Accurate prediction of protein structures and interactions using a three-track neural network.
ADAM Proteins
/ chemistry
Amino Acid Sequence
Computer Simulation
Cryoelectron Microscopy
Crystallography, X-Ray
Databases, Protein
Deep Learning
Membrane Proteins
/ chemistry
Models, Molecular
Multiprotein Complexes
/ chemistry
Neural Networks, Computer
Protein Conformation
Protein Folding
Protein Subunits
/ chemistry
Proteins
/ chemistry
Receptors, G-Protein-Coupled
/ chemistry
Sphingosine N-Acyltransferase
/ chemistry
Journal
Science (New York, N.Y.)
ISSN: 1095-9203
Titre abrégé: Science
Pays: United States
ID NLM: 0404511
Informations de publication
Date de publication:
20 08 2021
20 08 2021
Historique:
received:
07
06
2021
accepted:
07
07
2021
pubmed:
21
7
2021
medline:
28
8
2021
entrez:
20
7
2021
Statut:
ppublish
Résumé
DeepMind presented notably accurate predictions at the recent 14th Critical Assessment of Structure Prediction (CASP14) conference. We explored network architectures that incorporate related ideas and obtained the best performance with a three-track network in which information at the one-dimensional (1D) sequence level, the 2D distance map level, and the 3D coordinate level is successively transformed and integrated. The three-track network produces structure predictions with accuracies approaching those of DeepMind in CASP14, enables the rapid solution of challenging x-ray crystallography and cryo-electron microscopy structure modeling problems, and provides insights into the functions of proteins of currently unknown structure. The network also enables rapid generation of accurate protein-protein complex models from sequence information alone, short-circuiting traditional approaches that require modeling of individual subunits followed by docking. We make the method available to the scientific community to speed biological research.
Identifiants
pubmed: 34282049
pii: science.abj8754
doi: 10.1126/science.abj8754
pmc: PMC7612213
mid: EMS140725
doi:
Substances chimiques
Membrane Proteins
0
Multiprotein Complexes
0
Protein Subunits
0
Proteins
0
Receptors, G-Protein-Coupled
0
CERS1 protein, human
EC 2.3.1.24
Sphingosine N-Acyltransferase
EC 2.3.1.24
ADAM Proteins
EC 3.4.24.-
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
871-876Subventions
Organisme : Austrian Science Fund FWF
ID : P 29432
Pays : Austria
Organisme : NIGMS NIH HHS
ID : R35 GM127390
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM123089
Pays : United States
Organisme : NIGMS NIH HHS
ID : P01 GM063210
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI051321
Pays : United States
Organisme : Wellcome Trust
ID : 209407
Pays : United Kingdom
Organisme : NIH HHS
ID : DP5 OD026389
Pays : United States
Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.
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