|
61
|
215
|
1yk7A |
Cathepsin k complexed with a cyanopyrrolidine inhibitor |
|
100
|
303
|
1xkgA |
Crystal structure of the major house dust mite allergen der p 1 in its pro form at 1.61 a resolution |
|
116
|
357
|
1x9yA |
The prostaphopain b structure |
|
62
|
215
|
1vsnA |
Crystal structure of a potent small molecule inhibitor bound to cathepsin k |
|
115
|
397
|
1vjvA |
Crystal structure of ubiquitin carboxyl-terminal hydrolase 6 (yfr010w) from saccharomyces cerevisiae at 1.74 a resolution |
|
68
|
188
|
1ukfA |
Crystal structure of pseudomonas avirulence protein avrpphb |
|
63
|
215
|
1u9qX |
Crystal structure of cruzain bound to an alpha-ketoester |
|
62
|
215
|
1u9vA |
Crystal structure of the cysteine protease human cathepsin k in complex with the covalent inhibitor nvp-abe854 |
|
63
|
216
|
1u9xA |
Crystal structure of the cysteine protease human cathepsin k in complex with the covalent inhibitor nvp-abj688 |
|
161
|
699
|
1u5iA |
Crystal structure analysis of rat m-calpain mutant lys10 thr |
|
61
|
216
|
1u9wA |
Crystal structure of the cysteine protease human cathepsin k in complex with the covalent inhibitor nvp-abi491 |
|
64
|
215
|
1tu6A |
Cathepsin k complexed with a ketoamide inhibitor |
|
75
|
253
|
1theA |
Crystal structures of recombinant rat cathepsin b and a cathepsin b-inhibitor complex: implications for structure-based inhibitor design |
|
96
|
321
|
1tl9A |
High resolution crystal structure of calpain i protease core in complex with leupeptin |
|
95
|
322
|
1tloA |
High resolution crystal structure of calpain i protease core in complex with e64 |
|
63
|
212
|
1stfE |
The refined 2.4 angstroms x-ray crystal structure of recombinant human stefin b in complex with the cysteine proteinase papain: a novel type of proteinase inhibitor interaction |
|
49
|
205
|
1sp4B |
Crystal structure of ns-134 in complex with bovine cathepsin b: a two headed epoxysuccinyl inhibitor extends along the whole active site cleft |
|
64
|
214
|
1snkA |
Cathepsin k complexed with carbamate derivatized norleucine aldehyde |
|
65
|
224
|
1s4vA |
The 2.0 a crystal structure of the kdel-tailed cysteine endopeptidase functioning in programmed cell death of ricinus communis endosperm |
|
164
|
899
|
1qxpA |
Crystal structure of a mu-like calpain |
|
40
|
156
|
1qmyA |
Fmdv leader protease (lbshort-c51a-c133s) |
|
76
|
253
|
1qdqA |
X-ray crystal structure of bovine cathepsin b-ca074 complex |
|
38
|
173
|
1qolA |
Structure of the fmdv leader protease |
|
64
|
215
|
1q6kA |
Cathepsin k complexed with t-butyl(1s)-1-cyclohexyl-2-oxoethylcarbamate |
|
62
|
216
|
1ppoA |
Determination of the structure of papaya protease omega |
|
66
|
212
|
1pipA |
Crystal structure of papain-succinyl-gln-val-val-ala-ala-p-nitroanilide complex at 1.7 angstroms resolution: noncovalent binding mode of a common sequence of endogenous thiol protease inhibitors |
|
53
|
183
|
1pxvA |
The staphostatin-staphopain complex: a forward binding inhibitor in complex with its target cysteine protease |
|
70
|
212
|
1ppnA |
Structure of monoclinic papain at 1.60 angstroms resolution |
|
62
|
212
|
1pppA |
Crystal structure of papain-e64-c complex. binding diversity of e64-c to papain s2 and s3 subsites |
|
105
|
368
|
1pvjA |
Crystal structure of the streptococcal pyrogenic exotoxin b (speb)- inhibitor complex |
|
67
|
212
|
1ppdA |
Restrained least-squares refinement of the sulfhydryl protease papain to 2.0 angstroms |
|
66
|
212
|
1popA |
X-ray crystallographic structure of a papain-leupeptin complex |
|
70
|
212
|
1pe6A |
Refined x-ray structure of papain(dot)e-64-c complex at 2.1-angstroms resolution |
|
54
|
212
|
1padA |
Binding of chloromethyl ketone substrate analogues to crystalline papain |
|
54
|
311
|
1pciA |
Procaricain |
|
63
|
317
|
1pbhA |
Crystal structure of human recombinant procathepsin b at 3.2 angstrom resolution |
|
68
|
217
|
1npzA |
Crystal structures of cathepsin s inhibitor complexes |
|
68
|
208
|
1o0eA |
1.9 angstrom crystal structure of a plant cysteine protease ervatamin c |
|
54
|
215
|
1nl6A |
Crystal structure of the cysteine protease human cathepsin k in complex with a covalent azepanone inhibitor |
|
69
|
217
|
1nqcA |
Crystal structures of cathepsin s inhibitor complexes |
|
65
|
215
|
1nljA |
Crystal structure of the cysteine protease human cathepsin k in complex with a covalent azepanone inhibitor |
|
57
|
220
|
1nb3A |
Crystal structure of stefin a in complex with cathepsin h: n-terminal residues of inhibitors can adapt to the active sites of endo-and exopeptidases |
|
70
|
217
|
1ms6A |
Dipeptide nitrile inhibitor bound to cathepsin s. |
|
44
|
174
|
1mhwA |
Design of non-covalent inhibitors of human cathepsin l. from the 96-residue proregion to optimized tripeptides |
|
61
|
313
|
1mirA |
Rat procathepsin b |
|
62
|
215
|
1me4A |
High resolution crystal structure analysis of cruzain non-covalently bound to a hydroxymethyl ketone inhibitor (i) |
|
56
|
215
|
1memA |
Crystal structure of cathepsin k complexed with a potent vinyl sulfone inhibitor |
|
63
|
215
|
1me3A |
High resolution crystal structure analysis of cruzain non-covalently bound to a hydroxymethyl ketone inhibitor (ii) |
|
60
|
216
|
1megA |
Crystal structure of a caricain d158e mutant in complex with e-64 |
|
94
|
323
|
1mdwA |
Crystal structure of calcium-bound protease core of calpain ii reveals the basis for intrinsic inactivation |
