|
15
|
79
|
3uioB |
Complex between human rangap1-sumo2, ubc9 and the ir1 domain from ranbp2 containing ir2 motif ii |
|
18
|
78
|
3uipB |
Complex between human rangap1-sumo1, ubc9 and the ir1 domain from ranbp2 containing ir2 motif ii |
|
38
|
151
|
3ui3A |
Structural and biochemical characterization of hp0315 from helicobacter pylori as a vapd protein with an endoribonuclease activity |
|
75
|
293
|
3u8zA |
Human merlin ferm domain |
|
42
|
149
|
3u30A |
Crystal structure of a linear-specific ubiquitin fab bound to linear ubiquitin |
|
26
|
118
|
3u52E |
X-ray crystal structure of xenon-pressurized phenol hydroxylase from pseudomonas sp. ox1 |
|
250
|
950
|
3tjpA |
Crystal structure of pi3k gamma with n6-(3,4-dimethoxyphenyl)-2-morpholino-[4,5'-bipyrimidine]-2',6-diamine |
|
27
|
97
|
3u7zA |
Crystal structure of a putative metal binding protein rumgna_00854 (zp_02040092.1) from ruminococcus gnavus atcc 29149 at 1.30 a resolution |
|
258
|
949
|
3tl5A |
Discovery of gdc-0980: a potent, selective, and orally available class i phosphatidylinositol 3-kinase (pi3k)/mammalian target of rapamycin (mtor) kinase inhibitor for the treatment of cancer |
|
89
|
311
|
3u7dA |
Crystal structure of the krit1/ccm1 ferm domain in complex with the heart of glass (heg1) cytoplasmic tail |
|
19
|
122
|
3u4eG |
Crystal structure of pg9 fab in complex with v1v2 region from hiv-1 strain cap45 |
|
19
|
104
|
3tuoA |
Crystal structure of n-terminal domain of dna-binding protein satb1 |
|
63
|
190
|
3tssA |
Toxic shock syndrome toxin-1 tetramutant, p2(1) crystal form |
|
270
|
949
|
3t8mA |
Rational design of pi3k-alpha inhibitors that exhibit selectivity over the pi3k-beta isoform |
|
21
|
75
|
3tmpB |
The catalytic domain of human deubiquitinase duba in complex with ubiquitin aldehyde |
|
76
|
260
|
3tcaA |
Crystal structure of the ras-associating and pleckstrin-homology domains of riam |
|
69
|
222
|
3t9lA |
Structure of n-terminal dusp-ubl domains of human usp15 |
|
45
|
153
|
3tixA |
Crystal structure of the chp1-tas3 complex core |
|
197
|
701
|
3texA |
Crystal structure of anthrax protective antigen (membrane insertion loop deleted) to 1.7-a resolution |
|
9
|
72
|
3tblD |
Structure of mono-ubiquitinated pcna: implications for dna polymerase switching and okazaki fragment maturation |
|
177
|
570
|
3su8X |
Crystal structure of a truncated intracellular domain of plexin-b1 in complex with rac1 |
|
37
|
164
|
3sr6A |
Crystal structure of reduced bovine xanthine oxidase in complex with arsenite |
|
94
|
313
|
3shqA |
Crystal structure of ublcp1 |
|
61
|
239
|
3sfdB |
Crystal structure of porcine mitochondrial respiratory complex ii bound with oxaloacetate and pentachlorophenol |
|
73
|
238
|
3sebA |
Staphylococcal enterotoxin b |
|
37
|
151
|
3sdlC |
Crystal structure of human isg15 in complex with ns1 n-terminal region from influenza b virus, northeast structural genomics consortium target ids hx6481, hr2873, and or2 |
|
251
|
949
|
3sd5A |
Crystal structure of pi3k gamma with 5-(2,4-dimorpholinopyrimidin-6-yl)-4-(trifluoromethyl)pyridin-2-amine |
|
60
|
240
|
3sfeB |
Crystal structure of porcine mitochondrial respiratory complex ii bound with oxaloacetate and thiabendazole |
|
261
|
945
|
3s2aA |
Crystal structure of pi3k-gamma in complex with a quinoline inhibitor |
|
20
|
77
|
3rulA |
New strategy to analyze structures of glycopeptide-target complexes |
|
97
|
622
|
3rzfA |
Crystal structure of inhibitor of kappab kinase beta (i4122) |
|
146
|
613
|
3rytA |
The plexin a1 intracellular region in complex with rac1 |
|
20
|
75
|
3rzwC |
Crystal structure of the monobody ysmb-9 bound to human sumo1 |
|
30
|
113
|
3ruiB |
Crystal structure of atg7c-atg8 complex |
|
24
|
83
|
3rngC |
Structure of the toluene/o-xylene monooxygenase hydroxylase t201s/w167e double mutant |
|
25
|
84
|
3rn9C |
Structure of the toluene/o-xylene monooxygenase hydroxylase t201s/l272e double mutant |
|
25
|
85
|
3rnbC |
Structure of the toluene/o-xylene monooxygenase hydroxylase t201s/f176w double mutant |
|
24
|
83
|
3rneC |
Structure of the toluene/o-xylene monooxygenase hydroxylase t201s/i276e double mutant |
|
24
|
81
|
3rmkC |
Toluene 4 monooxygenase h with 4-bromophenol |
|
11
|
74
|
3rpfC |
Protein-protein complex of subunit 1 and 2 of molybdopterin-converting factor from helicobacter pylori 26695 |
|
23
|
83
|
3rncC |
Structure of the toluene/o-xylene monooxygenase hydroxylase t201s/i100a double mutant |
|
25
|
85
|
3rnfC |
Structure of the toluene/o-xylene monooxygenase hydroxylase t201s/v271a double mutant |
|
269
|
949
|
3r7qA |
Structure-based design of thienobenzoxepin inhibitors of pi3- kinase |
|
36
|
153
|
3rt3B |
Complex of influenza virus protein with host anti-viral factor |
|
24
|
83
|
3rnaC |
Structure of the toluene/o-xylene monooxygenase hydroxylase t201s/i100w double mutant |
|
18
|
74
|
3rczA |
Rad60 sld2 ubc9 complex |
|
16
|
82
|
3rd2A |
Nip45 sumo-like domain 2 |
|
24
|
83
|
3ri7C |
Toluene 4 monooxygenase hd mutant g103l |
|
268
|
949
|
3r7rA |
Structure-based design of thienobenzoxepin inhibitors of pi3-kinase |
|
70
|
236
|
3r8bA |
Crystal structure of staphylococcal enterotoxin b in complex with an affinity matured mouse tcr vbeta8.2 protein, g5-8 |
