacillus iheyensis |
7.1.2.2 | sequence comparison, overview | Geobacillus kaustophilus |
7.1.2.2 | sequence comparison, overview | Bacillus subtilis subsp. subtilis |
EC Number | Protein Variants | Comment | Organism |
---|---|---|---|
7.1.2.2 | additional information | polar deletion of atpI, atpZ or a double atpIZ deletion result in a defect in nonfermentative growth at pH 7.5 that is especially pronounced at suboptimal Mg2+ concentration | Alkalihalophilus pseudofirmus |
EC Number | Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|---|
7.1.2.2 | membrane | - |
Bacillus sp. (in: Bacteria) | 16020 | - |
7.1.2.2 | membrane | - |
Bacillus licheniformis | 16020 | - |
7.1.2.2 | membrane | - |
Bacillus amyloliquefaciens | 16020 | - |
7.1.2.2 | membrane | - |
Bacillus pumilus | 16020 | - |
7.1.2.2 | membrane | - |
Bacillus mycoides | 16020 | - |
7.1.2.2 | membrane | - |
Bacillus thuringiensis | 16020 | - |
7.1.2.2 | membrane | - |
Halalkalibacterium halodurans | 16020 | - |
7.1.2.2 | membrane | - |
Anoxybacillus flavithermus | 16020 | - |
7.1.2.2 | membrane | - |
Carboxydothermus hydrogenoformans | 16020 | - |
7.1.2.2 | membrane | - |
Geobacillus thermodenitrificans | 16020 | - |
7.1.2.2 | membrane | - |
Bacillus anthracis | 16020 | - |
7.1.2.2 | membrane | - |
Alkalihalobacillus clausii | 16020 | - |
7.1.2.2 | membrane | - |
Oceanobacillus iheyensis | 16020 | - |
7.1.2.2 | membrane | - |
Geobacillus kaustophilus | 16020 | - |
7.1.2.2 | membrane | - |
Pelotomaculum thermopropionicum | 16020 | - |
7.1.2.2 | membrane | - |
Bacillus subtilis subsp. subtilis | 16020 | - |
7.1.2.2 | membrane | - |
Desulforamulus reducens | 16020 | - |
7.1.2.2 | membrane | - |
Alkalihalophilus pseudofirmus | 16020 | - |
7.1.2.2 | membrane | - |
Candidatus Desulforudis audaxviator | 16020 | - |
7.1.2.2 | membrane | - |
Exiguobacterium sibiricum | 16020 | - |
EC Number | Metals/Ions | Comment | Organism | Structure |
---|---|---|---|---|
7.1.2.2 | Mg2+ | required | Bacillus sp. (in: Bacteria) | |
7.1.2.2 | Mg2+ | required | Bacillus licheniformis | |
7.1.2.2 | Mg2+ | required | Bacillus amyloliquefaciens | |
7.1.2.2 | Mg2+ | required | Bacillus pumilus | |
7.1.2.2 | Mg2+ | required | Bacillus mycoides | |
7.1.2.2 | Mg2+ | required | Bacillus thuringiensis | |
7.1.2.2 | Mg2+ | required | Halalkalibacterium halodurans | |
7.1.2.2 | Mg2+ | required | Anoxybacillus flavithermus | |
7.1.2.2 | Mg2+ | required | Carboxydothermus hydrogenoformans | |
7.1.2.2 | Mg2+ | required | Geobacillus thermodenitrificans | |
7.1.2.2 | Mg2+ | required | Bacillus anthracis | |
7.1.2.2 | Mg2+ | required | Alkalihalobacillus clausii | |
7.1.2.2 | Mg2+ | required | Oceanobacillus iheyensis | |
7.1.2.2 | Mg2+ | required | Geobacillus kaustophilus | |
7.1.2.2 | Mg2+ | required | Pelotomaculum thermopropionicum | |
7.1.2.2 | Mg2+ | required | Bacillus subtilis subsp. subtilis | |
7.1.2.2 | Mg2+ | required | Desulforamulus reducens | |
7.1.2.2 | Mg2+ | required | Alkalihalophilus pseudofirmus | |
7.1.2.2 | Mg2+ | required | Candidatus Desulforudis audaxviator | |
7.1.2.2 | Mg2+ | required | Exiguobacterium sibiricum |
EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
7.1.2.2 | ATP + H2O + H+/in | Bacillus sp. (in: Bacteria) | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Bacillus licheniformis | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Bacillus amyloliquefaciens | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Bacillus pumilus | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Bacillus mycoides | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Bacillus thuringiensis | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Halalkalibacterium halodurans | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Anoxybacillus flavithermus | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Carboxydothermus hydrogenoformans | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Geobacillus thermodenitrificans | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Bacillus anthracis | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Alkalihalobacillus clausii | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Oceanobacillus iheyensis | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Geobacillus kaustophilus | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Pelotomaculum thermopropionicum | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Bacillus subtilis subsp. subtilis | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Desulforamulus reducens | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Alkalihalophilus pseudofirmus | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Candidatus Desulforudis audaxviator | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Exiguobacterium sibiricum | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Bacillus sp. (in: Bacteria) TA2.A1 | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Bacillus anthracis Ames | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Exiguobacterium sibiricum 255-15 | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Carboxydothermus hydrogenoformans Z-2901 / DSM 6008 | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Pelotomaculum thermopropionicum SI | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Alkalihalophilus pseudofirmus OF4 | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Bacillus amyloliquefaciens FZB42 | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Bacillus pumilus SAFR-032 | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Oceanobacillus iheyensis HTE83 | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Candidatus Desulforudis audaxviator MP104C | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Bacillus thuringiensis Al Hakam | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Bacillus mycoides KBAB4 | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Desulforamulus reducens MI-1 | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Alkalihalobacillus clausii DSM 23117 | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Halalkalibacterium halodurans C-125 | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Anoxybacillus flavithermus WK1 | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Bacillus licheniformis ATCC 14580 | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Geobacillus thermodenitrificans NG80-2 | - |
ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | Bacillus subtilis subsp. subtilis 168 | - |
ADP + phosphate + H+/out | - |
r |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
7.1.2.2 | Alkalihalobacillus clausii | - |
- |
- |
7.1.2.2 | Alkalihalobacillus clausii DSM 23117 | - |
- |
- |
7.1.2.2 | Alkalihalophilus pseudofirmus | Q9EXJ9 | gene atpZ | - |
7.1.2.2 | Alkalihalophilus pseudofirmus OF4 | Q9EXJ9 | gene atpZ | - |
7.1.2.2 | Anoxybacillus flavithermus | - |
- |
- |
7.1.2.2 | Anoxybacillus flavithermus WK1 | - |
- |
- |
7.1.2.2 | Bacillus amyloliquefaciens | - |
- |
- |
7.1.2.2 | Bacillus amyloliquefaciens FZB42 | - |
- |
- |
7.1.2.2 | Bacillus anthracis | - |
- |
- |
7.1.2.2 | Bacillus anthracis Ames | - |
- |
- |
7.1.2.2 | Bacillus licheniformis | - |
DSM 13 | - |
7.1.2.2 | Bacillus licheniformis ATCC 14580 | - |
DSM 13 | - |
7.1.2.2 | Bacillus mycoides | - |
- |
- |
7.1.2.2 | Bacillus mycoides KBAB4 | - |
- |
- |
7.1.2.2 | Bacillus pumilus | - |
- |
- |
7.1.2.2 | Bacillus pumilus SAFR-032 | - |
- |
- |
7.1.2.2 | Bacillus sp. (in: Bacteria) | - |
- |
- |
7.1.2.2 | Bacillus sp. (in: Bacteria) TA2.A1 | - |
- |
- |
7.1.2.2 | Bacillus subtilis subsp. subtilis | - |
- |
- |
7.1.2.2 | Bacillus subtilis subsp. subtilis 168 | - |
- |
- |
7.1.2.2 | Bacillus thuringiensis | - |
- |
- |
7.1.2.2 | Bacillus thuringiensis Al Hakam | - |
- |
- |
7.1.2.2 | Candidatus Desulforudis audaxviator | - |
- |
- |
7.1.2.2 | Candidatus Desulforudis audaxviator MP104C | - |
- |
- |
7.1.2.2 | Carboxydothermus hydrogenoformans | - |
- |
- |
7.1.2.2 | Carboxydothermus hydrogenoformans Z-2901 / DSM 6008 | - |
- |
- |
7.1.2.2 | Desulforamulus reducens | - |
- |
- |
7.1.2.2 | Desulforamulus reducens MI-1 | - |
- |
- |
7.1.2.2 | Exiguobacterium sibiricum | - |
- |
- |
7.1.2.2 | Exiguobacterium sibiricum 255-15 | - |
- |
- |
7.1.2.2 | Geobacillus kaustophilus | - |
- |
- |
7.1.2.2 | Geobacillus thermodenitrificans | - |
- |
- |
7.1.2.2 | Geobacillus thermodenitrificans NG80-2 | - |
- |
- |
7.1.2.2 | Halalkalibacterium halodurans | - |
- |
- |
7.1.2.2 | Halalkalibacterium halodurans C-125 | - |
- |
- |
7.1.2.2 | Oceanobacillus iheyensis | - |
- |
- |
7.1.2.2 | Oceanobacillus iheyensis HTE83 | - |
- |
- |
7.1.2.2 | Pelotomaculum thermopropionicum | - |
- |
- |
7.1.2.2 | Pelotomaculum thermopropionicum SI | - |
- |
- |
EC Number | Reaction | Comment | Organism | Reaction ID |
---|---|---|---|---|
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Bacillus sp. (in: Bacteria) | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Bacillus licheniformis | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Bacillus amyloliquefaciens | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Bacillus pumilus | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Bacillus mycoides | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Bacillus thuringiensis | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Halalkalibacterium halodurans | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Anoxybacillus flavithermus | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Carboxydothermus hydrogenoformans | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Geobacillus thermodenitrificans | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Bacillus anthracis | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Alkalihalobacillus clausii | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Oceanobacillus iheyensis | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Geobacillus kaustophilus | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Pelotomaculum thermopropionicum | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Bacillus subtilis subsp. subtilis | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Desulforamulus reducens | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Alkalihalophilus pseudofirmus | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Candidatus Desulforudis audaxviator | |
7.1.2.2 | ATP + H2O + 4 H+[side 1] = ADP + phosphate + 4 H+[side 2] | reaction mechanism, cytoplasmic pH homeostasis and the problem it creates for protonmotive force-driven ATP synthesis, adaptive mechanisms, comparison of alkaliphiles and neutralophiles, detailed overview | Exiguobacterium sibiricum |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
7.1.2.2 | ATP + H2O + H+/in | - |
Bacillus sp. (in: Bacteria) | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Bacillus licheniformis | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Bacillus amyloliquefaciens | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Bacillus pumilus | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Bacillus mycoides | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Bacillus thuringiensis | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Halalkalibacterium halodurans | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Anoxybacillus flavithermus | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Carboxydothermus hydrogenoformans | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Geobacillus thermodenitrificans | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Bacillus anthracis | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Alkalihalobacillus clausii | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Oceanobacillus iheyensis | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Geobacillus kaustophilus | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Pelotomaculum thermopropionicum | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Bacillus subtilis subsp. subtilis | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Desulforamulus reducens | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Alkalihalophilus pseudofirmus | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Candidatus Desulforudis audaxviator | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Exiguobacterium sibiricum | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Bacillus sp. (in: Bacteria) | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Bacillus licheniformis | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Bacillus amyloliquefaciens | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Bacillus pumilus | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Bacillus mycoides | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Bacillus thuringiensis | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Halalkalibacterium halodurans | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Anoxybacillus flavithermus | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Carboxydothermus hydrogenoformans | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Geobacillus thermodenitrificans | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Bacillus anthracis | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Alkalihalobacillus clausii | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Oceanobacillus iheyensis | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Geobacillus kaustophilus | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Pelotomaculum thermopropionicum | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Bacillus subtilis subsp. subtilis | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Desulforamulus reducens | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Alkalihalophilus pseudofirmus | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Candidatus Desulforudis audaxviator | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Exiguobacterium sibiricum | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Bacillus sp. (in: Bacteria) TA2.A1 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Bacillus sp. (in: Bacteria) TA2.A1 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Bacillus anthracis Ames | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Bacillus anthracis Ames | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Exiguobacterium sibiricum 255-15 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Exiguobacterium sibiricum 255-15 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Carboxydothermus hydrogenoformans Z-2901 / DSM 6008 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Carboxydothermus hydrogenoformans Z-2901 / DSM 6008 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Pelotomaculum thermopropionicum SI | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Pelotomaculum thermopropionicum SI | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Alkalihalophilus pseudofirmus OF4 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Alkalihalophilus pseudofirmus OF4 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Bacillus amyloliquefaciens FZB42 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Bacillus amyloliquefaciens FZB42 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Bacillus pumilus SAFR-032 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Bacillus pumilus SAFR-032 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Oceanobacillus iheyensis HTE83 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Oceanobacillus iheyensis HTE83 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Candidatus Desulforudis audaxviator MP104C | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Candidatus Desulforudis audaxviator MP104C | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Bacillus thuringiensis Al Hakam | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Bacillus thuringiensis Al Hakam | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Bacillus mycoides KBAB4 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Bacillus mycoides KBAB4 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Desulforamulus reducens MI-1 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Desulforamulus reducens MI-1 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Alkalihalobacillus clausii DSM 23117 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Alkalihalobacillus clausii DSM 23117 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Halalkalibacterium halodurans C-125 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Halalkalibacterium halodurans C-125 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Anoxybacillus flavithermus WK1 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Anoxybacillus flavithermus WK1 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Bacillus licheniformis ATCC 14580 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Bacillus licheniformis ATCC 14580 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Geobacillus thermodenitrificans NG80-2 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Geobacillus thermodenitrificans NG80-2 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | - |
Bacillus subtilis subsp. subtilis 168 | ADP + phosphate + H+/out | - |
r | |
7.1.2.2 | ATP + H2O + H+/in | protonmotive force- or sodium motive force-dependent ATP synthesis by a rotary mechanism, overview | Bacillus subtilis subsp. subtilis 168 | ADP + phosphate + H+/out | - |
r |
EC Number | Subunits | Comment | Organism |
---|---|---|---|
7.1.2.2 | More | subunit organisation model, overview | Bacillus sp. (in: Bacteria) |
7.1.2.2 | More | subunit organisation model, overview | Bacillus licheniformis |
7.1.2.2 | More | subunit organisation model, overview | Bacillus amyloliquefaciens |
7.1.2.2 | More | subunit organisation model, overview | Bacillus pumilus |
7.1.2.2 | More | subunit organisation model, overview | Bacillus mycoides |
7.1.2.2 | More | subunit organisation model, overview | Bacillus thuringiensis |
7.1.2.2 | More | subunit organisation model, overview | Halalkalibacterium halodurans |
7.1.2.2 | More | subunit organisation model, overview | Anoxybacillus flavithermus |
7.1.2.2 | More | subunit organisation model, overview | Carboxydothermus hydrogenoformans |
7.1.2.2 | More | subunit organisation model, overview | Geobacillus thermodenitrificans |
7.1.2.2 | More | subunit organisation model, overview | Bacillus anthracis |
7.1.2.2 | More | subunit organisation model, overview | Alkalihalobacillus clausii |
7.1.2.2 | More | subunit organisation model, overview | Oceanobacillus iheyensis |
7.1.2.2 | More | subunit organisation model, overview | Geobacillus kaustophilus |
7.1.2.2 | More | subunit organisation model, overview | Pelotomaculum thermopropionicum |
7.1.2.2 | More | subunit organisation model, overview | Bacillus subtilis subsp. subtilis |
7.1.2.2 | More | subunit organisation model, overview | Desulforamulus reducens |
7.1.2.2 | More | subunit organisation model, overview | Alkalihalophilus pseudofirmus |
7.1.2.2 | More | subunit organisation model, overview | Candidatus Desulforudis audaxviator |
7.1.2.2 | More | subunit organisation model, overview | Exiguobacterium sibiricum |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
7.1.2.2 | AtpZ | - |
Alkalihalophilus pseudofirmus |
7.1.2.2 | F1F0-ATP synthase | - |
Geobacillus thermodenitrificans |
7.1.2.2 | F1F0-ATP synthase | - |
Desulforamulus reducens |
7.1.2.2 | F1FO-ATP synthase | - |
Bacillus sp. (in: Bacteria) |
7.1.2.2 | F1FO-ATP synthase | - |
Bacillus licheniformis |
7.1.2.2 | F1FO-ATP synthase | - |
Bacillus amyloliquefaciens |
7.1.2.2 | F1FO-ATP synthase | - |
Bacillus pumilus |
7.1.2.2 | F1FO-ATP synthase | - |
Bacillus mycoides |
7.1.2.2 | F1FO-ATP synthase | - |
Bacillus thuringiensis |
7.1.2.2 | F1FO-ATP synthase | - |
Halalkalibacterium halodurans |
7.1.2.2 | F1FO-ATP synthase | - |
Anoxybacillus flavithermus |
7.1.2.2 | F1FO-ATP synthase | - |
Carboxydothermus hydrogenoformans |
7.1.2.2 | F1FO-ATP synthase | - |
Bacillus anthracis |
7.1.2.2 | F1FO-ATP synthase | - |
Alkalihalobacillus clausii |
7.1.2.2 | F1FO-ATP synthase | - |
Oceanobacillus iheyensis |
7.1.2.2 | F1FO-ATP synthase | - |
Geobacillus kaustophilus |
7.1.2.2 | F1FO-ATP synthase | - |
Pelotomaculum thermopropionicum |
7.1.2.2 | F1FO-ATP synthase | - |
Bacillus subtilis subsp. subtilis |
7.1.2.2 | F1FO-ATP synthase | - |
Alkalihalophilus pseudofirmus |
7.1.2.2 | F1FO-ATP synthase | - |
Candidatus Desulforudis audaxviator |
7.1.2.2 | F1FO-ATP synthase | - |
Exiguobacterium sibiricum |
EC Number | General Information | Comment | Organism |
---|---|---|---|
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Bacillus sp. (in: Bacteria) |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Bacillus licheniformis |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Bacillus amyloliquefaciens |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Bacillus pumilus |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Bacillus mycoides |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Bacillus thuringiensis |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Halalkalibacterium halodurans |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Anoxybacillus flavithermus |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Carboxydothermus hydrogenoformans |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Geobacillus thermodenitrificans |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Bacillus anthracis |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Alkalihalobacillus clausii |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Oceanobacillus iheyensis |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Geobacillus kaustophilus |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Pelotomaculum thermopropionicum |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Bacillus subtilis subsp. subtilis |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Desulforamulus reducens |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Alkalihalophilus pseudofirmus |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Candidatus Desulforudis audaxviator |
7.1.2.2 | evolution | ATP synthases of alkaliphilic bacteria and, in particular, those that successfully overcome the bioenergetic challenges of achieving robust H+-coupled ATP synthesis at external pH values of over 10. ATP synthesis in alkaliphiles depends upon alkaliphile-specific adaptations of the ATP synthase and there is also evidence for alkaliphile-specific adaptations of respiratory chain components. The protonmotive force is lowered at a very high pH by the need to maintain a cytoplasmic pH well below the pH outside, which results in an energetically adverse pH gradient, overview | Exiguobacterium sibiricum |