SSGCID
Seattle Structural Genomics Center for Infectious Disease

Cited Structures: list of articles citing SSGCID structures

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.

Cited structures

Manually reviewed citations

# PDB Additional SSGCID structures cited Link Title Year Citation Highlighted abstract
1 5ez3 - https://www.mdpi.com/1422-0067/21/15/5391 Characterization of the Proteins Involved in the DNA Repair Mechanism in M. smegmatis 2020 A Di Somma, C Can, A Moretta, A Cirillo- International journal of, 2020 - mdpi.com The primary structure of the recombinant protein was verified by MALDI mapping strategy (Supplementary Materials, Table S4) and its correct folding assessed by circular The Acyl-CoA dehydrogenase from Brucella melitensis in complex with FAD ( PDB code 5EZ3 A) was
2 5v6d 4dut, 6ay1, 4ek2, 4hr2 https://www.mdpi.com/1422-0067/21/18/6779 Structure, Folding and Stability of Nucleoside Diphosphate Kinases 2020 F Georgescauld, Y Song, A Dautant- International Journal of Molecular, 2020 - mdpi.com So far, 162 structures from 30 different species have been deposited within the Protein Data Bank ( PDB ) which fall to tetramer type II and two are isolated dimers [23,24,25] (Table 1). The structure of most tetramers was recently solved by a structural genomics approach yet ... 5v6d Neisseria gonorrhoeae in complex with citrate (1.85 Å) Abendroth, J.; Mayclin, S.J.; Lorimer, D.D.; Edwards, T.E.
3 4hjh - https://www.mdpi.com/1422-0067/21/24/9341 Genomic Analysis of Natural Rough Brucella melitensis Rev. 1 Vaccine Strains: Identification and Characterization of Mutations in Key Genes Associated with 2020 D Kornspan, R Lubkovskaia, S Mathur- International journal of, 2020 - mdpi.com through all homologs (Figure 2A). To evaluate the possible effect of the detected mutation on protein functionality, we conducted a structural analysis of the amino acid sequence of GST based on the solved 3D structure of this protein from Sinorhizobium meliloti ( PDB ID 4MDC) ... we conducted a structural analysis of the amino acid sequence of phosphomannomutase based on the solved 3D structure of its paralog phosphoglucomutase (PDB ID 4HJH,
4 3tcq - https://www.mdpi.com/1422-0067/24/7/6298 Cheminformatics-Based Study Identifies Potential Ebola VP40 Inhibitors 2023 E Broni, C Ashley, J Adams, H Manu, E Aikins- International Journal of, 2023 - mdpi.com Modeller generated five models using the 3D structures of 3TCQ and 7K5L as templates. structure of the VP40 with PDB ID 1ES6 as the parent template for modelling. 1ES6s structure
5 3p96 - https://www.mdpi.com/1424-8247/12/2/66 Targeting the Serine Pathway: A Promising Approach against Tuberculosis? 2019 M Haufroid, J Wouters- Pharmaceuticals, 2019 - mdpi.com Structural differences can occur from one specie to another, ie, human phosphoserine phosphatase is only composed of the PSP domain while of the pathway in order to inhibit the reaction in an allosteric manner (Figure 7b).... Structure of M. avium (3P96) with domain ACT-I in orange, ACT-II in blue, the linker between two ACT domains in red, PSP catalytic domain in grey, linker between PSP domain and ACT-II in green (b). ...
6 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 [
7 6tys - https://www.mdpi.com/1999-4915/12/3/342 Structural insight into paramyxovirus and pneumovirus entry inhibition 2020 M Aggarwal, RK Plemper- Viruses, 2020 - mdpi.com 19,20,21] have furthermore created a novel opportunity for structure -informed mechanistic Structural information is very limited compared to that available for the paramyxovirus attachment Consequently, crystal structures of prefusion PIV5 and NiV F ectodomains could only be
8 6q04 6VXX https://www.mdpi.com/1999-4915/12/9/909 The sialoside-binding pocket of SARS-CoV-2 spike glycoprotein structurally resembles MERS-CoV 2020 M Awasthi, S Gulati, DP Sarkar, S Tiwari, S Kateriya- Viruses, 2020 - mdpi.com Multiple sequence alignment of the NTD domains was performed with the Clustal W program [15]. 2.2. Structure Prediction. The cryo-EM structures of SARS-CoV-2 ( PDB ID: 6VXX) [8] and MERS-CoV ( PDB ID: 6Q04 ) [11] spike glycoproteins were used as the starting point for
9 6nb3 - https://www.mdpi.com/1999-4915/13/8/1615 What Binds Cationic Photosensitizers Better: Brownian Dynamics Reveals Key Interaction Sites on Spike Proteins of SARS-CoV, MERS-CoV, and SARS-CoV-2 2021 V Fedorov, E Kholina, S Khruschev, I Kovalenko- Viruses, 2021 - mdpi.com M-protein defines the shape of the viral envelope organizing CoVs assembly in the interaction with all other major structural proteins [9 Computational virology tools contribute greatly to the understanding of viral structure , infectivity and pathogenesis, and design of antiviral drugs ... The models of S-proteins of SARS-CoV and MERS-CoV were based on cryo-EM structures from the Protein Data Bank (PDB) with IDs 6NB3 and 5X58, respectively.
10 3u0g - https://www.mdpi.com/2073-4344/10/9/1024 Counterbalance of Stability and Activity Observed for Thermostable Transaminase from Thermobaculum terrenum in the Presence of Organic Solvents 2020 EY Bezsudnova, AY Nikolaeva, SY Kleymenov- Catalysts, 2020 - mdpi.com the hydration shell and the interface of the enzyme molecules, thus defining the balance between the structural integrity and Somewhat counterintuitively, crystallographic studies of solvent-resistant enzymes did not reveal significant changes in structures obtained from crystals