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 |
|---|---|---|
| 5TE9 | 2016 | 0 |
| 5TF4 | 2016 | 0 |
| 5THK | 2016 | 0 |
| 5THX | 2016 | 0 |
| 5TP4 | 2017 | 0 |
| 8SBV | 2023 | 0 |
| 5TR9 | 2016 | 0 |
| 8SBX | 2023 | 0 |
| 5TT1 | 2016 | 0 |
| 5TVK | 2016 | 0 |
| # | PDB | Additional SSGCID structures cited | Link | Title | Year | Citation | Highlighted abstract |
|---|---|---|---|---|---|---|---|
| 1 | 5vn4 | - | https://www.nature.com/articles/s41598-021-91747-6 | Acyclic nucleoside phosphonates with adenine nucleobase inhibit Trypanosoma brucei adenine phosphoribosyltransferase in vitro | 2021 | E Doleelov, T Klejch, P paek, M Slapnikov- Scientific Reports, 2021 - nature.com | Acyclic nucleoside phosphonates (ANPs) represent a group of compounds whose biological activity is based on their structural resemblance to the natural nucleotides 8,9 . Their flexibility enables them to adopt a conformation suitable for the interaction with the active site ... To assess the probable binding modes of the most potent inhibitors, docking calculations were performed. Since T. brucei APRT1 has been slightly explored so far, the only experimental structure that is available for this enzyme |
| 2 | 4ewg | 3u0f | https://www.nature.com/articles/s41598-021-95890-y | Structural basis of the complementary activity of two ketosynthases in aryl polyene biosynthesis | 2021 | WC Lee, S Choi, A Jang, J Yeon, E Hwang, Y Kim- Scientific Reports, 2021 - nature.com | There is a protein structure in PDB ( 4EWG ), which shares ~ 59% identity with that of AbApeR. The two structures could be superposed with an rmsd of 0.574 . This ApeR homolog is |
| 3 | 4f2n | - | https://www.nature.com/articles/s41598-023-45448-x | Dual-target drugs against Leishmania donovani for potential novel therapeutics | 2023 | K Bora, M Sarma, SP Kanaujia, VK Dubey- Scientific Reports, 2023 - nature.com | For this study, the crystal structures of Leishmania major FeSODA ( PDB ID: 4F2N ) and ( PDB ID: 2JK6) were obtained from the PDB database 13,14 . The crystal structure of 4F2N was |
| 4 | 6d9y | - | https://www.nature.com/articles/s41598-024-65627-8 | Crystal structure of l-2-keto-3-deoxyfuconate 4-dehydrogenase reveals a unique binding mode as a -furanosyl hemiketal of substrates | 2024 | M Akagashi, S Watanabe, S Kwiatkowski, J Drozak- Scientific Reports, 2024 - nature.com | Although the crystal structure of l-KDRDH was unavailable, the closest related structure in the PDB , the hypothetical SDR protein from Burkholderia phymatum ( 6D9Y ; not yet published) |
| 5 | 4kam | - | https://www.nature.com/articles/s41598-024-79886-y | Targeting Candida albicans O-acetyl-L-homoserine sulfhydrylase (Met15p) in antifungal treatment | 2024 | A Kupliska, K Rzd, J Stefaniak-Skorupa- Scientific Reports, 2024 - nature.com | Several O-acetyl-L-homoserine or L-homocysteine structural analogs were analyzed as potential inhibitors of CaMet15p. In these studies, a newly developed RP-HPLC-MS method ... The quaternary structure of CaMet15p is therefore consistent with those of its S. cerevisiae29 (PDB code: 8OVH), Wolinella succinogenes13 (PDB code: 3RI6), and Mycobacterium marinum30 (PDB code: 4KAM) counterparts. |
| 6 | 7jzl | - | https://www.nature.com/articles/s41598-025-12444-2 | Fusion of SARS-CoV-2 neutralizing LCB1 peptide with Bacillus amyloliquefaciens RNase improves antiviral efficacy | 2025 | NN Kostin, TV Bobik, EV Konovalova- Scientific Reports, 2025 - nature.com | structural interaction with the trimeric spike ( PDB : 7JZL ). Its in vivo efficacy has been demonstrated in multiple studies, including in transgenic mouse models 14 . Moreover, its compact |
| 7 | 7l6s | - | https://www.nature.com/articles/s41598-025-93122-1 | Structural insights into fungal and human topoisomerase II with implications for in silico antifungal drug design | 2025 | S Sappati, K Kondaka, I Gabriel, M Baginski- Scientific Reports, 2025 - nature.com | Our analysis extended to include representative from Amoebozoa (Balamuthia mandrillaris), utilizing PDB ID 7L6S for a comprehensive comparative study. |
| 8 | 7l6c | - | https://www.nature.com/articles/s41598-025-97513-2 | Identification of novel inhibitors targeting Mycobacterium abscessus InhA through virtual screening, docking, and molecular dynamic simulations | 2025 | M Abbas, AR Alanzi, KI Sahibzada, M Nawaz- Scientific Reports, 2025 - nature.com | Enoyl-ACP reductase InhA ( PDB : 7L6 C) crystal structures were carefully chosen after an The possible binding modes of the top six hit compounds in the 7L6c binding pocket. Hit |
| 9 | 4kam | - | https://www.nature.com/articles/s42003-020-0954-9 | Adaptive laboratory evolution enhances methanol tolerance and conversion in engineered Corynebacterium glutamicum | 2020 | Y Wang, L Fan, P Tuyishime, J Liu, K Zhang- Communications, 2020 - nature.com | Synthetic methylotrophy has recently been intensively studied to achieve methanol-based biomanufacturing of fuels and chemicals. However, attempts to engineer platform microorganisms to utilize methanol mainly focus on enzyme and pathway engineering... The model structure of the wild-type Cgl0653 was constructed with the crystal structure of O-acetyl-L-homoserine sulfhydrylase from Mycobacterium marinum ATCC BAA-535 (PDB ID: 4KAM) as a template (54% sequence identity with Cgl0653) |
| 10 | 7m53 | - | https://www.nature.com/articles/s42003-022-03262-7 | Structural definition of a pan-sarbecovirus neutralizing epitope on the spike S2 subunit | 2022 | NK Hurlburt, LJ Homad, I Sinha, MF Jennewein- Communications, 2022 - nature.com | a Structural alignment of stem helix peptides to CV3-25 Fab and B6 Fab (PDBid: 7M53 ) shown The CV3-25/peptide structure has been deposited in the PDB (7RAQ). The negative stain |