We are actively tracking the number of publications by the scientific community which reference our structures, whether in the main text, figure captions or supplementary material. Selected articles are manually reviewed. Publications by SSGCID authors are excluded from the manually reviewed list. From our manual curation results, we estimate that the false positive rate might be as high as 50% for some structures.
This list was obtained from Google Scholar searches using an API provided by Christian Kreibich.
| Structure | Year released | #citations |
|---|---|---|
| 6Q04 | 2020 | 36 |
| 6NB7 | 2019 | 34 |
| 7K45 | 2020 | 32 |
| 2LWK | 2012 | 31 |
| 7N8H | 2021 | 28 |
| 7JZL | 2020 | 28 |
| 7JVC | 2021 | 27 |
| 6BFU | 2017 | 26 |
| 3LAA | 2010 | 26 |
| 7LXY | 2021 | 26 |
| # | PDB | Additional SSGCID structures cited | Link | Title | Year | Citation | Highlighted abstract |
|---|---|---|---|---|---|---|---|
| 1 | 5k85 | 5u29 | https://aaltodoc.aalto.fi/items/ef5fbad3-e949-4f46-8925-8ec058ca3b0b | Investigating the substrate promiscuity of acetyl-CoA synthetase from A. ethanivorans through a structural approach | 2025 | M Nikkanen - 2025 - aaltodoc.aalto.fi | Analogous and similarly spatially aligned residues residues seem to have the same function in Acs structures with PDB accession numbers 5u29 and 5k85 (figure 3) [27]. |
| 2 | 3fdz | 3gp5 | https://core.ac.uk/download/pdf/649473507.pdf | Revisiting the Plasmodium falciparum druggable genome using predicted structures | 2025 | K Godinez-Macias, D Chen, J Wallis- npj Drug Discovery, 2 (1), 2025 - core.ac.uk | To assess druggability evidence, we leveraged the AlphaFill database of predicted ligandtransplants based on homology of AlphaFold structures to all structures in the PDB REDO |
| 3 | 7m53 | 7skz | https://onlinelibrary.wiley.com/doi/abs/10.1111/imr.70000 | A Structural Voyage Toward the Landscape of Humoral and Cellular Immune Escapes of SARSCoV2 | 2025 | J Liu, Y Wu, GF Gao- Immunological Reviews, 2025 - Wiley Online Library | Herein, from the perspectives of structural immunology, we outline the characteristics and : 7M53 ), and S2P6 (blue, PDB : 7RNJ) are superimposed with the prefusion S trimer ( PDB : |
| 4 | 3o0m | 3oj7 | https://papers.ssrn.com/sol3/papers.cfm?abstract_id=5273447 | Biochemical and Biophysical Characterization, and 3d Structure Modeling of Human Hint3, a Hydrolase of the Hit Superfamily | 2025 | R Dolot, M Sirerant, A Mikoajczyk- Available at SSRN - papers.ssrn.com | Structure modelling of the HINT3 (Gly36) variant revealed that the enzyme exists mainly in absent in the structures of HINT1 and HINT2. Analysis of the HINT3 structure shows that there... In a first attempt, a homology model for HINT3 was generated based on eight crystallographic structures with the PDB IDs: 5UVM, 6D6J, 6CVS, 3OJ7, 3O0M, 4INC, 3TW2, and 3O1Z (see Table S2) using the MODELLER 10.5 software. |
| 5 | 7ki4 | 7ki6 | https://advanced.onlinelibrary.wiley.com/doi/abs/10.1002/advs.202501996 | Potent Crossneutralizing Antibodies Reveal Vulnerabilities of Henipavirus Fusion Glycoprotein | 2025 | Y Ren, P Fan, X Zhang, T Fang, Z Chen- Advanced, 2025 - Wiley Online Library | structure of LayV F ( PDB ID: 8FEL). The root mean square deviation between the model and the reference LayV F or an incomplete postfusion NiV F ( PDB from the PDB database onto This study also used 6TYS, 7KI4, 7KI6, 7UOP, 7UP9, 7UPA, 7UPK, 7UPB, 7UPD, 6T3F, 8FEL, 8DMJ, and 7FAB from the Protein Data Bank. The data that support the findings of this study are available from the corresponding author upon reasonable request. |
| 6 | 3ndn | - | https://www.nature.com/articles/s42003-025-08051-6 | A pH-dependent direct sulfhydrylation pathway is required for the pathogenesis of Mycobacterium tuberculosis | 2025 | VK Nain, V Barik, M Pandey, M Pareek- Communications, 2025 - nature.com | For system preparation, the crystal structure of putative O-succinyl homoserine sulfhydrylase of M. tuberculosis was retrieved from RCSB PDB 56 ( PDB -ID: 3NDN 57 ). The protein has 4 |
| 7 | 6tys | 7ki6, 7ki4 | https://www.sciencedirect.com/science/article/pii/S016635422500141X | A monoclonal antibody targeting conserved regions of pre-fusion protein cross-neutralizes Nipah and Hendra virus variants | 2025 | T Li, H Xu, M Zhang, J Nie, B Liao, J Xie, Y Jiang, Y Liu- Antiviral Research, 2025 - Elsevier | The mAbs developed in this study and their conserved cross-neutralizing epitopes elucidated by structural analysis may contribute to the control of highly pathogenic HNV outbreaks. ... Local resolution estimation and filtering were performed using CryoSPARC. The cryo-EM structure of the NiV-F ectodomain (Protein Data Bank [PDB]: 6TYS) and crystal structure of the Fab (PDB: 7EJY) were aligned with the cryo-EM density map using UCSF Chimera |
| 8 | 7luy | 6wct | https://www.nature.com/articles/s41467-025-61732-y | Comprehensive profiling of the catalytic conformations of human Guanylate kinase | 2025 | L Wang, Z Li, Y Xuan, J Qin, S Li, F Zhong- Nature, 2025 - nature.com | The atomic coordinates and structure factors for GMPK in its free form and substrate-bound forms generated in this study were deposited to the Protein Data Bank ( PDB ) ... The source data underlying Figs. 1i, 2c, 3i and Supplementary Fig. 6c–i, 9a–d, 11e are provided as a Source Data file. Previously published data for crystal structures of GMPK are available with PDB accession codes: 1EX6, 1EX7, 1LVG, 1S4Q, 1S96, 1ZNX, 1ZNW, 1GKY, 2ANB, 2ANC, 2QOR, 3TR0, 6WCT, 7LUY, 8PTS. |
| 9 | 4h3e | 4lsm | https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cmdc.202500408 | Sertraline as a Scaffold for Antitrypanosoma Cruzi Drug Development: Design of Novel Derivatives and Computational Target Screening | 2025 | AS Mijoba, Z Blanco, NJ ParraGimnez- , 2025 - Wiley Online Library | For this analysis, we selected a panel of 14 key therapeutic targets involved in T. cruzi's physiological functions. The studied target proteins included: ...glyceraldehyde-3-phosphate dehydrogenase (4LSM)... superoxide dismutase (4H3E), trypanothione reductase (1AOG), and phosphodiesterase C (3V94). |
| 10 | 4f40 | 4gie | https://www.mdpi.com/1424-8247/18/10/1489 | Computational Investigation of the Potential Antileishmanial Mechanism of the Nitroindazole Derivative VATR131 | 2025 | O Casanova-Alvarez, N Mollineda-Diogo- Pharmaceuticals, 2025 - mdpi.com | structural damage to the parasite, further supporting their therapeutic potential [17]. VATR131s leishmanicidal activity, causing both structural and ultrastructural damage to the parasite [ |