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Transketolase-like protein 2 (TKTL2) is one of three human genes encoding proteins structurally related to transketolase, an enzyme active in the non-oxidative branch of the pentose phosphate pathway[1][2]. TKTL2 is predicted—and supported by structural homology modeling—to act as a bona fide transketolase enzyme, with key active site residues and binding domains conserved, facilitating the transfer of two-carbon units between sugar phosphates via a thiamine pyrophosphate (TPP)-dependent mechanism[1]. The evidence suggests TKTL2 is cytoplasmic and can bind thiamine pyrophosphate, playing a putative role in cellular carbohydrate metabolism. Recent research supports TKTL2 as a novel therapeutic target, with altered expression or activity potentially relevant in the pathogenesis of diabetes and various cancers[1][2]. However, the physiological and clinical significance of TKTL2 remains under investigation; no drugs are currently known to selectively target it, but studies on the more established transketolase (TKT) enzyme suggest possible future avenues.
Enzyme inhibition (inferred from canonical transketolase targeting strategies, not specific to TKTL2)
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