letters to the editor\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

Journal logoSTRUCTURAL
BIOLOGY
ISSN: 2059-7983

Announcing the launch of Protein Data Bank China as an Associate Member of the Worldwide Protein Data Bank Partnership

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aProtein Data Bank China, ShanghaiTech University and National Facility for Protein Science in Shanghai, Shanghai, People's Republic of China, bProtein Data Bank in Europe, European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, United Kingdom, cElectron Microscopy Data Bank, European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, United Kingdom, dBiological Magnetic Resonance Data Bank, UConn Health, Farmington, CT 06030-3305, USA, eResearch Collaboratory for Structural Bioinformatics Protein Data Bank, Institute for Quantitative Biomedicine and Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA, fResearch Collaboratory for Structural Biology Protein Data Bank, San Diego Supercomputer Center, University of California San Diego, La Jolla, CA 92093, USA, gProtein Data Bank Japan, Institute for Protein Research, Osaka University, Osaka 565-0871, Japan, and hProtein Data Bank Japan, Protein Research Foundation, Minoh, Osaka 562-8686, Japan
*Correspondence e-mail: xuwq2@shanghaitech.edu.cn, sameer@ebi.ac.uk, stephen.burley@rcsb.org, gkurisu@protein.osaka-u.ac.jp

Edited by R. J. Read, University of Cambridge, United Kingdom (Received 1 July 2023; accepted 21 July 2023; online 10 August 2023)

This paper is dedicated to the International Union of Crystallography on the occasion of its 75th anniversary.

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.

In 1971, the Protein Data Bank (PDB) was established as a global public good jointly by Brookhaven National Laboratory (BNL) in the United States and Cambridge Crystallo­graphic Data Center in the United Kingdom (Protein Data Bank, 1971[Protein Data Bank (1971). Nature New Biol. 233, 223.]). It was managed by BNL until 1998, with continuous support from US federal funders. Between 1999 and 2003, the PDB was managed by the Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB; https://www.rcsb.org), headquartered at Rutgers University (Berman et al., 2000[Berman, H. M., Westbrook, J., Feng, Z., Gilliland, G., Bhat, T. N., Weissig, H., Shindyalov, I. N. & Bourne, P. E. (2000). Nucleic Acids Res. 28, 235-242.]), again with continuous support from US federal funders. Between 1999 and 2003, Protein Data Bank in Europe (PDBe; https://www.pdbe.org) and Protein Data Bank Japan (PDBj; https://www.pdbj.org) coordinated deposition and biocuration efforts with RCSB PDB.

Since 2003, the PDB archive has been managed by the wwPDB (Berman et al., 2003[Berman, H. M., Henrick, K. & Nakamura, H. (2003). Nat. Struct. Mol. Biol. 10, 980.]), an international nongovernmental organization founded by three regionally funded wwPDB data centers: RCSB PDB (United States), PDBe (United Kingdom and Europe) and PDBj (Japan). Two method-focused wwPDB data centers, the Biological Magnetic Resonance Bank (BMRB; https://bmrb.io) and the Electron Microscopy Data Bank (EMDB; https://www.ebi.ac.uk/emdb), joined the wwPDB in 2006 and 2021, respectively (wwPDB Consortium, 2019[wwPDB Consortium (2019). Nucleic Acids Res. 47, D520-D528.]). wwPDB partners adhere to the FAIR principles of Findability, Accessibility, Interoperability and Reusability (Wilkinson et al., 2016[Wilkinson, M. D., Dumontier, M., Aalbersberg, I. J. J., Appleton, G., Axton, M., Baak, A., Blomberg, N., Boiten, J.-W.., da Silva Santos, L. B., Bourne, P. E., Bouwman, J., Brookes, A. J., Clark, T., Crosas, M., Dillo, I., Dumon, O., Edmunds, S., Evelo, C. T., Finkers, R., Gonzalez-Beltran, A., Gray, A. J. G., Groth, P., Goble, C., Grethe, J. S., Heringa, J., 't Hoen, P. A. C., Hooft, R., Kuhn, T., Kok, R., Kok, J., Lusher, S. J., Martone, M. E., Mons, A., Packer, A. L., Persson, B., Rocca-Serra, P., Roos, M., van Schaik, R., Sansone, S.-A., Schultes, E., Sengstag, T., Slater, T., Strawn, G., Swertz, M. A., Thompson, M., van der Lei, J., van Mulligen, E., Velterop, J., Waagmeester, A., Wittenburg, P., Wolstencroft, K., Zhao, J. & Mons, B. (2016). Sci. Data, 3, 160018.]), and ensure that all archival data can be accessed at no charge and with no limitations on usage under the most permissive Creative Commons CC0 1.0 Universal License (https://creativecommons.org/publicdomain/zero/1.0/). At present, wwPDB members jointly manage three Core Archives overseen by wwPDB-designated Archive Keepers: the PDB (Archive Keeper: RCSB PDB), EMDB (Archive Keeper: EMDB) and BMRB (Archive Keeper: BMRB). wwPDB operations are guided by an international advisory committee (wwPDB AC; https://www.wwpdb.org/about/advisory) consisting of an independent chair, representatives appointed by each wwPDB data center and experts drawn from the macromolecular crystallography (MX), three-dimensional cryo-electron microscopy (3DEM) and nuclear magnetic resonance (NMR) spectroscopy communities. The wwPDB AC meets annually to review the health and wellbeing of the three Core Archives. Annual meeting presentations and reports are publicly available online.

With great foresight, PDB data were made freely available with no limitations on usage to the global scientific community (including for-profit users) at the time of launch in 1971. This pioneering online digital data resource, the first of its kind in biology, demonstrated the importance of free dissemination of scientific information to support both basic and applied researchers. A working group formed by the International Union of Crystallography (IUCr) defined the guidelines for 3D biostructure data deposition (Commission on Biological Macromolecules, 1989[Commission on Biological Macromolecules (1989). Acta Cryst. A45, 658.]). These guidelines formed the basis for the deposition of atomic coordinates and experimental data in the PDB. Today, most government and private bioscience funders and scientific journals mandate the deposition of 3D biostructure data as a condition for either funding or publication. The central role played by the PDB within the worldwide biodata ecosystem was recently recognized by its designation as a Global Core Biodata Resource `of fundamental importance to the wider biological and life sciences community and the long-term preservation of biological data' by the Global Biodata Coalition (https://globalbiodata.org).

When the wwPDB was launched 20 years ago, significant growth in the PDB archive was eagerly anticipated. At that time, each wwPDB data center accepted 3D biostructure depositions through independently operated data deposition/validation/biocuration (data-in) systems. To accommodate the increased demand for data archiving, wwPDB members initiated the development of a single global software system for data-in and started planning for the extension of the franchise to new PDB data centers for the management of depositions originating from emerging economies. Both steps were strongly endorsed by the wwPDB AC.

In 2015, the wwPDB launched OneDep (Young et al., 2017[Young, J. Y., Westbrook, J. D., Feng, Z., Sala, R., Peisach, E., Oldfield, T. J., Sen, S., Gutmanas, A., Armstrong, D. R., Berrisford, J. M., Chen, L., Chen, M., Di Costanzo, L., Dimitropoulos, D., Gao, G., Ghosh, S., Gore, S., Guranovic, V., Hendrickx, P. M. S., Hudson, B. P., Igarashi, R., Ikegawa, Y., Kobayashi, N., Lawson, C. L., Liang, Y., Mading, S., Mak, L., Mir, M. S., Mukhopadhyay, A., Patwardhan, A., Persikova, I., Rinaldi, L., Sanz-Garcia, E., Sekharan, M. R., Shao, C., Swaminathan, G. J., Tan, L., Ulrich, E. L., van Ginkel, G., Yamashita, R., Yang, H., Zhuravleva, M. A., Quesada, M., Kleywegt, G. J., Berman, H. M., Markley, J. L., Nakamura, H., Velankar, S. & Burley, S. K. (2017). Structure, 25, 536-545.]) as a single global system for complete deposition, rigorous validation (Gore et al., 2017[Gore, S., Sanz García, E., Hendrickx, P. M. S., Gutmanas, A., Westbrook, J. D., Yang, H., Feng, Z., Baskaran, K., Berrisford, J. M., Hudson, B. P., Ikegawa, Y., Kobayashi, N., Lawson, C. L., Mading, S., Mak, L., Mukhopadhyay, A., Oldfield, T. J., Patwardhan, A., Peisach, E., Sahni, G., Sekharan, M. R., Sen, S., Shao, C., Smart, O. S., Ulrich, E. L., Yamashita, R., Quesada, M., Young, J. Y., Nakamura, H., Markley, J. L., Berman, H. M., Burley, S. K., Velankar, S. & Kleywegt, G. J. (2017). Structure, 25, 1916-1927.]; Feng et al., 2021[Feng, Z., Westbrook, J. D., Sala, R., Smart, O. S., Bricogne, G., Matsubara, M., Yamada, I., Tsuchiya, S., Aoki-Kinoshita, K. F., Hoch, J. C., Kurisu, G., Velankar, S., Burley, S. K. & Young, J. Y. (2021). Structure, 29, 393-400.]) and expert biocuration of 3D biostructures (Young et al., 2018[Young, J. Y., Westbrook, J. D., Feng, Z., Peisach, E., Persikova, I., Sala, R., Sen, S., Berrisford, J. M., Swaminathan, G. J., Oldfield, T. J., Gutmanas, A., Igarashi, R., Armstrong, D. R., Baskaran, K., Chen, L., Chen, M., Clark, A. R., Costanzo, L. D., Dimitropoulos, D., Gao, G., Ghosh, S., Gore, S., Guranovic, V., Hendrickx, P. M. S., Hudson, B. P., Ikegawa, Y., Kengaku, Y., Lawson, C. L., Liang, Y., Mak, L., Mukhopadhyay, A., Narayanan, B., Nishiyama, K., Patwardhan, A., Sahni, G., Sanz-García, E., Sato, J., Sekharan, M. R., Shao, C., Smart, O. S., Tan, L., van Ginkel, G., Yang, H., Zhuravleva, M. A., Markley, J. L., Nakamura, H., Kurisu, G., Kleywegt, G. J., Velankar, S., Berman, H. M. & Burley, S. K. (2018). Database, 2018, bay002.]) in the PDB, EMDB and BMRB wwPDB Core Archives. The OneDep software system also supports the archive-wide remediation of existing structures (see, for example, Shao et al., 2021[Shao, C., Feng, Z., Westbrook, J. D., Peisach, E., Berrisford, J., Ikegawa, Y., Kurisu, G., Velankar, S., Burley, S. K. & Young, J. Y. (2021). Glycobiology, 31, 1204-1218.]) and the secure transfer of information among wwPDB data centers. Since it was launched, OneDep has been continuously maintained and upgraded by a wwPDB software developer team to ensure the robust capture of data from new and emerging structure-determination methods. At present, the wwPDB is working with major structural biology software providers to develop more automated and efficient deposition procedures and to capture data from standardized workflows commonly used within the MX and 3DEM communities.

Each wwPDB data center manages its own instance of OneDep. Initially, incoming structures were assigned to wwPDB data centers on a regional basis as follows: RCSB PDB, America and Oceania; PDBe/EMDB, Europe and Africa; PDBj, Asia and the Middle East. During 2017, RCSB PDB, PDBe/EMDB and PDBj processed 6206, 4044 and 2799 new depositions, respectively (a total of 13 049; MX, 11 915; 3DEM, 674; NMR, 460). In 2022, RCSB PDB, PDBe/EMDB and PDBj processed 7020, 4811 and 4214 new depositions, respectively (a total of 16 344; MX, 10 650; 3DEM, 5407; NMR, 287). Annual depositions of 3DEM experimental maps to EMDB were as follows: 1448 in 2017 (including 674 maps associated with PDB depositions and 774 maps without atomic coordinates) and 8519 in 2022 (including 5407 maps associated with PDB depositions and 3112 maps without atomic coordinates). Annual experimental data depositions to BMRB for NMR macromolecular structures were 460 in 2017 and 287 in 2022. The growth in the number of PDB depositions originating from Asia is primarily the result of increased investment in research and development within the People's Republic of China (PRC). In 2022, structural biologists working in the PRC contributed 3118 new PDB structures (accounting for ∼65% of all depositions originating from Asia). Reflecting the impact of the resolution revolution, 3DEM structure depositions to the PDB originating from the PRC in 2022 numbered 1538 (versus 1539 MX structure depositions and 41 NMR structure depositions originating from the PRC in 2022).

wwPDB operations are governed by an international agreement (https://www.wwpdb.org/about/agreement) that was most recently renewed at the beginning of 2021. The new `Charter of the wwPDB' defined all five existing members as Core Members of the wwPDB and established new processes for admitting new Associate Members and advancing them to Core Membership. These procedural changes were reviewed and endorsed by the wwPDB AC. Effective 1 February 2022, PDBc was admitted to the wwPDB partnership as its first Associate Member. During the remainder of 2022, to support the launch of PDBc, remote training, encompassing orientation and policy matters, was provided by RCSB PDB, PDBe and EMDB. Thereafter, PDBj provided full-time, hands-on training on-site for two PDBc biocurators in Osaka. RCSB PDB, PDBe and EMDB helped to mitigate the impact on PDBj by processing overflow depositions from Asia during PDBc on-site training.

Following two months of intensive training at PDBj, the PDBc biocurators returned to the National Facility for Protein Science in Shanghai and began processing PDB depositions originating from within the PRC using a new PDBc OneDep instance (currently managed by PDBj). As of the end of 2022, the PDBc biocurators had processed 297 new PDB depositions, representing ∼10% of the 3D biostructure depositions from the PRC for the year (∼7% of all Asian depositions). During 2023, it is expected that PDBc will process most, possibly all, depositions to all three wwPDB Core Archives made by structural biologists working in the PRC.

The wwPDB is excited to formally announce the launch of PDBc, coinciding with the 20th anniversary of continuous wwPDB operations serving more than 50 000 structural biolo­gists around the world and many millions of data consumers based in nearly every sovereign country recognized by the United Nations.

Acknowledgements

The authors thank the tens of thousands of structural biologists worldwide who have deposited structures and experimental data to the wwPDB Core Archives over the past 52 years, and the many millions of researchers, educators and students around the world who consume data from the wwPDB Core Archives: PDB, EMDB and BMRB. We also gratefully acknowledge the contributions to the success of the wwPDB and the wwPDB Core Archives made by past and present members of the wwPDB partner organizations RCSB PDB, PDBe, PDBj, PDBc, EMDB and BMRB. Finally, we thank Dr Helen M. Berman and Ms Christine Zardecki for consultation on the history of the PDB and the wwPDB.

Funding information

PDBc is supported by Shanghai Advanced Research Institute (SARI), Chinese Academy of Sciences and ShanghaiTech University. PDBe and EMDB are supported by the European Molecular Biology Laboratory–European Bioinformatics Institute and by the Wellcome Trust (104948/Z/14/Z and 221327/Z/20/Z). BMRB is supported by the US National Institutes of Health (R01GM109046, principal investigator J. C. Hoch). RCSB PDB is jointly funded by the National Science Foundation (DBI-1832184, principal investigator S. K. Burley), the US Department of Energy (DE-SC0019749, principal investigator S. K. Burley) and the National Cancer Institute, the National Institute of Allergy and Infectious Diseases and the National Institute of General Medical Sciences of the National Institutes of Health (R01GM133198, principal investigator S. K. Burley). PDBj is supported by grants from the Database Integration Coordination Program from the Department of NBDC program, Japan Science and Technology Agency (JPMJND2205, principal investigator G. Kurisu) and by the Platform Project for Supporting Drug Discovery and Life Science Research (Basis for Supporting Innovative Drug Discovery and Life Science Research; BINDS) from AMED (23ama121001, principal investigator G. Kurisu). Other funding awards to RCSB PDB by the NSF and to PDBe by the UK Biotechnology and Biological Research Council are jointly supporting the development of a Next Generation PDB archive (DBI-2019297, principal investigator S. K. Burley; BB/V004247/1, principal investigator S. Velankar) and new Mol* molecular-graphics tools (DBI-2129634, principal investigator S. K. Burley; BB/W017970/1, principal investigator S. Velankar).

References

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This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.

Journal logoSTRUCTURAL
BIOLOGY
ISSN: 2059-7983
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