Objective
Truncated versions of the erythromycin-producing polyketide synthase (PKS) will be engineered, in which specific active sites are mutated. The pattern of intersubunit protein-protein interaction in these giant multienzymes will be deduced by studying heterodimers of such mutants.
Call for proposal
Data not availableFunding Scheme
RGI - Research grants (individual fellowships)Coordinator
CB2 2QR Cambridge
United Kingdom