DoubleHelix: nucleic acid sequence identification, assignment and validation tool for cryo-EM and crystal structure models

被引:5
|
作者
Chojnowski, Grzegorz [1 ]
机构
[1] Hamburg Unit, European Mol Biol Lab, Notkestr 85, D-22607 Hamburg, Germany
关键词
REFINEMENT; MAPS; CRYSTALLOGRAPHY; ISOSTERICITY; PREDICTIONS; EXPANSION; ACCURACY; RIBOSOME; DATABASE; MOTIFS;
D O I
10.1093/nar/gkad553
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sequence assignment is a key step of the model building process in both cryogenic electron microscopy (cryo-EM) and macromolecular crystallography (MX). If the assignment fails, it can result in difficult to identify errors affecting the interpretation of a model. There are many model validation strategies that help experimentalists in this step of protein model building, but they are virtually non-existent for nucleic acids. Here, I present doubleHelix-a comprehensive method for assignment, identification, and validation of nucleic acid sequences in structures determined using cryo-EM and MX. The method combines a neural network classifier of nucleobase identities and a sequence-independent secondary structure assignment approach. I show that the presented method can successfully assist sequence-assignment step in nucleic-acid model building at lower resolutions, where visual map interpretation is very difficult. Moreover, I present examples of sequence assignment errors detected using doubleHelix in cryo-EM and MX structures of ribosomes deposited in the Protein Data Bank, which escaped the scrutiny of available model-validation approaches. The doubleHelix program source code is available under BSD-3 license at .
引用
收藏
页码:8255 / 8269
页数:15
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