The Journal of biological chemistry · 2012
Structural basis for the acyltransferase activity of lecithin:retinol acyltransferase-like proteins.
СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод пока не подготовлен
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.
Golczak Marcin, Kiser Philip D, Sears Avery E, Lodowski David T, Blaner William S, Palczewski Krzysztof
Аннотация
Lecithin:retinol acyltransferase-like proteins, also referred to as HRAS-like tumor suppressors, comprise a vertebrate subfamily of papain-like or NlpC/P60 thiol proteases that function as phospholipid-metabolizing enzymes. HRAS-like tumor suppressor 3, a representative member of this group, plays a key role in regulating triglyceride accumulation and energy expenditure in adipocytes and therefore constitutes a novel pharmacological target for treatment of metabolic disorders causing obesity. Here, we delineate a catalytic mechanism common to lecithin:retinol acyltransferase-like proteins and provide evidence for their alternative robust lipid-dependent acyltransferase enzymatic activity. We also determined high resolution crystal structures of HRAS-like tumor suppressor 2 and 3 to gain insight into their active site architecture. Based on this structural analysis, two conformational states of the catalytic Cys-113 were identified that differ in reactivity and thus could define the catalytic properties of these two proteins. Finally, these structures provide a model for the topology of these enzymes and allow identification of the protein-lipid bilayer interface. This study contributes to the enzymatic and structural understanding of HRAS-like tumor suppressor enzymes.
Предметные рубрики MeSH
AcylationAcyltransferasesAmino Acid SequenceBiocatalysisCatalytic DomainChromatography, High Pressure LiquidCrystallography, X-RayCysteineElectrophoresis, Polyacrylamide GelEnzyme StabilityHumansMass SpectrometryModels, MolecularMolecular Sequence DataPhospholipases A2Phospholipases A2, Calcium-IndependentPhospholipidsProtein BindingProtein Structure, TertiarySequence Homology, Amino AcidSubstrate SpecificityTumor Suppressor Proteins