Sandbox Reserved 689
From Proteopedia
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== Structural Elements == | == Structural Elements == | ||
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<scene name='Sandbox_Reserved_689/Monomer_rainbow/1'>N-->C Rainbow</scene> | <scene name='Sandbox_Reserved_689/Monomer_rainbow/1'>N-->C Rainbow</scene> | ||
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<scene name='Sandbox_Reserved_689/Secondary_structure/1'>Secondary Structure</scene> | <scene name='Sandbox_Reserved_689/Secondary_structure/1'>Secondary Structure</scene> | ||
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<scene name='Sandbox_Reserved_689/Rifampicin_in_acrb_polar_non/2'>Polar and Nonpolar</scene> interacting residues are shown here (Polar in blue, nonpolar in orange). | <scene name='Sandbox_Reserved_689/Rifampicin_in_acrb_polar_non/2'>Polar and Nonpolar</scene> interacting residues are shown here (Polar in blue, nonpolar in orange). | ||
+ | <scene name='Sandbox_Reserved_689/Rifampicin_in_acrb_sl/1'>in front of switch loop</scene> (switch loop is shown in orange). | ||
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+ | (Rifampicin crystal structure from Nakashima, et al. 2011) | ||
+ | '''Minocycline''' is a lower molecular weight drug (~400 g/mol) that has been crystallized in the distal binding pocket. | ||
== Energy Transduction == | == Energy Transduction == | ||
There are <scene name='Sandbox_Reserved_689/Proton_translocation_residues/1'>Four Titrateable Residues</scene> (Asp408, Asp407, Lys940, and Arg 971) whose protonation and deprotonation are suggested to play a large role in the conformational change between the L, T, and O states (Eicher, et al. 2009). PDB: 3D9B | There are <scene name='Sandbox_Reserved_689/Proton_translocation_residues/1'>Four Titrateable Residues</scene> (Asp408, Asp407, Lys940, and Arg 971) whose protonation and deprotonation are suggested to play a large role in the conformational change between the L, T, and O states (Eicher, et al. 2009). PDB: 3D9B |
Revision as of 14:29, 30 April 2013
This Sandbox is Reserved from 30/01/2013, through 30/12/2013 for use in the course "Biochemistry II" taught by Hannah Tims at the Messiah College. This reservation includes Sandbox Reserved 686 through Sandbox Reserved 700. |
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Contents |
The E. coli AcrB Efflux Pump
Structure
The AcrB efflux pump is part of a tripartite system used by E. Coli to remove antibiotic and other toxic molecules from the bacterial cell.
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Structural Elements
Substrates
Because of the large binding pockets in AcrB, it is able to bind and export a wide variety of antibiotic drugs and other toxins.
Rifampicin is a high molecular weight drug (~800 g/mol) that has been crystallized in the proximal binding pocket
, interacting residues (all residues within 4 Angstroms) highlighted and shown in ball-and-stick representation.
interacting residues are shown here (Polar in blue, nonpolar in orange).
(switch loop is shown in orange).
(Rifampicin crystal structure from Nakashima, et al. 2011)
Minocycline is a lower molecular weight drug (~400 g/mol) that has been crystallized in the distal binding pocket.
Energy Transduction
There are (Asp408, Asp407, Lys940, and Arg 971) whose protonation and deprotonation are suggested to play a large role in the conformational change between the L, T, and O states (Eicher, et al. 2009). PDB: 3D9B