|
329
|
889
|
4r5vA |
Structure of the m1 alanylaminopeptidase from malaria complexed with a hydroxamic acid-based inhibitor |
|
218
|
607
|
4rsyA |
Crystal structures of the human leukotriene a4 hydrolase complex with a potential inhibitor h7 |
|
304
|
867
|
4qpeA |
Crystal structure of aminopeptidase n in complex with n-cyclohexyl-1,2-diaminoethylphosphonic acid |
|
220
|
607
|
4r7lA |
Structure of human leukotriene a4 hydrolase in complex with inhibitor h1 |
|
131
|
378
|
4rcvA |
M. tuberculosis 1-deoxy-d-xylulose-5-phosphate reductoisomerase bound to 1-deoxy-l-erythrulose |
|
57
|
176
|
4nqwA |
Structure of mycobacterium tuberculosis extracytoplasmic function sigma factor sigk in complex with the cytosolic domain of its cognate anti-sigma factor rska |
|
339
|
888
|
4j3bA |
A naturally variable residue in the s1 subsite of m1-family aminopeptidases modulates catalytic properties and promotes functional specialization |
|
134
|
376
|
4ooeA |
M. tuberculosis 1-deoxy-d-xylulose-5-phosphate reductoisomerase w203y mutant bound to fosmidomycin and nadph |
|
222
|
608
|
4ms6A |
Human leukotriene a4 hydrolase in complex with pro-gly-pro analogue |
|
335
|
889
|
4k5mA |
Phosphonic arginine mimetics as inhibitors of the m1 aminopeptidases from plasmodium falciparum |
|
132
|
378
|
4oofA |
M. tuberculosis 1-deoxy-d-xylulose-5-phosphate reductoisomerase w203f mutant bound to fosmidomycin and nadph |
|
334
|
889
|
4k5nA |
Phosphonic arginine mimetics as inhibitors of the m1 aminopeptidases from plasmodium falciparum |
|
330
|
889
|
4k5oA |
Phosphonic arginine mimetics as inhibitors of the m1 aminopeptidases from plasmodium falciparum |
|
226
|
608
|
4mktA |
Human leukotriene a4 hydrolase in complex with pro-gly-pro analogue and 4-(4-benzylphenyl)thiazol-2-amine |
|
334
|
889
|
4k5lA |
Phosphonic arginine mimetics as inhibitors of the m1 aminopeptidases from plasmodium falciparum |
|
335
|
889
|
4k5pA |
Phosphonic arginine mimetics as inhibitors of the m1 aminopeptidases from plasmodium falciparum |
|
152
|
409
|
4kp7A |
Structure of plasmodium ispc in complex with a beta-thia-isostere derivative of fosmidomycin |
|
224
|
607
|
4l2lA |
Human leukotriene a4 hydrolase complexed with ligand 4-(4-benzylphenyl)thiazol-2-amine |
|
141
|
424
|
4jndA |
Structure of a c.elegans sex determining protein |
|
199
|
606
|
4gaaA |
Structure of leukotriene a4 hydrolase from xenopus laevis complexed with inhibitor bestatin |
|
143
|
416
|
4gaeA |
Crystal structure of plasmodium dxr in complex with a pyridine-containing inhibitor |
|
334
|
889
|
3q43A |
X-ray crystal structure of pfa-m1 bound to bestatin derivative 15 |
|
248
|
628
|
4flqA |
Crystal structure of amylosucrase double mutant a289p-f290i from neisseria polysaccharea. |
|
235
|
628
|
4flsA |
Crystal structure of amylosucrase inactive double mutant f290k-e328q from neisseria polysaccharea in complex with sucrose. |
|
248
|
628
|
4floA |
Crystal structure of amylosucrase double mutant a289p-f290c from neisseria polysaccharea |
|
325
|
866
|
3qjxA |
Crystal structure of e. coli aminopeptidase n in complex with l-serine |
|
243
|
628
|
4flrA |
Crystal structure of amylosucrase double mutant a289p-f290l from neisseria polysaccharea |
|
333
|
889
|
3q44A |
X-ray crystal structure of pfa-m1 bound to bestatin derivative 16 |
|
316
|
866
|
3puuA |
Crystal structure of glu121gln mutant of e. coli aminopeptidase n |
|
145
|
398
|
3r0iA |
Ispc in complex with an n-methyl-substituted hydroxamic acid |
|
147
|
482
|
4fcaA |
The crystal structure of a functionally unknown conserved protein from bacillus anthracis str. ames. |
|
315
|
866
|
3kedA |
Crystal structure of aminopeptidase n in complex with 2,4-diaminobutyric acid |
|
172
|
509
|
3jt1A |
Legionella pneumophila glucosyltransferase lgt1, udp-bound form |
|
165
|
520
|
3jszA |
Legionella pneumophila glucosyltransferase lgt1 n293a with udp-glc |
|
146
|
398
|
3iieA |
1-deoxy-d-xylulose 5-phosphate reductoisomerase from yersinia pestis. |
|
85
|
308
|
3hw2A |
Crystal structure of the sifa-skip(ph) complex |
|
210
|
606
|
3fuiA |
Leukotriene a4 hydrolase in complex with n-benzyl-4-[(2r)-pyrrolidin-2-ylmethoxy]aniline |
|
219
|
607
|
3fueA |
Leukotriene a4 hydrolase in complex with fragment 5-chloroindole and bestatin |
|
217
|
605
|
3fumA |
Leukotriene a4 hydrolase in complex with (r)-pyridin-4-yl[4-(2-pyrrolidin-1-ylethoxy)phenyl]methanol |
|
221
|
607
|
3fufA |
Leukotriene a4 hydrolase in complex with fragment 5-fluoroindole and bestatin |
|
217
|
607
|
3fuhA |
Leukotriene a4 hydrolase in complex with fragment 5-hydroxyindole and bestatin |
|
213
|
606
|
3fudA |
Leukotriene a4 hydrolase in complex with n-methyl-1-(2-thiophen-2-ylphenyl)methanamine |
|
218
|
607
|
3fu0A |
Leukotriene a4 hydrolase in complex with fragment 4-(4-fluorobenzoyl)pyridine |
|
223
|
607
|
3ftsA |
Leukotriene a4 hydrolase in complex with resveratrol |
|
216
|
606
|
3fu6A |
Leukotriene a4 hydrolase in complex with fragment (4-thiophen-2-ylphenyl)methanamine |
|
218
|
607
|
3ftvA |
Leukotriene a4 hydrolase in complex with fragment n-(pyridin-3-ylmethyl)aniline |
|
219
|
606
|
3fh5A |
Leukotriene a4 hydrolase complexed with inhibitor (2r)-2-[(4-benzylphenoxy)methyl]pyrrolidine. |
|
213
|
606
|
3fu5A |
Leukotriene a4 hydrolase in complex with (5-thiophen-2-ylthiophen-2-yl)methylamine |
|
220
|
607
|
3fh7A |
Leukotriene a4 hydrolase complexed with inhibitor 4-[(2s)-2-{[4-(4-chlorophenoxy)phenoxy]methyl}pyrrolidin-1-yl]butanoate. |
|
218
|
606
|
3ftyA |
Leukotriene a4 hydrolase in complex with fragment 3-(benzyloxy)pyridin-2-amine |
