2zxa Citations

Structural basis of alpha-fucosidase inhibition by iminocyclitols with K(i) values in the micro- to picomolar range.

Angew Chem Int Ed Engl 49 337-40 (2010)
Related entries: 2zwz, 2zx5, 2zx6, 2zx7, 2zx8, 2zx9, 2zxb, 2zxd

Cited: 17 times
EuropePMC logo PMID: 19967696

Articles - 2zxa mentioned but not cited (1)

  1. VaProS: a database-integration approach for protein/genome information retrieval. Gojobori T, Ikeo K, Katayama Y, Kawabata T, Kinjo AR, Kinoshita K, Kwon Y, Migita O, Mizutani H, Muraoka M, Nagata K, Omori S, Sugawara H, Yamada D, Yura K. J Struct Funct Genomics 17 69-81 (2016)


Reviews citing this publication (1)

  1. The dual role of fucosidases: tool or target. Jiménez-Pérez C, Guzmán-Rodríguez F, Cruz-Guerrero AE, Alatorre-Santamaría S. Biologia (Bratisl) 1-16 (2023)

Articles citing this publication (15)

  1. 1,3-1,4-α-L-fucosynthase that specifically introduces Lewis a/x antigens into type-1/2 chains. Sakurama H, Fushinobu S, Hidaka M, Yoshida E, Honda Y, Ashida H, Kitaoka M, Kumagai H, Yamamoto K, Katayama T. J Biol Chem 287 16709-16719 (2012)
  2. Design of an α-L-transfucosidase for the synthesis of fucosylated HMOs. Saumonneau A, Champion E, Peltier-Pain P, Molnar-Gabor D, Hendrickx J, Tran V, Hederos M, Dekany G, Tellier C. Glycobiology 26 261-269 (2016)
  3. Structural and thermodynamic analyses of α-L-fucosidase inhibitors. Lammerts van Bueren A, Popat SD, Lin CH, Davies GJ. Chembiochem 11 1971-1974 (2010)
  4. Assessing and improving the performance of consensus docking strategies using the DockBox package. Preto J, Gentile F. J Comput Aided Mol Des 33 817-829 (2019)
  5. Exploiting the hydrophobic terrain in fucosidases with aryl-substituted pyrrolidine iminosugars. Hottin A, Wright DW, Davies GJ, Behr JB. Chembiochem 16 277-283 (2015)
  6. Enhance the performance of current scoring functions with the aid of 3D protein-ligand interaction fingerprints. Liu J, Su M, Liu Z, Li J, Li Y, Wang R. BMC Bioinformatics 18 343 (2017)
  7. α-L-fucosidase inhibition by pyrrolidine-ferrocene hybrids: rationalization of ligand-binding properties by structural studies. Hottin A, Wright DW, Steenackers A, Delannoy P, Dubar F, Biot C, Davies GJ, Behr JB. Chemistry 19 9526-9533 (2013)
  8. Harnessing α-l-fucosidase for in vivo cellular senescence imaging. Koo S, Won M, Li H, Kim WY, Li M, Yan C, Sharma A, Guo Z, Zhu WH, Sessler JL, Lee JY, Kim JS. Chem Sci 12 10054-10062 (2021)
  9. The Staudinger/aza-Wittig/Grignard reaction as key step for the concise synthesis of 1-C-Alkyl-iminoalditol glycomimetics. Zoidl M, Gonzalez Santana A, Torvisco A, Tysoe C, Siriwardena A, Withers SG, Wrodnigg TM. Carbohydr Res 429 62-70 (2016)
  10. Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme. Chkioua L, Amri Y, Chaima S, Fenni F, Boudabous H, Ben Turkia H, Messaoud T, Tebib N, Laradi S. BMC Med Genomics 14 208 (2021)
  11. An F-type lectin domain directs the activity of Streptosporangium roseum alpha-l-fucosidase. Bishnoi R, Mahajan S, Ramya TNC. Glycobiology 28 860-875 (2018)
  12. Detection of Human α-L-Fucosidases by a Quinone Methide-Generating Probe: Enhanced Activities in Response to Helicobacter pylori Infection. Nandakumar M, Hsu YL, Lin JC, Lo C, Lo LC, Lin CH. Chembiochem 16 1555-1559 (2015)
  13. Development of Fluorogenic Substrates of α-l-Fucosidase Useful for Inhibitor Screening and Gene-expression Profiling. Miura K, Tsukagoshi T, Hirano T, Nishio T, Hakamata W. ACS Med Chem Lett 10 1309-1313 (2019)
  14. Arabinoamidine synthesis and its inhibition toward β-glucosidase (sweet almonds) in comparison to a library of galactonoamidines. Pickens JB, Striegler S, Fan QH. Bioorg Med Chem 24 3371-3377 (2016)
  15. Synthetic and Crystallographic Insight into Exploiting sp2 Hybridization in the Development of α-l-Fucosidase Inhibitors. Coyle T, Wu L, Debowski AW, Davies GJ, Stubbs KA. Chembiochem 20 1365-1368 (2019)