Cells that experience a devastating mutation in the gene that encodes g6p dehydrogenase are most likely to experience problems specifically connected to choose one: a. the krebs cycle. b. lipid transport. c. nucleotide biosynthesis. d. protein catabolism

The right answer is nucleotide biosynthesis.

Favism or deficiency of glucose-6-phosphate dehydrogenase, or deficiency of G6PD, is the most widespread enzymatic deficiency in the world. Of genetic origin, it is characterized by a destruction of the red blood cells (hemolysis) during the ingestion of beans or the taking of certain drugs (especially synthesized antimalarials).

The enzyme Glucose-6-phosphate dehydrogenase is involved in the pentose phosphate pathway that produces riboses that are part of the nucleotide composition.

we would need to see the picture to answer it