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(Show all)Enterobacteriaphage PRD1 - P12 protein filament in complex with poly(dT) ssDNA
E. coli 70S ribosome in situ structure for lamellae backside damage analysis: 1 - 2 microns from lamellae backside
E. coli 70S ribosome in situ structure for xenon damage layer determination: 10,000 particles (>45 nm)
E. coli 70S ribosome in situ structure for xenon damage layer determination: 10,000 particles (no depth constraint)
Human gamma-tubulin ring complex from purified centrosomes of CDK5RAP2-knockout cells
E. coli 70S ribosome in situ structure for lamellae backside damage analysis: 3 - 4 microns from lamellae backside
E. coli 70S ribosome in situ structure for lamellae backside damage analysis: 4 - 5 microns from lamellae backside
E. coli 70S ribosome in situ structure for xenon damage layer determination: 10,000 particles (no depth constraint)
Structure of the SARS-CoV-2 spike glycoprotein in complex with nanobody 7F
'Outwards conformation' of the human gamma-TuRC from purified centrosomes
E. coli 70S ribosome in situ structure for xenon damage layer determination: >15 nm matched control for 10 - 15 nm
Human gamma-tubulin ring complex in centrosomes of HCT116 and HeLa cells
E. coli 70S ribosome in situ structure for lamellae backside damage analysis: 2 - 3 microns from lamellae backside
Spoke 12-14 of the NEDD1-bound native vertebrate gamma-tubulin ring complex from Xenopus laevis
E. coli 70S ribosome in situ structure for xenon damage layer determination: 5 - 10 nm
Enterobacteriaphage PRD1 - P12 protein filament in complex with non-repetitive ssDNA
E. coli 70S ribosome in situ structure for xenon damage layer determination: >20 nm matched control for 15 - 20 nm
E. coli 70S ribosome in situ structure for xenon damage layer determination: 10,000 particles (>30 nm)
E. coli 70S ribosome in situ structure for xenon damage layer determination: >55 nm matched control for 50 - 55 nm
E. coli 70S ribosome in situ structure for xenon damage layer determination: >45 nm matched control for 40 - 45 nm
'Inwards conformation' of the human gamma-TuRC from purified centrosomes
E. coli 70S ribosome in situ structure for xenon damage layer determination: 10,000 particles (<30 nm)
E. coli 70S ribosome in situ structure for xenon damage layer determination: 25 - 30 nm
E. coli 70S ribosome in situ structure for xenon damage layer determination: >35 nm matched control for 30 - 35 nm
E. coli 70S ribosome in situ structure for xenon damage layer determination: >50 nm matched control for 45 - 50 nm
Cryo-EM structure of antibody T5-1E11 in complex with stabilized H1N1 Influenza Hemagglutinin Trimer (A/Kiev/1/57)
Structure of the 48S translation initiation complex assembled on the encephalomyocarditis virus IRES
The Cryo-EM structure of the yeast Dmc1-ssDNA nucleoprotein filament ADP bound state
Cryo-EM structure of the Strand displacement Complex (I) of Yeast Mitochondrial DNA polymerase Gamma (MIP1) with downstream DNA
Class 16 model for pre-reduction condition of Bacillus subtilis ribonucleotide reductase complex
Cryo-EM structure of yeast CMG helicase stalled at G4-containing DNA template, state 2
Class 10 model for product condition of Bacillus subtilis ribonucleotide reductase complex
Class 28 model for combined refinement of Bacillus subtilis ribonucleotide reductase complex
Cryo-EM Map of yeast Exportin Msn5 bound to cargo Pho4 and RanGTP (State 3-2)
Mycobacterium tuberculosis UvrD1 dimer: DNA-bound dimer, dsDNA masked map
Cryo-EM structure of the Strand displacement Complex (III) of Yeast Mitochondrial DNA polymerase Gamma (MIP1) with downstream DNA
Class 12 model for preturnover condition of Bacillus subtilis ribonucleotide reductase complex
Cryo-EM structure of the Strand displacement Complex (III) of Yeast Mitochondrial DNA polymerase Gamma (MIP1) with downstream DNA
Class 12 model for turnover condition of Bacillus subtilis ribonucleotide reductase complex
Consensus model for product condition of Bacillus subtilis ribonucleotide reductase complex
Consensus full-complex model for preturnover condition of Bacillus subtilis ribonucleotide reductase complex
Class 7 model for combined refinement of Bacillus subtilis ribonucleotide reductase complex
Cryo-EM structure of antibody T5-1E08 in complex with H7N9 Influenza Hemagglutinin Trimer (A/Shanghai/2/13)
Cryo-EM structure of antibody T5-1E08 in complex with stabilized H1N1 Influenza Hemagglutinin Trimer (A/Kiev/1/57)
Class 3 model for product condition of Bacillus subtilis ribonucleotide reductase complex
Cryo-EM structure of yeast Exportin Msn5 bound to RanGTP and Pho4 (not modeled) (State 2-1)
Class 50 model for combined refinement of Bacillus subtilis ribonucleotide reductase complex
Class 5 model for preturnover condition of Bacillus subtilis ribonucleotide reductase complex
Class 29 model for combined refinement of Bacillus subtilis ribonucleotide reductase complex
TrxA focus-classified model for re-reduction condition of Bacillus subtilis ribonucleotide reductase complex
Cryo-EM structure of antibody T5-1E08 UCA (unmutated common ancestor) in complex with stabilized H1N1 Influenza Hemagglutinin Trimer (A/Kiev/1/57)
Class 19 model for product condition of Bacillus subtilis ribonucleotide reductase complex
Structure of SARS-CoV spike in complex with CoV1-65 Fab (NTD-bound)
Class 11 model for product condition of Bacillus subtilis ribonucleotide reductase complex
Mycobacterium tuberculosis UvrD1 dimer: apo extended conformation.
Consensus full-complex model for re-reduction condition of Bacillus subtilis ribonucleotide reductase complex
Class 18 model for combined refinement of Bacillus subtilis ribonucleotide reductase complex
Impacts of ribosomal RNA sequence variation on gene expression and phenotype: Cryo-EM structure of the rrsH ribosome (HBB-70S)
C-ring Consensus map, 34-mer CCW flagellar switch complex - FliF, FliG, FliM, and FliN from Salmonella
Class 9 model for turnover condition of Bacillus subtilis ribonucleotide reductase complex
In situ human top-back di-ribosome structure (Focused on trailing ribosome)
The Cryo-EM structure of the yeast Rad51-ssDNA nucleoprotein filament ADP bound state
Cryo-EM structure of the Strand displacement Complex (IV) of Yeast Mitochondrial DNA polymerase Gamma (MIP1) with downstream DNA
Structure of Fab 297 in complex with influenza H1N1 A/Victoria/4897/2022 neuraminidase
Cryo-EM map of yeast Exportin Msn5 bound to cargo Pho4 (full-length) and RanGTP (State 1)
Class 16 model for product condition of Bacillus subtilis ribonucleotide reductase complex
Cryo-EM structure of AdnA(D934A)-AdnB(D1014A) in complex with AMPPNP and blunt end DNA
Consensus full-complex model for turnover condition of Bacillus subtilis ribonucleotide reductase complex
Cryo-EM structure of yeast Exportin Msn5 bound to cargo Pho4 and RanGTP
Class 23 model for combined refinement of Bacillus subtilis ribonucleotide reductase complex
Class 9 model for preturnover condition of Bacillus subtilis ribonucleotide reductase complex
Consensus model for re-reduction condition of Bacillus subtilis ribonucleotide reductase complex
Class 45 model for combined refinement of Bacillus subtilis ribonucleotide reductase complex
Class 9 model for product condition of Bacillus subtilis ribonucleotide reductase complex
Class 15 model for preturnover condition of Bacillus subtilis ribonucleotide reductase complex
Class 12 model for product condition of Bacillus subtilis ribonucleotide reductase complex
Cryo-EM map of yeast Exportin Msn5 bound to cargo Pho4 (full-length) and RanGTP (State 3)
Class 11 model for pre-reduction condition of Bacillus subtilis ribonucleotide reductase complex
Class 26 model for combined refinement of Bacillus subtilis ribonucleotide reductase complex
Class 15 model for combined refinement of Bacillus subtilis ribonucleotide reductase complex
Class 1 model for turnover condition of Bacillus subtilis ribonucleotide reductase complex
Class 31 model for combined refinement of Bacillus subtilis ribonucleotide reductase complex
Impacts of ribosomal RNA sequence variation on gene expression and phenotype: Cryo-EM structure of the rrsB ribosome (BBB-70S)
CCW Flagellar Switch Complex - FliF, FliG, FliM, and FliN forming 34-mer C-ring from Salmonella
Class 14 model for turnover condition of Bacillus subtilis ribonucleotide reductase complex
Class 2 model for preturnover condition of Bacillus subtilis ribonucleotide reductase complex
Class 4 model for turnover condition of Bacillus subtilis ribonucleotide reductase complex
Consensus model for preturnover condition of Bacillus subtilis ribonucleotide reductase complex
Class 43 model for combined refinement of Bacillus subtilis ribonucleotide reductase complex
Cryo-EM map of yeast Exportin Msn5 bound to cargo Pho4 and RanGTP (State 2-2)
Class 17 model for turnover condition of Bacillus subtilis ribonucleotide reductase complex
Consensus full-complex model for product condition of Bacillus subtilis ribonucleotide reductase complex
Mycobacterium tuberculosis UvrD1 dimer: apo compact conformation.
Class 8 model for turnover condition of Bacillus subtilis ribonucleotide reductase complex
Class 8 model for product condition of Bacillus subtilis ribonucleotide reductase complex
Class 15 model for pre-reduction condition of Bacillus subtilis ribonucleotide reductase complex
Consensus model for turnover condition of Bacillus subtilis ribonucleotide reductase complex
Class 40 model for combined refinement of Bacillus subtilis ribonucleotide reductase complex
Class 5 model for turnover condition of Bacillus subtilis ribonucleotide reductase complex
CABP-bound Decameric Rubisco from Candidatus Methanofastidiosum methylthiophilus
Cryo-EM structure of yeast Exportin Msn5 bound to RanGTP and Pho4 (not modeled) (State 3-1)
Cryo-EM map of yeast Exportin Msn5 bound to cargo Pho4 and RanGTP (State 1-2)
RNA-nsp9 bound to the NiRAN domain of the E-RTC with an empty G-pocket
Class 6 model for combined refinement of Bacillus subtilis ribonucleotide reductase complex
SARS-CoV-2 spike (Wuhan-Hu-1) in the closed conformation induced by Ad5-nCoV vaccine
Human lysine O-link glycosylation complex, LH3/ColGalT1 tetramer with bound UDP-galactose
Cryo-EM structure of docked mouse bestrophin-1 in a partial open state
CryoEM structure of M. tuberculosis ClpC1P1P2 complex bound to bortezomib, conformation 3
The piccolo NuA4 bound to the H2A.Z nucleosome-H4KQ complex without Ac-CoA at pre-H2A.Z-acetylation state
The piccolo NuA4 bound to the H2A.Z nucleosome-H4KQ Complex with Ac-CoA at resetting state
Human lysine O-link glycosylation complex, LH3/ColGalT1 with bound UDP-glucose
CODANIN-1 sequesters ASF1 by using a histone H3 mimic helix to regulate histone supply
CryoEM structure of M. tuberculosis ClpXP1P2 complex bound to bortezomib
The piccolo NuA4 bound to the H2A.Z nucleosome complex with Ac-CoA at resetting state
The class2 of piccolo NuA4 bound to the H2A.Z nucleosome complex at harboring state
Human lysine O-link glycosylation complex, LH3/ColGalT1 in its apo state
The piccolo NuA4 bound to the H2A.Z nucleosome complex at pre-H4-acetylation state
SARS-CoV-2 spike (Omicron) in the One-RBD-up conformation induced by Ad5-nCoV vaccine
CryoEM structure of M. tuberculosis ClpC1P1P2 complex bound to bortezomib, conformation 2
Cryo-EM map of 30S ribosomal subunit in complex with MetAP1c of Mycobacterium smegmatis
SARS-CoV-2 spike (Omicron) in the closed conformation induced by Ad5-nCoV vaccine
The class1 of piccolo NuA4 bound to the H2A.Z nucleosome complex at harboring state
Human lysine O-link glycosylation complex, LH3/ColGalT1 with bound UDP-galactose
SARS-CoV-2 spike (Wuhan-Hu-1) in the One-RBD-up conformation induced by Ad5-nCoV vaccine
CryoEM structure of M. tuberculosis ClpC1P1P2 complex bound to bortezomib, conformation 1
Structure of the wild-type AZG2 in Arabidopsis thaliana in the trans-Zeatin-bound state at pH 5.5
Chloroflexus aurantiacus ATP synthase, state 1, focused refinement of FO and peripheral stalk
Chloroflexus aurantiacus ATP synthase, state 2, focused refinement of FO
Cryo-EM structure of human TauT in the apo state, determined in an inward-facing open conformation
Chloroflexus aurantiacus ADP-bound ATP synthase, state 3, focused refinement of FO and peripheral stalk
Chloroflexus aurantiacus ADP-bound ATP synthase, state 1, focused refinement of FO
Chloroflexus aurantiacus ADP-bound ATP synthase, state 2, focused refinement of FO and peripheral stalk
Chloroflexus aurantiacus ATP synthase, state 3, focused refinement of FO and peripheral stalk
Cryo-EM structure of human TauT in presence of Taurocyamine, determined in an inward-facing occluded conformation
Structure of the wild-type AZG2 in Arabidopsis thaliana in the trans-Zeatin-bound state-2 at pH 7.4
Chloroflexus aurantiacus ADP-bound ATP synthase, state 2, focused refinement of FO
Cryo-EM structure of human TauT in presence of taurine, determined in an inward-facing occluded conformation
Chloroflexus aurantiacus ADP-bound ATP synthase, state 3, focused refinement of FO
Chloroflexus aurantiacus ATP synthase, state 2, focused refinement of FO and peripheral stalk
ATP bound Chlamydia pneumoniae ATP/ADP translocator NTT1(Inward open state)
Cryo-EM structure of Delta RBD complexed with ConD-852, P2C-1F11 and S304 Fabs
Chloroflexus aurantiacus ATP synthase, state 3, focused refinement of FO
Structure of the wild-type AZG2 in Arabidopsis thaliana in the trans-Zeatin-bound state-1 at pH 7.4
Cryo-EM structure of human TauT in presence of Piperidine-4-sulfonate, determined in an inward-facing occluded conformation
Structure of the wild-type AZG2 in Arabidopsis thaliana in the apo state at pH 5.5
Structure of the wild-type AZG2 in Arabidopsis thaliana in the adenine-bound state at pH 5.5
Chlamydia pneumoniae ATP/ADP translocator NTT1(Outward open state)
Single particle cryo-EM reconstruction of Oryza sativa recombinant human serum albumin
Structure of the wild-type AZG2 in Arabidopsis thaliana in the adenine-bound state at pH 7.4
Chloroflexus aurantiacus ADP-bound ATP synthase, state 1, focused refinement of FO and peripheral stalk
Cryo-EM structure of human TauT in presence of taurine, observed only one sodium ion, determined in an inward-occluded conformation
Structure of the wild-type AZG2 in Arabidopsis thaliana in the apo state at pH 7.4
Chloroflexus aurantiacus ATP synthase, state 1, focused refinement of FO
Human gamma-tubulin ring complex from purified centrosomes of RPE1 cells
E. coli 70S ribosome in situ structure for xenon damage layer determination: 30 - 35 nm
E. coli 70S ribosome in situ structure for xenon damage layer determination: >40 nm matched control for 35 - 40 nm
13pf E254Q microtubule from recombinant human tubulin decorated with EB3
'Consensus refinement' of the human gamma-tubulin ring complex in purified centrosomes
E. coli 70S ribosome in situ structure for xenon damage layer determination: >30 nm matched control for 25 - 30 nm
Structure of the SARS-CoV-2 spike glycoprotein in complex with nanobody 7F (local refinement)
E. coli 70S ribosome in situ structure for xenon damage layer determination: 55 - 60 nm
Undecorated 13pf mosaic 20%E254Q - 80% E254QN microtubule from recombinant human tubulin
Structure of Edeine-30S-IF1-IF3-mRNA-tRNA translation pre-initiation complex, open form
13pf mosaic 20%E254Q - 80% E254N microtubule from recombinant human tubulin decorated with EB3
E. coli 70S ribosome in situ structure for xenon damage layer determination: >60 nm matched control for 55 - 60 nm
E. coli 70S ribosome in situ structure for xenon damage layer determination: >25 nm matched control for 20 - 25 nm
E. coli 70S ribosome in situ structure for xenon damage layer determination: >10nm matched control for 5 - 10 nm
E. coli 70S ribosome in situ structure for lamellae backside damage analysis: 0 - 1 micron from lamellae backside
E. coli 70S ribosome in situ structure for xenon damage layer determination: 10 - 15 nm
NEDD1-bound native vertebrate gamma-tubulin ring complex from Xenopus laevis
E. coli 70S ribosome in situ structure for xenon damage layer determination: 10,000 particles (<=45 nm)
E. coli 70S ribosome in situ structure for xenon damage layer determination: 20 - 25 nm
E. coli 70S ribosome in situ structure for xenon damage layer determination: 15 - 20 nm
Enterobacteriaphage PRD1 - P12 protein filament in complex with repetitive (ATGCT) ssDNA
Structure of Kasugamycin-30S-IF1-IF3-mRNA-tRNA translation pre-initiation complex, open form
E. coli 70S ribosome in situ structure for xenon damage layer determination: 50 - 55 nm
E. coli 70S ribosome in situ structure for xenon damage layer determination: 35 - 40 nm
NEDD1-bound native vertebrate gamma-tubulin ring complex from Xenopus laevis, focused reconstruction
E. coli 70S ribosome in situ structure for xenon damage layer determination: 45 - 50 nm
E. coli 70S ribosome in situ structure for xenon damage layer determination: 40 - 45 nm