Figure 5 - full size

 

Figure 5.
Figure 5. Conformational changes. (a) Conformational change at residue 73 due to crystal contacts. A stereo view of the crystal contact environment for glutamine 73 of subunit B in the tetragonal structure (shown in yellow) is shown with the cubic structure (shown in cyan) superimposed. Bonds are shown as thin tubes and polar or charged atoms of interest are shown as spheres colored according to atom type (nitrogen blue and oxygen red). Proposed hydrogen bonds are shown as broken gray lines. Glutamine 73 from subunit B of the tetragonal structure is hydrogen bonding with lysine 65 and asparagine 83 of subunit C of a symmetry-related molecule in the crystal packing of the tetragonal struc- ture. Glutamine 73 from the cubic structure clashes severely with atoms in the symmetry-related molecules in the crystal packing of the tetragonal structure. Gluta- mine 73 from subunit C (not shown) is also involved in crystal contacts, hydrogen bonding with asparagine 83 of a symmetry-related subunit A and to a water mol- ecule hydrogen bonding to lysine 65 of subunit A. This Figure was generated with MIDAS (UCSF & MGL, 1995). (b) Conformational change at residue 42 due to crystal contacts. Shown in cyan, residues 39, 42, and 45 are shown with the backbone helical segment and superimposed with the same residues of the tetragonal structure (shown in yellow). Backbone C a trace is shown as thick tubes while bonds are shown as thin tubes and polar or charged atoms of interest are shown as spheres colored according to atom type (nitrogen blue and oxy- gen red). Proposed hydrogen bonds are shown as bro- ken gray lines. Also shown are two symmetry-related residues 39 and a proposed sodium ion coordinated to the three acid groups that approach each other in the crystal packing. A thin green line is shown which is coincident with the crystallographic 3-fold axis. The con- formational change in residue 42 is due to shielding of the charge on the acidic group of aspartate 39 upon binding to the ammonium ion, which causes the charge

The above figure is reprinted by permission from Elsevier: J Mol Biol (1998, 279, 223-232) copyright 1998.