|
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 |
