|
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 |
|
170
|
526
|
6i0cA |
Human butyrylcholinesterase in complex with the r enantiomer of a chlorotacrine-tryptophan multi-target inhibitor. |
|
167
|
533
|
6h0tA |
Crystal structure of native recombinant human bile salt activated lipase |
|
177
|
534
|
6h18A |
Crystal structure of sarin surrogate nimp inhibited recombinant human bile salt activated lipase |
|
183
|
532
|
6h12A |
Crystal structure of tcache complexed to 1-(6-oxo-1,2,3,4,6,10b-hexahydropyrido[2,1-a]isoindol-10-yl)-3-(4-(((1-(2-((1,2,3,4-tetrahydroacridin-9-yl)amino)ethyl)-1h-1,2,3-triazol-4-yl)methoxy)methyl)pyridin-2-yl)urea |
|
177
|
534
|
6h1aA |
Crystal structure of vx surrogate nemp inhibited recombinant human bile salt activated lipase |
|
191
|
532
|
6h14A |
Crystal structure of tcache complexed to 1-(6-oxo-1,2,3,4,6,10b-hexahydropyrido[2,1-a]isoindol-10-yl)-3-(4-(1-(2-((1,2,3,4-tetrahydroacridin-9-yl)amino)ethyl)-1h-1,2,3-triazol-4-yl)pyridin-2-yl)urea |
|
177
|
532
|
6h13A |
Crystal structure of tcache complexed to1-(4-((methyl((1-(2-((1,2,3,4-tetrahydroacridin-9-yl)amino)ethyl)-1h-1,2,3-triazol-4-yl)methyl)amino)methyl)pyridin-2-yl)-3-(6-oxo-1,2,3,4,6,10b-hexahydropyrido[2,1-a]isoindol-10-yl)urea |
|
154
|
537
|
5ydiA |
Crystal structure of acetylcholinesterase catalytic subunits of the malaria vector anopheles gambiae, new crystal packing |
|
179
|
569
|
5ikxA |
Crystal structure of the alpha-esterase-7 carboxyl esterase (dimer), e3, from lucilia cuprina |
|
150
|
531
|
1amnA |
Transition state analog: acetylcholinesterase complexed with m-(n,n,n-trimethylammonio)trifluoroacetophenone |
|
184
|
532
|
5nauA |
Torpedo californica acetylcholinesterase in complex with a non-chiral donepezil-like compound 20 |
|
185
|
532
|
5napA |
Torpedo californica acetylcholinesterase in complex with a non-chiral donepezil-like inhibitor 17 |
|
179
|
527
|
5lkrA |
Human butyrylcholinesterase complexed with n-propargyliperidines |
|
175
|
527
|
5k5eA |
Discovery and structure-activity relationships of a highly selective butyrylcholinesterase inhibitor by structure-based virtual screening |
