Structural genomics and the Protein Data Bank

被引:10
|
作者
Michalska, Karolina [1 ,2 ]
Joachimiak, Andrzej [1 ,2 ,3 ]
机构
[1] Univ Chicago, Ctr Struct Genom Infect Dis, Chicago, IL 60637 USA
[2] Argonne Natl Lab, Xray Sci Div, Struct Biol Ctr, Lemont, IL 60439 USA
[3] Univ Chicago, Dept Biochem & Mol Biol, 920 E 58Th St, Chicago, IL 60637 USA
基金
美国国家卫生研究院;
关键词
BIOLOGY KNOWLEDGEBASE; TARGET SELECTION; DRUG DISCOVERY; DIFFRACTION; VALIDATION; PDB; AI;
D O I
10.1016/j.jbc.2021.100747
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
The field of Structural Genomics arose over the last 3 decades to address a large and rapidly growing divergence between microbial genomic, functional, and structural data. Several international programs took advantage of the vast genomic sequence information and evaluated the feasibility of structure determination for expanded and newly discovered protein families. As a consequence, structural genomics has developed structure-determination pipelines and applied them to a wide range of novel, uncharacterized proteins, often from "microbial dark matter," and later to proteins from human pathogens. Advances were especially needed in protein production and rapid de novo structure solution. The experimental three-dimensional models were promptly made public, facilitating structure determination of other members of the family and helping to understand their molecular and biochemical functions. Improvements in experimental methods and databases resulted in fast progress in molecular and structural biology. The Protein Data Bank structure repository played a central role in the coordination of structural genomics efforts and the structural biology community as a whole. It facilitated development of standards and validation tools essential for maintaining high quality of deposited structural data.
引用
收藏
页数:9
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