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Open data
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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 informationnitric 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
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Citation | Journal: Biorxiv / Year: 2025Title: Conformational analysis of liganded human hemoglobin by cryo electron microscopy Authors: Takahashi K / Lee Y / Nishizawa T / Tame JRH | |||||||||
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Structure visualization
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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 |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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| Related items in Molecule of the Month |
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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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| Density Histograms |
-Half map: #2
| File | emd_65083_half_map_1.map | ||||||||||||
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| Density Histograms |
-Half map: #1
| File | emd_65083_half_map_2.map | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : human haemoglobin in carboxy form
| Entire | Name: human haemoglobin in carboxy form |
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| Components |
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-Supramolecule #1: human haemoglobin in carboxy form
| Supramolecule | Name: human haemoglobin in carboxy form / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#2 |
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| 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 |
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| 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 |
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| 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 |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Buffer | pH: 7.5 |
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| Grid | Model: Quantifoil / Support film - Material: CARBON / Support film - topology: HOLEY |
| Vitrification | Cryogen name: ETHANE / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
| Microscope | TFS KRIOS |
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| 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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About Yorodumi




Keywords
Homo sapiens (human)
Authors
Japan, 1 items
Citation





















Z (Sec.)
Y (Row.)
X (Col.)














































Processing
FIELD EMISSION GUN


