相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Molecular modelling and molecular dynamics of CFTR
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CELLULAR AND MOLECULAR LIFE SCIENCES (2016)
Anion conductance selectivity mechanism of the CFTR chloride channel
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Functional Architecture of the Cytoplasmic Entrance to the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore
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Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) CLOSED AND OPEN STATE CHANNEL MODELS
Valentina Corradi et al.
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Full-open and closed CFTR channels, with lateral tunnels from the cytoplasm and an alternative position of the F508 region, as revealed by molecular dynamics
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State-dependent blocker interactions with the CFTR chloride channel: implications for gating the pore
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Tuning of CFTR Chloride Channel Function by Location of Positive Charges within the Pore
Yassine El Hiani et al.
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Alignment of transmembrane regions in the cystic fibrosis transmembrane conductance regulator chloride channel pore
Wuyang Wang et al.
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Structural basis for the channel function of a degraded ABC transporter, CFTR (ABCC7)
Yonghong Bai et al.
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Changes in Accessibility of Cytoplasmic Substances to the Pore Associated with Activation of the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel
Yassine El Hiani et al.
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Regulation of conductance by the number of fixed positive charges in the intracellular vestibule of the CFTR chloride channel pore
Jing-Jun Zhou et al.
JOURNAL OF GENERAL PHYSIOLOGY (2010)
ABC transporters: the power to change
Douglas C. Rees et al.
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Identification of a second blocker binding site at the cytoplasmic mouth of the cystic fibrosis transmembrane conductance regulator chloride channel pore
Chantal N. St Aubin et al.
MOLECULAR PHARMACOLOGY (2007)
Direct and indirect effects of mutations at the outer mouth of the cystic fibrosis transmembrane conductance regulator chloride channel pore
Jing-Jun Zhou et al.
JOURNAL OF MEMBRANE BIOLOGY (2007)
Positive charges at the intracellular mouth of the pore regulate anion conduction in the CFTR chloride channel
Chantal N. St. Aubin et al.
JOURNAL OF GENERAL PHYSIOLOGY (2006)
The ABC protein turned chloride channel whose failure causes cystic fibrosis
DC Gadsby et al.
NATURE (2006)
Location of a common inhibitor binding site in the cytoplasmic vestibule of the cystic fibrosis transmembrane conductance regulator chloride channel pore
P Linsdell
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Direct comparison of the functional roles played by different transmembrane regions in the cystic fibrosis transmembrane conductance regulator chloride channel pore
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JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
The human ATP-binding cassette (ABC) transporter superfamily
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