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5L9H

Crystal structure of T. brucei PDE-B1 catalytic domain with inhibitor NPD-340

Summary for 5L9H
Entry DOI10.2210/pdb5l9h/pdb
DescriptorPhosphodiesterase, ZINC ION, MAGNESIUM ION, ... (7 entities in total)
Functional Keywordsparasitic pde, african trypanosomiasis, sleeping sickness, hydrolase
Biological sourceTrypanosoma brucei
Total number of polymer chains2
Total formula weight82779.58
Authors
Singh, A.K.,Brown, D.G. (deposition date: 2016-06-10, release date: 2018-03-14, Last modification date: 2018-05-23)
Primary citationBlaazer, A.R.,Singh, A.K.,de Heuvel, E.,Edink, E.,Orrling, K.M.,Veerman, J.J.N.,van den Bergh, T.,Jansen, C.,Balasubramaniam, E.,Mooij, W.J.,Custers, H.,Sijm, M.,Tagoe, D.N.A.,Kalejaiye, T.D.,Munday, J.C.,Tenor, H.,Matheeussen, A.,Wijtmans, M.,Siderius, M.,de Graaf, C.,Maes, L.,de Koning, H.P.,Bailey, D.S.,Sterk, G.J.,de Esch, I.J.P.,Brown, D.G.,Leurs, R.
Targeting a Subpocket in Trypanosoma brucei Phosphodiesterase B1 (TbrPDEB1) Enables the Structure-Based Discovery of Selective Inhibitors with Trypanocidal Activity.
J. Med. Chem., 61:3870-3888, 2018
Cited by
PubMed: 29672041
DOI: 10.1021/acs.jmedchem.7b01670
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.25 Å)
Structure validation

218500

数据于2024-04-17公开中

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