Spontaneous conformational changes in the E. coli GroEL subunit from all-atom molecular dynamics simulations.

ABSTRACT: The Escherichia coli chaperonin GroEL is a complex of identical subunit proteins (57 kDa each) arranged in a back-to-back stacking of two heptameric rings. Its hallmarks include nested positive intra-ring and negative inter-ring cooperativity in adenosine trisphosphate (ATP) binding and the ability to mediate the folding of newly transcribed and/or denatured substrate proteins. We performed unbiased molecular dynamics simulations of the GroEL subunit protein in explicit water both with and without the nucleotide KMgATP to understand better the details of the structural transitions that enable these behaviors. Placing KMgATP in the equatorial domain binding pocket of a t state subunit, which corresponds to a low ATP-affinity state, produced a short-lived (6 ns) state that spontaneously tran

SUBMITTER: Sliozberg Y 

PROVIDER: S-EPMC1959553 | biostudies-literature | 2007 Sep

REPOSITORIES: biostudies-literature