4JFW
Crystal structure of a bacterial fucosidase with iminosugar inhibitor (2S,3S,4R,5S)-2-[N-(propylferrocene)]aminoethyl-5-methylpyrrolidine-3,4-diol
Summary for 4JFW
Entry DOI | 10.2210/pdb4jfw/pdb |
Related | 2WVV 4J27 4J28 4JFS 4JFT 4JFU 4JFV |
Descriptor | alpha-L-fucosidase, (3alpha)-[3-({2-[(2S,3S,4R,5S)-3,4-dihydroxy-5-methylpyrrolidin-2-yl]ethyl}amino)propyl]ferrocene, SULFATE ION, ... (5 entities in total) |
Functional Keywords | alpha-l-fucosidase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
Biological source | Bacteroides thetaiotaomicron |
Total number of polymer chains | 4 |
Total formula weight | 210817.74 |
Authors | Wright, D.W.,Davies, G.J. (deposition date: 2013-02-28, release date: 2013-09-18, Last modification date: 2023-09-20) |
Primary citation | Hottin, A.,Wright, D.W.,Steenackers, A.,Delannoy, P.,Dubar, F.,Biot, C.,Davies, G.J.,Behr, J.B. alpha-L-fucosidase inhibition by pyrrolidine-ferrocene hybrids: rationalization of ligand-binding properties by structural studies. Chemistry, 19:9526-9533, 2013 Cited by PubMed: 23740878DOI: 10.1002/chem.201301001 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.1 Å) |
Structure validation
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