Found 1040 chains in Genus chains table. Displaying 751 - 800. Applied filters: Proteins

Search results query ec: 5.2.1.8

Total Genus Sequence Length pdb Title
45 157 3kaiA Structure-guided design of alpha-amino acid-derived pin1 inhibitors
44 157 3kadA Structure-guided design of alpha-amino acid-derived pin1 inhibitors
41 157 3kafA Structure-guided design of alpha-amino acid-derived pin1 inhibitors
39 113 3kacA Structure-guided design of alpha-amino acid-derived pin1 inhibitors
44 158 3kceA Structure-guided design of alpha-amino acid-derived pin1 inhibitors
42 157 3kahA Structure-guided design of alpha-amino acid-derived pin1 inhibitors
49 157 3kagA Structure-guided design of alpha-amino acid-derived pin1 inhibitors
45 157 3kabA Structure-guided design of alpha-amino acid-derived pin1 inhibitors
46 162 3k0pA Cryogenic structure of cypa mutant ser99thr
46 164 3k0mA Cryogenic structure of cypa
49 164 3k0qA Cryogenic structure of cypa mutant ser99thr (2)
40 113 3jyjA Structure-based design of novel pin1 inhibitors (ii)
46 164 3k0oA Room temperature structure of cypa mutant ser99thr
57 239 3jxvA Crystal structure of the 3 fkbp domains of wheat fkbp73
62 354 3jymA Crystal structure of the 3 fkbp domains of wheat fkbp73
51 176 3k2cA Crystal structure of peptidyl-prolyl cis-trans isomerase from encephalitozoon cuniculi at 1.9 a resolution
47 164 3k0rA Cryogenic structure of cypa mutant arg55lys
45 163 3k0nA Room temperature structure of cypa
41 113 3ikgA Structure-based design of novel pin1 inhibitors (i)
36 113 3ikdA Structure-based design of novel pin1 inhibitors (i)
50 180 3ichA Crystal structure of cyclophilin b at 1.2 a resolution
50 188 3iciA Crystal structure of cyclophilin b in complex with calmegin fragment
37 113 3ik8A Structure-based design of novel pin1 inhibitors (i)
42 113 3i6cA Structure-based design of novel pin1 inhibitors (ii)
27 107 3h9rB Crystal structure of the kinase domain of type i activin receptor (acvr1) in complex with fkbp12 and dorsomorphin
30 108 3gpkA Crystal structure of ppic-type peptidyl-prolyl cis-trans isomerase domain at 1.55a resolution.
114 414 3gtyX Promiscuous substrate recognition in folding and assembly activities of the trigger factor chaperone
95 406 3gu0A Promiscuous substrate recognition in folding and assembly activities of the trigger factor chaperone
24 107 3fapA Atomic structures of the rapamycin analogs in complex with both human fkbp12 and frb domain of frap
43 166 3eovA Crystal structure of cyclophilin from leishmania donovani ligated with cyclosporin a
29 118 3ey6A Crystal structure of the fk506-binding domain of human fkbp38
28 165 3cysA Determination of the nmr solution structure of the cyclophilin a-cyclosporin a complex
53 164 3cyhA Cyclophilin a complexed with dipeptide ser-pro
28 151 3cgnA Crystal structure of thermophilic slyd
35 157 3cgmA Crystal structure of thermophilic slyd
45 166 3bt8A Crystal structure of mutant cyclophilin (r147a) from leishmania donovani
17 65 3b09A Crystal structure of the n-domain of fkbp22 from shewanella sp. sib1
29 125 3b7xA Crystal structure of human fk506-binding protein 6
45 158 2zr4A Crystal structure of a mutant pin1 peptidyl-prolyl cis-trans isomerase
47 158 2zqtA Crystal structure of a mutant pin1 peptidyl-prolyl cis-trans isomerase
42 158 2zquA Crystal structure of a mutant pin1 peptidyl-prolyl cis-trans isomerase
45 158 2zqvA Crystal structure of a mutant pin1 peptidyl-prolyl cis-trans isomerase
39 158 2zr6A Crystal structure of a mutant pin1 peptidyl-prolyl cis-trans isomerase
44 158 2zr5A Crystal structure of a mutant pin1 peptidyl-prolyl cis-trans isomerase
42 158 2zqsA Crystal structure of a mutant pin1 peptidyl-prolyl cis-trans isomerase
57 164 2z6wA Crystal structure of human cyclophilin d in complex with cyclosporin a
29 122 2y78A Crystal structure of bpss1823, a mip-like chaperone from burkholderia pseudomallei
43 157 2xp8A Discovery of cell-active phenyl-imidazole pin1 inhibitors by structure-guided fragment evolution
53 165 2xgyB Complex of rabbit endogenous lentivirus (relik)capsid with cyclophilin a
47 157 2xpbA Discovery of cell-active phenyl-imidazole pin1 inhibitors by structure-guided fragment evolution