Happy Holidays and New year from the EMDB! Please be advised that the EMDB team will be operating at reduced capacity between December 15th - January 12th. With this in mind we would ask that you be prepared for longer reply times through both our helpdesk system and the OneDep deposition system. well done on a productive 2025, wishing you all the best and we will see you in 2026!
FAQ
EM map deposition questions
- How do I begin a map deposition to EMDB?
- What map formats are accepted by EMDB?
- What is the difference between a deposition session id and an EMDB accession id?
- We have two maps for one submitted manuscript, one native, one with cofactor protein. Do we need to complete two separate depositions?
- Can I deposit a composite map to EMDB?
- How can we deposit multiple 3D volumes generated from imaging of a single specimen?
- How can I request a change/correction/citation update to my EMDB entry?
- Our manuscript has not been officially accepted yet, so please do not release our entry.
- I received an email stating that my map is being released. When will it be available in the EM Data Bank?
- The journal I am targetting requires editors and referees access to the structure while my manuscript is under review. Does EMDB provide confidential access to editors or referees if a structure is "on hold"?
EM map-derived coordinate model deposition questions
- I have fitted coordinates for my map, can I include them with my map entry?
- I obtained coordinates from PDB and used rigid-body fitting to place them into my map. Can I deposit these coordinates to PDB?
- My fitted coordinates correspond to a protein homolog. During the PDB deposition, should I provide the species information/sequence information for the EM sample or for the protein homolog?
- How are coordinates derived from EM reconstructions validated?
- We have a new coordinate model fitted into an EMDB map entry authored by another research group. Can we deposit our coordinates?
EM map, model and metadata access questions
- How can I find/download a map or browse the EMDB database?
- How can I view EMDB maps?
- How can I download a map that has already been deposited and released?
- Can I use maps and/or map images from EMDB in my thesis/publication?
- How can I download EMDB map entry metadata?
EM map deposition answers
How do I begin a map deposition to EMDB?
EMDB maps can be deposited through the wwPDB OneDep system. Tutorials for which can be found here.
What map formats are accepted by EMDB?
Maps can be deposited in mrc and ccp4 formats; they are converted to standard ccp4 format for redistribution in the EMDB.
What is the difference between a deposition session id and an EMDB accession id ?
When you initiate a deposition session you are assigned a session id (reference code). The session id is a "private" identifier known only to the depositor and the deposition site. When you complete your deposition and submit it to the EMDB, you are assigned a public accession code ("EMD-" followed by a four or five digit number). The public accession code is the id you should provide to journals when indicating your EMDB submission; it is also the code by which you can access to your entry in the publicly available EMDB search and atlas pages.
We have two maps for one submitted manuscript, one native, one with cofactor protein. Do we need to complete two separate depositions?
If the maps were generated from different specimen preparations/imaging experiments you will need to make two separate depositions.
Time saving tip: complete the submission for the first map (deposition session 1), and then for the second map (deposition session 2) select the option "based on previous submission." You will need to provide the 1st deposition session id and password in order to use this option.
Can I deposit a composite map to EMDB?
A composite map is here defined as a map constructed by piecing together two or more experimentally derived component EM maps together. A composite map may be deposited to EMDB if the component maps share the same specimen preparations/imaging experiments (see also "We have two maps for one submitted manuscript, one native, one with cofactor protein. Do we need to complete two separate depositions?”). For composite map depositions we ask that you: a) also provide each of the component maps as individual EMDB entries, in addition to the composite map entry; b) add the following suffix to the composite map entry title: “(composite structure).”
How can we deposit multiple 3D volumes generated from imaging of a single specimen?
EM reconstruction methods are beginning to yield ensembles of maps representing multiple conformations/enzymatic states within a heterogeneous population of imaged particles. If you need to deposit multiple maps of this type you can do so either within a single submission, in which case one map must be designated at the primary map, or a separate submissions (please see answer above).
How can I request a change/correction/citation update to my EMDB entry?
Please log into your OneDep deposition and make the request using the communication module.
Our manuscript has not been officially accepted yet, so please do not release our entry.
The only part of an EMDB submission that is released immediately is the experimental information in the header. The header information will only be released after you have had an opportunity to comment on the curated data. The map will not be released until the hold period has elapsed which can be on publication (HPUB), or 1 year from deposition. The map will only be released immediately if you have requested this at the release option stage.
I received an email stating that my map is being released. When will it be available in the EM Data Bank?
EMDB follows the same weekly release cycle as PDB. Maps queued for release before Thursday at 5pm (UK) will be available from EMDB on the following Wednesday.
The journal I am targeting requires editors and referees access to the structure while my manuscript is under review. Does EMDB provide confidential access to editors or referees if a structure is "on hold"?
Unreleased structural data on hold, both maps and coordinate sets, are kept strictly confidential. After deposition, you will immediately receive EMDB ids for your map entries and PDB ids for your map-derived model entries, which you may include in your manuscript. In addition, for PDB model entries you can obtain validation reports that provide assessments of model quality while keeping the coordinate file confidential. We encourage journal editors and referees to request validation reports from depositors as part of the manuscript submission and review process. The reports are date-stamped, and display the wwPDB processing site logo. For more information see https://www.wwpdb.org/validation.html.
EM map-derived coordinate model deposition answers
I have fitted coordinates for my map, can I include them with my map entry?
Fitted coordinate models for EM entries may be deposited along with your map; they will be assigned a PDB id.
I obtained coordinates from PDB and used rigid-body fitting to place them into my map. Can I deposit these coordinates to PDB?
You can deposit coordinates derived from any fitting protocol, including rigid-body fitting, flexible fitting, or de novo tracing. The deposited coordinates must be aligned and in-frame with the map.
My fitted coordinates correspond to a protein homolog. During the PDB deposition, should I provide the species information/sequence information for the EM sample or for the protein homolog?
The species information should correspond to your EM sample, but the sequence information should correspond to the protein homolog/fitted model.
How are coordinates derived from EM reconstructions validated?
Currently, model fit to an EMDB map is validated through visual inspection of the deposited map + model pair using a 3D graphics program. Models are also checked for correct stereochemistry and clashes; a validation report is issued for every submitted model.
We have a new coordinate model fitted into an EMDB map entry authored by another research group. Can we deposit our coordinates?
Yes, you can deposit your coordinates. Provide the EMDB map accession id (EMD-XXXX) as the associated EM volume of your coordinate deposition. The PDB policy regarding re-refined entries applies: "A re-refined entry may be deposited prior to publication but will not be processed (will have REFI status) or released until the associated publication has become publicly available." No changes will be made to the EMDB map entry.
EM map, model and metadata access answers
How can I find/download a map or browse the EMDB archive?
You can use the advanced search link on the top of the page.
To view the map on your own computer, you will first need to download the map from the EMDB atlas page and view the map with locally installed software. ChimeraX, Pymol, Coot (v. 0.6.2 or later), and other graphics programs can display EMDB maps when loaded as "ccp4" format maps.
How can I download a map that has already been deposited and released?
Released maps can be downloaded either from the 'downloads' tab of the atlas page for the entry or from one of the three wwPDB ftp distribution sites: ftp://ftp.ebi.ac.uk/pub/databases/emdb, https://ftp.wwpdb.org/pub/emdb or https://data.pdbj.org/pub/emdb. Some strategies to retrieve files from the ftp sites are posted here: https://www.wwpdb.org/download/downloads.php
Can I use maps and/or map images from EMDB in my thesis/publication?
Data files contained in the EMDB are free of all copyright restrictions and made fully and freely available for both non-commercial and commercial use. Users of the data should attribute the original authors of the structural data and the EMDB accession id. Many of the static EM map images shown on atlas pages have been contributed by the original deposition authors in which case they may also be protected by copyright law, even though we provide free access to them. The respective copyright holders of author-provided images retain rights for reproduction, redistribution and reuse. Users are responsible for compliance with copyright restrictions and are expected to adhere to the terms and conditions defined by the copyright holder.
How can I download EMDB map entry metadata?
The EMDB is distributed as a branch of the wwPDB archive, and is available via all of the wwPDB ftp sites. Instructions to retrieve EMDB xml metadata files are posted here: https://www.wwpdb.org/download/downloads.php
Quick links
Recent Entries
(Show all)Group II intron assembly intermediate Domain 1, 2, 3 and 4 "Fully open" state
Respiratory supercomplex CI2-CIII2-CIV2 (megacomplex, C1 symmetry) from alphaproteobacterium
Sub-tomogram average of the wild-type C. elegans I1III2 respiratory supercomplex
Influenza Neuraminidase in complex with N-Acyl Oseltamivir inhibitor
Influenza Neuraminidase in complex with N-Acyl Oseltamivir inhibitor
Influenza Neuraminidase in complex with N-Acyl Oseltamivir inhibitor
Soft-landed and rehydrated beta-galactosidase (averaged structure)
Translational activators Aep1, Aep2 and Atp25 in complex with mRNA and the yeast mitochondrial ribosome (consensus)
Sub-tomogram average of the wild-type C. elegans ATP synthase dimer (narrow membrane curvature)
Sub-tomogram average of nduf-11(RNAi) C. elegans respiratory complex I
Sub-tomogram average of the nduf-11(RNAi) C. elegans ATP synthase dimer (intermediate membrane curvature)
Sub-tomogram average of the wild-type C. elegans ATP synthase dimer (intermediate membrane curvature)
Sub-tomogram average of the wild-type C. elegans ATP synthase dimer (wide membrane curvature)
Sub-tomogram average of the nduf-11(RNAi) C. elegans ATP synthase dimer (wide membrane curvature)
Sub-tomogram average of the nduf-11(RNAi) C. elegans ATP synthase dimer (narrow membrane curvature)
Cryo-EM Structure of the Vaccinia Virus Entry/Fusion Complex (EFC) Lacking the F9 Subunit
Cryo-EM structure of soluble methane monooxygenase hydroxylase from Methylosinus sporium 5
Cryo-EM Structure of the Vaccinia Virus Entry/Fusion Complex (EFC) Including the F9 Subunit
Cryo-EM structure of human lipid phosphate phosphatase 1 complexed with LPA
Cryo-EM structure of the light-driven sodium pump ErNaR in the pentameric form
Cryo-EM structure of the light-driven sodium pump ErNaR in the monomeric form in the O2 state
Translational activators Aep1, Aep2 and Atp25 in complex with mRNA and the yeast mitochondrial ribosome (focused on the LSU)
Translational activators Aep1, Aep2 and Atp25 in complex with mRNA and the yeast mitochondrial ribosome (focused on the SSU head)
Translational activator Aep3 in complex with mRNA and the yeast mitochondrial ribosome (consensus map)
Translational activators Aep1, Aep2 and Atp25 in complex with mRNA and the yeast mitochondrial ribosome (focused on Aep1-Aep2-Atp25)
Translational activator Aep3 in complex with mRNA and the yeast mitochondrial ribosome (focused on Aep3)
Translational activators Aep1, Aep2 and Atp25 in complex with mRNA and the yeast mitochondrial ribosome (focused on the SSU body)
Translational activator Aep3 in complex with mRNA and the yeast mitochondrial ribosome (focused on the SSU)
Translational activator Aep3 in complex with mRNA and the yeast mitochondrial ribosome (focused on the SSU head)
Translational activator Aep3 in complex with mRNA and the yeast mitochondrial ribosome (focused on the LSU)
Translational activator Aep3 in complex with mRNA and the yeast mitochondrial ribosome
Translational activators Aep1, Aep2 and Atp25 in complex with mRNA and the yeast mitochondrial ribosome
High resolution structure of the thermophilic 60S ribosomal subunit of Chaetomium thermophilum
Connexin-32 (Cx32) gap junction channel in POPC-containing nanodiscs in the absence of CHS
Connexin-32 (Cx32) W3S mutant gap junction channel in POPC-containing MSP2N2 nanodiscs
Cryo-EM structure of the light-driven sodium pump ErNaR in the monomeric form in the K2 state
Deconvolved piDPC tomogram of lift-out lamellae from cell-derived matrices recorded on the Opal detector
Deconvolved piDPC tomogram of lift-out lamellae from cell-derived matrices
Deconvolved piDPC tomogram of lift-out lamellae from cell-derived matrices
Cryo-EM structure of E.coli transcription initiation complex with Escherichia phage Mu late transcription activator C focusing on C region
Cryo-EM structure of E.coli transcription initiation complex with Escherichia phage Mu late transcription activator C focusing on RNA polymerase region
Cryo-EM structure of E.coli transcription initiation complex with Escherichia phage Mu middle transcription activator Mor focusing on RNA polymerase region
Cryo-EM structure of E.coli transcription initiation complex with Escherichia phage Mu middle transcription activator Mor focusing on Mor region
Motor domain with ADP AAA1 and ADP AAA3 from yeast full-length dynein-1 in 0.1 mM ATP condition
Motor domain with Apo AAA1 and ADP AAA3 from yeast full-length dynein-1 in 0.1 mM ATP condition
Motor domain alone with Apo AAA1 and ADP AAA3 from yeast full-length dynein-1 and Pac1 in 0.1 mM ATP condition
Cryo-EM structure of rabbit TRPM3 in apo resting state at 37 degrees Celsius
Motor domain-Pac1 complex with ADP AAA1 and Apo AAA3 from yeast full-length dynein-1 and Pac1 in 0.1 mM ATP condition
Cryo-EM structure of rabbit TRPM3 in apo activated state at 18 degrees Celsius
Cryo-EM structure of rabbit TRPM3 in apo activated state at 37 degrees Celsius
Cryo-EM structure of rabbit TRPM3 in complex with CIM0216 in resting state at 18 degrees Celsius
Cryo-EM structure of rabbit TRPM3 in complex with primidone in resting state at 18 degrees Celsius
Cryo-EM structure of rabbit TRPM3 in complex with CIM0216 in activated state at 18 degrees Celsius
Cryo-EM structure of rabbit TRPM3 in complex with primidone in activated state at 18 degrees Celsius
Cryo-EM structure of rabbit TRPM3 in complex with CIM0216 at 18 degrees Celsius
Cryo-EM structure of apo rabbit TRPM3 having 2 resting and 2 activated subunits (ortho position) at 18 degrees Celsius
Cryo-EM structure of apo rabbit TRPM3 having 2 resting and 2 activated subunits (para position) at 18 degrees Celsius
Cryo-EM structure of apo rabbit TRPM3 having 1 resting and 3 activated subunits at 18 degrees Celsius
Cryo-EM structure of apo rabbit TRPM3 having 3 resting and 1 activated subunits at 18 degrees Celsius
Cryo-EM structure of apo rabbit TRPM3 having 2 resting and 2 activated subunits (para position) at 37 degrees Celsius
Cryo-EM structure of apo rabbit TRPM3 having 2 resting and 2 activated subunits (ortho position) at 37 degrees Celsius
Cryo-EM structure of apo rabbit TRPM3 having 3 resting and 1 activated subunits at 37 degrees Celsius
Cryo-EM structure of CIM0216-bound rabbit TRPM3 having 3 resting and 1 activated subunits at 18 degrees Celsius
Cryo-EM structure of apo rabbit TRPM3 having 1 resting and 3 activated subunits at 37 degrees Celsius
Cryo-EM structure of primidone-bound rabbit TRPM3 having 3 resting and 1 activated subunits at 18 degrees Celsius
Cryo-EM structure of CIM0216-bound rabbit TRPM3 having 2 resting and 2 activated subunits (ortho position) at 18 degrees Celsius
Cryo-EM structure of CIM0216-bound rabbit TRPM3 having 2 resting and 2 activated subunits (para position) at 18 degrees Celsius
Cryo-EM structure of CIM0216-bound rabbit TRPM3 having 1 resting and 3 activated subunits at 18 degrees Celsius
Cryo-EM structure of primidone-bound rabbit TRPM3 having 1 resting and 3 activated subunits at 18 degrees Celsius
Cryo-EM structure of primidone-bound rabbit TRPM3 having 2 resting and 2 activated subunits (para position) at 18 degrees Celsius
Helical assembly of the IL-17RA/RB/ACT1 complex upper part focused map
Helical assembly of the IL-17RA/RB/ACT1 complex lower part focused map
Masked Classification of Prohibitin Complexes Showing the Prohibitin complex with an Additional Matrix-Facing Density (Class 1)
Masked Classification of Prohibitin Complexes Showing the Prohibitin complex without an Additional Matrix-Facing Density (Class 2)
Human quaternary complex of a translating 80S ribosome, NAC, MetAP1 and NatD
S. thermophilus class III ribonucleotide reductase focused refined core
S. thermophilus class III ribonucleotide reductase with dATP and TTP
S. thermophilus class III ribonucleotide reductase with ATP and TTP
S. thermophilus class III ribonucleotide reductase signal subtracted cone domains and core
S. thermophilus class III ribonucleotide reductase signal subtracted cone domains and core
S. thermophilus class III ribonucleotide reductase focused refined core
Cryo-EM structure of the glycosyltransferase GtrB in the substrate-bound state
Cryo-EM structure of the glycosyltransferase GtrB in the pre-catalysis and product-bound state
Cryo-EM structure of the glycosyltransferase GtrB (tetramer volume)
Cryo-EM structure of the glycosyltransferase GtrB in the apo state (octamer volume)
Cryo-EM structure of the glycosyltransferase GtrB in the pre-intermediate state
Tomogram of bacteriophage NF5-infected Brochothrix thermosphacta cell (1 out of 2)
Tomogram of bacteriophage NF5-infected Brochothrix thermosphacta cell (2 out of 2)
Cryo-EM map of apo-XPF-ERCC1-SLX4(330-555)-SLX4IP from a DNA-containing sample.
Cryo-EM structure of a DNA-bound XPF-ERCC1-SLX4(330-555)-SLX4IP complex
In-situ structure of the flagellar motor of Campylobacter jejuni pflA deletion mutant
In-situ structure of the flagellar motor of Campylobacter jejuni rpoN deletion mutant
In-situ structure of the flagellar motor of Campylobacter jejuni pflC deletion mutant
In-situ structure of the flagellar motor of Campylobacter jejuni pflB deletion mutant
Cryo-EM structure of human sortilin ectodomain in complex with a thyroglobulin C-terminal peptide
Focused refinement map of in situ E-ring structure in Campylobacter jejuni flagellar motor
In-situ structure of the flagellar motor of Campylobacter jejuni flgY deletion mutant
In-situ structure of the flagellar motor of Campylobacter jejuni fcpMNO deletion mutant
Half of Campylobacter jejuni motA deletion mutant flagellar motor structure in situ
Focused refinement map of in situ spoke-rim structure in Campylobacter jejuni flagellar motor
Half of Campylobacter jejuni pflD deletion mutant flagellar motor structure in situ
In-situ structure of the flagellar motor of Campylobacter jejuni pflD deletion mutant
Half of Campylobacter jejuni fcpMNO deletion mutant flagellar motor structure in situ
beta-barrel assembly machine from Escherichia coli in an early state of substrate assembly
Focused refinement of the barrel region of beta-barrel assembly machine from Escherichia coli in an late state of substrate assembly
beta-barrel assembly machine from Escherichia coli in a late state of substrate assembly
beta-barrel assembly machine from Escherichia coli in a middle state of substrate assembly
Consensus refinement of the barrel region of beta-barrel assembly machine from Escherichia coli in an late state of substrate assembly
Native GluN1/GluN2A/GluNx in complex with 5F11 and 3D2 Fabs (class 2), glycine and glutamate-bound state
Cryo-EM structure of Spinacia oleracea cytochrome b6f complex with bound plastocyanin
GluN1/GluN2A in complex with 3D2 Fab, glycine and glutamate-bound state
Native GluN1/GluNx in complex with 5F11 Fab (class 5), glycine and glutamate-bound state
Native GluN1/GluN2A/GluN2B in complex with 5F11 and 3D2 Fabs (class 1), glycine and glutamate bound state
GluN1/GluN2A in complex with polyclonal autoantibody Fab fragments (class 1), glycine- and glutamate-bound state
Native GluN1/GluN2A in complex with 5F11 and 3D2 Fabs, local ATD dimer
GluN1/GluN2A in complex with polyclonal autoantibody Fab fragments (class 2), glycine- and glutamate-bound state
Native GluN1/GluN2B in complex with 5F11 Fab (class 4), glycine and glutamate-bound state
Native GluN1/GluN2A in complex with 5F11 and 3D2 Fabs (class 3), glycine and glutamate-bound state
Sampling-mismatch-uncorrected ptychographic SPA reconstruction of the Thermoplasma acidophilum 20S proteasome
Sampling-mismatch-corrected ptychographic SPA reconstruction of the Thermoplasma acidophilum 20S proteasome
Single-particle cryo-EM structure of the first variant of mobilized colistin resistance (MCR-1) in its ligand-bound state
Rabbit muscle aldolase cryo-EM reconstruction obtained from Krios 5 with Selectris-X Falcon 4i detector
Cryo-EM structure of J601-1B2 Fab in complex with HIV-1 BG505 DS-SOSIP Env trimer
Cryo-EM structure of K001-A1 Fab in complex with HIV-1 459C-OPT RnS DS-SOSIP Env trimer
Cryo-EM structure of J601-A6 Fab in complex with HIV-1 BG505 DS-SOSIP Env trimer
Cryo-EM structure of Vibrio cholerae RNA polymerase holoenzyme bound to an ompU promoter DNA fragment
Focused map #2 of the cryo-EM structure of Vibrio cholerae RNA polymerase Transcription Activation Complex with ToxR and TcpP transcription factors and bound to a toxT promoter DNA fragment
Cryo-EM structure of Vibrio cholerae RNA polymerase Transcription Activation Complex with TcpP transcription factor and a toxT promoter DNA fragment
Focused map #1 of the cryo-EM structure of Vibrio cholerae RNA polymerase Transcription Activation Complex with ToxR and TcpP transcription factors and bound to a toxT promoter DNA fragment
Consensus map of the cryo-EM structure of Vibrio cholerae RNA polymerase Transcription Activation Complex with ToxR transcription factor and bound to an ompU promoter DNA fragment
Cryo-EM structure of Vibrio cholerae RNA polymerase holoenzyme bound to an ompU promoter DNA fragment and 5-mer RNA
Consensus map of the cryo-EM structure of Vibrio cholerae RNA polymerase Transcription Activation Complex with TcpP transcription factor and bound to a toxT promoter DNA fragment
Focused map #1 of the cryo-EM structure of Vibrio cholerae RNA polymerase Transcription Activation Complex with TcpP transcription factor and bound to a toxT promoter DNA fragment
Cryo-EM structure of Vibrio cholerae RNA polymerase Transcription Activation Complex with ToxR and TcpP transcription factors and a toxT promoter DNA fragment
Cryo-EM structure of Vibrio cholerae RNA polymerase dimer with ToxR and TcpP transcription factors and a toxT promoter DNA fragment
Focused map #1 of the cryo-EM structure of Vibrio cholerae RNA polymerase Transcription Activation Complex with ToxR transcription factor and bound to an ompU promoter DNA fragment
Focused map #2 of the cryo-EM structure of Vibrio cholerae RNA polymerase Transcription Activation Complex with TcpP transcription factor and bound to a toxT promoter DNA fragment
Focused map #2 of the cryo-EM structure of Vibrio cholerae RNA polymerase Transcription Activation Complex with ToxR transcription factor and bound to an ompU promoter DNA fragment
Cryo-EM structure of Vibrio cholerae RNA polymerase Transcription Activation Complex with ToxR transcription factor and ompU promoter DNA
Consensus map of the cryo-EM structure of Vibrio cholerae RNA polymerase Transcription Activation Complex with ToxR and TcpP transcription factors and bound to a toxT promoter DNA fragment
Cryo-EM map of respirasome open state bound by proguanil (SC-ProgO), complex I distal membrane arm focused
Cryo-EM map of respirasome open state 1 in presence of metformin (SC-MetO1), complex I distal membrane arm focused
Cryo-EM map of respirasome open state 1 in presence of metformin (SC-MetO1)
Cryo-EM map of respirasome open state bound by proguanil (SC-ProgO), complex I proximal membrane arm focused
Cryo-EM map of respirasome open state 1 in presence of metformin (SC-MetO1), complex IV focused
Cryo-EM map of respirasome open state 1 in presence of metformin (SC-MetO1), complex I peripheral arm focused
Cryo-EM map of respirasome open state 1 in presence of metformin (SC-MetO1), complex I proximal membrane arm focused
Cryo-EM map of respirasome open state bound by proguanil (SC-ProgO), complex I peripheral arm focused
Cryo-EM map of respirasome open state 1 in presence of metformin (SC-MetO1), complex III2 focused
Cryo-EM map of respirasome open state bound by proguanil (SC-ProgO)
Cryo-EM structure of the ICT01-BTN3A1/BTN3A2 complex, local refinement
Cryo-EM structure of the ICT01-BTN2A1/BTN3A1/BTN3A2 complex, local refinement
Cryo-EM structure of the ICT01-BTN2A1/BTN3A1/BTN3A2 complex (2 fabs)
Cryo-EM structure of the SPS3-FBN5 complex in a 2:2 state (class 3)
Cryo-EM structure of amyloid peptide-silk block protein fibril, Type 1
Cryo-EM structure of amyloid peptide-silk block protein fibril, Type 3
Complex I form respirasome open state bound by proguanil (SC-ProgO)
Cryo-EM structure of E.coli transcription initiation complex with Escherichia phage Mu late transcription activator C
Cryo-EM structure of E.coli transcription initiation complex with Escherichia phage Mu middle transcription activator Mor
Cryo-EM structure of the SPS3-FBN5 complex from Oryza sativa in complex with cobalt and geranylgeranyl S-thiodiphosphate (GGSPP)
