Found 400 chains in Genus chains table. Displaying 1 - 50. Applied filters: Proteins

Search results query: COesterase

Total Genus Sequence Length pdb Title
181 539 6wvoA Crystal structure of recombinant human acetylcholinesterase in complex with gd and hi-6
183 531 7b2wA Torpedo californica acetylcholinesterase complexed with uo2
187 532 7b8eA Torpedo californica acetylcholinesterase complexed with ca+2
168 573 7ceeA Crystal structure of mouse neuroligin-3
189 532 7b38A Torpedo californica acetylcholinesterase complexed with mg+2
179 539 6wuzA Crystal structure of recombinant human acetylcholinesterase inhibited by gb
145 579 7cegB Crystal structure of the complex between mouse ptp delta and neuroligin-3
180 540 6wv1A Crystal structure of recombinant human acetylcholinesterase in complex with gb and hi-6
172 539 6wvpA Crystal structure of recombinant human acetylcholinesterase inhibited by gf
176 540 6wvqA Crystal structure of recombinant human acetylcholinesterase inhibited by gp
172 539 6wuvA Crystal structure of recombinant human acetylcholinesterase inhibited by ga
177 540 6wvcA Crystal structure of recombinant human acetylcholinesterase inhibited by gd
179 539 6wuyA Crystal structure of recombinant human acetylcholinesterase in complex with ga and hi-6
171 527 6xtaA Recombinant human butyrylcholinesterase in complex with (2s)-n-[2-(1-benzylazepan-4-yl)ethyl]-2-(butylamino)-3-(1h-indol-3-yl)propanamide
169 532 6tt0A Crystal structure of a potent and reversible dual binding site acetylcholinesterase chiral inhibitor
168 526 6t9sA Human butyrylcholinesterase in complex with 2-(n-hydroxyimino)-n-[(1s)-3-{4-[(2-methyl-1h-imidazol-1-yl)methyl]-1h-1,2,3-triazol-1-yl}-1- phenylpropyl]acetamide
168 526 6t9pA Human butyrylcholinesterase in complex with 2-(n-hydroxyimino)-n-[(1r)-3-{4-[(2-methyl-1h-imidazol-1-yl)methyl]-1h-1,2,3-triazol-1-yl}-1- phenylpropyl]acetamide
178 540 6ntoA Crystal structure of recombinant human acetylcholinesterase inhibited by a-230
170 540 6ntkA Crystal structure of recombinant human acetylcholinesterase inhibited by a-232
177 539 6ntnA Crystal structure of recombinant human acetylcholinesterase inhibited by a-230 in complex with the reactivator, hi-6
171 539 6ntgA Crystal structure of recombinant human acetylcholinesterase inhibited by a-234 in complex with reactivator, hi-6
179 540 6ntlA Crystal structure of recombinant human acetylcholinesterase inhibited by a-234
176 540 6nthA Crystal structure of recombinant human acetylcholinesterase inhibited by (s) stereoisomer of a-232
175 566 5ivhA The alpha-esterase-7 carboxylesterase, e3, from the blowfly lucilia cuprina: apo-enzyme ensemble refinement
181 566 5ivkA The alpha-esterase-7 carboxylesterase, e3, from the blowfly lucilia cuprina: phosphorylated-enzyme ensemble refinement
169 558 6i2tA Cryoem reconstruction of full-length, fully-glycosylated human butyrylcholinesterase tetramer
174 539 6cqyA Crystal structure of recombinant human acetylcholinesterase in complex with empa and hi-6
175 540 6cquA Crystal structure of recombinant human acetylcholinesterase with reactivator hi-6
170 540 6cqvA Crystal structure of recombinant human acetylcholinesterase in complex with vx(+) and hi-6
177 540 6cqzA Crystal structure of recombinant human acetylcholinesterase inhibited by vx
181 540 6cqtA Crystal structure of recombinant human acetylcholinesterase inhibited by (-) stereoisomer of vx
168 542 6fsdA Mus musculus acetylcholinesterase in complex with 2-(4-biphenylyloxy)-n-[3-(1-piperidinyl)propyl]-acetamide hydrochloride (10)
186 532 6ezgA Torpedo californica ache in complex with indolic multi-target directed ligand
185 532 6ewkA T. californica ache in complex with a 3-hydroxy-2-pyridine aldoxime.
179 540 6cqxA Crystal structure of recombinant human acetylcholinesterase inhibited by vx(+)
167 542 6fseA Mus musculus acetylcholinesterase in complex with 1-(4-(4-ethylpiperazin-1-yl)piperidin-1-yl)-2-((4'-methoxy-[1,1'-biphenyl]-4-yl)oxy)ethanone dihydrochloride (15)
185 532 6eucA Reactivating oxime bound to tc ache's catalytic gorge.
173 540 6cqwA Crystal structure of recombinant human acetylcholinesterase in complex with vx(-) and hi-6
184 532 6ezhA Torpedo californica ache in complex with indolic multi-target directed ligand
183 532 6eueA Rivastigmine analogue bound to tc ache.
168 539 6f25A Crystal structure of human acetylcholinesterase in complex with c35.
163 526 6qacA Human butyrylcholinesterase in complex with (s)-2-(butylamino)-n-(3-cycloheptylpropyl)-3-(1h-indol-3-yl)propanamide
174 526 6qaaA Human butyrylcholinesterase in complex with (s)-2-(butylamino)-n-(2-cycloheptylethyl)-3-(1h-indol-3-yl)propanamide
173 526 6qabA Human butyrylcholinesterase in complex with (s)-n-(1-((2-cycloheptylethyl)amino)-3-(1h-indol-3-yl)-1-oxopropan-2-yl)-n,n-dimethylbutan-1-aminium
170 526 6qaeA Human butyrylcholinesterase in complex with (s)-n2-butyl-n1-(2-cycloheptylethyl)-3-(1h-indol-3-yl)-n1,n2-dimethylpropane-1,2-diamine
173 526 6i0bA Human butyrylcholinesterase in complex with the s enantiomer of a chlorotacrine-tryptophan multi-target inhibitor.
170 526 6qadA Human butyrylcholinesterase in complex with ((s)-2-(butylamino)-n-(2-(4-(dimethylamino)cyclohexyl)ethyl)-3-(1h-indol-3-yl)propanamide
176 537 6o69A Crystal structure of double mutant l380r/f535k of human acetylcholinesterase
174 534 6h19A Crystal structure of ethyl-paraoxon inhibited recombinant human bile salt activated lipase (aged form)
167 533 6h0vA Crystal structure of tabun surrogate nedpa inhibited recombinant human bile salt activated lipase