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!
Composite Map Guide
Introduction
The deposition of a composite map entry set follows the recommendations laid out by the community in 2020 (https://doi.org/10.48550/arXiv.2311.17640). In accordance with these recommendations we require the composite map, all constituent maps (henceforth referred to as focused refinements), and the un-focused full structure (henceforth known as a consensus map) to be deposited as their own entries so that validation can be carried out for each of the deposited maps. In addition, the composite map entry must appropriately reference the focused refinements and consensus map. In this tutorial we will summarise the workflow to deposit a composite map set of entries in the most efficient manner possible.
In this tutorial we will use publicly available data EMDB: EMD-43299 and PDB: 8VK3.
Graphical Overview
To complete a deposition of a composite map set you will need several maps. These maps are described graphically below and EMD-IDs are included for an example composite map deposition set that can be found on the EMDB website.
Summary
Reminder: A composite map deposition must consist of separate depositions describing the composite map, consensus map, and focused map(s).
- Create a composite map deposition (Do not submit).
- Create focused refinement and consensus depositions (after completing composite map deposition). Pull the metadata from the composite map deposition.
- Associate the focused refinement and consensus depositions to the composite map deposition by filling the IDs in the “related entries” and submit.
Deposition Table
| Composite Map | Consensus Map | Focused Map(s) | |
|---|---|---|---|
| Primary Map |
Required |
Required |
Required |
| Half-maps |
Optional (If provided they must be composite half-maps)* |
Required |
Required |
| Entry Image |
Required |
Required |
Required |
| mmCIF file |
Optional (unless also depositing a model) |
Optional (unless also depositing a model) |
Optional (unless also depositing a model) |
| FSC Curve file |
Optional (If provided it should be calculated from the composite half-maps and described appropriately)** |
Optional |
Optional |
| Mask(s) |
Optional |
Optional |
Optional |
| Additional Map(s) |
Optional |
Optional |
Optional |
| Layer line file |
Not expected |
Not expected |
Not expected |
*If depositing half-maps as part of a composite-map deposition, only composite half-maps should be provided. Consensus and focused half-maps should be provided with the relevant, separate, depositions.
**EMDB recommends using the mean resolution of the focused maps as the resolution of the composite map
Step by Step
-
Start the composite map deposition
We recommend you start by creating the composite map deposition. This entry should contain all the metadata relevant to the other entries and we will be able to copy this across to those entries later. The deposition setup for this can be seen in Figure 1. Don’t forget to sign in with ORCID to enable easy access to all your depositions later on. In this example the model has been built into the composite map, therefore the composite map and model will be deposited together so that map-model validation can be carried out in this entry.
Figure 1: Setting up a composite map deposition.
Once the setup is complete and you have clicked ‘start deposition’ you should receive the details to login to the deposition via email and find it in your ORCID list of depositions if you were signed in with ORCID. The first step is to upload your files, an example of which can be seen in Figure 2, since this is a composite map deposition no half-maps are expected. Don’t forget that the mmCIF file format is also a metadata file format. All metadata provided in the uploaded mmCIF will automatically be used to fill the deposition interface. For users who wish to learn more about mmCIF files the mmCIF dictionary is available online (https://mmcif.wwpdb.org/) and example mmCIF files with EM metadata are available from the EMDB (e.g. https://www.ebi.ac.uk/emdb/EMD-43299?tab=links) under the Metadata section as a cif.gz download.
Figure 2: File upload page for a composite map entry.
After completing this section, the deposition interface will allow all metadata to be entered. Anything that was in the mmCIF file should already be in the deposition interface. Once all metadata sections are filled the entry should look similar to Figure 3.
DO NOT SUBMIT THE DEPOSITION YET!
Figure 3: a completed composite map deposition user-interface
We can now log out of this entry and start the deposition of the other entries.
2. Focused/Consensus map deposition
Now we are going to deposit the focused map(s) and consensus map. There should be one or more focused refinements and one consensus map deposited for every composite map deposited. In this example we will show you the deposition of a single focused refinement map, the method for depositing the others should be identical.
Once again we start by setting up the deposition (Figure 4). This time we will approach it as a regular map deposition (not composite). We have also already deposited coordinates with the composite map, as a result we will deposit the focused refinement(s) and consensus map without a coordinate model. If you have good reason to deposit portions of the model with the focused refinement(s) you are free to do so but where efficiency of deposition is concerned depositing the maps alone will be quicker.
Figure 4: Setting up a deposition for a focused/consensus map
As before, once the deposition is started you will get to the file upload screen. This time you can use the ‘based on a previous wwPDB deposition’ (Figure 5) option during the file upload process. This allows you to copy across various metadata from a previous deposition. Once the file upload is complete you should now see that, where possible, metadata has been transferred to the new deposition (Figure 6). This deposition can now be completed and submitted. Once submitted you will receive an EMD accession code which is needed for the next step.
Figure 5: Copying metadata from the composite map deposition
Figure 6: Metadata pulled from a previous deposition automatically fills relevant pages, in some cases already providing all required information (green tick).
3. Complete the composite map deposition
Now that you have completed all your focused refinement and consensus map depositions we can return to the composite map deposition and associate the new depositions to them. To do this we are going to go to the ‘Related entries’ page and fill the table out. The ‘content type’ drop-down menu will allow you to define the maps as focused or consensus. An example of this can be seen, including how it will be displayed on the EMDB website, in Figure 7. Once this is complete you are ready to submit the composite map deposition. If the composite map is accidentally submitted prematurely, or more entries are generated that you wish to be associated with the composite map after its submission, this can be corrected by contacting a wwPDB biocurator through the communication tab in OneDep.
Figure 7: Filling in the related entries for the composite map deposition.
Recommendation from EMDB: It is advised to use correlated yet distinct titles for entries related to a composite map.
Quick links
Recent Entries
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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
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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)
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)
