![]() | PDB-3j2l![]() ![]() ![]() ![]() Promiscuous behavior of proteins in archaeal ribosomes revealed by cryo-EM: implications for evolution of eukaryotic ribosomes (50S ribosomal RNA) |
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![]() | PDB-2ymr![]() ![]() ![]() ![]() The cryo-EM structure of a 3D DNA-origami object |
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![]() | PDB-3j2k![]() ![]() ![]() ![]() Cryo-EM structure of the mammalian eRF1-eRF3-associated termination complex |
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![]() | PDB-2ymf![]() ![]() ![]() ![]() The cryo-EM structure of a 3D DNA-origami object |
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![]() | PDB-2ymg![]() ![]() ![]() ![]() The cryo-EM structure of a 3D DNA-origami object |
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![]() | PDB-2ymh![]() ![]() ![]() ![]() The cryo-EM structure of a 3D DNA-origami object |
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![]() | PDB-2ymi![]() ![]() ![]() ![]() The cryo-EM structure of a 3D DNA-origami object |
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![]() | EMDB-2210![]() ![]() ![]() ![]() The cryo-EM structure of a 3D DNA-origami object |
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![]() | EMDB-5518![]() ![]() ![]() ![]() eRF1-eRF3-bound 80S ribosome |
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![]() | EMDB-5513![]() ![]() ![]() ![]() Structure of late pre-60S ribosomal subunits with nuclear export factor Arx1 bound at the peptide exit tunnel |
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![]() | PDB-3j2i![]() ![]() ![]() ![]() Structure of late pre-60S ribosomal subunits with nuclear export factor Arx1 bound at the peptide exit tunnel |
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![]() | EMDB-5500![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | EMDB-5501![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | EMDB-5502![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | EMDB-5503![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | EMDB-5504![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | EMDB-5506![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | EMDB-5507![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | EMDB-5508![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | EMDB-5509![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | EMDB-5510![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | PDB-3j28![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | PDB-3j29![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | PDB-3j2a![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | PDB-3j2b![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | PDB-3j2c![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | PDB-3j2d![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | PDB-3j2e![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | PDB-3j2f![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | PDB-3j2g![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | PDB-3j2h![]() ![]() ![]() ![]() Dissecting the in vivo assembly of the 30S ribosomal subunit reveals the role of RimM |
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![]() | EMDB-2198![]() ![]() ![]() ![]() Architecture of human translation initiation factor 3 |
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![]() | EMDB-2199![]() ![]() ![]() ![]() Architecture of human translation initiation factor 3 |
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![]() | EMDB-2183![]() ![]() ![]() ![]() Structural basis for TetM-mediated tetracycline resistance |
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![]() | PDB-3j25![]() ![]() ![]() ![]() Structural basis for TetM-mediated tetracycline resistance |
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![]() | EMDB-2179![]() ![]() ![]() ![]() Electron cryo-microscopy of C. thermophilum RAC bound to the 80S ribosome |
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![]() | EMDB-2170![]() ![]() ![]() ![]() Thermococcus kodakaraensis 70S ribosome |
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![]() | EMDB-2171![]() ![]() ![]() ![]() Staphylothermus marinus 50S ribosomal subunit |
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![]() | EMDB-2172![]() ![]() ![]() ![]() Methanococcus igneus 70S ribosome |
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![]() | PDB-3j20![]() ![]() ![]() ![]() Promiscuous behavior of proteins in archaeal ribosomes revealed by cryo-EM: implications for evolution of eukaryotic ribosomes (30S ribosomal subunit) |
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![]() | PDB-3j21![]() ![]() ![]() ![]() Promiscuous behavior of proteins in archaeal ribosomes revealed by cryo-EM: implications for evolution of eukaryotic ribosomes (50S ribosomal proteins) |
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![]() | PDB-4b6b![]() ![]() ![]() ![]() Cryo-EM Structure of the 60S Ribosomal Subunit in Complex with Arx1 and Rei1 |
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![]() | EMDB-2167![]() ![]() ![]() ![]() Cryo-EM structure of the 60S-Arx1-Rei1-Jjj1 complex |
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![]() | EMDB-2168![]() ![]() ![]() ![]() Cryo-EM structure of the 60S-Rei1 complex |
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![]() | EMDB-2169![]() ![]() ![]() ![]() Cryo-EM structure of the 60S-Arx1-Rei1 complex |
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![]() | PDB-4b6a![]() ![]() ![]() ![]() Cryo-EM Structure of the 60S Ribosomal Subunit in Complex with Arx1 and Rei1 |
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![]() | EMDB-2166![]() ![]() ![]() ![]() Architecture of human translation initiation factor 3 |
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![]() | EMDB-2103![]() ![]() ![]() ![]() Heritable yeast prions have a highly organized 3-dimensional architecture with inter-fiber structures |
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![]() | EMDB-2104![]() ![]() ![]() ![]() Heritable yeast prions have a highly organized 3-dimensional architecture with inter-fiber structures |
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![]() | EMDB-2099![]() ![]() ![]() ![]() Structure of ER membrane associated ribosomes in situ |
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