4A82
Fitted model of staphylococcus aureus sav1866 model ABC transporter in the human cystic fibrosis transmembrane conductance regulator volume map EMD-1966.
Summary for 4A82
Entry DOI | 10.2210/pdb4a82/pdb |
EMDB information | 1966 |
Descriptor | CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR (1 entity in total) |
Functional Keywords | cystic fibrosis, cftr, ion channel, transport protein, cassette protein |
Biological source | HOMO SAPIENS (HUMAN) |
Total number of polymer chains | 4 |
Total formula weight | 259735.86 |
Authors | Rosenberg, M.F.,ORyan, L.P.,Hughes, G.,Zhao, Z.,Aleksandrov, L.A.,Riordan, J.R.,Ford, R.C. (deposition date: 2011-11-18, release date: 2012-01-11, Last modification date: 2024-05-08) |
Primary citation | Rosenberg, M.F.,O'Ryan, L.,Hughes, G.,Zhao, Z.,Aleksandrov, L.A.,Riordan, J.R.,Ford, R.C. The Cystic Fibrosis Transmembrane Conductance Regulator (Cftr):3D Structure and Localisation of a Channel Gate. J.Biol.Chem., 286:42647-, 2011 Cited by PubMed Abstract: Cystic fibrosis affects about 1 in 2500 live births and involves loss of transmembrane chloride flux due to a lack of a membrane protein channel termed the cystic fibrosis transmembrane conductance regulator (CFTR). We have studied CFTR structure by electron crystallography. The data were compared with existing structures of other ATP-binding cassette transporters. The protein was crystallized in the outward facing state and resembled the well characterized Sav1866 transporter. We identified regions in the CFTR map, not accounted for by Sav1866, which were potential locations for the regulatory region as well as the channel gate. In this analysis, we were aided by the fact that the unit cell was composed of two molecules not related by crystallographic symmetry. We also identified regions in the fitted Sav1866 model that were missing from the map, hence regions that were either disordered in CFTR or differently organized compared with Sav1866. Apart from the N and C termini, this indicated that in CFTR, the cytoplasmic end of transmembrane helix 5/11 and its associated loop could be partly disordered (or alternatively located). PubMed: 21931164DOI: 10.1074/JBC.M111.292268 PDB entries with the same primary citation |
Experimental method | ELECTRON CRYSTALLOGRAPHY (9 Å) |
Structure validation
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