6OHS
Structure of compound 3 (ML299) bound human Phospholipase D2 catalytic domain
Summary for 6OHS
| Entry DOI | 10.2210/pdb6ohs/pdb |
| Descriptor | Phospholipase D2, 4-bromo-N-{(2S)-1-[1-(3-fluorophenyl)-4-oxo-1,3,8-triazaspiro[4.5]decan-8-yl]propan-2-yl}benzamide (2 entities in total) |
| Functional Keywords | phosphodiesterase, hydrolase, hkd motif, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
| Biological source | Homo sapiens (Human) |
| Total number of polymer chains | 4 |
| Total formula weight | 293344.65 |
| Authors | Metrick, C.M.,Chodaparambil, J.V. (deposition date: 2019-04-06, release date: 2020-02-19, Last modification date: 2023-10-11) |
| Primary citation | Metrick, C.M.,Peterson, E.A.,Santoro, J.C.,Enyedy, I.J.,Murugan, P.,Chen, T.,Michelsen, K.,Cullivan, M.,Spilker, K.A.,Kumar, P.R.,May-Dracka, T.L.,Chodaparambil, J.V. Human PLD structures enable drug design and characterization of isoenzyme selectivity. Nat.Chem.Biol., 16:391-399, 2020 Cited by PubMed: 32042197DOI: 10.1038/s41589-019-0458-4 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (3.2 Å) |
Structure validation
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