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6RZ9

Crystal structure of the human cysteinyl leukotriene receptor 2 in complex with ONO-2770372

Summary for 6RZ9
Entry DOI10.2210/pdb6rz9/pdb
DescriptorCysteinyl leukotriene receptor 2,Soluble cytochrome b562,Cysteinyl leukotriene receptor 2, (2~{S})-8-[[4-[4-(5-fluoranyl-2-methyl-phenyl)butoxy]phenyl]carbonylamino]-4-(4-oxidanyl-4-oxidanylidene-butyl)-2,3-dih ydro-1,4-benzoxazine-2-carboxylic acid, CHOLESTEROL, ... (7 entities in total)
Functional Keywordsgpcr, lcp, membrane protein, cysteinyl leukotriene, cyslt2, cysltr2, cyslt2r, asthma, bril, cysteinyl leukotriene receptor 2
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains1
Total formula weight53797.74
Authors
Primary citationGusach, A.,Luginina, A.,Marin, E.,Brouillette, R.L.,Besserer-Offroy, E.,Longpre, J.M.,Ishchenko, A.,Popov, P.,Patel, N.,Fujimoto, T.,Maruyama, T.,Stauch, B.,Ergasheva, M.,Romanovskaia, D.,Stepko, A.,Kovalev, K.,Shevtsov, M.,Gordeliy, V.,Han, G.W.,Katritch, V.,Borshchevskiy, V.,Sarret, P.,Mishin, A.,Cherezov, V.
Structural basis of ligand selectivity and disease mutations in cysteinyl leukotriene receptors.
Nat Commun, 10:5573-5573, 2019
Cited by
PubMed Abstract: Cysteinyl leukotriene G protein-coupled receptors CysLT and CysLT regulate pro-inflammatory responses associated with allergic disorders. While selective inhibition of CysLTR has been used for treating asthma and associated diseases for over two decades, CysLTR has recently started to emerge as a potential drug target against atopic asthma, brain injury and central nervous system disorders, as well as several types of cancer. Here, we describe four crystal structures of CysLTR in complex with three dual CysLTR/CysLTR antagonists. The reported structures together with the results of comprehensive mutagenesis and computer modeling studies shed light on molecular determinants of CysLTR ligand selectivity and specific effects of disease-related single nucleotide variants.
PubMed: 31811124
DOI: 10.1038/s41467-019-13348-2
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.73 Å)
Structure validation

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건을2024-11-06부터공개중

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