|
192
|
595
|
3v6qA |
Crystal structure of the complex of bovine lactoperoxidase with carbon monoxide at 2.0 a resolution |
|
42
|
100
|
3vh5A |
Crystal structure of the chicken cenp-t histone fold/cenp-w/cenp-s/cenp-x heterotetrameric complex, crystal form i |
|
83
|
289
|
3vfdA |
Human spastin aaa domain |
|
75
|
262
|
3v5lA |
Crystal structure of interleukin-2 inducible t-cell kinase itk catalytic domain with thienopyrazolylindole inhibitor 542 |
|
71
|
190
|
5hbuA |
Structure of the e. coli nucleoid occlusion protein slma bound to dna and the c-terminal tail of the cytoskeletal cell division protein ftsz |
|
79
|
272
|
3vf9A |
Crystal structure of spleen tyrosine kinase syk catalytic domain with thienopyrazolylindole inhibitor 027 |
|
157
|
566
|
3utoA |
Twitchin kinase region from c.elegans (fn31-nl-kin-crd-ig26) |
|
148
|
465
|
3v5tA |
Calcium-dependent protein kinase 1 from toxoplasma gondii (tgcdpk1) in complex with inhibitor uw1299 |
|
134
|
410
|
3v8fA |
Crystal structure of crosslinked gltph v216c-m385c mutant |
|
331
|
1071
|
3tw6A |
Structure of rhizobium etli pyruvate carboxylase t882a with the allosteric activator, acetyl coenzyme-a |
|
103
|
322
|
3v7cA |
Cystal structure of sabpl in complex with inhibitor |
|
83
|
301
|
3vb4A |
Crystal structure of sars-cov 3c-like protease with b4z |
|
83
|
291
|
3uysA |
Crystal structure of apo human ck1d |
|
102
|
271
|
3v9tA |
Crystal structure of the ppargamma-lbd complexed with a cercosporamide derivative modulator |
|
80
|
301
|
3vb7A |
Crystal structure of sars-cov 3c-like protease with m4z |
|
82
|
301
|
3vb3A |
Crystal structure of sars-cov 3c-like protease in apo form |
|
88
|
306
|
3v3mA |
Severe acute respiratory syndrome coronavirus (sars-cov) 3cl protease in complex with n-[(1r)-2-(tert-butylamino)-2-oxo-1-(pyridin-3-yl)ethyl]-n-(4-tert-butylphenyl)furan-2-carboxamide inhibitor. |
|
98
|
322
|
3v8jA |
Crystal structure of staphylococcus aureus biotin protein ligase |
|
135
|
438
|
3vdxA |
Structure of a 16 nm protein cage designed by fusing symmetric oligomeric domains |
|
106
|
348
|
3uvpA |
Human p38 map kinase in complex with a benzamide substituted benzosuberone |
|
94
|
325
|
3uxnA |
Crystal structure of rat dna polymerase beta, wild type apoenzyme |
|
80
|
271
|
3vbqA |
Exploitation of hydrogen bonding constraints and flat hydrophobic energy landscapes in pim-1 kinase needle screening and inhibitor design |
|
65
|
265
|
3v8wA |
Crystal structure of interleukin-2 inducible t-cell kinase itk catalytic domain with thienopyrazolylindole inhibitor 469 |
|
103
|
359
|
3vheA |
Crystal structure of human vegfr2 kinase domain with a novel pyrrolopyrimidine inhibitor. |
|
218
|
581
|
3useL |
Crystal structure of e. coli hydrogenase-1 in its as-isolated form |
|
116
|
390
|
3v76A |
The crystal structure of a flavoprotein from sinorhizobium meliloti |
|
85
|
322
|
3v01A |
Discovery of novel allosteric mek inhibitors possessing classical and non-classical bidentate ser212 interactions. |
|
88
|
356
|
3vidA |
Crystal structure of human vegfr2 kinase domain with compound a. |
|
134
|
475
|
3vbbA |
Crystal structure of seryl-trna synthetase from human at 2.9 angstroms |
|
81
|
271
|
3vbtA |
Exploitation of hydrogen bonding constraints and flat hydrophobic energy landscapes in pim-1 kinase needle screening and inhibitor design |
|
87
|
238
|
3v3eA |
Crystal structure of the human nur77 ligand-binding domain |
|
90
|
290
|
3uytA |
Crystal structure of ck1d with pf670462 from p1 crystal form |
|
28
|
81
|
3vc8A |
Crystal structure of the c-terminal cytoplasmic domain of non-structural protein 4 from mouse hepatitis virus a59 |
|
243
|
714
|
3uw8A |
Crystal structure analysis of the ser305thr variants of katg from haloarcula marismortui |
|
151
|
456
|
3v2wA |
Crystal structure of a lipid g protein-coupled receptor at 3.35a |
|
85
|
301
|
3vb5A |
Crystal structure of sars-cov 3c-like protease with c4z |
|
143
|
335
|
3vjaA |
Crystal structure of the human squalene synthase |
|
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 |
|
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 |
|
56
|
325
|
3v7lA |
Apo structure of rat dna polymerase beta k72e variant |
|
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 |
|
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 |
|
98
|
322
|
3v7rA |
Crystal structure of staphylococcus aureus biotin protein ligase in complex with inhibitor |
|
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 |
