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. 2017 Oct 16;8(12):8384–8399. doi: 10.1039/c7sc03336b

Fig. 2. FTIR spectra of (a) wild-type InhA (b) S94A–InhA, (c) P193A–InhA and (d) W222A–InhA. In each panel red corresponds to the apo-enzyme, blue to the enzyme with NADH cofactor present and green to the enzyme with the INH–NAD inhibitor present. The arrow in (a) marks the increased amplitude near 1620–1630 cm–1 observed upon binding of the co-factor and inhibitor to the wild-type enzyme discussed in the text. All spectra are normalised to the peak of absorbance. Uncertainty due to measurement error in each individual spectrum is indicated by the width of the line.

Fig. 2