Skip to main content
. 2005 Nov 24;61(Pt 12):1069–1074. doi: 10.1107/S1744309105036559

Table 2. Revised Fast Screen crystallization hit count by position.

        Hits
        Alanine Glutamine  
Position Mutated Secondary structure Exposure 277K RT 277K RT Total
17 A, Q Helix I 0 2 9 2 13
76   Coil E          
78 A, Q Helix I 8 4 9 3 24
82   Helix I          
192 A, Q Sheet I 4 2 3 4 13
196 A, Q Coil E 6 3 14 5 28
203 A, Q Coil E 0 1 5 1 7
206 A, Q Sheet E 4 3 9 3 19
232 A, Q Sheet I 7 1 8 4 20
250 A, Q Helix E 7 1 8 5 21
283   Helix B          
301 A, Q Sheet E 4 2 9 6 21
304   Disordered NA          
312   Sheet E          
376   Helix E          
379   Coil I          
390   Sheet B          
392   Coil B          
404 A, Q Helix E 7 4 8 5 24
421   Sheet B          
473   Helix I          
477   Helix I          
483 Q Helix E     5 5 10
501 Q Coil E     2 1 3
506   Sheet B          
522   Helix B          
619   Sheet E          
653 A, Q Helix E 11 3 5 5 24
665 A, Q Helix E 8 3 11 4 26
691   Helix I          
702 A, Q Coil E 7 3 4 3 17
720   Helix I          
Total§       73 32 109 56 270

Secondary-structural classification was performed using the program DSSP (Kabsch Sander, 1983). Both 310- and -helices are denoted as Helix; Coil corresponds to all secondary-structural elements except helices and sheets. Residue 304 was disordered in all structures.

Disordered lysines were automatically modeled by the Swiss-Pdb Viewer (Guex Peitsch, 1997) and lysine side-chain solvent accessibility was calculated using the CCP4 program AREAIMOL, which was subsequently classified as B for buried, I for intermediate and E for exposed after Rost Sander (1994).

§

Wild-type E. coli malate synthase G produced seven crystals at 277K and five at room temperature and is not included in the table.