A fragment of the Trypanosoma brucei ZC3H41 protein encompassing the ATP-dependent RNA helicase domain was successfully subcloned for expression in a bacterial system (Escherichia coli). Following expression, the protein was purified and crystallized using the vapor-diffusion method. The protein crystals were optimized at a 1:1 protein:reservoir solution ratio using PPGBA 2000. The optimized crystals diffracted to a d of 3.15 Å. The collected data revealed preliminary structural information regarding this newly discovered protein.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716258 | PMC |
http://dx.doi.org/10.1107/S2053230X20015204 | DOI Listing |
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