|
323
|
866
|
4xn7A |
Crystal structure of e. coli aminopeptidase n in complex with l-2,3-diaminopropionic acid |
|
317
|
866
|
4xn5A |
Crystal structure of met260ala mutant of e. coli aminopeptidase n in complex with l-phenylalanine |
|
324
|
866
|
4xn2A |
Crystal structure of met260ala mutant of e. coli aminopeptidase n in complex with l-leucine |
|
329
|
866
|
4xn8A |
Crystal structure of e. coli aminopeptidase n in complex with l-alanine |
|
324
|
867
|
4xmzA |
Crystal structure of met260ala mutant of e. coli aminopeptidase n in complex with 2,4-diaminobutyric acid |
|
329
|
866
|
4xmxA |
Crystal structure of met260ala mutant of e. coli aminopeptidase n in complex with bestatin |
|
328
|
867
|
4xmwA |
Crystal structure of met260ala mutant of e. coli aminopeptidase n in complex with l-aspartic acid |
|
321
|
887
|
4wz9A |
Apn1 from anopheles gambiae |
|
306
|
866
|
4qhpA |
Crystal structure of aminopeptidase n in complex with the phosphinic dipeptide analogue ll-(r,s)-hphep[ch2]phe(4-ch2nh2) |
|
302
|
865
|
4quoA |
Crystal structure of aminopeptidase n in complex with the phosphinic dipeptide analogue ll-(r,s)-hphep[ch2]phe(3-ch2nh2) |
|
325
|
866
|
4q4iA |
Crystal structure of e.coli aminopeptidase n in complex with amastatin |
|
300
|
864
|
4pu2A |
Crystal structure of aminopeptidase n in complex with the phosphonic acid analogue of leucine l-(r)-leup |
|
326
|
889
|
4r5tA |
Structure of the m1 alanylaminopeptidase from malaria complexed with a hydroxamic acid-based inhibitor |
|
114
|
316
|
4tlnA |
Binding of hydroxamic acid inhibitors to crystalline thermolysin suggests a pentacoordinate zinc intermediate in catalysis |
|
303
|
866
|
4qmeA |
Crystal structure of aminopeptidase n in complex with the phosphinic dipeptide analogue ll-(r,s)-hphep[ch2]phe |
|
330
|
888
|
4r5xA |
Structure of the m1 alanylaminopeptidase from malaria complexed with a hydroxamic acid-based inhibitor |
|
219
|
607
|
4rvbA |
Crystal structure analysis of the human leukotriene a4 hydrolase |
|
117
|
316
|
4tmnE |
Slow-and fast-binding inhibitors of thermolysin display different modes of binding. crystallographic analysis of extended phosphonamidate transition-state analogues |
|
307
|
864
|
4qirA |
Crystal structure of aminopeptidase n in complex with the phosphinic dipeptide analogue ll-(r,s)-2-(pyridin-3-yl)ethylglyp[ch2]phe |
|
123
|
316
|
4tliA |
Thermolysin (25% isopropanol soaked crystals) |
|
310
|
865
|
4pw4A |
Crystal structure of aminopeptidase n in complex with phosphonic acid analogue of homophenylalanine l-(r)-hphep |
|
322
|
866
|
4q4eA |
Crystal structure of e.coli aminopeptidase n in complex with actinonin |
|
112
|
316
|
4tnlA |
1.8 a resolution room temperature structure of thermolysin recorded using an xfel |
|
218
|
607
|
4rsyA |
Crystal structures of the human leukotriene a4 hydrolase complex with a potential inhibitor h7 |
|
329
|
889
|
4r5vA |
Structure of the m1 alanylaminopeptidase from malaria complexed with a hydroxamic acid-based inhibitor |
|
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 |
|
308
|
901
|
4naqA |
Crystal structure of porcine aminopeptidase-n complexed with poly-alanine |
|
317
|
902
|
4ou3A |
Crystal structure of porcine aminopeptidase n complexed with cngrcg tumor-homing peptide |
|
296
|
867
|
4pj6A |
Crystal structure of human insulin regulated aminopeptidase with lysine in active site |
|
289
|
867
|
4p8qA |
Crystal structure of human insulin regulated aminopeptidase with alanine in active site |
|
311
|
901
|
4nz8A |
Crystal structure of porcine aminopeptidase-n complexed with cleaved poly-alanine |
|
110
|
316
|
4ow3A |
Thermolysin structure determined by free-electron laser |
|
120
|
316
|
4n5pE |
Thermolysin in complex with ubtln20 |
|
120
|
316
|
4n4eE |
Thermolysin in complex with ubtln58 |
|
119
|
316
|
4n66E |
Thermolysin in complex with ubtln37 |
|
313
|
879
|
4kxdA |
Crystal structure of human aminopeptidase a complexed with glutamate and calcium |
|
339
|
888
|
4j3bA |
A naturally variable residue in the s1 subsite of m1-family aminopeptidases modulates catalytic properties and promotes functional specialization |
|
334
|
889
|
4k5nA |
Phosphonic arginine mimetics as inhibitors of the m1 aminopeptidases from plasmodium falciparum |
|
316
|
879
|
4kx9A |
Crystal structure of human aminopeptidase a complexed with arginine |
|
121
|
316
|
4oi5E |
Glycerol-free structure of thermolysin in complex with ubtln58 |
|
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 |
|
119
|
316
|
4mtwE |
Thermolysin in complex with ubtln36 |
|
119
|
316
|
4mxjE |
Thermolysin in complex with ubtln35 |
|
119
|
316
|
4mznE |
Thermolysin in complex with ubtln59 |
|
226
|
608
|
4mktA |
Human leukotriene a4 hydrolase in complex with pro-gly-pro analogue and 4-(4-benzylphenyl)thiazol-2-amine |
|
309
|
879
|
4kxcA |
Crystal structure of human aminopeptidase a complexed with glutamate |
|
334
|
889
|
4k5lA |
Phosphonic arginine mimetics as inhibitors of the m1 aminopeptidases from plasmodium falciparum |
|
314
|
879
|
4kx7A |
Crystal structure of human aminopeptidase a |
