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Exploiting Structural Modelling Tools to Explore Host-Translocated Effector Proteins

Journal

Publisher

MDPI
DOI: 10.3390/ijms222312962

Keywords

effector proteins; fungi; oomycetes; protein modelling; RoseTTafold; AlphaFold2

Funding

  1. University of Canterbury PhD scholarship
  2. New Zealand Tertiary Education Commission CoRE grant to the Bioprotection Aoteroa
  3. [BioRender [105]]

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Interactions between pathogenic fungi and oomycetes with plants can have different impacts on plant health, with effector proteins playing a key role in successful colonization of the host plant. Investigating the biological and functional roles of effectors through bioinformatics and experimental approaches is crucial for understanding plant-microbe interactions. The use of next generation protein modeling software like RoseTTafold and AlphaFold2, which utilize novel machine-learning algorithms, has advanced the field of effector biology and made these methods more accessible to users.
Oomycete and fungal interactions with plants can be neutral, symbiotic or pathogenic with different impact on plant health and fitness. Both fungi and oomycetes can generate so-called effector proteins in order to successfully colonize the host plant. These proteins modify stress pathways, developmental processes and the innate immune system to the microbes' benefit, with a very different outcome for the plant. Investigating the biological and functional roles of effectors during plant-microbe interactions are accessible through bioinformatics and experimental approaches. The next generation protein modeling software RoseTTafold and AlphaFold2 have made significant progress in defining the 3D-structure of proteins by utilizing novel machine-learning algorithms using amino acid sequences as their only input. As these two methods rely on super computers, Google Colabfold alternatives have received significant attention, making the approaches more accessible to users. Here, we focus on current structural biology, sequence motif and domain knowledge of effector proteins from filamentous microbes and discuss the broader use of novel modelling strategies, namely AlphaFold2 and RoseTTafold, in the field of effector biology. Finally, we compare the original programs and their Colab versions to assess current strengths, ease of access, limitations and future applications.

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