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Yorodumi- EMDB-62194: Cryo-EM structure of MjHKU4r-CoV-1 receptor-binding domain comple... -
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Basic information
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| Title | Cryo-EM structure of MjHKU4r-CoV-1 receptor-binding domain complexed with human CD26 | |||||||||
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Keywords | Complex / VIRAL PROTEIN/HYDROLASE / VIRAL PROTEIN-HYDROLASE complex | |||||||||
| Function / homology | Function and homology informationglucagon processing / negative regulation of neutrophil chemotaxis / regulation of cell-cell adhesion mediated by integrin / Synthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP) / negative regulation of extracellular matrix disassembly / dipeptidyl-peptidase IV / chemorepellent activity / psychomotor behavior / intercellular canaliculus / dipeptidyl-peptidase activity ...glucagon processing / negative regulation of neutrophil chemotaxis / regulation of cell-cell adhesion mediated by integrin / Synthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP) / negative regulation of extracellular matrix disassembly / dipeptidyl-peptidase IV / chemorepellent activity / psychomotor behavior / intercellular canaliculus / dipeptidyl-peptidase activity / peptide hormone processing / locomotory exploration behavior / lamellipodium membrane / endocytic vesicle / aminopeptidase activity / endothelial cell migration / behavioral fear response / T cell costimulation / receptor-mediated endocytosis of virus by host cell / serine-type peptidase activity / T cell activation / Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) / lamellipodium / virus receptor activity / protease binding / membrane fusion / host cell endoplasmic reticulum-Golgi intermediate compartment membrane / response to hypoxia / receptor-mediated virion attachment to host cell / cell adhesion / apical plasma membrane / membrane raft / endocytosis involved in viral entry into host cell / signaling receptor binding / lysosomal membrane / fusion of virus membrane with host plasma membrane / serine-type endopeptidase activity / focal adhesion / fusion of virus membrane with host endosome membrane / positive regulation of cell population proliferation / viral envelope / symbiont entry into host cell / host cell plasma membrane / virion membrane / cell surface / protein homodimerization activity / proteolysis / extracellular exosome / extracellular region / identical protein binding / membrane / plasma membrane Similarity search - Function | |||||||||
| Biological species | Mammalia (mammals) / Homo sapiens (human) / Tylonycteris bat coronavirus HKU4 | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 2.61 Å | |||||||||
Authors | Sun JQ / Han P | |||||||||
| Funding support | China, 1 items
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Citation | Journal: Hlife / Year: 2025Title: Rational design of human CD26 receptor for a strong neutralizing ability against MjHKU4r-CoV-1 and MERS-CoV Authors: Zhang Y / Tian M / Han Y / Sun J / Li W / Bai C / Su C / Han P | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_62194.map.gz | 161.4 MB | EMDB map data format | |
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| Header (meta data) | emd-62194-v30.xml emd-62194.xml | 16.1 KB 16.1 KB | Display Display | EMDB header |
| Images | emd_62194.png | 46.3 KB | ||
| Filedesc metadata | emd-62194.cif.gz | 6.3 KB | ||
| Others | emd_62194_half_map_1.map.gz emd_62194_half_map_2.map.gz | 301.9 MB 301.9 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-62194 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-62194 | HTTPS FTP |
-Validation report
| Summary document | emd_62194_validation.pdf.gz | 886.1 KB | Display | EMDB validaton report |
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| Full document | emd_62194_full_validation.pdf.gz | 885.6 KB | Display | |
| Data in XML | emd_62194_validation.xml.gz | 17.2 KB | Display | |
| Data in CIF | emd_62194_validation.cif.gz | 20.5 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-62194 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-62194 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9k9nMC 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_62194.map.gz / Format: CCP4 / Size: 325 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: 0.69 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: #2
| File | emd_62194_half_map_1.map | ||||||||||||
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| Density Histograms |
-Half map: #1
| File | emd_62194_half_map_2.map | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : Cryo-EM structure of MjHKU4r-CoV-1 receptor-binding domain comple...
| Entire | Name: Cryo-EM structure of MjHKU4r-CoV-1 receptor-binding domain complexed with human CD26 |
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| Components |
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-Supramolecule #1: Cryo-EM structure of MjHKU4r-CoV-1 receptor-binding domain comple...
| Supramolecule | Name: Cryo-EM structure of MjHKU4r-CoV-1 receptor-binding domain complexed with human CD26 type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#2 |
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| Source (natural) | Organism: Mammalia (mammals) |
-Macromolecule #1: Dipeptidyl peptidase 4 soluble form
| Macromolecule | Name: Dipeptidyl peptidase 4 soluble form / type: protein_or_peptide / ID: 1 / Number of copies: 2 / Enantiomer: LEVO |
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| Source (natural) | Organism: Homo sapiens (human) |
| Molecular weight | Theoretical: 88.445375 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: MGILPSPGMP ALLSLVSLLS VLLMGCVAET GTSRKTYTLT DYLKNTYRLK LYSLRWISDH EYLYKQENNI LVFNAEYGNS SVFLENSTF DEFGHSINDY SISPDGQFIL LEYNYVKQWR HSYTASYDIY DLNKRQLITE ERIPNNTQWV TWSPVGHKLA Y VWNNDIYV ...String: MGILPSPGMP ALLSLVSLLS VLLMGCVAET GTSRKTYTLT DYLKNTYRLK LYSLRWISDH EYLYKQENNI LVFNAEYGNS SVFLENSTF DEFGHSINDY SISPDGQFIL LEYNYVKQWR HSYTASYDIY DLNKRQLITE ERIPNNTQWV TWSPVGHKLA Y VWNNDIYV KIEPNLPSYR ITWTGKEDII YNGITDWVYE EEVFSAYSAL WWSPNGTFLA YAQFNDTEVP LIEYSFYSDE SL QYPKTVR VPYPKAGAVN PTVKFFVVNT DSLSSVTNAT SIQITAPASM LIGDHYLCDV TWATQERISL QWLRRIQNYS VMD ICDYDE SSGRWNCLVA RQHIEMSTTG WVGRFRPSEP HFTLDGNSFY KIISNEEGYR HICYFQIDKK DCTFITKGTW EVIG IEALT SDYLYYISNE YKGMPGGRNL YKIQLSDYTK VTCLSCELNP ERCQYYSVSF SKEAKYYQLR CSGPGLPLYT LHSSV NDKG LRVLEDNSAL DKMLQNVQMP SKKLDFIILN ETKFWYQMIL PPHFDKSKKY PLLLDVYAGP CSQKADTVFR LNWATY LAS TENIIVASFD GRGSGYQGDK IMHAINRRLG TFEVEDQIEA ARQFSKMGFV DNKRIAIWGW SYGGYVTSMV LGSGSGV FK CGIAVAPVSR WEYYDSVYTE RYMGLPTPED NLDHYRNSTV MSRAENFKQV EYLLIHGTAD DNVHFQQSAQ ISKALVDV G VDFQAMWYTD EDHGIASSTA HQHIYTHMSH FIKQCFSLPH HHHHH UniProtKB: Dipeptidyl peptidase 4 |
-Macromolecule #2: Spike protein S1
| Macromolecule | Name: Spike protein S1 / type: protein_or_peptide / ID: 2 Details: Sequence reference for strain 'Tylonycteris bat coronavirus HKU4' is not available in UniProt at the time of biocuration. Current sequence reference is from UniProt id A0AAE8ZFM2. Number of copies: 1 / Enantiomer: LEVO |
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| Source (natural) | Organism: Tylonycteris bat coronavirus HKU4 |
| Molecular weight | Theoretical: 25.60725 KDa |
| Recombinant expression | Organism: Homo sapiens (human) |
| Sequence | String: MHSSALLCCL VLLTGVRAKE CDFTPMLVGV PPQVYNFKRL VFTNCNYNLT KLLSLFMVNE FSCNGISPDA IARGCYSSLT VDYFAYPLS MRSYIQPGSA GDISLYNYKQ SFANPTCRVL ATAPANLTLT KPSAYGYFQK CSRVSGEHNS VETPLYINPG E YSICRSFS ...String: MHSSALLCCL VLLTGVRAKE CDFTPMLVGV PPQVYNFKRL VFTNCNYNLT KLLSLFMVNE FSCNGISPDA IARGCYSSLT VDYFAYPLS MRSYIQPGSA GDISLYNYKQ SFANPTCRVL ATAPANLTLT KPSAYGYFQK CSRVSGEHNS VETPLYINPG E YSICRSFS PYGFSEDGEV FRRQLTQYEG GGILVGVGAK LAMTDKLEMG FIISVQYGTD TNSVCPMHHH HHH UniProtKB: Spike glycoprotein |
-Macromolecule #6: 2-acetamido-2-deoxy-beta-D-glucopyranose
| Macromolecule | Name: 2-acetamido-2-deoxy-beta-D-glucopyranose / type: ligand / ID: 6 / Number of copies: 10 / Formula: NAG |
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| Molecular weight | Theoretical: 221.208 Da |
| Chemical component information | ![]() ChemComp-NAG: |
-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: 8 |
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| Vitrification | Cryogen name: ETHANE |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 60.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.0 µm / Nominal defocus min: 1.0 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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About Yorodumi



Keywords
Homo sapiens (human)
Tylonycteris bat coronavirus HKU4
Authors
China, 1 items
Citation



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Processing
FIELD EMISSION GUN
