Abstract
Apd1,
a cytosolic yeast protein, and Aim32, its counterpart in the mitochondrial
matrix, have a C-terminal thioredoxinlike ferredoxin domain and a widely
divergent N-terminal domain. These proteins are found in bacteria, plants,
fungi and unicellular pathogenic eukaryotes, but not in Metazoa. Our
chemogenetic experiments demonstrate that the highly conserved cysteine and
histidine residues within the C-X8-C-X24-75-H-X-G-G-H motif of the TLF domain
of Apd1 and Aim32 proteins are essential for viability upon treatment of yeast
cells with the redox potentiators gallobenzophenone or pyrogallol,
respectively. UV-Vis, EPR and Mössbauer spectroscopy of purified wild type Apd1
and three His to Cys variants demonstrated that Cys207 and Cys216 are the
ligands of the ferric ion and His255 and His259 are the ligands of the
reducible iron ion of the [2Fe-2S]2+/1+ cluster. The [2Fe-2S] center of Apd1
(Em,7 = -164±5 mV, pKox1,2=7.9±0.1 and 9.7±0.1) differs from both dioxygenase
(Em,7 ≈ -150 mV, pKox1,2=9.8 and 11.5) and cytochrome
bc1/b6f Rieske clusters (Em,7 ≈
+300 mV, pKox1,2= 7.7 and 9.8). Apd1 and its engineered variants represent an
unprecedented flexible system for which a stable [2Fe-2S] cluster with two
histidine ligands, (two different) single histidine ligands or only cysteinyl
ligands is possible in the same protein fold. Our results define a remarkable
example of convergent evolution of [2Fe-2S] cluster containing proteins with
bis-histidinyl coordination and proton-coupled electron transfer.