|
20
|
69
|
5trbA |
Crystal structure of the rnf20 ring domain |
|
35
|
102
|
5trfA |
Mdm2 in complex with sar405838 |
|
18
|
70
|
5tdbA |
Crystal structure of the human ubr-box domain from ubr2 in complex with asymmetrically double methylated arginine peptide |
|
17
|
70
|
5tdcA |
Crystal structure of the human ubr-box domain from ubr1 in complex with monomethylated arginine peptide. |
|
19
|
72
|
5tddA |
Human ubr-box from ubr2 in complex with hifs peptide |
|
34
|
132
|
5olmA |
Trim21 |
|
30
|
106
|
5oqwA |
Xiap in complex with small molecule |
|
119
|
385
|
5o76A |
Structure of phosphoy371 c-cbl in complex with zap70-peptide and ubv.pcbl ubiquitin variant |
|
69
|
260
|
5o6cA |
Crystal structure of a threonine-selective rcr e3 ligase |
|
20
|
71
|
5o75A |
Ube4b u-box domain |
|
29
|
93
|
5oc8A |
Hdm2 (17-111, wild type) complexed with nvp-hdm201 at 1.56a |
|
14
|
64
|
5o6tA |
Birc4 ring in complex with dimeric ubiquitin variant |
|
74
|
173
|
5nt1A |
Complex of influenza a ns1 effector domain with trim25 coiled coil |
|
78
|
173
|
5nt2A |
Complex of influenza a ns1 with trim25 coiled coil domain |
|
32
|
107
|
5c84A |
Fragment-based drug discovery targeting inhibitor of apoptosis proteins: compound 20 |
|
30
|
95
|
5layA |
Discovery of new natural-product-inspired spiro-oxindole compounds as orally active inhibitors of the mdm2-p53 interaction: hdm2 (mdm2) in complex with compound 6g |
|
26
|
92
|
5c5aA |
Crystal structure of hdm2 in complex with nutlin-3a |
|
28
|
94
|
5lawA |
Novel spiro[3h-indole-3,2 -pyrrolidin]-2(1h)-one inhibitors of the mdm2-p53 interaction: hdm2 (mdm2) in complex with compound 14 |
|
32
|
104
|
5c0kA |
Fragment-based drug discovery targeting inhibitor of apoptosis proteins: compound 3 |
|
29
|
93
|
5lavA |
Novel spiro[3h-indole-3,2 -pyrrolidin]-2(1h)-one inhibitors of the mdm2-p53 interaction: hdm2 (mdm2) in complex with compound 6b |
|
29
|
94
|
5lazA |
Novel spiro[3h-indole-3,2 -pyrrolidin]-2(1h)-one inhibitors of the mdm2-p53 interaction: hdm2 (mdm2) in complex with compound bi-0252 |
|
122
|
389
|
5j3xA |
Structure of c-cbl y371f |
|
108
|
306
|
4z30A |
Crystal structure of the roq domain of human roquin-2 |
|
32
|
94
|
5j7gA |
Structure of mdm2 with low molecular weight inhibitor with aliphatic linker. |
|
11
|
43
|
5k3qA |
Rhesus macaques trim5alpha bbox2 domain |
|
30
|
96
|
5hmiA |
Hdm2 in complex with a 3,3-disubstituted piperidine |
|
101
|
303
|
5hl0A |
Crystal structure of c-cbl tkbd in complex with spry2 peptide (54-60, py55) refined to 2.2a resolution |
|
68
|
341
|
5hqgA |
Wd40 domain of human e3 ubiquitin ligase cop1 (rfwd2) |
|
19
|
60
|
5im8A |
Solution structure of the microtubule-targeting cos domain of mid1 |
|
106
|
302
|
5hkwA |
Crystal structure of apo c-cbl tkbd refined to 2.25 a resolution |
|
128
|
382
|
5hkxA |
Crystal structure of c-cbl tkbd-ring domains (y371e mutant) refined to 1.85 a resolution |
|
45
|
190
|
5h9mA |
Crystal structure of siah2 sbd domain |
|
82
|
321
|
5igoA |
Wd40 domain of arabidopsis thaliana e3 ubiquitin ligase cop1 in complex with peptide from trib1 |
|
26
|
124
|
5h7sB |
Structural basis of the flanking zinc-finger motifs crucial for the e3 ligase activity of the lnx1 ring domain |
|
103
|
303
|
5hkzA |
Crystal structure of c-cbl tkbd in complex with spry2 peptide (36-60, py55) refined to 1.8 a resolution (p21 form) |
|
24
|
124
|
5h7rD |
Structural basis of the flanking zinc-finger motifs crucial for the e3 ligase activity of the lnx1 ring domain |
|
106
|
305
|
5axiA |
Crystal structure of cbl-b tkb domain in complex with cblin |
|
60
|
224
|
5b0nA |
Structure of shigella effector lrr domain |
|
50
|
182
|
5h1vA |
Complex structure of trim24 phd-bromodomain and inhibitor 6 |
|
55
|
224
|
5b0tA |
Structure of shigella effector lrr domain |
|
16
|
84
|
5feyA |
Trim32 ring |
|
145
|
406
|
5fg1A |
Structure of the conserved yeast listerin (ltn1) selenomethionine-substituted n-terminal domain, trigonal form |
|
84
|
360
|
4zb4A |
Spliceosome component |
|
160
|
407
|
5fg0A |
Structure of the conserved yeast listerin (ltn1) n-terminal domain, monoclinic form |
|
0
|
12
|
4ztdD |
Crystal structure of human pcna in complex with a traip peptide |
|
51
|
134
|
5eiuA |
Mini trim5 b-box 2 dimer c2 crystal form |
|
21
|
76
|
5eyaF |
Trim25 ring domain in complex with ubc13-ub conjugate |
|
29
|
96
|
5dkaA |
A c2hc zinc finger is essential for the activity of the ring ubiquitin ligase rnf125 |
|
49
|
183
|
4zqlA |
Crystal structure of trim24 with 3,4-dimethoxy-n-(6-(4-methoxyphenoxy)-1,3-dimethyl-2-oxo-2,3-dihydro-1h-benzo[d]imidazol-5-yl)benzenesulfonamide inhibitor |
|
28
|
127
|
5d1lB |
Crystal structure of ubch5b in complex with the ring-u5br fragment of ao7 (y165a) |
