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Highly Accurate and Efficient Deep Learning Paradigm for Full-Atom Protein Loop Modeling with KarmaLoop.

Tianyue WangXujun ZhangOdin ZhangGuangyong ChenPeichen PanErcheng WangJike WangJialu WuDonghao ZhouLangcheng WangRuofan JinShicheng ChenChao ShenYu KangChang-Yu HsiehTing-Jun Hou
Published in: Research (Washington, D.C.) (2024)
Protein loop modeling is a challenging yet highly nontrivial task in protein structure prediction. Despite recent progress, existing methods including knowledge-based, ab initio, hybrid, and deep learning (DL) methods fall substantially short of either atomic accuracy or computational efficiency. To overcome these limitations, we present KarmaLoop, a novel paradigm that distinguishes itself as the first DL method centered on full-atom (encompassing both backbone and side-chain heavy atoms) protein loop modeling. Our results demonstrate that KarmaLoop considerably outperforms conventional and DL-based methods of loop modeling in terms of both accuracy and efficiency, with the average RMSDs of 1.77 and 1.95 Å for the CASP13+14 and CASP15 benchmark datasets, respectively, and manifests at least 2 orders of magnitude speedup in general compared with other methods. Consequently, our comprehensive evaluations indicate that KarmaLoop provides a state-of-the-art DL solution for protein loop modeling, with the potential to hasten the advancement of protein engineering, antibody-antigen recognition, and drug design.
Keyphrases
  • deep learning
  • protein protein
  • amino acid
  • binding protein
  • healthcare
  • machine learning
  • small molecule
  • artificial intelligence
  • convolutional neural network
  • drug induced
  • electronic health record