Salbutamol
From Proteopedia
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The β2 adrenergic receptor has seven <scene name='96/968805/Hydrophobic_hydrophilic/1'> mostly hydrophobic </scene> (shown in grey; hydrophilic residues are shown in pink) alpha helices that cross the cell membrane. When shown in a <scene name='96/968805/N_to_c_rainbow/1'>N to C rainbow</scene>, where the N terminus is shown in blue, the C terminus in red, and the intervening segments following the colors of the rainbow, the seven long helices that form a diagonal bundle, with shorter helices forming "caps" on either end can be seen more clearly. | The β2 adrenergic receptor has seven <scene name='96/968805/Hydrophobic_hydrophilic/1'> mostly hydrophobic </scene> (shown in grey; hydrophilic residues are shown in pink) alpha helices that cross the cell membrane. When shown in a <scene name='96/968805/N_to_c_rainbow/1'>N to C rainbow</scene>, where the N terminus is shown in blue, the C terminus in red, and the intervening segments following the colors of the rainbow, the seven long helices that form a diagonal bundle, with shorter helices forming "caps" on either end can be seen more clearly. | ||
- | The <scene name='96/968805/Binding_site/1'>Salbutamol binding site</scene> shows many intermolecular interactions between the protein and the drug. The phenyl ring of the salbutamol is sandwiched by <scene name='96/968805/Hydrophobic_pocket/1'>hydrophobic residues</scene>, while the N and O in salbutamol form <scene name='96/968805/ | + | The <scene name='96/968805/Binding_site/1'>Salbutamol binding site</scene> shows many intermolecular interactions between the protein and the drug. The phenyl ring of the salbutamol is sandwiched by <scene name='96/968805/Hydrophobic_pocket/1'>hydrophobic residues</scene>, while the N and O in salbutamol form <scene name='96/968805/H_bonds/1'>hydrogen bonds</scene> with nearby asparagine (Asn) and aspartate (Asp) residues. |
Adrenergic agonists share structural characteristics, including ~<scene name='96/968805/N_o_distance/1'>0.3 nm between the N and the O</scene>, approximately 0.5 nm from the <scene name='96/968805/O_para_c_distance/1'>O to the C</scene> in the para position on the phenyl ring, and o.65 nm from the <scene name='96/968805/N_para_c_distance/1'>N to the C</scene> in the para position on the phenyl ring. The OH group and the phenyl ring are in the same plane, while the four atom <scene name='96/968805/Torsion_angles/1'>dihedral or torsion</scene> angle between the O and the N is approximately 70 degrees. | Adrenergic agonists share structural characteristics, including ~<scene name='96/968805/N_o_distance/1'>0.3 nm between the N and the O</scene>, approximately 0.5 nm from the <scene name='96/968805/O_para_c_distance/1'>O to the C</scene> in the para position on the phenyl ring, and o.65 nm from the <scene name='96/968805/N_para_c_distance/1'>N to the C</scene> in the para position on the phenyl ring. The OH group and the phenyl ring are in the same plane, while the four atom <scene name='96/968805/Torsion_angles/1'>dihedral or torsion</scene> angle between the O and the N is approximately 70 degrees. |
Revision as of 12:53, 30 October 2024
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