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 3p96 - https://pure.unamur.be/ws/files/51548461/publi_marinum_postprint.pdf researchportal. unamur. be 2020 E Pierson, J Wouters - pure.unamur.be avium (MavSerB, based on the surrounding residues in PDB structures 5JLR and 5JLP) are The superimposition of MmaSerB2 model with the structures of MavSerB 3P96 and
2 3p96 - http://link.springer.com/article/10.1007/s00018-016-2177-2 The M. tuberculosis HAD phosphatase (Rv3042c) interacts with host proteins and is inhibited by Clofazimine 2016 S Shree, AK Singh, R Saxena, H Kumar - Cellular and Molecular , 2016 - Springer ... SanyalAffiliated withBiochemistry Division, CSIR-Central Drug Research Institute; and 1 more: ,Ravishankar RamachandranAffiliated withMolecular and Structural Biology Division ... Homologymodels of MtSerB2 based on M. avium SerB (PDB code 3P96) were generated ...
3 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). ...
4 3p96 - http://onlinelibrary.wiley.com/doi/10.1002/prot.24238/full Identification of a novel ligand binding site in phosphoserine phosphatase from the hyperthermophilic archaeon Thermococcus onnurineus 2013 TY Jung, YS Kim, BH Oh, E Woo - Proteins: Structure, Function, and Bioinformatics, 2013 - Wiley Online Library ... Flexible movement between the open structure (PDB ID: 1L8L, 1RKV, 2FEA, and 3M1Y), colored in bright orange, and closed structures (PDB ID: 1F5S, 1L7M, 1J97, 1L7P, 3P96, and 3KD3), colored in bluewhite, were analyzed by the program DynDom. ...
5 3p96 - https://www.nature.com/articles/s42003-023-05402-z A morpheein equilibrium regulates catalysis in phosphoserine phosphatase SerB2 from Mycobacterium tuberculosis 2023 E Pierson, F De Pol, M Fillet, J Wouters- Communications Biology, 2023 - nature.com structure 14 ( PDB : 3P96 ). The residues are exposed to solvent and not engaged in intramolecular interactions. The difference in numbering comes from the fact that MaSerB bears two
6 3p96 - https://www.mdpi.com/1420-3049/25/2/415 Identification and Repurposing of Trisubstituted Harmine Derivatives as Novel Inhibitors of Mycobacterium tuberculosis Phosphoserine Phosphatase 2020 E Pierson, M Haufroid, TP Gosain, P Chopra, R Singh- Molecules, 2020 - mdpi.com SerB2 model generated by homology modeling based on the crystal structure of Mycobacterium avium SerB (Protein Data Bank ( PDB ) entry 3P96 ) is in The docked structure of the best inhibitor, compound 124, is shown in Figure 4. Analysis of those structures shows that
7 3p96 - http://pubs.acs.org/doi/abs/10.1021/acs.biochem.7b01082 Regulatory Mechanism of Mycobacterium tuberculosis Phosphoserine Phosphatase SerB2 2017 GA Grant- Biochemistry, 2017 - ACS Publications figure Figure 1. Ribbon diagram of the structure of M. avium phosphoserine phosphatase (maPSP, Protein Data Bank entry 3p96 ) (right panel). The enzyme is a dimer with each subunit consisting of a catalytic domain (dark
8 3p4t - http://search.proquest.com/openview/daf8fc817648cf5585c39f0c60983d2f/1?pq-origsi... Mycobacterium tuberculosis cholesterol catabolism utilizes a structurally and evolutionarily discrete class of acyl-Coenzyme A dehydrogenase 2015 MF Wipperman - 2015 - search.proquest.com This image (grey) shows the crystal structure of tetrameric FadE13 from M smegmatis (pdb: 3P4T) using the DAMAVER modeling algorithm.
9 3p4i 4dq8 http://uir.unisa.ac.za/handle/10500/19148 Mycobacterium tuberculosis kinases as potential drug targets: production of recombinant kinases in E. coli for functional characterization and enzyme inhibition 2015 V Lukman - 2015 - uir.unisa.ac.za ... Other mycobacterial AKs have been deposited in the Protein Data Bank (www.pdb.org), with high levels of similarity to the putative Mtb AK (M. avum, pdb 3P4I at 74.4% and M. marinum pdb 4DQ8 at 75.1%). ...
10 3p4i - http://www.biomedcentral.com/1472-6807/12/24/ Structural and mechanistic investigations on Salmonella typhimurium acetate kinase (AckA): identification of a putative ligand binding pocket at the dimeric interface 2012 S Chittori, H Savithri, M Murthy - BMC structural biology, 2012 - biomedcentral.com ... Crystal structures of two archeal acetate kinases, from Thermotoga maritima (PDB:2IIR, unpublished results) and Methanosarcina thermophila[15] and one from Mycobacterium avium (PDB:3P4I, unpublished results) have been determined earlier. ...