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 3p0x - http://onlinelibrary.wiley.com/doi/10.1111/j.1476-5381.2011.01629.x/full Lifting the lid on GPCRs: the role of extracellular loops 2012 M Wheatley, D Wootten, MT Conner… - British journal of …, 2012 - Wiley Online Library ... Family A GPCRs: ECL structural aspects. ... 2RH1); B, D3R (yellow; PDB accession 3PBL); C, A2A R (orange; PDB accession 2YDO); D, CXCR4 (green; PDB accession 3OE0). ... In contrast, theECL2 of the β 2 AR possess a radically different structure comprising a short α-helix that ...
2 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)
3 6nb7 6nb8, 6wps, 6wpt, 6ws6 https://www.sciencedirect.com/science/article/pii/S1471490620302118 Structural basis of SARS-CoV-2 and SARS-CoVantibody interactions 2020 E Gavor, YK Choong, SY Er, H Sivaraman- Trends in, 2020 - Elsevier While the binding of COV21 to the S-glycoprotein resembles the binding of the SARS-CoV S230( PDB : 6NB7 )[73], the binding interface SARS-CoV-2-S-S309-Fab[12] complex ( PDB : 6WPS/6WPT/6WS6) and the crystal structure of SARS
4 3o0m 4lsm https://link.springer.com/content/pdf/10.1038/srep13652.pdf Dimeric interactions and complex formation using direct coevolutionary couplings 2015 RN Dos Santos, F Morcos, B Jana, AD Andricopulo- Scientific reports, 2015 - Springer Structural Modeling. All the homodimers used in this study were retrieved from Protein Data Bank ( PDB )60. The PDB accession code for each structure is shown in Table 1. ... Histidine triad protein 3O0M 149 ... GAPDH 4LSM 346 Gp_dh_N
5 6xdh - https://academic.oup.com/bib/article-abstract/22/2/1476/6146769 A molecular modelling approach for identifying antiviral selenium-containing heterocyclic compounds that inhibit the main protease of SARS-CoV-2: an in silico 2021 A Rakib, Z Nain, SA Sami, S Mahmud- Briefings in, 2021 - academic.oup.com Abstract. Coronavirus disease 2019 (COVID-19), an infectious disease caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has been declar. ... For docking analysis, the following receptors were selected: PDB ID 6M3M for N protein, PDB ID 2GHV for the RBD of the S protein, PDB ID 6W9C for PLpro, PDB ID 6 M71 for RdRp, PDB ID 6ZSL for SARS-CoV-2 helicase (nsp13), 6WC1 for nsp9 RNA-replicase, and 6XDH for nsp15
6 3eon - http://pubs.acs.org/doi/pdf/10.1021/cr900368a Update 1 of: Proteases universally recognize beta strands in their active sites 2011 PK Madala, JDA Tyndall, T Nall, DP Fairlie - Chemical Reviews, 2011 - ACS Publications ... All endoprotease complexes deposited in the Protein Data Bank (PDB http://www.rcsb.org/pdb mir- rored at http://oca.wehi.edu.au:8383/oca/22) through July 2009 were included in this study, updated with only a few key structures beyond that date. ...
7 6wps 6vxx https://academic.oup.com/nar/article-abstract/49/D1/D282/5901966 CoV3D: a database of high resolution coronavirus protein structures 2021 R Gowthaman, JD Guest, R Yin- Nucleic acids, 2021 - academic.oup.com (A) Visualization of the superposed spike RBD complexes with antibody S309 ( PDB code 6WPS ) ( 20 ) and (B) A trimeric spike structure in RBD-closed conformation ( 5 ) ( PDB code 6VXX Park YJ, Tortorici MA, Wall A., McGuire AT and Veesler D. (2020) Structure , Function, and
8 7r7n - https://www.thelancet.com/journals/laninf/article/PIIS1473-3099(22)00311-5/fullt... Monoclonal antibody therapies against SARS-CoV-2 2022 D Focosi, S McConnell, A Casadevall- The Lancet Infectious, 2022 - thelancet.com PDB 7K8M). Antibody binding classes 14 are displayed as mesh space-filling. (C) Structures in complex with a single RBD domain ( PDB 6XEY). Antibody binding classes RBS-A, RBS- ... S2D10633 7r7n RBM class III*
9 3f9i 3grp https://www.cell.com/cell-chemical-biology/pdf/S1074-5521(15)00442-1.pdf Human ISPD is a cytidyltransferase required for dystroglycan O-mannosylation 2015 M Riemersma, DS Froese, W van Tol, UF Engelke- Chemistry & biology, 2015 - cell.com To provide molecular insight into hISPD properties, we determined the crystal structure of structure factors have been deposited with the PDB under the accession code PDB : 4CVH. Structure similarity of hISPD C-terminal domain, identified using DALI 3f9i 11.7 3.3 137 220 12 FabG R. prowazekii ... 3grp 11.4 3.2 131 209 15 B. henseliae
10 6vyb - https://www.tandfonline.com/doi/abs/10.1080/07391102.2020.1778537 Ethnomedicines of Indian origin for combating COVID-19 infection by hampering the viral replication: using structure-based drug discovery approach 2021 S Alagu Lakshmi, RMB Shafreen, A Priya- Structure and, 2021 - Taylor & Francis CoV-2 main protease ( PDB ID: 5R82. pdb ), spike protein ( PDB ID: 6VYB . pdb ) and human In order to minimize the energy, PDB structures of the target proteins were refined through for combating COVID-19 infection by hampering the viral replication: using structure -based drug