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)Cryo-EM structure of hemagglutinin from the A/Malaysia/1706215/2007 (H1N1) influenza virus with stabilizing mutations
Cryo-EM structure of hemagglutinin from the A/swine/Hong Kong/2106/98 (H9N2) influenza virus with stabilizing mutations
Structure of a circMbl 48S translation initiation complex in the AUG recognition state
Structure of a circMbl 48S translation initiation complex in the scanning state
Cryo-EM structure of Vibrio cholerae divisome complex FtsWIQLB (periplasmic conformation 2)
Cryo-electron tomogram of Chroococcidiopsis thermalis PCC 7203 in white light
Cryo-EM structure of Vibrio cholerae divisome complex FtsWIQLB (periplasmic conformation 1)
Cryo-EM structure of Vibrio cholerae divisome complex FtsWIQLB (consensus)
Chimeric Hepatitis B Virus Core Antigen (HBc) Virus-like Particles (VLP) Incorporating SARS-CoV-2 Spike Protein Epitopes
AHA hibernation factor bound to the 70S ribosome of Haloferax volcanii
Cryo-EM focused map of the active-state GPR55-N171Q mutant in complex with G13 and BI-6229
Structure of the Plant mitochondrial initiation complex, (SSU, LSU, initiator tRNA, mRNA)
Structure of the Plant mitochondrial pre-initiation complex 1, (SSU,mtIF3)
Cryo-EM focused map of inactive-state GPR55-bRIL-Fab-Nb bound to BI-8310
Cryo-EM consensus map of inactive-state GPR55-bRIL-Fab-Nb bound to BI-6229
Active-state structure of the GPR55-N171Q mutant in complex with G13 and BI-6229
Cryo-EM focused map of inactive-state GPR55-bRIL-Fab-Nb bound to BI-6229
Cryo-EM consensus map of inactive-state GPR55-bRIL-Fab-Nb bound to BI-8310
Cryo-EM consensus map of the active-state GPR55-N171Q mutant in complex with G13 and BI-6229
Structure of the Plant mitochondrial pre-initiation complex 3, (SSU,mtIF3,mRNA,tRNA)
Structure of the Plant mitochondrial pre-initiation complex 2, (SSU,mtIF3,mRNA)
Escherichia coli transhydrogenase double dIIIs detached to dIIs state in the presence of both NADPH and NADP+
Cryo-EM structure of SKF-83566 bound dopamine receptor DRD1-Gs signaling complex.
Type Ia alpha-synuclein filament amplified by One-Spin RT-QuIC from human plasma
Type Ib alpha-synuclein filament amplified by One-Spin RT-QuIC from human plasma
Type Ic alpha-synuclein filament amplified by One-Spin RT-QuIC from human plasma
Cryo-EM structure of Saccharomyces cerevisiae Mitochondrial Respiratory Complex II in YF241131B-bound state
Type IIb alpha-synuclein filament amplified by One-Spin RT-QuIC from human plasma
Type III alpha-synuclein filament amplified by One-Spin RT-QuIC from human plasma
Type I alpha-synuclein filament amplified from EV extraction buffer as a blank control for One-Spin RT-QuIC
Type A 2N4R human tau filaments induced by heparan sulfate with a double-protofilament fold
Type II alpha-synuclein filament amplified from EV extraction buffer as a blank control for One-Spin RT-QuIC
Type B 2N4R human tau filaments induced by heparan sulfate with a double-protofilament fold
Type B 2N4R human tau filaments induced by heparan sulfate with a single-protofilament fold
The cryo-EM structure of F-BF227 bound type1 amyloid beta 42 fibril
The cryo-EM structure of Congored bound type1 amyloid beta 42 fibril
Alpha-synuclein filament amplified from preformed fibrils as a positive control for One-Spin RT-QuIC
First-generation 2N4R human tau filaments seeded by Alzheimer's disease tau
The cryo-EM structure of F-PI2620 bound type1 amyloid beta 42 fibril
Second-generation 2N4R human tau filaments seeded by Alzheimer's disease tau in the presence of heparan sulfate
The cryo-EM structure of F-FDDNP bound type1 amyloid beta 42 fibril
SARS-CoV-2 Omicron LP.8.1 spike trimer (S-6P) in complex with 3 ZL58 Fabs and 3 ZL525 Fabs
factor VIIa-tissue factor-factor X-ixolaris complex in calcium ion-containing buffer
EBV gB trimer with "delta" mutations (intermediate-2 conformation)
EBV gB trimer with "deliDoP" mutations and flexibly attached I5350A (prefusion-like conformation)
EBV gB trimer with "deliDoP" mutations and I5350A2h (prefusion conformation) - I5350A2h local refinement
EBV gB trimer with "deliDoP" mutations and I5350A2h (prefusion conformation) - DIII-DV local refinement
EBV gB trimer with "deliDoP" mutations and I5350A2h (prefusion conformation) - Global refinement
EBV gB trimer with "deliDoP" mutations and I5350A2hN (prefusion conformation) - I5350A2hN local refinement
EBV gB trimer with "deliDoP" mutations and I5350A2hN (prefusion conformation) - DI-DV local refinement
SARS-CoV-2 S 2P with C-terminal 4X oP3h motif (RINAIET) - local refinement
SARS-CoV-2 S 2P with C-terminal 3X oP3h motif (RINEIER) - local refinement
HSV1 gB dimer of prefusion-1 trimer and prefusion-2 trimer with "deliD" mutations
CMV gB trimer with "deliDoP" mutations and I5350A2hN (prefusion conformation)
3A3 and 3A5 plus EBV gB trimer with "deliDoP" mutations and I5350A2hN (prefusion conformation) - 3A5 local refinement
EBV gB trimer with "deliDoP" mutations and I5350A2hN (prefusion conformation) - DII-DV local refinement
EBV gB trimer with "deliDoP" mutations and I5350A2h (prefusion conformation) - DII-DV local refinement
3A3 and 3A5 plus EBV gB trimer with "deliDoP" mutations and I5350A2hN (prefusion conformation) - 3A3 local refinement
3D reconstruction of a cross section of the Indo-Pacific bottlenose dolphin sperm midpiece
Cryo-EM structure of hACE2 in complex with antibodies F9-12S and F9-64
Cryo-EM structure of hACE2 in complex with antibodies F9-26 and F9-8S
Cryo-EM structure of hACE2 in complex with NeoCoV RBD_MU3 and antibodies F9-63 and F9-64
Cryo-EM structure of hACE2 in complex with antibodies F9-43 and F9-64
Cryo-EM structure of hACE2 in complex with antibodies F9-3S and F9-21
Bovine complex I at pH 9.2 in the deactive state (proximal membrane domain)
CryoEM structure of human 20S proteasome in complex with proteasome inhibitor Carmaphycin B
Structure of stacked allo-activated CBS conformer by allosteric SAM - by Helical approach
Bovine complex I at pH 6.0 in the deactive state (peripheral domain)
Structure of trans-basal conformer of human CBS encompassing 16-18 dimer repeating units (in absence of substrate and allosteric ligand)- by Helical approach
Expanded Coxsackievirus B1 (CVB1) virus-like particle delta-PALXA
Bovine complex I at pH 6.0 in the deactive state (proximal membrane domain)
Bovine complex I at pH 6.0 in the deactive state (distal membrane domain)
Bovine complex I at pH 9.2 in the deactive state (peripheral domain)
Bovine complex I at pH 9.2 in the deactive state (distal membrane domain)
CRYO-EM CONSENSUS MAP OF EKVX HUMAN CANCER CELL LINE RIBOSOME : CLASS 4
Ribosome of algae-fed tardigrade (R. varieornatus) - consensus map
Translating ribosome of algae-fed tardigrade (R. varieornatus) - eEF1A and tRNA (A/T-, P-, E-site) bound
Hibernating ribosome of rehydrated tardigrade (R. varieornatus) - eEF2, eIF5A, Cyp1 bound
Hibernating ribosome of algae-fed tardigrade (R. varieornatus) - eEF2, eIF5A bound
Membrane bound hibernating ribosome of unfed tardigrade (R. varieornatus) - eEF2, eIF5A, Cyp1 bound
Translating ribosome of unfed tardigrade (R. varieornatus) - eEF1A, tRNA (A/T-, P-, E-site) bound
Ribosome of unfed tardigrade (R. varieornatus) - unassigned state
Hibernating ribosome of unfed tardigrade (R. varieornatus) - eEF2, eIF5A bound - derived from classification with focused mask on membrane
Translating ribosome of unfed tardigrade (R. varieornatus) - tRNA (A-, P- site) bound
Hibernating ribosome of algae-fed tardigrade (R. varieornatus) - eEF2, eIF5A, Cyp1 bound
Membrane bound ribosome of unfed tardigrade (R. varieornatus) - eEF1A, tRNA (A/T-, P-, E-site) bound
Hibernating ribosome of rehydrated tardigrade (R. varieornatus) - eEF2, eIF5A bound
Hibernating ribosome of unfed tardigrade (R. varieornatus) - eEF2, eIF5A bound - derived from classification with focused mask on A/P/E sites
Hibernating ribosome of rehydrated tardigrade (R. varieornatus) - eEF2 bound
Ribosome of unfed tardigrade (R. varieornatus) - ebp1, eEF2, eIF5A bound
Translating ribosome of algae-fed tardigrade (R. varieornatus) - tRNA (P-, E-site) bound
Translating ribosome of unfed tardigrade (R. varieornatus) - eEF1A, tRNA (A/T-, P-site) bound
Membrane bound ribosome of unfed tardigrade (R. varieornatus) - consensus map
Cryo-EM structure of unnatural-base aptamer AptD1c with DENV1 NS1 tetramer
Structure of recombinant RyR2 in complex with Ryanozole in the closed conformation (Ca2+ dataset)
Structure of recombinant RyR2 in complex with Ryanozole in the closed conformation (EGTA dataset)
Translating ribosome of rehydrated tardigrade (R. varieornatus) - tRNA (A-, P-site) bound
Cryo-EM structure of the 198 bp human nucleosome containing H3.2 C110A mutant
Translating ribosome of rehydrated tardigrade (R. varieornatus) - eEF1A and tRNA (A/T-, P-, E-site) bound
Ribosome of rehydrated tardigrade (R. varieornatus) - consensus map
Cryo-EM structure of unnatural-base aptamer AptD1 with DENV1 NS1 hexamer
Structure of recombinant RyR2 in complex with Ryanozole in the open conformation (Ca2+ dataset)
Translating ribosome of rehydrated tardigrade (R. varieornatus) - tRNA (P- , E-site) bound
Membrane bound translating ribosome of unfed tardigrade (R. varieornatus) - eEF1A, tRNA (A/T-, P-site) bound
Structure of recombinant RyR2 in complex with Ryanozole in the closed conformation (EGTA dataset, Local refinement of Core domain)
Structure of recombinant RyR2 in the closed state (EGTA dataset, Local refinement of Core domain)
Cryo-EM structure of GAPDH on a silane-functionalized graphene grid
Structure of recombinant RyR2 in complex with Ryanozole in the closed conformation (Ca2+ dataset, Local refinement of Core domain)
Structure of recombinant RyR2 in the open state (Ca2+ dataset, Local refinement of Core domain)
Structure of recombinant RyR2 in complex with Ryanozole in the open conformation (Ca2+ dataset, Local refinement of Core domain)
Cryo-EM map of the 70S ribosome from stationary-phase Methanolobus in complex with P/E-tRNA
Cryo-EM map of the native ARC-bound 70S ribosome from stationary-phase Methanolobus
Cryo-EM map of the 70S ribosome from oxygen-stressed Methanolobus in complex with A/P-tRNA and P/E-tRNA
Cryo-EM map of the 70S ribosome from oxygen-stressed Methanolobus
Cryo-EM map of the 70S ribosome from oxygen-stressed Methanolobus in complex with P/P-tRNA
Cryo-EM map of the native ARC-bound 70S ribosome from oxygen-stressed Methanolobus
Cryo-EM map of the 50S ribosomal subunit from stationary-phase Methanolobus
Cryo-EM map of the 70S ribosome from oxygen-stressed Methanolobus in complex with P/E-tRNA
Cryo-EM map of the 50S ribosomal subunit from oxygen-stressed Methanolobus
Single protofilament with the Alzheimer tau fold and the V337M mutation from seeded primary murine neurons
Paired helical filament from Alzheimer's disease brain (AD seed)
Paired helical filament with the V337M mutation from seeded primary murine neurons
Structure of the ATPalphaS-bound soluble domain of human Adenylyl cyclase 9 in complex with stimulatory G protein, ATPalphaS, and forskolin
Structure of the occluded-state soluble domain of human Adenylyl cyclase 9 in complex with stimulatory G protein, ATPalphaS, and forskolin
Structure of the soluble domain of chimeric Adenylyl cyclase 95 in complex with stimulatory G protein, ATPalphaS, and forskolin
Cryo-EM Structure of Tetrameric EcCaspase Filament Bound to N7-cADPR
HIV-1 CA hexamer-hexamer interface from purified viral cores (consensus)
HIV-1 CA hexamer-hexamer interface from purified viral cores tilt 23.0 twist -4.7
HIV-1 CA hexamer-hexamer interface from purified viral cores tilt 16.6 twist -1.5
HIV-1 CA hexamer-hexamer interface from purified viral cores tilt 9.8 twist 1.9
HIV-1 CA hexamer-hexamer interface from purified viral cores tilt 21.1 twist 4.1
Structure of E04 Fab in complex with B/Lee40/1940 influenza B virus hemagglutinin
HIV-1 CA hexamer-hexamer interface from purified viral cores tilt 17.4 twist -2.1
Hypomethylated nucleoplasmic pre-60S intermediate containing Nog2 at Rsa4-arrested 5S post-rotation state
Closed state of D-ornithine 4,5-aminomutase from Fervidobacterium nodosum
Open state of D-ornithine 4,5-aminomutase from Fervidobacterium nodosum
Cryo-EM structure of human Fibroblast Activation Protein alpha in complex with H4 VNAR
Cryo-EM structure of human Fibroblast Activation Protein alpha in complex with F7 VHH
Cryo-EM structure of human Fibroblast Activation Protein alpha in complex with huB12 IgG
Candida albicans ribosome in the hibernating state reconstructed using 2D template matching from in-situ micrographs
Amino-terminal domain for GluK2 in the apo state with asymmetric ligand binding domain
Ligand-binding and transmembrane domains for GluK2 in the apo state with asymmetric ligand binding domain
Amino-terminal domain for GluK2 in the apo state with 2-fold symmetrical ligand-binding domain
Ligand-binding and transmembrane domains for GluK2 in the apo state with 2-fold symmetrical ligand binding domain
Consensus map for GluK2 in the apo state with 2-fold symmetrical ligand-binding domain
Consensus map for GluK2 in the apo state with asymmetric ligand binding domain
SSU processome maturation and disassembly, State A - Bfr2Kre33 focused map
Structure of aptamer in complex with SARS-CoV-2 BA.2 S protein, open
Cryo-EM structure of UL5/UL8/UL52 from Herpes Simplex Virus 1 in the presence of ATP-gamma-S
Cryo-EM focus refinement of UL5 and UL52 subunits of UL5/UL8/UL52 complex
Cryo-EM structure of UL5/UL52 heterodimer from Herpes Simplex Virus 1 in complex with Pritelivir and ssDNA
Cryo-EM structure of UL52 catalytic core in complex with UL8 subunit from Herpes Simplex Virus 1
Subtomogram Averaged Cryo-ET Structure of the 96-nm Axonemal Repeat in RSP3B-KO Tetrahymena thermophila
PC68_L31_570 Fab in complex with HIV-1 Env BG505 SOSIP.664 and RM20A3 Fab (negative stain)
Cryo-EM structure of the cytochrome bc complex (CIII2) from Bacillus subtilis
PC68_L31_391 Fab in complex with HIV-1 Env BG505 SOSIP.664 and RM20A3 Fab (negative stain)
PC68_L31_570 Fab in complex with HIV-1 Env BG505 SOSIP.664 and RM20A3 Fab
High-resolution cryo-EM structure of the CIII2CIV1 respiratory supercomplex from Bacillus subtilis (composite)
Cryo-EM structure of the CIII2 featuring FES in c-position from Bacillus subtilis
Cryo-EM structure of the CIII2CIV1 respiratory supercomplex from Bacillus subtilis
Cryo-EM structure of the cytochrome bc complex (CIII2) from Bacillus subtilis with multiple Qi site menaquinone binding
High-resolution cryo-EM structure of the cytochrome bc complex (CIII2) from Bacillus subtilis (composite)
Cryo-EM structure of the CIII2 featuring FES in b-position from Bacillus subtilis
HHV6B gB trimer with "deliDoP" mutations and I5350A2h (prefusion conformation) - DII-DV local refinement
Hibernating ribosome of unfed tardigrade (R. varieornatus) - eEF2, eIF5A, Cyp1 bound
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-5 (catalytic, composite)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-3 (catalytic, composite)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-5 (catalytic-FHA, composite)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-3 (catalytic-FHA, composite)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-3 (FHA, composite)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-3 (catalytic, consensus)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-3 (catalytic-FHA, PNKP/DNA local refine)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-3 (catalytic-FHA, FHA local refine)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-5 (FHA, composite)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-3 (FHA, consensus)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-3 (catalytic, PNKP/DNA local refine)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-3 (catalytic-FHA, consensus)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-3 (FHA, FHA local refine)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-5 (FHA, consensus)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-5 (catalytic-FHA, PNKP/DNA local refine)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-5 (catalytic-FHA, consensus)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-4 (catalytic-FHA, PNKP/DNA local refine)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-4 (FHA, consensus)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-5 (catalytic, consensus)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-4 (catalytic-FHA, consensus)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-5 (catalytic, PNKP/DNA local refine)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-5 (FHA, FHA local refine)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-5 (catalytic-FHA, FHA local refine)
Cryo-EM structure of the CIII2 without YlbA from Bacillus subtilis
Cryo-EM structure of pSTAT1 bound to importin alpha 5 (4:2 assembly)
Nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-3
Cryo-EM structure of the human mitochondrial transcription initiation complex on HSP with TFAM
Cryo-EM structure of the human mitochondrial transcription initiation complex on HSP without TFAM
Nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-4
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-4 (catalytic, composite)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-4 (catalytic-FHA, composite)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-4 (catalytic, consensus)
Nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-5
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-4 (FHA, composite)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-4 (catalytic, PNKP/DNA local refine)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-4 (FHA, FHA local refine)
Polynucleotide kinase phosphatase bound to a nucleosome containing a nick with a 3'-phosphate and 5'-OH at SHL-4 (catalytic-FHA, FHA local refine)
Cryo-EM structure of Acinetobacter baumannii LolDF bound to abaucin with lipoprotein
Cryo-EM map of Escherichia coli GroEL bound to denatured luciferase
Cryo-EM structure of full-length molybdoenzyme ergothioneine synthase from Caldithrix abyssi
Cryo-EM structure of the persulfide-bound metallopterin-binding domain of molybdoenzyme ergothioneine synthase from Caldithrix abyssi
Cryo-EM structure of the native metallopterin-binding domain of molybdoenzyme ergothioneine synthase from Caldithrix abyssi
Cryo-EM structure of the L. pneumophila Ceg14 effector in complex with AnkJ
Cryo-EM structure of the L. pneumophila Ceg14 effector in complex with G-actin and AnkJ
Cryo-EM Structure of Hybrid NRPS-PKS Enzyme CorA from the myxobacterium Corallococcus exiguus
Cryo-EM of the sarco(endo)plasmic reticulum calcium ATPase (SERCA) in presence of calcium and compound UM-52 (bound)
Cryo-EM of the sarco(endo)plasmic reticulum calcium ATPase (SERCA) in presence of calcium and compound UM-52 (unbound)
Cryo-EM of the sarco(endo)plasmic reticulum calcium ATPase (SERCA) in presence of calcium and CDN1163
CryoEM structure of substrate engaged p97 in complex with Ufd1/Npl4 and C-terminal FAF1- State II
CryoEM structure of substrate engaged p97 in complex with Ufd1/Npl4 and C-terminal FAF1- State III
Consensus map of substrate engaged p97 in complex with Ufd1/Npl4 and C-terminal FAF1- State II
Focused map of substrate engaged p97 in complex with Ufd1/Npl4 and C-terminal FAF1- State II (Npl4)
Focused map of substrate engaged p97 in complex with Ufd1/Npl4 and C-terminal FAF1 (FAF1)
Focused map of substrate engaged p97 in complex with Ufd1/Npl4 and C-terminal FAF1-State I (Npl4)
Cryo-EM structure of HKU1 spike with antibody HKU1-2 (conformation 1)
Cryo-EM structure of HKU1 spike with antibody HKU1-11 (local refinement of CTD, NTD, and Fab variable domain)
Cryo-EM structure of HKU1 spike with antibody HKU1-2 (conformation 2)
Focused map of substrate engaged p97 in complex with Ufd1/Npl4 and C-terminal FAF1- State IV (Npl4)
Focused map of substrate engaged p97 in complex with Ufd1/Npl4 and C-terminal FAF1- State III (Npl4)
CryoEM structure of substrate engaged p97 in complex with Ufd1/Npl4 and C-terminal FAF1-State II (non-normalized map)
Cryo-EM structure of Acinetobacter baylyi LolDF bound AMP-PNP (closed NBDs)
CryoEM structure of substrate engaged p97 in complex with Ufd1/Npl4 and Delta-N-FAF1
Consensus map of substrate engaged p97 in complex with Ufd1/Npl4 and C-terminal FAF1- State III
Consensus map of substrate engaged p97 in complex with Ufd1/Npl4 and C-terminal FAF1- State IV
Cryo-EM structure of Acinetobacter baumannii LolDF bound abaucin (wide cavity)
Focused map of substrate engaged p97 in complex with Ufd1/Npl4 and C-terminal FAF1- State IV (FAF1)
Cryo-EM structure of Acinetobacter baumannii LolDF bound abaucin (narrow cavity)
CryoEM structure of substrate engaged p97 in complex with Ufd1/Npl4 and C-terminal FAF1-State I (non-normalized map)
CryoEM structure of substrate engaged p97 in complex with Ufd1/Npl4 and C-terminal FAF1-State III (non-normalized map)
CryoEM structure of substrate engaged p97 in complex with Ufd1/Npl4 and C-terminal FAF1-State IV (non-normalized map)
CryoEM structure of substrate engaged p97 in complex with Ufd1/Npl4 and C-terminal FAF1- State IV
Cryo-EM structure of Acinetobacter baylyi LolA bound LolDF with lipoprotein
Cryo-EM structure of Acinetobacter baylyi endogenous LolDF with lipoprotein
Cryo-EM structure of human beta-cardiac myosin carrying the E525K mutation in the Interacting-Heads Motif state
Human beta-cardiac myosin S1 motor domain with the essential light chain in the pre-powerstroke state
Human beta-cardiac myosin S1 motor domain carrying the E525K mutation with the essential light chain in the pre-powerstroke state
Cryo-EM Structure of RSV Polymerase (L:P) Bound to Tr3-mimic RNA (TrC12-4U-Tr3), Unreacted Tr3-mimic Form B
Interferon-alpha8 complexed with IFA002 monoclonal antibody and IFNAR2, global cryoEM
Cryo-EM Structure of RSV Polymerase (L:P) Bound to Tr3-mimic RNA (TrC12-4U-Tr3), Unreacted Tr3-mimic Form A
Cryo-EM structure of pSTAT1 bound to importin alpha 5 (2:1 assembly)
Cryo-EM ternary structure of CD1c presenting a mycobacterial lipid to a T cell receptor
Cdc48-Ufd1-Npl4 complex processing polyUbEOS in the presence of ubx2
Focus refined map of ncBAF bound to nucleosome on the SnAC domain of SAMRCA4
Focus refined map of ncBAF bound to nucleosome on BRD9 grip helix
Cryo-EM structure of human UHRF1 bound to mononucleosome with hemimethylated DNA at superhelical location -6.2.
Cryo-EM structure of hemagglutinin from the A/California/04/2009 (H1N1) influenza virus with stabilizing mutations
Focus refinem map of ncBAF bound to nucleosome on the SMARCA4 motor domain
