TY - JOUR
T1 - Molecular mechanisms of cytochrome c biogenesis
T2 - Three distinct systems
AU - Kranz, Robert
AU - Lill, Roland
AU - Goldman, Barry
AU - Bonnard, Géraldine
AU - Merchant, Sabeeha
PY - 1998
Y1 - 1998
N2 - The past 10 years have heralded remarkable progress In the understanding of the biogenesis of c-type cytochromes. The hallmark of c-type cytochrome synthesis is the covalent ligation of haem vinyl groups to two cysteinyl residues of the apocytochrome (at a Cys-Xxx-Yyy-Cys-His signature motif). From genetic, genomic and biochemical studies, it is clear that three distinct systems have evolved in nature to assemble this ancient protein. In this review, common principles of assembly for all systems and the molecular mechanisms predicted for each system are summarized. Prokaryotes, plant mitochondria and chloroplasts use either system I or II, which are each predicted to use dedicated mechanisms for haem delivery, apocytochrome ushering and thioreduction. Accessory proteins of systems I and II co-ordinate the positioning of these two substrates at the membrane surface for covalent ligation, The third system has evolved specifically in mitochondria of fungi, invertebrates and vertebrates, For system III, a pivotal role is played by an enzyme called cytochrome c haem lyase (CCHL) in the mitochondrial intermembrane space.
AB - The past 10 years have heralded remarkable progress In the understanding of the biogenesis of c-type cytochromes. The hallmark of c-type cytochrome synthesis is the covalent ligation of haem vinyl groups to two cysteinyl residues of the apocytochrome (at a Cys-Xxx-Yyy-Cys-His signature motif). From genetic, genomic and biochemical studies, it is clear that three distinct systems have evolved in nature to assemble this ancient protein. In this review, common principles of assembly for all systems and the molecular mechanisms predicted for each system are summarized. Prokaryotes, plant mitochondria and chloroplasts use either system I or II, which are each predicted to use dedicated mechanisms for haem delivery, apocytochrome ushering and thioreduction. Accessory proteins of systems I and II co-ordinate the positioning of these two substrates at the membrane surface for covalent ligation, The third system has evolved specifically in mitochondria of fungi, invertebrates and vertebrates, For system III, a pivotal role is played by an enzyme called cytochrome c haem lyase (CCHL) in the mitochondrial intermembrane space.
UR - http://www.scopus.com/inward/record.url?scp=0031875674&partnerID=8YFLogxK
U2 - 10.1046/j.1365-2958.1998.00869.x
DO - 10.1046/j.1365-2958.1998.00869.x
M3 - Review article
C2 - 9720859
AN - SCOPUS:0031875674
SN - 0950-382X
VL - 29
SP - 383
EP - 396
JO - Molecular Microbiology
JF - Molecular Microbiology
IS - 2
ER -