Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

2ZJV

Crystal Structure of Lymnaea stagnalis Acetylcholine Binding Protein (Ls-AChBP) Complexed with Clothianidin

Summary for 2ZJV
Entry DOI10.2210/pdb2zjv/pdb
Related2ZJU
DescriptorAcetylcholine-binding protein, 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3-methyl-2-nitroguanidine (3 entities in total)
Functional Keywordsacetylcholine binding protein, neonicotinoids, nicotinic acetylcholine receptor, clothianidin, cell junction, glycoprotein, immunoglobulin domain, secreted, synapse, signaling protein
Biological sourceLymnaea stagnalis (Great pond snail)
Cellular locationSecreted: P58154
Total number of polymer chains5
Total formula weight122357.45
Authors
Okajima, T.,Ihara, M.,Yamashita, A.,Oda, T.,Morimoto, T.,Matsuda, K. (deposition date: 2008-03-10, release date: 2008-04-08, Last modification date: 2024-10-30)
Primary citationIhara, M.,Okajima, T.,Yamashita, A.,Oda, T.,Hirata, K.,Nishiwaki, H.,Morimoto, T.,Akamatsu, M.,Ashikawa, Y.,Kuroda, S.,Mega, R.,Kuramitsu, S.,Sattelle, D.B.,Matsuda, K.
Crystal structures of Lymnaea stagnalis AChBP in complex with neonicotinoid insecticides imidacloprid and clothianidin
Invert.Neurosci., 8:71-81, 2008
Cited by
PubMed Abstract: Neonicotinoid insecticides, which act on nicotinic acetylcholine receptors (nAChRs) in a variety of ways, have extremely low mammalian toxicity, yet the molecular basis of such actions is poorly understood. To elucidate the molecular basis for nAChR-neonicotinoid interactions, a surrogate protein, acetylcholine binding protein from Lymnaea stagnalis (Ls-AChBP) was crystallized in complex with neonicotinoid insecticides imidacloprid (IMI) or clothianidin (CTD). The crystal structures suggested that the guanidine moiety of IMI and CTD stacks with Tyr185, while the nitro group of IMI but not of CTD makes a hydrogen bond with Gln55. IMI showed higher binding affinity for Ls-AChBP than that of CTD, consistent with weaker CH-pi interactions in the Ls-AChBP-CTD complex than in the Ls-AChBP-IMI complex and the lack of the nitro group-Gln55 hydrogen bond in CTD. Yet, the NH at position 1 of CTD makes a hydrogen bond with the backbone carbonyl of Trp143, offering an explanation for the diverse actions of neonicotinoids on nAChRs.
PubMed: 18338186
DOI: 10.1007/s10158-008-0069-3
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.7 Å)
Structure validation

227111

PDB entries from 2024-11-06

PDB statisticsPDBj update infoContact PDBjnumon