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6LUQ

Haloperidol bound D2 dopamine receptor structure inspired discovery of subtype selective ligands

Summary for 6LUQ
Entry DOI10.2210/pdb6luq/pdb
Descriptorchimera of D(2) dopamine receptor and Endolysin, 4-[4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl]-1-(4-fluorophenyl)butan-1-one, OLEIC ACID, ... (4 entities in total)
Functional Keywordsgpcr, dopamine receptor, haloperidol, d2 dopamine receptor, membrane protein
Biological sourceHomo sapiens (Human)
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Total number of polymer chains1
Total formula weight50385.11
Authors
Fan, L.,Tan, L.,Chen, Z.,Qi, J.,Nie, F.,Luo, Z.,Cheng, J.,Wang, S. (deposition date: 2020-01-30, release date: 2020-03-04, Last modification date: 2023-11-29)
Primary citationFan, L.,Tan, L.,Chen, Z.,Qi, J.,Nie, F.,Luo, Z.,Cheng, J.,Wang, S.
Haloperidol bound D2dopamine receptor structure inspired the discovery of subtype selective ligands.
Nat Commun, 11:1074-1074, 2020
Cited by
PubMed: 32103023
DOI: 10.1038/s41467-020-14884-y
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.1 Å)
Structure validation

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