3TIF: Dimeric structure of a post-hydrolysis state of the ATP-binding cassette MJ0796 bound to ADP and Pi

Most ATP binding cassette (ABC) proteins are pumps that transport substrates across biological membranes using the energy of ATP hydrolysis. Functional ABC proteins have two nucleotide-binding domains (NBDs) that bind and hydrolyze ATP, but the molecular mechanism of nucleotide hydrolysis is unresolved. This is due in part to the limited kinetic information on NBD association and dissociation. Here, we show dimerization of a catalytically active NBD and follow in real time the association and dissociation of NBDs from the changes in fluorescence emission of a tryptophan strategically located at the center of the dimer interface. Spectroscopic and structural studies demonstrated that the tryptophan can be used as dimerization probe, and we showed that under hydrolysis conditions (millimolar MgATP), not only the dimer dissociation rate increases, but also the dimerization rate. Neither dimer formation or dissociation are clearly favored, and the end result is a dynamic equilibrium where the concentrations of monomer and dimer are very similar. We proposed that based on their variable rates of hydrolysis, the rate-limiting step of the hydrolysis cycle may differ among full-length ABC proteins.
PDB ID: 3TIFDownload
MMDB ID: 98151
PDB Deposition Date: 2011/8/20
Updated in MMDB: 2018/03
Experimental Method:
x-ray diffraction
Resolution: 1.7995  Å
Source Organism:
Similar Structures:
Biological Unit for 3TIF: dimeric; determined by author and by software (PISA)
Molecular Components in 3TIF
Label Count Molecule
Proteins (2 molecules)
Uncharacterized ABC Transporter Atp-binding Protein Mj0796(Gene symbol: MJ_RS04255)
Molecule annotation
Chemicals (9 molecules)
* Click molecule labels to explore molecular sequence information.

Citing MMDB