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6OHP

Structure of compound 1 (halopemide) bound human Phospholipase D2 catalytic domain

Summary for 6OHP
Entry DOI10.2210/pdb6ohp/pdb
DescriptorPhospholipase D2, N-{2-[4-(5-chloro-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)piperidin-1-yl]ethyl}-4-fluorobenzamide, SULFATE ION, ... (5 entities in total)
Functional Keywordsphosphodiesterase, hydrolase, hkd motif, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceHomo sapiens (Human)
Total number of polymer chains4
Total formula weight294131.13
Authors
Metrick, C.M.,Chodaparambil, J.V. (deposition date: 2019-04-06, release date: 2020-02-19, Last modification date: 2023-11-15)
Primary citationMetrick, 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: 32042197
DOI: 10.1038/s41589-019-0458-4
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.6 Å)
Structure validation

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