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 3q8n - http://www.sciencedirect.com/science/article/pii/S0734975014001992 Bioinformatic analysis of a PLP-dependent enzyme superfamily suitable for biocatalytic applications 2015 F Steffen-Munsberg, C Vickers, H Kohls, H Land… - Biotechnology …, 2015 - Elsevier In this review we analyse structure/sequence-function relationships for the superfamily ofPLP-dependent enzymes with special emphasis on class III transaminase.
2 3iml 3tde, 3s82, 3rv2 https://febs.onlinelibrary.wiley.com/doi/abs/10.1111/febs.12784 Understanding molecular recognition of promiscuity of thermophilic methionine adenosyltransferase sMAT from Sulfolobussolfataricus 2014 F Wang, S Singh, J Zhang, TD Huber- The FEBS, 2014 - Wiley Online Library containing a nonnative product, and cumulatively these structures add new structural insight into the analysis here are the numbers from the AdoEth bound structure ( PDB code 4L2Z). To date, MAT structures from Escherichia coli [3, 4], Campylobacter jejuni [5], Burkholderia pseudomallei (PDB code 3IML), Entamoeba histolytica (PDB code 3SO4), Mycobacterium marinum (PDB code 3RV2), Mycobacterium avium (PDB code 3S82), Mycobacterium tuberculosis (PDB code 3TDE), Thermococcus kodakarensis [6], ...
3 7jv2 7jva https://www.cell.com/cell-reports/pdf/S2211-1247(21)01652-1.pdf Structural analysis of receptor binding domain mutations in SARS-CoV-2 variants of concern that modulate ACE2 and antibody binding 2021 D Mannar, JW Saville, X Zhu, SS Srivastava- Cell reports, 2021 - cell.com See Table S2 for PDB entries included in this analysis. (D) Structural overlap of all antibodies selected on the SARSCoV-2 RBD. Mutational positions within the RBD are highlighted. (E)
4 4tv4 - https://www.sciencedirect.com/science/article/pii/S0092867419302028 Cryo-EM Structure and Assembly of an Extracellular Contractile Injection System 2019 F Jiang, N Li, X Wang, J Cheng, Y Huang, Y Yang- Cell, 2019 - Elsevier Overall, the PVC particle displays a simplified structure of the bacterial phage A simplified architecture of T4 phage baseplate lies in the PVC syringe: Pvc5, Pvc7, Pvc8, and Pvc10 form a continuous central spike extending from the inner tube; Pvc11 (D) Initial models of Pvc1, Pvc2, Pvc9 and Pvc11 were built based onPDB: 4TV4, 3J9Q, 2IA7, 5HX2, respectively
5 6mg6 - https://www.tandfonline.com/doi/abs/10.1080/07388551.2020.1827367 Nitrilase: a promising biocatalyst in industrial applications for green chemistry 2021 JD Shen, X Cai, ZQ Liu, YG Zheng- Critical Reviews in, 2021 - Taylor & Francis 6I00), Saccharomyces cerevisiae ( PDB : 4H5U and 1F89), Pyrococcus abyssi ( PDB : 3KLC), Helicobacter pylori ( PDB : 6MG6 ) and Synechocystis ( PDB : 3WUY) has been obtained However, with most of the nitrilases, the crystal structure had been resolved, came from eukaryotes
6 5u25 - https://www.mdpi.com/2077-0383/8/12/2117 FAD/NADH Dependent Oxidoreductases: From Different Amino Acid Sequences to Similar Protein Shapes for Playing an Ancient Function 2019 L Trisolini, N Gambacorta, R Gorgoglione- Journal of Clinical, 2019 - mdpi.com Here, we present a structural comparative analysis showing that the investigated flavoprotein oxidoreductases have a highly similar overall structure , although the investigated Similarly, AIF-crystallized structure hosts a FAD and two NADH molecules (4bur. pdb , [26]) and
7 7lxz 7ly2 https://www.cell.com/cell-reports/pdf/S2211-1247(21)01401-7.pdf Neutralizing antibody 5-7 defines a distinct site of vulnerability in SARS-CoV-2 spike N-terminal domain 2021 G Cerutti, Y Guo, P Wang, MS Nair, M Wang, Y Huang- Cell reports, 2021 - cell.com We produced a structural superposition of all NTD-directed antibodies deposited in the PDB , superposed on NTD Ca atoms, in the context of SARS-CoV-2 spike trimer (Figure 2A). ... Figure S1. Sequence alignment for 5-7 with their corresponding germline genes, Related to Figures 1 and 2. 7LXZ McCallum et al., 2021
8 6vxx - https://www.tandfonline.com/doi/abs/10.1080/07391102.2020.1852117 Virtual screening of phytoconstituents from miracle herb nigella sativa targeting nucleocapsid protein and papain-like protease of SARS-CoV-2 for COVID-19 2022 S Siddiqui, S Upadhyay, R Ahmad- Structure and, 2022 - Taylor & Francis spike glycoprotein (closed state, PDB ID: 6VXX ), spike glycoprotein (open state, PDB ID: structures were subjected to refinements and energy minimizations. Whole pdb structures of
9 6d6j 3oj7 https://pubs.acs.org/doi/abs/10.1021/acs.jcim.9b00407 Upgrading and Validation of the AMBER Force Field for Histidine and Cysteine Zinc (II)-Binding Residues in Sites with Four Protein Ligands 2019 M Macchiagodena, M Pagliai, C Andreini- Journal of chemical, 2019 - ACS Publications quantum mechanical calculations on a training set of high-quality protein structures , encompassing the in the catalytic reaction of enzymes, by stabilizing the tertiary/quaternary structure of a cells.(5,7) The high thermodynamic stability of the tetrahedral zinc(II) structural sites in
10 6q07 - https://www.ncbi.nlm.nih.gov/pmc/articles/pmc8219949/ In-Silico evidence for a two receptor based strategy of SARS-CoV-2 2021 E Milanetti, M Miotto, L Di Rienzo- Frontiers in molecular, 2021 - ncbi.nlm.nih.gov Complex between MERS spike protein and sialic acid: PDB code 6Q07 Unbound SARS-CoV spike protein: PDB code 6CRV We use DMS (Richards, 1977) to compute the solvent accessible surface for all proteins structure , given their x-ray structure in PDB format (Berman et al