Figure 2 - full size

 

Figure 2.
Fig. 2. Structural features of GA modules. Panel A, stereo representation of 30 G148-GA3 NMR solution structures superimposed onto their unminimized average coordinates by minimizing the r.m.s. deviations for the backbone atoms of helices. Panel B, ribbon representation of the structure closest to the mean of the 30 structures representing G148-GA3. Panel C, ribbon representation of the structure closest to the mean of the 20 structures (the atomic coordinates are available in the Research Collaboratory for Structural Bioinformatics Protein Data Bank under PDB 1GAB (13)). The whole protein fragment of ALB8-GA (53 residues) is shown, and the corresponding residues of G148-GA3 are shown in panel B, although not all residues belong to the intact protein G sequence. Panel D, tube representation of ALB8-GA (light gray) and G148-GA3 (dark gray) with backbone atoms of helical regions superimposed. Residue Thr-18 in ALB8-GA is indicated with an arrow, and at the corresponding position in G148-GA3 there is a deletion. Structures (all oriented with their N terminus upward) in panels A-D were visualized using MOLMOL (40). Panel E, graphical DDM comparing the two GA modules in this study. The average distance differences between C^ and C^ in the 30 conformers of G148-GA3 and the 20 structures of ALB8-GA (PDB 1GAB (13) were calculated to generate the DDM (29). Only residues belonging to the defined GA module sequence were analyzed. Residue Thr-18 in ALB8-GA was excluded because there is a deletion at the corresponding position in the G148-GA3 sequence, and these locations are marked by arrows. The lower right half of the matrix shows the average distance differences for all residue pairs; the upper left part shows only the average distance differences that are larger than 2 S.D. The distance differences are coded using a gradient from white to black with gray representing interatomic distances that are the same in both ensembles. Interatomic distances that become larger in G148-GA3 tend toward white, whereas distances that become smaller tend toward black.

The above figure is reprinted by permission from the ASBMB: J Biol Chem (2002, 277, 8114-8120) copyright 2002.