PT  - JOURNAL ARTICLE
AU  - Alexander Derry
AU  - Kristy A. Carpenter
AU  - Russ B. Altman
TI  - Training data composition affects performance of protein structure analysis algorithms
AID  - 10.1101/2021.09.30.462647
DP  - 2021 Jan 01
TA  - bioRxiv
PG  - 2021.09.30.462647
4099  - http://biorxiv.org/content/early/2021/10/20/2021.09.30.462647.short
4100  - http://biorxiv.org/content/early/2021/10/20/2021.09.30.462647.full
AB  - The three-dimensional structures of proteins are crucial for understanding their molecular mechanisms and interactions. Machine learning algorithms that are able to learn accurate representations of protein structures are therefore poised to play a key role in protein engineering and drug development. The accuracy of such models in deployment is directly influenced by training data quality. The use of different experimental methods for protein structure determination may introduce bias into the training data. In this work, we evaluate the magnitude of this effect across three distinct tasks: estimation of model accuracy, protein sequence design, and catalytic residue prediction. Most protein structures are derived from X-ray crystallography, nuclear magnetic resonance (NMR), or cryo-electron microscopy (cryo-EM); we trained each model on datasets consisting of either all three structure types or of only X-ray data. We find that across these tasks, models consistently perform worse on test sets derived from NMR and cryo-EM than they do on test sets of structures derived from X-ray crystallography, but that the difference can be mitigated when NMR and cryo-EM structures are included in the training set. Importantly, we show that including all three types of structures in the training set does not degrade test performance on X-ray structures, and in some cases even increases it. Finally, we examine the relationship between model performance and the biophysical properties of each method, and recommend that the biochemistry of the task of interest should be considered when composing training sets.Competing Interest StatementThe authors have declared no competing interest.