宣布中国蛋白质数据库成为全球蛋白质数据库合作伙伴关系的准会员。

IF 2.6 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Wenqing Xu, Sameer Velankar, Ardan Patwardhan, Jeffrey C Hoch, Stephen K Burley, Genji Kurisu
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引用次数: 0

摘要

蛋白质数据库(PDB)是通过大分子晶体学、核磁共振谱或三维冷冻电镜实验确定的生物大分子原子级三维结构的全球唯一档案库。蛋白质数据库正在不断扩大,最近来自亚洲的新结构沉积物迅速增加。2022 年,全球蛋白质数据库(wwPDB; https://www.wwpdb.org/)合作伙伴欢迎中国蛋白质数据库(PDBc; https://www.pdbc.org.cn)作为准会员加入该组织。PDBc 位于上海的国家蛋白质科学设施内,该设施与中国科学院上海高等研究院、上海高级免疫化学研究所和上海理工大学 iHuman 研究所有联系。这封信介绍了wwPDB的历史、最近建立的增加新的wwPDB数据中心的机制以及将PDBc纳入伙伴关系的过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Announcing the launch of Protein Data Bank China as an Associate Member of the Worldwide Protein Data Bank Partnership.

The Protein Data Bank (PDB) is the single global archive of atomic-level, three-dimensional structures of biological macromolecules experimentally determined by macromolecular crystallography, nuclear magnetic resonance spectroscopy or three-dimensional cryo-electron microscopy. The PDB is growing continuously, with a recent rapid increase in new structure depositions from Asia. In 2022, the Worldwide Protein Data Bank (wwPDB; https://www.wwpdb.org/) partners welcomed Protein Data Bank China (PDBc; https://www.pdbc.org.cn) to the organization as an Associate Member. PDBc is based in the National Facility for Protein Science in Shanghai which is associated with the Shanghai Advanced Research Institute of Chinese Academy of Sciences, the Shanghai Institute for Advanced Immunochemical Studies and the iHuman Institute of ShanghaiTech University. This letter describes the history of the wwPDB, recently established mechanisms for adding new wwPDB data centers and the processes developed to bring PDBc into the partnership.

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来源期刊
Acta Crystallographica. Section D, Structural Biology
Acta Crystallographica. Section D, Structural Biology BIOCHEMICAL RESEARCH METHODSBIOCHEMISTRY &-BIOCHEMISTRY & MOLECULAR BIOLOGY
CiteScore
4.50
自引率
13.60%
发文量
216
期刊介绍: Acta Crystallographica Section D welcomes the submission of articles covering any aspect of structural biology, with a particular emphasis on the structures of biological macromolecules or the methods used to determine them. Reports on new structures of biological importance may address the smallest macromolecules to the largest complex molecular machines. These structures may have been determined using any structural biology technique including crystallography, NMR, cryoEM and/or other techniques. The key criterion is that such articles must present significant new insights into biological, chemical or medical sciences. The inclusion of complementary data that support the conclusions drawn from the structural studies (such as binding studies, mass spectrometry, enzyme assays, or analysis of mutants or other modified forms of biological macromolecule) is encouraged. Methods articles may include new approaches to any aspect of biological structure determination or structure analysis but will only be accepted where they focus on new methods that are demonstrated to be of general applicability and importance to structural biology. Articles describing particularly difficult problems in structural biology are also welcomed, if the analysis would provide useful insights to others facing similar problems.
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