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Figure 2 | BMC Microbiology

Figure 2

From: The crystal structure of alanine racemase from Streptococcus pneumoniae, a target for structure-based drug design

Figure 2

Structure-based sequence alignment of the five solved alanine racemase structures from Gram-positive bacteria. Structures are from S. pneumoniae, G. stearothermophilus [29], E. faecalis [38], B. anthracis [36] and S. lavendulae [33]. The black box encloses the conserved PLP binding site, the asterisks (*) mark the PLP-bound Lys residue and the catalytic Tyr residue, the diamond (♦) marks the location of the carbamylated Lys residue, and the residues constituting the entryway to the active site are marked with either I (inner layer) or M (middle layer). Residues that form intermonomer interfaces are highlighted in light green. The purple shading is proportional to the degree of sequence identity across the alignment.

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