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KINESIN SARA VAN NORTWICK GEOMETRIC COMPUTATIONS IN MOLECULAR BIOLOGY SS 2007 ETH THE STRUCTURE X-ray crystallography by Kull et al. (1996) Resolution Dimer = 1.8 A LET’S MOTOR! The Family of Motor Proteins Large and varied responsibilities Unidirectional movement Fuel = ATP Share motor “head” domain (structural core, common ancestor) WHERE ARE WE GOING AND WHY? Center Periphery Compass = Microtubule Polarity Anterograde Transport (towards the positive) Point A to Point B Kinesin > Diffusion Alignment Mitosis (cell division) HOW FAST ARE WE TALKING? 2 um/sec 8 nm per step (spacing of tubulin dimers along the microtubule) = 250 steps/second! Protein head = 7.5 X 4.5 X 4.5 nm ≈ speed and thrust of the supersonic car 60% efficiency THE MOTOR IN ACTION Kinesin Movement Video: http://www.scripps.edu/cb/milligan/research/movies/kinesin_mov.html MANY VARIETIES… Motor domain conserved @ N-terminus 40 known variations in Humans Differences in adaptor structure between motor and the object to be moved BREAKING IT DOWN Two heavy chains comprise globular head • Light Chains comprise cargo binding region • KINESIN VS. MYOSIN Motor domain is similar in both motor proteins Very little amino acid similarity Kinesin is 340 aa while myosin is 850 aa RMS of 3.5 A for 183 aa of kinesin motor domain STRUCTURE ISN’T ALWAYS ENOGUH… REFERENCES Kozeilski, Sack, et al. The Crystal Structure of Dimeric Kinesin and Implication fo Microtubule-Dependent Motility. Cell, Vol 91, 985-994. December, 26, 1997. Molecular Biology of the Cell http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=mboc4.figgrp .3054 PDB Molecule of the Month Kull, Sablin, et al.(1996). Crystal structure of the kinesin motor domains reveals a structural similarity to myosin. Nature 380, 550-554. Wikipedia Block, Steve. Kinesin: What Gives? Cell, Vol 93 5-8. April, 1998. WE’VE ARRIVED… Questions?