The Journal of biological chemistry · 2003
Cys32 and His105 are the critical residues for the calcium-dependent cysteine proteolytic activity of CvaB, an ATP-binding cassette transporter.
СтатьяПоддержка исследования: вне правительства СШАПоддержка службы здравоохранения СШАНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Wu Kai-Hui, Tai Phang C
Аннотация
CvaB, a member of the ATP-binding cassette transporter superfamily, is the central membrane transporter of the colicin V secretion system in Escherichia coli. Cys32 and His105 in the N-terminal domain of CvaB were identified as critical residues for both colicin V secretion and cysteine proteolytic activity. By inhibiting degradation with N-ethylmaleimide and a mixture of protease inhibitors, a stable wild-type N-terminal domain (which showed cysteine protease activity when activated) was purified. Such protease activity was Ca2+- and concentration-dependent and could be inhibited by antipain, N-ethylmaleimide, EDTA, and EGTA. At low concentrations, the Ca2+ analogs Tb3+ and La3+ (but not Fe3+) significantly enhanced proteolytic activity, suggesting that the size of the cations is important for activity. Together with comparisons of the sequences of members of the cysteine protease family, these results indicate that Cys32 and His105 are the critical residues in the CvaB N-terminal domain for the calcium-dependent cysteine protease activity and secretion of colicin V.
Предметные рубрики MeSH
ATP-Binding Cassette TransportersAmino Acid SequenceAnimalsBlotting, WesternCalciumCalpainCell DivisionColicinsCulture MediaCysteineCysteine EndopeptidasesDose-Response Relationship, DrugEdetic AcidEgtazic AcidEscherichia coli ProteinsEthylmaleimideHistidineHumansHydrogen-Ion ConcentrationMolecular Sequence DataMutagenesis, Site-DirectedMutationPeptidesPlasmidsProtease InhibitorsProtein BindingProtein Structure, TertiaryRatsSequence Homology, Amino AcidTime Factors