RT Journal Article
SR Electronic
T1 Analysis of distance-based protein structure prediction by deep learning in CASP13
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 624460
DO 10.1101/624460
A1 Jinbo Xu
A1 Sheng Wang
YR 2019
UL http://biorxiv.org/content/early/2019/05/02/624460.abstract
AB This paper reports the CASP13 results of distance-based contact prediction, threading and folding methods implemented in three RaptorX servers, which are built upon the powerful deep convolutional residual neural network (ResNet) method initiated by us for contact prediction in CASP12. On the 32 CASP13 FM (free-modeling) targets with a median MSA (multiple sequence alignment) depth of 36, RaptorX yielded the best contact prediction among 46 groups and almost the best 3D structure modeling among all server groups without time-consuming conformation sampling. In particular, RaptorX achieved top L/5, L/2 and L long-range contact precision of 70%, 58% and 45%, respectively, and predicted correct folds (TMscore>0.5) for 18 of 32 targets. Although on average underperforming AlphaFold in 3D modeling, RaptorX predicted correct folds for all FM targets with >300 residues (T0950-D1, T0969-D1 and T1000-D2) and generated the best 3D models for T0950-D1 and T0969-D1 among all groups. This CASP13 test confirms our previous findings: (1) predicted distance is more useful than contacts for both template-based and free modeling; and (2) structure modeling may be improved by integrating alignment and co-evolutionary information via deep learning. This paper will discuss progress we have made since CASP12, the strength and weakness of our methods, and why deep learning performed much better in CASP13.