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- EMDB-40408: Cryo-EM structure of a double loaded human UBA7-UBE2L6-ISG15 thio... -

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Entry
Database: EMDB / ID: EMD-40408
TitleCryo-EM structure of a double loaded human UBA7-UBE2L6-ISG15 thioester mimetic complex (Form 1)
Map data
Sample
  • Complex: Cryo-EM structure of a double loaded human UBA7-UBE2L6-ISG15 thioester mimetic complex (Form 1)
    • Protein or peptide: Ubiquitin-like modifier-activating enzyme 7
    • Protein or peptide: Ubiquitin-like protein ISG15
    • Protein or peptide: Ubiquitin/ISG15-conjugating enzyme E2 L6
  • Ligand: ADENOSINE MONOPHOSPHATE
KeywordsLigase / Signaling Protein
Function / homology
Function and homology information


ISG15 activating enzyme activity / ISG15 transferase activity / Ligases; Forming carbon-sulfur bonds; Acid-thiol ligases / positive regulation of protein oligomerization / ISG15-protein conjugation / regulation of type II interferon production / protein localization to mitochondrion / NS1 Mediated Effects on Host Pathways / response to type I interferon / negative regulation of type I interferon-mediated signaling pathway ...ISG15 activating enzyme activity / ISG15 transferase activity / Ligases; Forming carbon-sulfur bonds; Acid-thiol ligases / positive regulation of protein oligomerization / ISG15-protein conjugation / regulation of type II interferon production / protein localization to mitochondrion / NS1 Mediated Effects on Host Pathways / response to type I interferon / negative regulation of type I interferon-mediated signaling pathway / negative regulation of viral genome replication / E2 ubiquitin-conjugating enzyme / RSV-host interactions / ubiquitin conjugating enzyme activity / positive regulation of interleukin-10 production / positive regulation of bone mineralization / ubiquitin ligase complex / negative regulation of protein ubiquitination / positive regulation of interferon-beta production / positive regulation of erythrocyte differentiation / ubiquitin binding / integrin-mediated signaling pathway / Negative regulators of DDX58/IFIH1 signaling / Termination of translesion DNA synthesis / protein modification process / DDX58/IFIH1-mediated induction of interferon-alpha/beta / response to virus / PKR-mediated signaling / ISG15 antiviral mechanism / modification-dependent protein catabolic process / protein polyubiquitination / positive regulation of type II interferon production / ubiquitin-protein transferase activity / protein tag activity / Interferon alpha/beta signaling / integrin binding / Antigen processing: Ubiquitination & Proteasome degradation / ubiquitin-dependent protein catabolic process / defense response to virus / protein ubiquitination / defense response to bacterium / Amyloid fiber formation / innate immune response / DNA damage response / ubiquitin protein ligase binding / SARS-CoV-2 activates/modulates innate and adaptive immune responses / extracellular region / nucleoplasm / ATP binding / nucleus / cytosol / cytoplasm
Similarity search - Function
: / Ubiquitin-activating enzyme E1 / Ubiquitin-activating enzyme E1, C-terminal / Ubiquitin-activating enzyme E1, FCCH domain / Ubiquitin-activating enzyme E1, four-helix bundle / Ubiquitin-activating enzyme E1, C-terminal domain superfamily / Ubiquitin-activating enzyme E1, SCCH domain / Ubiquitin-activating enzyme E1, FCCH domain superfamily / Ubiquitin fold domain / Ubiquitin-activating enzyme E1 FCCH domain ...: / Ubiquitin-activating enzyme E1 / Ubiquitin-activating enzyme E1, C-terminal / Ubiquitin-activating enzyme E1, FCCH domain / Ubiquitin-activating enzyme E1, four-helix bundle / Ubiquitin-activating enzyme E1, C-terminal domain superfamily / Ubiquitin-activating enzyme E1, SCCH domain / Ubiquitin-activating enzyme E1, FCCH domain superfamily / Ubiquitin fold domain / Ubiquitin-activating enzyme E1 FCCH domain / Ubiquitin-activating enzyme E1 four-helix bundle / Ubiquitin-activating enzyme e1 C-terminal domain / Ubiquitin-activating enzyme, SCCH domain / Ubiquitin-activating enzyme, SCCH domain / Ubiquitin/SUMO-activating enzyme E1-like / Ubiquitin-activating enzyme E1, inactive adenylation domain, subdomain 1 / Ubiquitin-activating enzyme E1, Cys active site / Ubiquitin-activating enzyme active site. / ThiF/MoeB/HesA family / THIF-type NAD/FAD binding fold / ThiF family / Ubiquitin-activating enzyme / : / Ubiquitin-conjugating enzyme, active site / Ubiquitin-conjugating (UBC) active site signature. / Ubiquitin-conjugating enzyme E2 / Ubiquitin-conjugating enzyme / Ubiquitin-conjugating (UBC) core domain profile. / Ubiquitin-conjugating enzyme E2, catalytic domain homologues / Ubiquitin-conjugating enzyme/RWD-like / Ubiquitin domain / Ubiquitin family / Ubiquitin homologues / Ubiquitin domain profile. / Ubiquitin-like domain / Ubiquitin-like domain superfamily
Similarity search - Domain/homology
Ubiquitin/ISG15-conjugating enzyme E2 L6 / Ubiquitin-like protein ISG15 / Ubiquitin-like modifier-activating enzyme 7
Similarity search - Component
Biological speciesHomo sapiens (human)
Methodsingle particle reconstruction / cryo EM / Resolution: 3.4 Å
AuthorsAfsar M / Jia L / Ruben EA / Olsen SK
Funding support United States, 1 items
OrganizationGrant numberCountry
National Institutes of Health/National Institute of General Medical Sciences (NIH/NIGMS) United States
CitationJournal: Nat Commun / Year: 2023
Title: Cryo-EM structures of Uba7 reveal the molecular basis for ISG15 activation and E1-E2 thioester transfer.
Authors: Mohammad Afsar / GuanQun Liu / Lijia Jia / Eliza A Ruben / Digant Nayak / Zuberwasim Sayyad / Priscila Dos Santos Bury / Kristin E Cano / Anindita Nayak / Xiang Ru Zhao / Ankita Shukla / ...Authors: Mohammad Afsar / GuanQun Liu / Lijia Jia / Eliza A Ruben / Digant Nayak / Zuberwasim Sayyad / Priscila Dos Santos Bury / Kristin E Cano / Anindita Nayak / Xiang Ru Zhao / Ankita Shukla / Patrick Sung / Elizabeth V Wasmuth / Michaela U Gack / Shaun K Olsen /
Abstract: ISG15 plays a crucial role in the innate immune response and has been well-studied due to its antiviral activity and regulation of signal transduction, apoptosis, and autophagy. ISG15 is a ubiquitin- ...ISG15 plays a crucial role in the innate immune response and has been well-studied due to its antiviral activity and regulation of signal transduction, apoptosis, and autophagy. ISG15 is a ubiquitin-like protein that is activated by an E1 enzyme (Uba7) and transferred to a cognate E2 enzyme (UBE2L6) to form a UBE2L6-ISG15 intermediate that functions with E3 ligases that catalyze conjugation of ISG15 to target proteins. Despite its biological importance, the molecular basis by which Uba7 catalyzes ISG15 activation and transfer to UBE2L6 is unknown as there is no available structure of Uba7. Here, we present cryo-EM structures of human Uba7 in complex with UBE2L6, ISG15 adenylate, and ISG15 thioester intermediate that are poised for catalysis of Uba7-UBE2L6-ISG15 thioester transfer. Our structures reveal a unique overall architecture of the complex compared to structures from the ubiquitin conjugation pathway, particularly with respect to the location of ISG15 thioester intermediate. Our structures also illuminate the molecular basis for Uba7 activities and for its exquisite specificity for ISG15 and UBE2L6. Altogether, our structural, biochemical, and human cell-based data provide significant insights into the functions of Uba7, UBE2L6, and ISG15 in cells.
History
DepositionApr 8, 2023-
Header (metadata) releaseOct 11, 2023-
Map releaseOct 11, 2023-
UpdateOct 11, 2023-
Current statusOct 11, 2023Processing site: RCSB / Status: Released

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Structure visualization

Supplemental images

emd_40408.png

Downloads & links

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Map

FileDownload / File: emd_40408.map.gz / Format: CCP4 / Size: 178 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)
Projections & slices

Image control

Size
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AxesZ (Sec.)Y (Row.)X (Col.)
0.83 Å/pix.
x 360 pix.
= 299.952 Å		0.83 Å/pix.
x 360 pix.
= 299.952 Å		0.83 Å/pix.
x 360 pix.
= 299.952 Å

Surface

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Images are generated by Spider.

Voxel sizeX=Y=Z: 0.8332 Å
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Histogram

Histogram (log scale)
Contour LevelBy AUTHOR: 0.1
Minimum - Maximum-0.80281883 - 1.2337745
Average (Standard dev.)-0.000078561476 (±0.020251507)
SymmetrySpace group: 1
Details

EMDB XML:

Map geometry
Axis orderXYZ
Origin000
Dimensions360360360
Spacing360360360
CellA=B=C: 299.952 Å
α=β=γ: 90.0 °

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Supplemental data

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Mask #1

Fileemd_40408_msk_1.map
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Half map: #1

Fileemd_40408_half_map_1.map
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Half map: #2

Fileemd_40408_half_map_2.map
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Sample components

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Entire : Cryo-EM structure of a double loaded human UBA7-UBE2L6-ISG15 thio...

EntireName: Cryo-EM structure of a double loaded human UBA7-UBE2L6-ISG15 thioester mimetic complex (Form 1)
Components
  • Complex: Cryo-EM structure of a double loaded human UBA7-UBE2L6-ISG15 thioester mimetic complex (Form 1)
    • Protein or peptide: Ubiquitin-like modifier-activating enzyme 7
    • Protein or peptide: Ubiquitin-like protein ISG15
    • Protein or peptide: Ubiquitin/ISG15-conjugating enzyme E2 L6
  • Ligand: ADENOSINE MONOPHOSPHATE

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Supramolecule #1: Cryo-EM structure of a double loaded human UBA7-UBE2L6-ISG15 thio...

SupramoleculeName: Cryo-EM structure of a double loaded human UBA7-UBE2L6-ISG15 thioester mimetic complex (Form 1)
type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#3
Source (natural)Organism: Homo sapiens (human)

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Macromolecule #1: Ubiquitin-like modifier-activating enzyme 7

MacromoleculeName: Ubiquitin-like modifier-activating enzyme 7 / type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO
Source (natural)Organism: Homo sapiens (human)
Molecular weightTheoretical: 111.822102 KDa
Recombinant expressionOrganism: Trichoplusia ni (cabbage looper)
SequenceString: MDALDASKLL DEELYSRQLY VLGSPAMQRI QGARVLVSGL QGLGAEVAKN LVLMGVGSLT LHDPHPTCWS DLAAQFLLSE QDLERSRAE ASQELLAQLN RAVQVVVHTG DITEDLLLDF QVVVLTAAKL EEQLKVGTLC HKHGVCFLAA DTRGLVGQLF C DFGEDFTV ...String:
MDALDASKLL DEELYSRQLY VLGSPAMQRI QGARVLVSGL QGLGAEVAKN LVLMGVGSLT LHDPHPTCWS DLAAQFLLSE QDLERSRAE ASQELLAQLN RAVQVVVHTG DITEDLLLDF QVVVLTAAKL EEQLKVGTLC HKHGVCFLAA DTRGLVGQLF C DFGEDFTV QDPTEAEPLT AAIQHISQGS PGILTLRKGA NTHYFRDGDL VTFSGIEGMV ELNDCDPRSI HVREDGSLEI GD TTTFSRY LRGGAITEVK RPKTVRHKSL DTALLQPHVV AQSSQEVHHA HCLHQAFCAL HKFQHLHGRP PQPWDPVDAE TVV GLARDL EPLKRTEEEP LEEPLDEALV RTVALSSAGV LSPMVAMLGA VAAQEVLKAI SRKFMPLDQW LYFDALDCLP EDGE LLPSP EDCALRGSRY DGQIAVFGAG FQEKLRRQHY LLVGAGAIGC ELLKVFALVG LGAGNSGGLT VVDMDHIERS NLSRQ FLFR SQDVGRPKAE VAAAAARGLN PDLQVIPLTY PLDPTTEHIY GDNFFSRVDG VAAALDSFQA RRYVAARCTH YLKPLL EAG TSGTWGSATV FMPHVTEAYR APASAAASED APYPVCTVRY FPSTAEHTLQ WARHEFEELF RLSAETINHH QQAHTSL AD MDEPQTLTLL KPVLGVLRVR PQNWQDCVAW ALGHWKLCFH YGIKQLLRHF PPNKVLEDGT PFWSGPKQCP QPLEFDTN Q DTHLLYVLAA ANLYAQMHGL PGSQDWTALR ELLKLLPQPD PQQMAPIFAS NLELASASAE FGPEQQKELN KALEVWSVG PPLKPLMFEK DDDSNFHVDF VVAAASLRCQ NYGIPPVNRA QSKRIVGQII PAIATTTAAV AGLLGLELYK VVSGPRPRSA FRHSYLHLA ENYLIRYMPF APAIQTFHHL KWTSWDRLKV PAGQPERTLE SLLAHLQEQH GLRVRILLHG SALLYAAGWS P EKQAQHLP LRVTELVQQL TGQAPAPGQR VLVLELSCEG DDEDTAFPPL HYEL

UniProtKB: Ubiquitin-like modifier-activating enzyme 7

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Macromolecule #2: Ubiquitin-like protein ISG15

MacromoleculeName: Ubiquitin-like protein ISG15 / type: protein_or_peptide / ID: 2 / Number of copies: 2 / Enantiomer: LEVO
Source (natural)Organism: Homo sapiens (human)
Molecular weightTheoretical: 17.147637 KDa
Recombinant expressionOrganism: Escherichia coli (E. coli)
SequenceString:
MGWDLTVKML AGNEFQVSLS SSMSVSELKA QITQKIGVHA FQQRLAVHPS GVALQDRVPL ASQGLGPGST VLLVVDKSDE PLSILVRNN KGRSSTYEVR LTQTVAHLKQ QVSGLEGVQD DLFWLTFEGK PLEDQLPLGE YGLKPLSTVF MNLRLRGG

UniProtKB: Ubiquitin-like protein ISG15

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Macromolecule #3: Ubiquitin/ISG15-conjugating enzyme E2 L6

MacromoleculeName: Ubiquitin/ISG15-conjugating enzyme E2 L6 / type: protein_or_peptide / ID: 3 / Number of copies: 1 / Enantiomer: LEVO / EC number: E2 ubiquitin-conjugating enzyme
Source (natural)Organism: Homo sapiens (human)
Molecular weightTheoretical: 17.643377 KDa
Recombinant expressionOrganism: Escherichia coli (E. coli)
SequenceString:
MASMRVVKEL EDLQKKPPPY LRNLSSDDAN VLVWHALLLP DQPPYHLKAF NLRISFPPEY PFKPPMIKFT TKIYHPNVDE NGQICLPII SSENWKPSTK TSQVLEALNV LVNRPNIREP KRMDLADLLT QNPELFRKNA EEFTLRFGVD RPS

UniProtKB: Ubiquitin/ISG15-conjugating enzyme E2 L6

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Macromolecule #4: ADENOSINE MONOPHOSPHATE

MacromoleculeName: ADENOSINE MONOPHOSPHATE / type: ligand / ID: 4 / Number of copies: 1 / Formula: AMP
Molecular weightTheoretical: 347.221 Da
Chemical component information

ChemComp-AMP:
ADENOSINE MONOPHOSPHATE / AMP*YM

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Experimental details

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Structure determination

Methodcryo EM
Processingsingle particle reconstruction
Aggregation stateparticle

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Sample preparation

BufferpH: 7.5
VitrificationCryogen name: ETHANE

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Electron microscopy

MicroscopeFEI TITAN KRIOS
Image recordingFilm or detector model: GATAN K3 (6k x 4k) / Average electron dose: 80.0 e/Å2
Electron beamAcceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN
Electron opticsIllumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.888 µm / Nominal defocus min: 0.1 µm
Experimental equipment
Model: Titan Krios / Image courtesy: FEI Company

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Image processing

Startup modelType of model: INSILICO MODEL
Final reconstructionResolution.type: BY AUTHOR / Resolution: 3.4 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 76089
Initial angle assignmentType: ANGULAR RECONSTITUTION
Final angle assignmentType: ANGULAR RECONSTITUTION
FSC plot (resolution estimation)

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