Journal of Biological Chemistry
Volume 289, Issue 6, 7 February 2014, Pages 3724-3735
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Protein Structure and Folding
Structure of the TbBILBO1 Protein N-terminal Domain from Trypanosoma brucei Reveals an Essential Requirement for a Conserved Surface Patch*

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TbBILBO1 is the only known component of the flagellar pocket collar, a cytoskeletal barrier element found in trypanosomes. The N-terminal domain (NTD) of TbBILBO1 was found to be dispensable for targeting of the protein in vivo. However, overexpression of constructs lacking the NTD caused complete growth inhibition, implying an essential requirement for this domain. A high resolution structure of the NTD of TbBILBO1 showed that it forms a ubiquitin-like fold with a conserved surface patch. Mutagenesis of this patch recapitulated the phenotypic effects of deleting the entire domain and was found to cause cell death. The surface patch on the NTD of TbBILBO1 is therefore a potential drug target.

Cytoskeleton
Infectious Diseases
Molecular Cell Biology
Nuclear Magnetic Resonance
Parasite
Protein Structure
Structural Biology
Trypanosoma brucei
TbBILBO1
Flagellar Pocket Collar

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The atomic coordinates and structure factors (code 2MEK) have been deposited in the Protein Data Bank (http://wwpdb.org/).

*

This work was supported by funding from the Max F. Perutz Laboratories and Grant P24383-B21 from the Austrian Science Fund (to G. D.).

1

Supported by an Österreichischer Austauschdienst (OeAD) graduate scholarship during 2009–2012.