Sequence-assignment validation in protein crystal structure models with checkMySequence

被引:1
|
作者
Chojnowski, Grzegorz [1 ]
机构
[1] European Mol Biol Lab, Hamburg Unit, Notkestr 85, D-22607 Hamburg, Germany
来源
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY | 2023年 / 79卷
关键词
macromolecular crystallography; register shifts; findMySequence; model validation; checkMySequence; sequence validation; REFINEMENT; ACCURACY;
D O I
10.1107/S2059798323003765
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Sequence-register shifts remain one of the most elusive errors in experimental macromolecular models. They may affect model interpretation and propagate to newly built models from older structures. In a recent publication, it was shown that register shifts in cryo-EM models of proteins can be detected using a systematic reassignment of short model fragments to the target sequence. Here, it is shown that the same approach can be used to detect register shifts in crystal structure models using standard, model-bias-corrected electron-density maps (2mF(o) - DFc). Five register-shift errors in models deposited in the PDB detected using this method are described in detail.
引用
收藏
页码:559 / 568
页数:10
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