|
35
|
148
|
3v6zE |
Crystal structure of hepatitis b virus e-antigen |
|
76
|
262
|
3vapA |
Synthesis and sar studies of imidazo-[1,2-a]-pyrazine aurora kinase inhibitors with improved off target kinase selectivity |
|
143
|
335
|
3vjaA |
Crystal structure of the human squalene synthase |
|
56
|
325
|
3v7lA |
Apo structure of rat dna polymerase beta k72e variant |
|
52
|
197
|
3vduA |
Structure of recombination mediator protein recrk21g mutant |
|
28
|
75
|
3vh5W |
Crystal structure of the chicken cenp-t histone fold/cenp-w/cenp-s/cenp-x heterotetrameric complex, crystal form i |
|
81
|
271
|
3vbvA |
Exploitation of hydrogen bonding constraints and flat hydrophobic energy landscapes in pim-1 kinase needle screening and inhibitor design |
|
79
|
271
|
3vbwA |
Exploitation of hydrogen bonding constraints and flat hydrophobic energy landscapes in pim-1 kinase needle screening and inhibitor design |
|
98
|
322
|
3v7rA |
Crystal structure of staphylococcus aureus biotin protein ligase in complex with inhibitor |
|
82
|
301
|
3vb6A |
Crystal structure of sars-cov 3c-like protease with c6z |
|
21
|
62
|
3vfzA |
Crystal structure of -35 promoter binding domain of sigd of mycobacterium tuberculosis |
|
27
|
89
|
3vcbA |
C425s mutant of the c-terminal cytoplasmic domain of non-structural protein 4 from mouse hepatitis virus a59 |
|
98
|
322
|
3v7sA |
Crystal structure of staphylococcus aureus biotin protein ligase in complex with inhibitor 0364 |
|
82
|
271
|
3vbxA |
Exploitation of hydrogen bonding constraints and flat hydrophobic energy landscapes in pim-1 kinase needle screening and inhibitor design |
|
216
|
581
|
3uscL |
Crystal structure of e. coli hydrogenase-1 in a ferricyanide-oxidized form |
|
164
|
482
|
3v8dA |
Crystal structure of human cyp7a1 in complex with 7-ketocholesterol |
|
69
|
172
|
3v6gA |
Crystal structure of transcriptional regulator |
|
235
|
581
|
3v08A |
Crystal structure of equine serum albumin |
|
41
|
120
|
3vb1A |
Crystal structure of anopholes gambiae odorant binding protein 20 in open state |
|
60
|
152
|
3v2zA |
Nitrite bound chlorin substituted myoglobin- method 2 |
|
137
|
331
|
3v9bA |
Crystal structure of the catalytic domain of pde4d2 with (s)-n-(3-{1-[1-(3-cyclopropylmethoxy-4-difluoromethoxyphenyl)-2-(1-oxypyridin-4-yl)-ethyl]-1h-pyrazl-3-yl}phenyl)acetamide |
|
46
|
136
|
3uijA |
Crystal structure of human survivin k62y/h80w mutant in complex with smac/diablo(1-15) peptide |
|
56
|
174
|
3uleE |
Structure of bos taurus arp2/3 complex with bound inhibitor ck-869 and atp |
|
203
|
514
|
3unvA |
Pantoea agglomerans phenylalanine aminomutase |
|
59
|
288
|
3uiuA |
Crystal structure of apo-pkr kinase domain |
|
103
|
329
|
3u87A |
Structure of a chimeric construct of human ck2alpha and human ck2alpha' in complex with a non-hydrolysable atp-analogue |
|
45
|
135
|
3uiiA |
Crystal structure of human survivin in complex with h3(1-10) peptide |
|
85
|
276
|
3uqgA |
C-src kinase domain in complex with bumpless bki analog uw1243 |
|
87
|
244
|
3uuaA |
Crystal structure of hera-lbd (y537s) in complex with bisphenol-af |
|
65
|
145
|
3uhqA |
Hbi (l36a) deoxy |
|
63
|
145
|
3uhnA |
Hbi (f80y) deoxy |
|
52
|
131
|
3ubvA |
Oxygen-bound hell's gate globin i by classical hanging drop |
|
67
|
264
|
3uohA |
Aurora a in complex with rpm1722 |
|
66
|
145
|
3uhcA |
Hbi (n79a) co bound |
|
47
|
135
|
3uigA |
Crystal structure of human survivin in complex with t3 phosphorylated h3(1-15) peptide |
|
63
|
145
|
3uhwA |
Hbi (n79a) deoxy |
|
20
|
63
|
3ul4B |
Crystal structure of coh-olpa(cthe_3080)-doc918(cthe_0918) complex: a novel type i cohesin-dockerin complex from clostridium thermocellum attc 27405 |
|
115
|
291
|
3ucaA |
Crystal structure of isoprenoid synthase (target efi-501974) from clostridium perfringens |
|
65
|
145
|
3uhbA |
Hbi (r104k) co bound |
|
185
|
656
|
3ur3C |
Structure of the cmr2 subunit of the crispr rna silencing complex |
|
71
|
264
|
3uo6A |
Aurora a in complex with yl5-083 |
|
77
|
302
|
3uimA |
Structural basis for the impact of phosphorylation on plant receptor-like kinase bak1 activation |
|
82
|
266
|
3um7A |
Crystal structure of the human two pore domain k+ ion channel traak (k2p4.1) |
|
62
|
145
|
3uhtA |
Hbi (l36v) deoxy |
|
51
|
129
|
3ulrA |
Lysozyme contamination facilitates crystallization of a hetero-trimericcortactin:arg:lysozyme complex |
|
153
|
465
|
3ua5A |
Crystal structure of p450 2b6 (y226h/k262r) in complex with two molecules of amlodipine |
|
45
|
137
|
3ueiA |
Crystal structure of human survivin e65a mutant |
|
78
|
269
|
3uixA |
Crystal structure of pim1 kinase in complex with small molecule inhibitor |
|
88
|
225
|
3um9A |
Crystal structure of the defluorinating l-2-haloacid dehalogenase bpro0530 |
|
79
|
270
|
3ue4A |
Structural and spectroscopic analysis of the kinase inhibitor bosutinib binding to the abl tyrosine kinase domain |
