“…Tyr54 and Tyr101 278 (T. aquaticus amylomaltase numbering [9]), since both were identified 279 as the aromatic positions involved in the secondary glucan-binding 280 site of the enzyme[49,57,58]. While the former was determined to con-281 trol the hydrolytic activity[57,59], the latter was shown to be responsi-282 ble rather for disproportionating activity of the amylomaltase[58,60].283 Interestingly, the residues of the secondary glucan-binding site from 284 T. aquaticus amylomaltase were found to be not strictly conserved 285 among its counterparts [27,61]. A detailed inspection of the alignment 286 of all 416 4-α-glucanotransferases compared in the present study con-287 firmed that neither Tyr54, nor Tyr101 does represent a conserved posi-288 tion in the family GH77 (Fig.…”