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
(Show all)Tubulin Cofactors D,E,G,C and Tubulin complex -- TBCC N Terminus Bound to Tubulin. TBC E Refinement
Tubulin cofactors D,E,G,C bound to tubulin dimer -- TBCC N terminus unbound. Core Refinement
Tubulin Cofactors D,E,G,C and Tubulin complex -- TBCC N Terminus Bound to Tubulin Core Refinement
Tubulin Cofactors D,E,G,C and Tubulin complex -- TBCC N Terminus Bound to Tubulin. TBCC Focused
Hepatitis C virus sE1E2.Cut1+2.SPYdeltaN bound to antibodies AR4A and AR3C
Hepatitis C virus sE1E2.Cut1+2.SPYdeltaN bound to antibodies AR4A and HEPC74
Tubulin cofactors D,E,G,C bound to tubulin dimer -- TBCC N terminus unbound. TBCE Refinement
Focused refinement map of the periplasmic part of the Legionella pneumophila T4SS.
Human uPAR bound to the Fab fragment of targeted cancer therapeutic antibody FL1
Focused refinement map of the cytoplasmic region of the Legionella pneumophila T4SS.
Cryo-EM structure of the human TRPM4 channel in complex with EGTA and DAB at 37 degrees Celsius
Cryo-EM structure of the human TRPM4 channel in complex with calcium and DAB at 37 degrees Celsius
The structure of TMD with 3 TARPs and 1 CNIH from all native AMPA receptor subtypes
Soluble ectodomain of Herpes simplex virus 2 (HSV-2) glycoprotein B (gB) in the prefusion conformation in complex with 2c and D48 Fabs
Structure of SpyCas9 in complex with the anti-CRISPR protein AcrIIA26
Cryo-EM structure of the SAH domain of Caenorhabditis elegans ICP-1 bound to the paclitaxel-stabilized microtubule
Cryo EM structure of LukAB (LukGH) toxin from Staphylococcus aureus in complex with neutralizing Fab STAU-15
Cryo-EM structure of the human Hec1-Nuf2 dimer bound to the paclitaxel-stabilized microtubule
Cryo-EM structure of the SAH domain of human INCENP bound to the paclitaxel-stabilized microtubule
Cryo-EM structure of the Xenopus laevis mitotic centromere-associated kinesin (MCAK) bound to the paclitaxel-stabilized microtubule
Cryo-EM structure of the Xenopus laevis mitotic centromere-associated kinesin (MCAK) bound to the paclitaxel-stabilized microtubule
Cryo-EM structure of the Xenopus laevis mitotic centromere-associated kinesin (MCAK) bound to the paclitaxel-stabilized microtubule
Cryo-EM structure of human UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase (DPAGT1) in complex with APPB, Chain B map
Co-transcriptional histone H3K36 methylation complex containing RNA polymerase II elongation complex, Set2, and the upstream nucleosome. (temp115, Spt6-Set2(AID) reconstruction)
Co-transcriptional histone H3K36 methylation complex containing RNA polymerase II elongation complex, Set2, and the upstream nucleosome. (temp115, Spt6 reconstruction)
Cryo-EM structure of human UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase (DPAGT1) in complex with APPB, consensus map
Cryo-EM structure of human UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase (DPAGT1) in complex with APPB, composite map
Cryo-EM structure of human UDP-N-acetylglucosamine-dolichyl-phosphate N-acetylglucosaminephosphotransferase (DPAGT1) in complex with APPB, Chain A map
Co-transcriptional histone H3K36 methylation complex containing RNA polymerase II elongation complex, Set2, and the upstream nucleosome. (temp115, Nucleosome-Set2(CD) reconstruction)
Focused map 'CI-Q' from the alphaproteobacterial respiratory supercomplex CI1-CIII2-CIV2
Consensus map of the alphaproteobacterial respiratory supercomplex CI1-CIII2-CIV2
Structural characterisation of chromatin remodelling intermediates supports linker DNA dependent product inhibition as a mechanism for nucleosome spacing.
Dissociation-state-3 of 9-subunit CSN and SCF (SKP1-SKP2-CKS1) complex
Dissociation-state-4 of 9-subunit CSN and SCF (SKP1-SKP2-CKS1) complex
Local refinement map of Gi-coupled NPFF2R in complex with GUB08248
Negative stain EM map 3 of polyclonal serum from mouse immunized with H5 TX24-membrane anchored in complex with TX24-I53_dn5B.
Negative stain EM map 1 of polyclonal serum from mouse immunized with H5 TX24-FMLMI-membrane anchored in complex with TX24-I53_dn5B.
Negative stain EM map 2 of polyclonal serum from mouse immunized with H5 TX24-membrane anchored in complex with TX24-I53_dn5B.
Negative stain EM map 3 of polyclonal serum from mouse immunized with H5 TX24-FMLMI-RC_I_1 in complex with TX24-I53_dn5B.
Negative stain EM map 3 of polyclonal serum from mouse immunized with H5 TX24-FMLMI-membrane anchored in complex with TX24-I53_dn5B.
Negative stain EM map 1 of polyclonal serum from mouse immunized with H5 TX24-FMLMI-RC_I_1 in complex with TX24-I53_dn5B.
Negative stain EM map 1 of polyclonal serum from mouse immunized with H5 TX24-membrane anchored in complex with TX24-I53_dn5B.
Negative stain EM map 2 of polyclonal serum from mouse immunized with H5 TX24-FMLMI-membrane anchored in complex with TX24-I53_dn5B.
Negative stain EM map 1 of polyclonal serum from mouse immunized with H5 TX24-FMLMI-foldon in complex with TX24-I53_dn5B.
Negative stain EM map 2 of polyclonal serum from mouse immunized with H5 TX24-FMLMI-RC_I_1 in complex with TX24-I53_dn5B.
Negative stain EM map of polyclonal serum from mouse immunized with H5 TX24-foldon in complex with TX24-I53_dn5B.
Negative stain EM map 4 of polyclonal serum from mouse immunized with H5 TX24-membrane anchored in complex with TX24-I53_dn5B.
Negative stain EM map 3 of polyclonal serum from mouse immunized with H5 TX24-FMLMI-foldon in complex with TX24-I53_dn5B.
Negative stain EM map 2 of polyclonal serum from mouse immunized with H5 TX24-FMLMI-foldon in complex with TX24-I53_dn5B.
Negative stain EM map 4 of polyclonal serum from mouse immunized with H5 TX24-FMLMI-membrane anchored in complex with TX24-I53_dn5B.
attPsym bound large serine integrase and RDF complex in the dimeric state
Cryo-tomogram of a patch-like NLRP3 inflammasome condensate at the MTOC
Patch-like NLRP3 inflammasome condensate formed above or below the MTOC
Cryo-tomogram of a matured NLRP3 inflammasome condensate at the MTOC
Apoferritin single-particle cryo-EM reconstruction using a Volta phase plate
Cryo-tomogram of a solid-like NLRP3 inflammasome condensate at the MTOC
Cryo-tomogram of NLRP3-associated vesicles residing at the Golgi following LPS treatment
Cryo-EM structure of stabilized H5N1 A/Texas/37/2024 hemagglutinin fused to foldon
Apoferritin single-particle cryo-EM reconstruction under matched conditions without a phase plate
Cryo-EM structure of the human BK channel bound to the agonist NS1619
Structural characterisation of chromatin remodelling intermediates supports linker DNA dependent product inhibition as a mechanism for nucleosome spacing.
Cryo-EM structure of Ro60/La/minimal misfolded pre-5S rRNA complex with Fab, composite map
Cryo-EM structure of Ro60/La/minimal misfolded pre-5S rRNA complex with Fab, consensus map
Cryo-EM structure of Ro60/La/truncated misfolded human pre-5S rRNA complex with Fab, focused map
Cryo-EM structure of Ro60/La/truncated misfolded human pre-5S rRNA complex with Fab, consensus map
Cryo-EM structure of Ro60/La/truncated misfolded human pre-5S rRNA complex with Fab, composite map
Cryo-EM structure of Ro60/La/minimal misfolded pre-5S rRNA complex with Fab, N-term La/Fab focused map
Cryo-EM structure of Ro60/La/minimal misfolded pre-5S rRNA complex with Fab, C-term La focused map
Muscle-type nicotinic acetylcholine receptor bound to conotoxin ImII
Structure of human Fab 245 in complex with influenza H1N1 A/Solomon Island/3/2006 hemagglutinin
Structure of human Fab 604 in complex with influenza H1N1 A/Solomon Island/3/2006 hemagglutinin
Hexameric AAV2 Rep40-dsDNA (ITR) duplex complex in presence of ATPyS
Hexameric AAV2 Rep40-dsDNA (ITR) melting complex in presence of ATPyS
Cryo-EM structure of NI06063_d30_103 Fab in complex with influenza virus hemagglutinin from A/Hong Kong/485197/2014 (H3N2)
Cryo-EM structure of NI06063_d30_103 Fab in complex with influenza virus hemagglutinin from A/Michigan/45/2015 (H1N1)
Cryo-EM structure of NI04359_d30_240 Fab in complex with influenza virus hemagglutinin from A/Hong Kong/485197/2014 (H3N2)
Cryo-EM structure of NI04359_d30_240 Fab in complex with influenza virus hemagglutinin from A/Michigan/45/2015 (H1N1)
Cryo-EM Structure of the Escherichia phage HK446 Rip1 in complex with the Enterobacteria phage T6 small terminase
CryoEM structure of MraZ in complex with its promoter from Mycoplasma genitalium
Type I-F_HNH variant Cascade bound to dsDNA, HNH domain in middle position
Type I-F_HNH variant Cascade target-free RNP, HNH domain in inwards position
Type I-F_HNH variant Cascade RNP bound to dsDNA with trace of target strand into HNH domain rotated in middle position
Type I-F_HNH variant Cascade target-free RNP, HNH domain in middle position
Cryo-EM structure of horse spleen apoferritin using the cryoWriter automated grid preparation system with one-time writing with spiral pattern
Cryo-EM structure of horse spleen apoferritin using the cryoWriter automated grid preparation system with one-time writing with a line pattern
Cryo-EM structure of the transient receptor potential melastatin 4 (TRPM4) channel prepared using the cryoWriter automated grid preparation system with spiral-pattern writing
Cryo-EM structure of the desthiobiotin-bound streptavidin prepared using the cryoWriter automated grid preparation system with line pattern writing
Cryo-EM structure of Tobacco Mosaic Virus (TMV) prepared using the cryoWriter automated grid preparation system with spiral writing.
Cryo-EM Structure of Horse Spleen Apoferritin using cryoWriter with On-Grid Protein Mixing
Cryo-EM structure of horse spleen apoferritin using the cryoWriter automated grid preparation system with two-time writing with spiral pattern
CryoEM structure of the octamer MraZ in complex with 1 box promoter from Mycoplasma genitalium
CryoEM structure of MraZ in complex with 4 box promoter from Mycoplasma genitalium
The cryo-EM structure of HerA-NurA complex with AMPPNP from Thermococcus kodakarensis
The cryo-EM structure of HerA-NurA complex with ATPgammaS and dsDNA from Thermococcus kodakarensis (State 3)
Subtomogram average of GEM-mCherry-nanobody labeled EGFR on A549 cell membranes
The cryo-EM structure of HerA-NurA complex with ATPgammaS and dsDNA from Thermococcus kodakarensis (State 1)
The cryo-EM structure of HerA-NurA complex with ATPgammaS and dsDNA from Thermococcus kodakarensis (State 2)
CryoEM structure of anti-MHC-I mAb B1.23.2 complex with HLA-B44:05
Cryo-EM structure of Hydrogenivirga sp. MraY in complex with APPB
The cryo-EM structure of HerA-NurA complex with AMPPNP and dsDNA from Thermococcus kodakarensis
Cryo-EM structure of human V1aR bound with SRX246 at a resolution of 2.6 angstrom
Cryo-EM structure of human V1aR bound with balovaptan at a resolution of 3.0 angstrom
Cryo-EM structure of human V1aR in apo state at a resolution of 2.8 angstrom
Structure of recombinantly assembled E83Q alpha-synuclein fibrils
Structure of minor species of Abeta fibrils from AppNL-FPsen1P117L mice
Focused map 'CI-N' from the alphaproteobacterial respiratory supercomplex CI1-CIII2-CIV2
Focussed map 'cbb3-Half-CIII2' from the alphaproteobacterial respiratory supercomplex CI1-CIII2-CIV2-(cbb3)1
Ribosome STA of particles classified by pytom-match-pick using the dual-constraint strategy.
Respiratory supercomplex CI1-CIII2-CIV2-(cbb3)1 from alphaproteobacterium
Focused map 'CIII2 + 2c' from the alphaproteobacterial respiratory supercomplex CI1-CIII2-CIV2
Focused map 'CIV-D' from the alphaproteobacterial respiratory supercomplex CI1-CIII2-CIV2
Respiratory supercomplex CI2-CIII2-CIV2 (megacomplex) from alphaproteobacterium
Structure of the Arabidopsis thaliana 80S ribosome in complex with P- and E-site tRNAs, mRNA, and thermospermine
Structure of the Arabidopsis thaliana 80S ribosome OVAC mutant in complex with P- and E-site tRNAs, mRNA, and thermospermine
Focused map 'CIV-P' from the alphaproteobacterial respiratory supercomplex CI1-CIII2-CIV2
Structure of the Arabidopsis thaliana 80S ribosome OVAC mutant in complex with P- and E-site tRNAs and mRNA
Structure of the Arabidopsis thaliana 80S ribosome in complex with P- and E-site tRNAs and mRNA
Respiratory supercomplex CI1-CIII2-CIV1 (respirasome) from alphaproteobacterium
Form II Rubisco inside EPYC1-formed liquid-liquid phase separated condensates with bound Magnesium and CABP
Photosynthetic A10B10 glyceraldehyde-3-phospahte dehydrogenase from Spinacia oleracea.
Complex of voltage-gated sodium channel NavPaS from American cockroach Periplaneta americana and sea anemone toxin Av3
Complex of voltage-gated sodium channel NavPaS from American cockroach Periplaneta americana and scorpion alpha toxin LqhaIT
Cryo-EM structure of the JN241-9-bound state 1a of APLNR homodimer
Cryo-EM structure of the JN241-9-bound state 1c of APLNR homodimer
Cryo-EM structure of the JN241-9-bound state 1b of APLNR homodimer
Cryo-EM structure of the AMG986-bound state 2a of APLNR homodimer
Cryo-EM structure of the AMG986-bound state 2b of APLNR homodimer
Cryo-EM structure of Rubisco from Arabidopsis thaliana with the 1A small subunit isoform
Cryo-EM structure of bacteriophage P22 gp1-gp5-gp4 complex at 2.76 angstrom
Structure of E.coli ribosome with filamin mutant Y719E nascent chain at linker length of 47 amino acids, with tRNA
Cryo-EM structure of the human TRPM4 channel subunit in complex with calcium and DAB at 37 degrees Celsius
Mutant human uPAR bound to the Fab fragment of the targeted cancer therapeutic antibody FL1
Cryo-EM structure of CDK2/CyclinE1 in complex with CRBN/DDB1 and Cpd 24
Stabilized tandem antigen chimera of Pfs230 and Pfs48/45 bound by potent mAbs
Tubulin Cofactors D,E,G,C and Tubulin complex -- TBCC N Terminus Bound to Tubulin
Tubulin cofactors D,E,G,C bound to tubulin dimer -- TBCC N terminus unbound
The structure of TMD with 2 TARPs and 2 CNIHs from all native AMPA receptor subtypes
The structure of TMD with 4 TARPs from all native AMPA receptor subtypes
Cryo-EM map of TMD with 2 TARPs from all native AMPA receptor subtypes
CryoEM structure of GluK2 bound to glutamate in the deep desensitized state 2
CryoEM structure of GluK2 bound to glutamate in the deep desensitized state 3
CryoEM structure of GluK2 bound to glutamate in the deep desensitized state 1
CryoEM structure of GluK2 bound to glutamate in the transition state
CryoEM structure of GluK2 bound to glutamate in the shallow desensitized state, consensus map
Structure of Native Bovine Rhodopsin in Complex with Mb7 in the Dark State
CryoEM structure of GluK2 bound to glutamate in the shallow desensitized state, composite map
