[English] 日本語
Yorodumi
- EMDB-10676: Human Coronavirus HKU1 Haemagglutinin-Esterase -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: EMDB / ID: EMD-10676
TitleHuman Coronavirus HKU1 Haemagglutinin-Esterase
Map dataHuman coronavirus-HKU1 haemagglutinin esterase (local resolution filtered map).
Sample
  • Complex: Human Coronavirus HKU1 Haemagglutinin-Esterase
    • Protein or peptide: Hemagglutinin-esteraseHemagglutinin esterase
  • Ligand: 2-acetamido-2-deoxy-beta-D-glucopyranose
Function / homology
Function and homology information


sialate O-acetylesterase activity / sialate 9-O-acetylesterase activity / sialate 4-O-acetylesterase activity / sialate O-acetylesterase / membrane => GO:0016020 / host cell surface receptor binding / fusion of virus membrane with host plasma membrane / viral envelope / host cell plasma membrane / virion membrane
Similarity search - Function
Hemagglutinin-esterase / Haemagglutinin-esterase glycoprotein, haemagglutinin domain / Haemagglutinin-esterase glycoprotein, core / Hemagglutinin domain of haemagglutinin-esterase-fusion glycoprotein / Hemagglutinin esterase / Viral capsid/haemagglutinin protein
Similarity search - Domain/homology
Hemagglutinin-esterase
Similarity search - Component
Biological speciesHuman coronavirus HKU1
Methodsingle particle reconstruction / cryo EM / Resolution: 3.39 Å
AuthorsHurdiss DL / Drulyte I
Citation
Journal: Nat Commun / Year: 2020
Title: Cryo-EM structure of coronavirus-HKU1 haemagglutinin esterase reveals architectural changes arising from prolonged circulation in humans.
Authors: Daniel L Hurdiss / Ieva Drulyte / Yifei Lang / Tatiana M Shamorkina / Matti F Pronker / Frank J M van Kuppeveld / Joost Snijder / Raoul J de Groot /
Abstract: The human betacoronaviruses HKU1 and OC43 (subgenus Embecovirus) arose from separate zoonotic introductions, OC43 relatively recently and HKU1 apparently much longer ago. Embecovirus particles ...The human betacoronaviruses HKU1 and OC43 (subgenus Embecovirus) arose from separate zoonotic introductions, OC43 relatively recently and HKU1 apparently much longer ago. Embecovirus particles contain two surface projections called spike (S) and haemagglutinin-esterase (HE), with S mediating receptor binding and membrane fusion, and HE acting as a receptor-destroying enzyme. Together, they promote dynamic virion attachment to glycan-based receptors, specifically 9-O-acetylated sialic acid. Here we present the cryo-EM structure of the ~80 kDa, heavily glycosylated HKU1 HE at 3.4 Å resolution. Comparison with existing HE structures reveals a drastically truncated lectin domain, incompatible with sialic acid binding, but with the structure and function of the esterase domain left intact. Cryo-EM and mass spectrometry analysis reveals a putative glycan shield on the now redundant lectin domain. The findings further our insight into the evolution and host adaptation of human embecoviruses, and demonstrate the utility of cryo-EM for studying small, heavily glycosylated proteins.
#1: Journal: Biorxiv / Year: 2020
Title: Cryo-EM structure of coronavirus-HKU1 haemagglutinin esterase reveals architectural changes arising from prolonged circulation in humans
Authors: Hurdiss DL / Drulyte I / Lang Y / Shamorkina TM / Pronker MF / van Kuppeveld FJM / Snijder J / de Groot RJ
History
DepositionFeb 19, 2020-
Header (metadata) releaseApr 8, 2020-
Map releaseApr 8, 2020-
UpdateDec 2, 2020-
Current statusDec 2, 2020Processing site: PDBe / Status: Released

-
Structure visualization

Movie
  • Surface view with section colored by density value
  • Surface level: 0.0601
  • Imaged by UCSF Chimera
  • Download
  • Surface view colored by cylindrical radius
  • Surface level: 0.0601
  • Imaged by UCSF Chimera
  • Download
  • Surface view with fitted model
  • Atomic models: PDB-6y3y
  • Surface level: 0.0601
  • Imaged by UCSF Chimera
  • Download
Movie viewer
Structure viewerEM map:
SurfViewMolmilJmol/JSmol
Supplemental images

Downloads & links

-
Map

FileDownload / File: emd_10676.map.gz / Format: CCP4 / Size: 125 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)
AnnotationHuman coronavirus-HKU1 haemagglutinin esterase (local resolution filtered map).
Voxel sizeX=Y=Z: 0.805 Å
Density
Contour LevelBy AUTHOR: 0.0601 / Movie #1: 0.0601
Minimum - Maximum-0.17708412 - 0.29912442
Average (Standard dev.)-0.0000526704 (±0.005566763)
SymmetrySpace group: 1
Details

EMDB XML:

Map geometry
Axis orderXYZ
Origin000
Dimensions320320320
Spacing320320320
CellA=B=C: 257.6 Å
α=β=γ: 90.0 °

CCP4 map header:

modeImage stored as Reals
Å/pix. X/Y/Z0.8050.8050.805
M x/y/z320320320
origin x/y/z0.0000.0000.000
length x/y/z257.600257.600257.600
α/β/γ90.00090.00090.000
MAP C/R/S123
start NC/NR/NS000
NC/NR/NS320320320
D min/max/mean-0.1770.299-0.000

-
Supplemental data

-
Mask #1

Fileemd_10676_msk_1.map
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

-
Additional map: Human coronavirus-HKU1 haemagglutinin esterase (Gaussian filtered N-glycan difference...

Fileemd_10676_additional_1.map
AnnotationHuman coronavirus-HKU1 haemagglutinin esterase (Gaussian filtered N-glycan difference map).
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

-
Additional map: Human coronavirus-HKU1 haemagglutinin esterase (unsharpened map).

Fileemd_10676_additional_2.map
AnnotationHuman coronavirus-HKU1 haemagglutinin esterase (unsharpened map).
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

-
Additional map: Human coronavirus-HKU1 haemagglutinin esterase (sharpened map).

Fileemd_10676_additional_3.map
AnnotationHuman coronavirus-HKU1 haemagglutinin esterase (sharpened map).
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

-
Half map: Human coronavirus-HKU1 haemagglutinin esterase (half map 2).

Fileemd_10676_half_map_1.map
AnnotationHuman coronavirus-HKU1 haemagglutinin esterase (half map 2).
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

-
Half map: Human coronavirus-HKU1 haemagglutinin esterase (half map 1).

Fileemd_10676_half_map_2.map
AnnotationHuman coronavirus-HKU1 haemagglutinin esterase (half map 1).
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

-
Sample components

-
Entire : Human Coronavirus HKU1 Haemagglutinin-Esterase

EntireName: Human Coronavirus HKU1 Haemagglutinin-Esterase
Components
  • Complex: Human Coronavirus HKU1 Haemagglutinin-Esterase
    • Protein or peptide: Hemagglutinin-esteraseHemagglutinin esterase
  • Ligand: 2-acetamido-2-deoxy-beta-D-glucopyranose

-
Supramolecule #1: Human Coronavirus HKU1 Haemagglutinin-Esterase

SupramoleculeName: Human Coronavirus HKU1 Haemagglutinin-Esterase / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1 / Details: Dimeric complex
Source (natural)Organism: Human coronavirus HKU1
Recombinant expressionOrganism: Homo sapiens (human)
Molecular weightExperimental: 30.777 KDa

-
Macromolecule #1: Hemagglutinin-esterase

MacromoleculeName: Hemagglutinin-esterase / type: protein_or_peptide / ID: 1 / Number of copies: 2 / Enantiomer: LEVO / EC number: sialate O-acetylesterase
Source (natural)Organism: Human coronavirus HKU1
Molecular weightTheoretical: 40.432648 KDa
Recombinant expressionOrganism: Homo sapiens (human)
SequenceString: LAFNEPLNVV SHLNHDWFLF GDSRSDCNHI NNLKIKNFDY LDIHPSLCNN GKISSSAGDS IFKSFHFTRF YNYTGEGDQI IFYEGVNFN PYHRFKCFPN GSNDVWLLNK VRFYRALYSN MAFFRYLTFV DIPYNVSLSK FNSCKSDILS LNNPIFINYS K EVYFTLLG ...String:
LAFNEPLNVV SHLNHDWFLF GDSRSDCNHI NNLKIKNFDY LDIHPSLCNN GKISSSAGDS IFKSFHFTRF YNYTGEGDQI IFYEGVNFN PYHRFKCFPN GSNDVWLLNK VRFYRALYSN MAFFRYLTFV DIPYNVSLSK FNSCKSDILS LNNPIFINYS K EVYFTLLG CSLYLVPLCL FKSNFSQYYY NIDTGSVYGF SNVVYPDLDC IYISLKPGSY KVSTTAPFLS LPTKALCFDK SK QFVPVQV VDSRWNNERA SDISLSVACQ LPYCYFRNSS ANYVGKYDIN HGDSGFISIL SGLLYNVSCI SYYGVFLYDN FTS IWPYYS FGRCPTSSII KHPICVYDSD PLVPR

-
Macromolecule #6: 2-acetamido-2-deoxy-beta-D-glucopyranose

MacromoleculeName: 2-acetamido-2-deoxy-beta-D-glucopyranose / type: ligand / ID: 6 / Number of copies: 6 / Formula: NAG
Molecular weightTheoretical: 221.208 Da
Chemical component information

ChemComp-NAG:
2-acetamido-2-deoxy-beta-D-glucopyranose / N-Acetylglucosamine

-
Experimental details

-
Structure determination

Methodcryo EM
Processingsingle particle reconstruction
Aggregation stateparticle

-
Sample preparation

Concentration4 mg/mL
BufferpH: 8
Component:
ConcentrationFormulaName
10.0 mMC4H11NO3Trisaminomethane
50.0 mMNaClSodium chlorideSodium chloride
GridModel: Quantifoil R1.2/1.3 / Material: COPPER / Mesh: 200 / Support film - Material: CARBON / Support film - topology: HOLEY / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Atmosphere: AIR / Details: 20 mA
VitrificationCryogen name: ETHANE / Chamber humidity: 95 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV / Details: Blot force = 1 Blot time = 5.5 seconds.

-
Electron microscopy

MicroscopeTFS KRIOS
Electron beamAcceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN
Electron opticsC2 aperture diameter: 50.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELDBright-field microscopy / Cs: 2.7 mm / Nominal defocus max: -2.5 µm / Nominal defocus min: -1.0 µm / Nominal magnification: 96000
Sample stageSpecimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN
DetailsTitan Krios G4 was used with fringe-free imaging and aberration-free image shift.
Image recordingFilm or detector model: OTHER / Digitization - Dimensions - Width: 4096 pixel / Digitization - Dimensions - Height: 4096 pixel / Digitization - Sampling interval: 14.0 µm / Number grids imaged: 1 / Number real images: 6029 / Average exposure time: 5.6 sec. / Average electron dose: 40.0 e/Å2 / Details: Falcon 4 Direct Electron Detector
Experimental equipment
Model: Titan Krios / Image courtesy: FEI Company

-
Image processing

Particle selectionNumber selected: 936260 / Details: Relion autopicking
CTF correctionSoftware - Name: Gctf (ver. 1.18)
Startup modelType of model: INSILICO MODEL
In silico model: A homology model of the dimeric HCoV-HKU1 HE (uniprot ID: Q5MQD1) was generated using the phyre2 server. The molmap command in UCSF chimera, was then used to create a 40 angstrom ...In silico model: A homology model of the dimeric HCoV-HKU1 HE (uniprot ID: Q5MQD1) was generated using the phyre2 server. The molmap command in UCSF chimera, was then used to create a 40 angstrom resolution starting model.
Initial angle assignmentType: NOT APPLICABLE / Software - Name: RELION (ver. 3.1)
Final 3D classificationNumber classes: 4 / Avg.num./class: 141000 / Software - Name: RELION (ver. 3.0.1)
Final angle assignmentType: NOT APPLICABLE / Software - Name: RELION (ver. 3.1)
Final reconstructionApplied symmetry - Point group: C2 (2 fold cyclic) / Algorithm: BACK PROJECTION / Resolution.type: BY AUTHOR / Resolution: 3.39 Å / Resolution method: FSC 0.143 CUT-OFF / Software - Name: RELION (ver. 3.1) / Number images used: 119717
DetailsFalcon 4 Direct Electron Detector
FSC plot (resolution estimation)

-
Atomic model buiding 1

DetailsA homology model of HCOV-HKU1 HE (uniprot ID: Q5MQD1) was generated using the phyre2 server
RefinementSpace: REAL / Protocol: RIGID BODY FIT / Target criteria: Correlation coefficient
Output model

PDB-6y3y:
Human Coronavirus HKU1 Haemagglutinin-Esterase

+
About Yorodumi

-
News

-
Feb 9, 2022. New format data for meta-information of EMDB entries

New format data for meta-information of EMDB entries

  • Version 3 of the EMDB header file is now the official format.
  • The previous official version 1.9 will be removed from the archive.

Related info.:EMDB header

External links:wwPDB to switch to version 3 of the EMDB data model

-
Aug 12, 2020. Covid-19 info

Covid-19 info

URL: https://pdbj.org/emnavi/covid19.php

New page: Covid-19 featured information page in EM Navigator.

Related info.:Covid-19 info / Mar 5, 2020. Novel coronavirus structure data

+
Mar 5, 2020. Novel coronavirus structure data

Novel coronavirus structure data

Related info.:Yorodumi Speices / Aug 12, 2020. Covid-19 info

External links:COVID-19 featured content - PDBj / Molecule of the Month (242):Coronavirus Proteases

+
Jan 31, 2019. EMDB accession codes are about to change! (news from PDBe EMDB page)

EMDB accession codes are about to change! (news from PDBe EMDB page)

  • The allocation of 4 digits for EMDB accession codes will soon come to an end. Whilst these codes will remain in use, new EMDB accession codes will include an additional digit and will expand incrementally as the available range of codes is exhausted. The current 4-digit format prefixed with “EMD-” (i.e. EMD-XXXX) will advance to a 5-digit format (i.e. EMD-XXXXX), and so on. It is currently estimated that the 4-digit codes will be depleted around Spring 2019, at which point the 5-digit format will come into force.
  • The EM Navigator/Yorodumi systems omit the EMD- prefix.

Related info.:Q: What is EMD? / ID/Accession-code notation in Yorodumi/EM Navigator

External links:EMDB Accession Codes are Changing Soon! / Contact to PDBj

+
Jul 12, 2017. Major update of PDB

Major update of PDB

  • wwPDB released updated PDB data conforming to the new PDBx/mmCIF dictionary.
  • This is a major update changing the version number from 4 to 5, and with Remediation, in which all the entries are updated.
  • In this update, many items about electron microscopy experimental information are reorganized (e.g. em_software).
  • Now, EM Navigator and Yorodumi are based on the updated data.

External links:wwPDB Remediation / Enriched Model Files Conforming to OneDep Data Standards Now Available in the PDB FTP Archive

-
Yorodumi

Thousand views of thousand structures

  • Yorodumi is a browser for structure data from EMDB, PDB, SASBDB, etc.
  • This page is also the successor to EM Navigator detail page, and also detail information page/front-end page for Omokage search.
  • The word "yorodu" (or yorozu) is an old Japanese word meaning "ten thousand". "mi" (miru) is to see.

Related info.:EMDB / PDB / SASBDB / Comparison of 3 databanks / Yorodumi Search / Aug 31, 2016. New EM Navigator & Yorodumi / Yorodumi Papers / Jmol/JSmol / Function and homology information / Changes in new EM Navigator and Yorodumi

Read more