+ Open data
Open data
- Basic information
Basic information
| Entry |  | |||||||||
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| Title | cryo-EM structure of human haemoglobin in the R conformation | |||||||||
|  Map data | ||||||||||
|  Sample | 
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|  Keywords | haemoglobin / OXYGEN BINDING | |||||||||
| Function / homology |  Function and homology information nitric oxide transport / hemoglobin alpha binding / cellular oxidant detoxification / hemoglobin binding / haptoglobin-hemoglobin complex / renal absorption / hemoglobin complex / oxygen transport / Scavenging of heme from plasma / endocytic vesicle lumen ...nitric oxide transport / hemoglobin alpha binding / cellular oxidant detoxification / hemoglobin binding / haptoglobin-hemoglobin complex / renal absorption / hemoglobin complex / oxygen transport / Scavenging of heme from plasma / endocytic vesicle lumen / blood vessel diameter maintenance / hydrogen peroxide catabolic process / oxygen carrier activity / carbon dioxide transport / response to hydrogen peroxide / Heme signaling / Erythrocytes take up oxygen and release carbon dioxide / Erythrocytes take up carbon dioxide and release oxygen / Late endosomal microautophagy / Cytoprotection by HMOX1 / oxygen binding / regulation of blood pressure / platelet aggregation / Chaperone Mediated Autophagy / positive regulation of nitric oxide biosynthetic process / tertiary granule lumen / Factors involved in megakaryocyte development and platelet production / blood microparticle / ficolin-1-rich granule lumen / iron ion binding / inflammatory response / heme binding / Neutrophil degranulation / extracellular space / extracellular exosome / extracellular region / metal ion binding / membrane / cytosol Similarity search - Function | |||||||||
| Biological species |  Homo sapiens (human) | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 2.45 Å | |||||||||
|  Authors | Takahashi K / Lee Y / Nishizawa T / Tame JRH | |||||||||
| Funding support |  Japan, 1 items 
 | |||||||||
|  Citation |  Journal: Biorxiv / Year: 2025 Title: Conformational analysis of liganded human hemoglobin by cryo electron microscopy Authors: Takahashi K / Lee Y / Nishizawa T / Tame JRH | |||||||||
| History | 
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- Structure visualization
Structure visualization
| Supplemental images | 
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- Downloads & links
Downloads & links
-EMDB archive
| Map data |  emd_65083.map.gz | 59.6 MB |  EMDB map data format | |
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| Header (meta data) |  emd-65083-v30.xml  emd-65083.xml | 17.4 KB 17.4 KB | Display Display |  EMDB header | 
| FSC (resolution estimation) |  emd_65083_fsc.xml | 8.4 KB | Display |  FSC data file | 
| Images |  emd_65083.png | 117 KB | ||
| Masks |  emd_65083_msk_1.map | 64 MB |  Mask map | |
| Filedesc metadata |  emd-65083.cif.gz | 5.7 KB | ||
| Others |  emd_65083_half_map_1.map.gz  emd_65083_half_map_2.map.gz | 59.3 MB 59.3 MB | ||
| Archive directory |  http://ftp.pdbj.org/pub/emdb/structures/EMD-65083  ftp://ftp.pdbj.org/pub/emdb/structures/EMD-65083 | HTTPS FTP | 
-Validation report
| Summary document |  emd_65083_validation.pdf.gz | 830.7 KB | Display |  EMDB validaton report | 
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| Full document |  emd_65083_full_validation.pdf.gz | 830.3 KB | Display | |
| Data in XML |  emd_65083_validation.xml.gz | 16.3 KB | Display | |
| Data in CIF |  emd_65083_validation.cif.gz | 21.2 KB | Display | |
| Arichive directory |  https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-65083  ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-65083 | HTTPS FTP | 
-Related structure data
| Related structure data |  9vicMC  9vibC  9vidC  9vieC M: atomic model generated by this map C: citing same article ( | 
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| Similar structure data | Similarity search - Function & homology  F&H Search | 
- Links
Links
| EMDB pages |  EMDB (EBI/PDBe) /  EMDataResource | 
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| Related items in Molecule of the Month | 
- Map
Map
| File |  Download / File: emd_65083.map.gz / Format: CCP4 / Size: 64 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Projections & slices | Image control
 
 Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 1.02 Å | ||||||||||||||||||||||||||||||||||||
| Density | 
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML: 
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-Supplemental data
-Mask #1
| File |  emd_65083_msk_1.map | ||||||||||||
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| Projections & Slices | 
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| Density Histograms | 
-Half map: #2
| File | emd_65083_half_map_1.map | ||||||||||||
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| Projections & Slices | 
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| Density Histograms | 
-Half map: #1
| File | emd_65083_half_map_2.map | ||||||||||||
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| Projections & Slices | 
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| Density Histograms | 
- Sample components
Sample components
-Entire : human haemoglobin in carboxy form
| Entire | Name: human haemoglobin in carboxy form | 
|---|---|
| Components | 
 | 
-Supramolecule #1: human haemoglobin in carboxy form
| Supramolecule | Name: human haemoglobin in carboxy form / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#2 | 
|---|---|
| Source (natural) | Organism:  Homo sapiens (human) | 
| Molecular weight | Theoretical: 100 KDa | 
-Macromolecule #1: Hemoglobin subunit alpha
| Macromolecule | Name: Hemoglobin subunit alpha / type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO | 
|---|---|
| Source (natural) | Organism:  Homo sapiens (human) | 
| Molecular weight | Theoretical: 15.28155 KDa | 
| Sequence | String: MVLSPADKTN VKAAWGKVGA HAGEYGAEAL ERMFLSFPTT KTYFPHFDLS HGSAQVKGHG KKVADALTNA VAHVDDMPNA  LSALSDLHA HKLRVDPVNF KLLSHCLLVT LAAHLPAEFT PAVHASLDKF LASVSTVLTS KYR UniProtKB: Hemoglobin subunit alpha | 
-Macromolecule #2: Hemoglobin subunit beta
| Macromolecule | Name: Hemoglobin subunit beta / type: protein_or_peptide / ID: 2 / Number of copies: 1 / Enantiomer: LEVO | 
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| Source (natural) | Organism:  Homo sapiens (human) | 
| Molecular weight | Theoretical: 16.021396 KDa | 
| Sequence | String: MVHLTPEEKS AVTALWGKVN VDEVGGEALG RLLVVYPWTQ RFFESFGDLS TPDAVMGNPK VKAHGKKVLG AFSDGLAHLD  NLKGTFATL SELHCDKLHV DPENFRLLGN VLVCVLAHHF GKEFTPPVQA AYQKVVAGVA NALAHKYH UniProtKB: Hemoglobin subunit beta | 
-Macromolecule #3: PROTOPORPHYRIN IX CONTAINING FE
| Macromolecule | Name: PROTOPORPHYRIN IX CONTAINING FE / type: ligand / ID: 3 / Number of copies: 2 / Formula: HEM | 
|---|---|
| Molecular weight | Theoretical: 616.487 Da | 
| Chemical component information |  ChemComp-HEM:  | 
-Macromolecule #4: CARBON MONOXIDE
| Macromolecule | Name: CARBON MONOXIDE / type: ligand / ID: 4 / Number of copies: 2 / Formula: CMO | 
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| Molecular weight | Theoretical: 28.01 Da | 
| Chemical component information |  ChemComp-CMO:  | 
-Experimental details
-Structure determination
| Method | cryo EM | 
|---|---|
|  Processing | single particle reconstruction | 
| Aggregation state | particle | 
- Sample preparation
Sample preparation
| Buffer | pH: 7.5 | 
|---|---|
| Grid | Model: Quantifoil / Support film - Material: CARBON / Support film - topology: HOLEY | 
| Vitrification | Cryogen name: ETHANE / Instrument: FEI VITROBOT MARK IV | 
- Electron microscopy
Electron microscopy
| Microscope | TFS KRIOS | 
|---|---|
| Specialist optics | Energy filter - Name: GIF Bioquantum / Energy filter - Slit width: 15 eV | 
| Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 58.4 e/Å2 | 
| Electron beam | Acceleration voltage: 300 kV / Electron source:  FIELD EMISSION GUN | 
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 1.2 µm / Nominal defocus min: 0.4 µm / Nominal magnification: 165000 | 
| Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN | 
| Experimental equipment |  Model: Titan Krios / Image courtesy: FEI Company | 
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