5LBO
Crystal structure of human phosphodiesterase 4D2 catalytic domain with inhibitor NPD-001
Summary for 5LBO
Entry DOI | 10.2210/pdb5lbo/pdb |
Related | 5G2B 5G57 5G5V 5L8C 5L8Y 5L9H 5LAQ |
Descriptor | cAMP-specific 3',5'-cyclic phosphodiesterase 4D, ZINC ION, MAGNESIUM ION, ... (9 entities in total) |
Functional Keywords | phosphodiesterase, hydrolase, camp hydrolysis, alternative splicing |
Biological source | Homo sapiens (Human) |
Cellular location | Apical cell membrane : Q08499 |
Total number of polymer chains | 4 |
Total formula weight | 172820.16 |
Authors | Singh, A.K.,Brown, D.G. (deposition date: 2016-06-16, release date: 2018-03-14, Last modification date: 2024-01-10) |
Primary citation | Blaazer, 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: 29672041DOI: 10.1021/acs.jmedchem.7b01670 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.25 Å) |
Structure validation
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