TY - JOUR
T1 - Live and let die
T2 - insights into pseudoenzyme mechanisms from structure
AU - Murphy, James M.
AU - Mace, Peter D.
AU - Eyers, Patrick A.
N1 - Funding Information:
JMM thanks the National Health and Medical Research Council of Australia for supporting work in this field in his laboratory (1105754, 1057905, 1067289, 1124735, 1124737; IRIISS 9000220), and the Victorian State Government Operational Infrastructure Support. PDM acknowledges support of research in this field from the Health Research Council of New Zealand and a Rutherford Discovery Fellowship from the New Zealand government administered by the Royal Society of New Zealand. PAE acknowledges support from The Royal Society, North West Cancer Research (CR1037) and a UK BBSRC tools and technology grant (BB/N021703/1). We apologize to colleagues whose work we were unable to cite due to space constraints.
Publisher Copyright:
© 2017
PY - 2017/12
Y1 - 2017/12
N2 - Pseudoenzymes were first described more than 50 years ago, when it was recognised that a subset of proteins that are structurally homologous to active enzymes lack amino acids necessary for catalytic activity. Recently, interest in pseudoenzymes has surged as it has become apparent that they constitute ∼10% of proteomes and perform essential metabolic and signalling functions that can be experimentally distinguished from catalytic outputs of enzymes. Here, we highlight recent structural studies of pseudoenzymes, which have revealed the molecular basis for roles as allosteric regulators of conventional enzymes, as molecular switches and integrators, as hubs for assembling protein complexes, and as competitors of substrate availability and holoenzyme assembly. As structural studies continue to illuminate pseudoenzyme molecular mechanisms, we anticipate that our knowledge of the breadth of their biological functions will expand in parallel.
AB - Pseudoenzymes were first described more than 50 years ago, when it was recognised that a subset of proteins that are structurally homologous to active enzymes lack amino acids necessary for catalytic activity. Recently, interest in pseudoenzymes has surged as it has become apparent that they constitute ∼10% of proteomes and perform essential metabolic and signalling functions that can be experimentally distinguished from catalytic outputs of enzymes. Here, we highlight recent structural studies of pseudoenzymes, which have revealed the molecular basis for roles as allosteric regulators of conventional enzymes, as molecular switches and integrators, as hubs for assembling protein complexes, and as competitors of substrate availability and holoenzyme assembly. As structural studies continue to illuminate pseudoenzyme molecular mechanisms, we anticipate that our knowledge of the breadth of their biological functions will expand in parallel.
UR - https://www.scopus.com/pages/publications/85026735431
U2 - 10.1016/j.sbi.2017.07.004
DO - 10.1016/j.sbi.2017.07.004
M3 - Review Article
C2 - 28787627
AN - SCOPUS:85026735431
SN - 0959-440X
VL - 47
SP - 95
EP - 104
JO - Current Opinion in Structural Biology
JF - Current Opinion in Structural Biology
ER -