73
|
422
|
6fecS |
Human cap-dependent 48s pre-initiation complex |
72
|
393
|
5wdtz |
70s ribosome-ef-tu h84a complex with gppnhp |
69
|
393
|
5we6z |
70s ribosome-ef-tu h84a complex with gtp and cognate trna |
70
|
393
|
5wfkz |
70s ribosome-ef-tu h84a complex with gtp and near-cognate trna (complex c3) |
70
|
393
|
5we4z |
70s ribosome-ef-tu wt complex with gppnhp |
69
|
393
|
5wf0z |
70s ribosome-ef-tu h84a complex with gtp and near-cognate trna (complex c2) |
68
|
393
|
5wfsz |
70s ribosome-ef-tu h84a complex with gtp and near-cognate trna (complex c4) |
198
|
874
|
5zwmC |
Cryo-em structure of the yeast pre-b complex at an average resolution of 3.4~4.6 angstrom (tri-snrnp and u2 snrnp part) |
110
|
840
|
6gq1AZ |
Cryo-em reconstruction of yeast 80s ribosome in complex with mrna, trna and eef2 (gmppcp/sordarin) |
229
|
888
|
5yzgC |
The cryo-em structure of human catalytic step i spliceosome (c complex) at 4.1 angstrom resolution |
188
|
702
|
6n0iA |
2.60 angstrom resolution crystal structure of elongation factor g 2 from pseudomonas putida. |
135
|
571
|
6gawBC |
Unique features of mammalian mitochondrial translation initiation revealed by cryo-em. this file contains the complete 55s ribosome. |
195
|
874
|
5zwoC |
Cryo-em structure of the yeast b complex at average resolution of 3.9 angstrom |
52
|
430
|
6fyxk |
Structure of a partial yeast 48s preinitiation complex with eif5 n-terminal domain (model c1) |
145
|
832
|
6ah0C |
The cryo-em structure of the precusor of human pre-catalytic spliceosome (pre-b complex) |
219
|
888
|
5z57C |
Cryo-em structure of the human activated spliceosome (late bact) at 6.5 angstrom |
219
|
888
|
5z56C |
Cryo-em structure of a human activated spliceosome (mature bact) at 5.1 angstrom. |
56
|
422
|
3jaqk |
Structure of a partial yeast 48s preinitiation complex in open conformation |
192
|
899
|
6qdvC |
Human post-catalytic p complex spliceosome |
177
|
694
|
6notA |
Crystal structure of a full length elongation factor g (ef-g) from rickettsia prowazekii |
63
|
422
|
3japk |
Structure of a partial yeast 48s preinitiation complex in closed conformation |
202
|
897
|
5ganC |
The overall structure of the yeast spliceosomal u4/u6.u5 tri-snrnp at 3.7 angstrom |
199
|
897
|
5gamC |
Foot region of the yeast spliceosomal u4/u6.u5 tri-snrnp |
175
|
888
|
6id1C |
Cryo-em structure of a human intron lariat spliceosome after prp43 loaded (ils2 complex) at 2.9 angstrom resolution |
171
|
888
|
6id0C |
Cryo-em structure of a human intron lariat spliceosome prior to prp43 loaded (ils1 complex) at 2.9 angstrom resolution |
185
|
894
|
6iczC |
Cryo-em structure of a human post-catalytic spliceosome (p complex) at 3.0 angstrom |
106
|
414
|
6i5mA |
Gamma subunit of the translation initiation factor 2 from sulfolobus solfataricus in complex with gdp and formate ion |
103
|
902
|
6ff7B |
Human bact spliceosome core structure |
50
|
449
|
6o81S |
Electron cryo-microscopy of the eukaryotic translation initiation factor 2b bound to translation initiation factor 2 from homo sapiens |
225
|
942
|
6j6hC |
Cryo-em structure of the yeast b*-a1 complex at an average resolution of 3.6 angstrom |
6
|
26
|
3jcdx |
Structure of escherichia coli ef4 in posttranslocational ribosomes (post ef4) |
103
|
595
|
3jcex |
Structure of escherichia coli ef4 in pretranslocational ribosomes (pre ef4) |
191
|
925
|
5mq0C |
Structure of a spliceosome remodeled for exon ligation |
59
|
596
|
5imqB |
Structure of ribosome bound to cofactor at 3.8 angstrom resolution |
38
|
598
|
5imrC |
Structure of ribosome bound to cofactor at 5.7 angstrom resolution |
74
|
501
|
5me0W |
Structure of the 30s pre-initiation complex 1 (30s ic-1) stalled by ge81112 |
65
|
639
|
5kcs1w |
Cryo-em structure of the escherichia coli 70s ribosome in complex with antibiotic evernimycin, mrna, tetm and p-site trna at 3.9a resolution |
74
|
501
|
5me1W |
Structure of the 30s pre-initiation complex 2 (30s ic-2) stalled by ge81112 |
93
|
422
|
5k0yS |
M48s late-stage initiation complex, purified from rabbit reticulocytes lysates, displaying eif2 ternary complex and eif3 i and g subunits relocated to the intersubunit face |
71
|
392
|
5uynZ |
70s ribosome bound with near-cognate ternary complex not base-paired to a site codon (structure i-nc) |
77
|
392
|
5uylZ |
70s ribosome bound with cognate ternary complex base-paired to a site codon (structure ii) |
74
|
392
|
5uykZ |
70s ribosome bound with cognate ternary complex not base-paired to a site codon (structure i) |
82
|
409
|
5jbh7 |
Cryo-em structure of a full archaeal ribosomal translation initiation complex in the p-in conformation |
52
|
449
|
6o85S |
Electron cryo-microscopy of the eukaryotic translation initiation factor 2b bound to eukaryotic translation initiation factor 2 from homo sapiens |
45
|
421
|
6jlxP |
Eif2(ap) - eif2b complex |
203
|
942
|
6j6qC |
Cryo-em structure of the yeast b*-b2 complex at an average resolution of 3.7 angstrom |
47
|
421
|
6jlwP |
Eif2 - eif2b complex |
212
|
942
|
6j6nC |
Cryo-em structure of the yeast b*-b1 complex at an average resolution of 3.86 angstrom |
98
|
414
|
6h6kA |
The structure of the fkr mutant of the archaeal translation initiation factor 2 gamma subunit in complex with gdpcp, obtained in the absence of magnesium salts in the crystallization solution. |
75
|
687
|
5ot7U |
Elongation factor g-ribosome complex captures in the absence of inhibitors. |