The induced-fit motion of an active-site loop (residues 706–710) including the catalytic acid/base residue Glu706 in pullulanase from Klebsiella pneumoniae (KPP) belonging to glycoside hydrolase family 13 subfamily 13 was examined by mutational and structural analysis. Analysis of the structure and activity of recombinant pullulanase from K. pneumoniae ATCC 9621 (rKPP) and its G680L mutant indicated that the side chain of residue 680 is important for the conformational change of the loop 706–710 in the ligand-free form, resulting in the altered binding affinity of the substrate.