|
97
|
312
|
4nz6A |
Steroid receptor rna activator (sra) modification by the human pseudouridine synthase 1 (hpus1p): rna binding, activity, and atomic model |
|
45
|
160
|
4nezA |
Crystal structure of an engineered protein with ferredoxin fold, northeast structural genomics consortium (nesg) target or276 |
|
206
|
562
|
4mk8A |
Hepatitis c virus polymerase ns5b genotype 1b (bk) in complex with inhibitor 4 (n-(4-{2-[3-tert-butyl-2-methoxy-5-(2-oxo-1,2-dihydropyridin-3-yl)phenyl]ethyl}phenyl)methanesulfonamide) |
|
29
|
102
|
4nypA |
The 2.0 angstrom crystal structure of pyrococcus horikoshii cuta1 complexed with na+ |
|
118
|
420
|
4ohwA |
C. elegans clp1 bound to atp, and mn2+(atp-bound state) |
|
29
|
102
|
4npoA |
Crystal structure of protein with unknown function from deinococcus radiodurans at p61 spacegroup |
|
24
|
90
|
4oj3A |
The crystal structure of v84p mutant of s. solfataricus acylphosphatase |
|
24
|
90
|
4oj1A |
Crystal structure of truncated acylphosphatase from s. sulfataricus |
|
140
|
461
|
4nlqA |
Poliovirus polymerase - c290f loop mutant |
|
21
|
81
|
4oi3A |
Crystal structure analysis of sco4226 from streptomyces coelicolor a3(2) |
|
165
|
556
|
4ncgA |
Discovery of doravirine, an orally bioavailable non-nucleoside reverse transcriptase inhibitor potent against a wide range of resistant mutant hiv viruses |
|
151
|
460
|
4nyzA |
The emcv 3dpol structure with altered motif a conformation at 2.15a resolution |
|
25
|
99
|
4n8oA |
Crystal structure of mycobacterial ftsx extracellular domain, bromide derivative |
|
28
|
102
|
4nyoA |
The 1.8 angstrom crystal structure of the periplasmic divalent cation tolerance protein cuta from pyrococcus horikoshii ot3 |
|
21
|
102
|
4oloA |
Ligand-free structure of the grpu microcompartment shell protein from clostridiales bacterium 1_7_47faa |
|
146
|
461
|
4nlwA |
Poliovirus polymerase - g289a/c290i loop mutant |
|
140
|
552
|
4o44A |
Crystal structure of hiv-1 reverse transcriptase in complex with 4-((4-(mesitylamino)-6-(3-morpholinopropoxy)-1,3,5-triazin-2-yl)amino)benzonitrile (jlj529), a non-nucleoside inhibitor |
|
121
|
420
|
4ohxA |
C. elegans clp1 bound to adp and mg2+ (rna released state) |
|
80
|
257
|
4nmlA |
2.60 angstrom resolution crystal structure of putative ribose 5-phosphate isomerase from toxoplasma gondii me49 in complex with dl-malic acid |
|
99
|
427
|
4o44B |
Crystal structure of hiv-1 reverse transcriptase in complex with 4-((4-(mesitylamino)-6-(3-morpholinopropoxy)-1,3,5-triazin-2-yl)amino)benzonitrile (jlj529), a non-nucleoside inhibitor |
|
108
|
425
|
4ncgB |
Discovery of doravirine, an orally bioavailable non-nucleoside reverse transcriptase inhibitor potent against a wide range of resistant mutant hiv viruses |
|
156
|
500
|
4nrtA |
Human norovirus polymerase bound to compound 6 (suramin derivative) |
|
51
|
238
|
4n77A |
Crystal structure of cas protein |
|
21
|
93
|
4olpA |
Ligand-free structure of the grpu microcompartment shell protein from pectobacterium wasabiae |
|
139
|
461
|
4nlpA |
Poliovirus polymerase - c290v loop mutant |
|
119
|
421
|
4oi2A |
C. elegans clp1 and adp and mg2+ (turnover state) |
|
24
|
90
|
4oixA |
Crystal structure of truncated acylphosphatase from s. sulfataricus |
|
22
|
92
|
4nmxA |
Pcsk9(deltacrd) in complex with phage-derived inhibitory peptide 2-8 |
|
94
|
277
|
4nx9A |
Crystal structure of pseudomonas aeruginosa flagellin flic |
|
25
|
102
|
4n8nA |
Crystal structure of mycobacterial ftsx extracellular domain |
|
156
|
486
|
4nruA |
Murine norovirus rna-dependent-rna-polymerase in complex with compound 6, a suramin derivative |
|
280
|
1039
|
4mt1A |
Crystal structure of the neisseria gonorrhoeae mtrd inner membrane multidrug efflux pump |
|
23
|
91
|
4ojgA |
The crystal structure of v84d mutant of s. solfataricus acylphosphatase |
|
140
|
461
|
4nlsA |
Poliovirus polymerase - s288a loop mutant |
|
110
|
421
|
4ohvA |
C. elegans clp1 bound to amp-pnp, and mg2+ |
|
143
|
461
|
4nloA |
Poliovirus polymerase - c290i loop mutant |
|
100
|
428
|
4o4gB |
Crystal structure of hiv-1 reverse transcriptase in complex with 4-((4-(mesitylamino)-1,3,5-triazin-2-yl)amino)benzonitrile (jlj527), a non-nucleoside inhibitor |
|
17
|
101
|
4nl5A |
Mycobacterium tuberculosis heme-degrading protein mhud in complex with heme and cyanide |
|
203
|
614
|
4mtpA |
Rdrp from japanesese encephalitis virus |
|
99
|
312
|
4nz7A |
Steroid receptor rna activator (sra) modification by the human pseudouridine synthase 1 (hpus1p): rna binding, activity, and atomic model |
|
156
|
683
|
4mytA |
Crystal structure of elongation factor g (efg) |
|
54
|
192
|
4ni2A |
Crystal structure of the heterodimeric catalytic domain of wild-type human soluble guanylate cyclase |
|
204
|
612
|
4na1A |
Crystal structure of the second ketosynthase from the bacillaene polyketide synthase |
|
142
|
461
|
4nlrA |
Poliovirus polymerase - c290s loop mutant |
|
41
|
172
|
4neyA |
Crystal structure of an engineered protein with ferredoxin fold, northeast structural genomics consortium (nesg) target or277 |
|
166
|
505
|
4nldA |
Crystal structure of the hepatitis c virus ns5b rna-dependent rna polymerase complex with bms-791325 also known as (1ar,12bs)-8-cyclohexyl-n-(dimethylsulfamoyl)-11-methoxy-1a-{[(1r,5s)-3-methyl-3,8-diazabicyclo[3.2.1]oct-8-yl]carbonyl}-1,1a,2,12b-tetrahydrocyclopropa[d]indolo[2,1-a][2]benzazepine-5-carboxamide and 2-(4-fluorophenyl)-n-methyl-6-[(me |
|
33
|
167
|
4nohA |
1.5 angstrom crystal structure of putative lipoprotein from bacillus anthracis. |
|
135
|
461
|
4nltA |
Poliovirus polymerase - s291p loop mutant |
|
132
|
429
|
4ofzA |
Structure of unliganded trehalose-6-phosphate phosphatase from brugia malayi |
|
49
|
153
|
4o0nA |
2.4 angstrom resolution crystal structure of putative nucleoside diphosphate kinase from toxoplasma gondii. |
