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- EMDB-43738: Cryo-EM structure of human tankyrase 2 SAM-PARP filament bound to... -

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Entry
Database: EMDB / ID: EMD-43738
TitleCryo-EM structure of human tankyrase 2 SAM-PARP filament bound to compound, TDI-2804 (consensus map).
Map dataLocal resolution filtered map
Sample
  • Complex: Tankyrase 2 SAM-PARP filament bound to compound TDI-2804.
    • Protein or peptide: Maltose/maltodextrin-binding periplasmic protein,Poly [ADP-ribose] polymerase tankyrase-2
  • Ligand: ZINC ION
  • Ligand: N-{2-[4-(2-hydroxypropan-2-yl)phenyl]-4-oxo-1,4-dihydroquinazolin-7-yl}-4-methoxy-6-phenylpyridine-3-carboxamide
KeywordsNAD+ ADP-ribosyltransferase / WNT signaling / inhibitor / SIGNALING PROTEIN / SIGNALING PROTEIN-INHIBITOR complex
Function / homology
Function and homology information


XAV939 stabilizes AXIN / positive regulation of telomere capping / NAD+ ADP-ribosyltransferase / negative regulation of telomere maintenance via telomere lengthening / protein auto-ADP-ribosylation / protein localization to chromosome, telomeric region / NAD+-protein-aspartate ADP-ribosyltransferase activity / protein poly-ADP-ribosylation / NAD+-protein-glutamate ADP-ribosyltransferase activity / pericentriolar material ...XAV939 stabilizes AXIN / positive regulation of telomere capping / NAD+ ADP-ribosyltransferase / negative regulation of telomere maintenance via telomere lengthening / protein auto-ADP-ribosylation / protein localization to chromosome, telomeric region / NAD+-protein-aspartate ADP-ribosyltransferase activity / protein poly-ADP-ribosylation / NAD+-protein-glutamate ADP-ribosyltransferase activity / pericentriolar material / NAD+-protein mono-ADP-ribosyltransferase activity / NAD+ poly-ADP-ribosyltransferase activity / Transferases; Glycosyltransferases; Pentosyltransferases / carbohydrate transmembrane transporter activity / maltose binding / maltose transport / maltodextrin transmembrane transport / ATP-binding cassette (ABC) transporter complex, substrate-binding subunit-containing / positive regulation of telomere maintenance via telomerase / nucleotidyltransferase activity / TCF dependent signaling in response to WNT / Degradation of AXIN / Wnt signaling pathway / Regulation of PTEN stability and activity / protein polyubiquitination / positive regulation of canonical Wnt signaling pathway / nuclear envelope / outer membrane-bounded periplasmic space / chromosome, telomeric region / Ub-specific processing proteases / Golgi membrane / perinuclear region of cytoplasm / enzyme binding / metal ion binding / nucleus / cytosol / cytoplasm
Similarity search - Function
Ankyrin repeat / Poly(ADP-ribose) polymerase catalytic domain / Poly(ADP-ribose) polymerase, catalytic domain / PARP catalytic domain profile. / SAM domain (Sterile alpha motif) / Maltose/Cyclodextrin ABC transporter, substrate-binding protein / Solute-binding family 1, conserved site / Bacterial extracellular solute-binding proteins, family 1 signature. / SAM domain profile. / Sterile alpha motif. ...Ankyrin repeat / Poly(ADP-ribose) polymerase catalytic domain / Poly(ADP-ribose) polymerase, catalytic domain / PARP catalytic domain profile. / SAM domain (Sterile alpha motif) / Maltose/Cyclodextrin ABC transporter, substrate-binding protein / Solute-binding family 1, conserved site / Bacterial extracellular solute-binding proteins, family 1 signature. / SAM domain profile. / Sterile alpha motif. / Sterile alpha motif domain / Bacterial extracellular solute-binding protein / Bacterial extracellular solute-binding protein / Sterile alpha motif/pointed domain superfamily / Ankyrin repeat / Ankyrin repeats (3 copies) / Ankyrin repeat profile. / Ankyrin repeat region circular profile. / ankyrin repeats / Ankyrin repeat / Ankyrin repeat-containing domain superfamily
Similarity search - Domain/homology
Maltose/maltodextrin-binding periplasmic protein / Poly [ADP-ribose] polymerase tankyrase-2
Similarity search - Component
Biological speciesHomo sapiens (human)
Methodsingle particle reconstruction / cryo EM / Resolution: 2.28 Å
AuthorsMalone BF / Zimmerman JL / Dow LE / Hite RK
Funding support1 items
OrganizationGrant numberCountry
Not funded
CitationJournal: bioRxiv / Year: 2025
Title: A potent and selective TNKS2 inhibitor for tumor-selective WNT suppression.
Authors: Jill Zimmerman / Brandon F Malone / Efrat Finkin-Groner / Shan Sun / Rui Liang / Miguel Foronda / Emma M Schatoff / Elizabeth Granowsky / Sukanya Goswami / Alyna Katti / Benjamin Leach / ...Authors: Jill Zimmerman / Brandon F Malone / Efrat Finkin-Groner / Shan Sun / Rui Liang / Miguel Foronda / Emma M Schatoff / Elizabeth Granowsky / Sukanya Goswami / Alyna Katti / Benjamin Leach / Heather Alcorn / Tuomas Tammela / Yoshiyuki Fukase / Tanweer Khan / David J Huggins / John Ginn / Nigel Liverton / Richard K Hite / Lukas E Dow /
Abstract: Hyperactive WNT signaling is a potent cancer driver, but clinical translation of WNT inhibitors has been hampered by on-target toxicities. WNT signaling can be constrained through inhibition of the ...Hyperactive WNT signaling is a potent cancer driver, but clinical translation of WNT inhibitors has been hampered by on-target toxicities. WNT signaling can be constrained through inhibition of the PARP family enzymes Tankyrase 1 (TNKS1) and Tankyrase 2 (TNKS2), however, existing TNKS inhibitors suppress WNT signaling in both tumor and healthy tissues. In this study, we show that the loss of chromosome 8p that occurs in approximately half of advanced epithelial malignancies, creates a collateral vulnerability that enables tumor-selective inhibition of Tankyrase activity. 8p loss depletes expression of TNKS1 and creates a tumor-specific dependency on the functionally redundant TNKS2 protein. Through structure-guided drug design, we identify a first-in-class TNKS2-selective inhibitor that can drive selective WNT inhibition in TNKS1-deficient oncogenic cell and organoid models. This work demonstrates a targetable vulnerability in multiple cancer types, providing a new approach to potent and selective WNT-targeted therapies.
History
DepositionFeb 19, 2024-
Header (metadata) releaseJul 9, 2025-
Map releaseJul 9, 2025-
UpdateJul 9, 2025-
Current statusJul 9, 2025Processing site: RCSB / Status: Released

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Structure visualization

Supplemental images

emd_43738.png

Downloads & links

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Map

FileDownload / File: emd_43738.map.gz / Format: CCP4 / Size: 512 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)
AnnotationLocal resolution filtered map
Projections & slices

Image control

Size
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AxesZ (Sec.)Y (Row.)X (Col.)
0.83 Å/pix.
x 512 pix.
= 422.912 Å		0.83 Å/pix.
x 512 pix.
= 422.912 Å		0.83 Å/pix.
x 512 pix.
= 422.912 Å

Surface

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Slices (2/3)

Images are generated by Spider.

Voxel sizeX=Y=Z: 0.826 Å
Density

Histogram

Histogram (log scale)
Contour LevelBy AUTHOR: 0.22
Minimum - Maximum-1.3701599 - 1.9334424
Average (Standard dev.)0.0005521626 (±0.037052426)
SymmetrySpace group: 1
Details

EMDB XML:

Map geometry
Axis orderXYZ
Origin000
Dimensions512512512
Spacing512512512
CellA=B=C: 422.912 Å
α=β=γ: 90.0 °

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Supplemental data

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Additional map: B-factor sharpened map

Fileemd_43738_additional_1.map
AnnotationB-factor sharpened map
Projections & Slices
AxesZYX

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Additional map: Raw map

Fileemd_43738_additional_2.map
AnnotationRaw map
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Half map: Half map A

Fileemd_43738_half_map_1.map
AnnotationHalf map A
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Half map: Half map B

Fileemd_43738_half_map_2.map
AnnotationHalf map B
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Sample components

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Entire : Tankyrase 2 SAM-PARP filament bound to compound TDI-2804.

EntireName: Tankyrase 2 SAM-PARP filament bound to compound TDI-2804.
Components
  • Complex: Tankyrase 2 SAM-PARP filament bound to compound TDI-2804.
    • Protein or peptide: Maltose/maltodextrin-binding periplasmic protein,Poly [ADP-ribose] polymerase tankyrase-2
  • Ligand: ZINC ION
  • Ligand: N-{2-[4-(2-hydroxypropan-2-yl)phenyl]-4-oxo-1,4-dihydroquinazolin-7-yl}-4-methoxy-6-phenylpyridine-3-carboxamide

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Supramolecule #1: Tankyrase 2 SAM-PARP filament bound to compound TDI-2804.

SupramoleculeName: Tankyrase 2 SAM-PARP filament bound to compound TDI-2804.
type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1
Source (natural)Organism: Homo sapiens (human)

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Macromolecule #1: Maltose/maltodextrin-binding periplasmic protein,Poly [ADP-ribose...

MacromoleculeName: Maltose/maltodextrin-binding periplasmic protein,Poly [ADP-ribose] polymerase tankyrase-2
type: protein_or_peptide / ID: 1
Details: Construct shown is the N-terminally tagged TNKS2 SAM-PARP (amino acids 850 - 1166). The N-terminal tag is twin-strep fused to maltose-binding protein. The modelled structure features ...Details: Construct shown is the N-terminally tagged TNKS2 SAM-PARP (amino acids 850 - 1166). The N-terminal tag is twin-strep fused to maltose-binding protein. The modelled structure features residues 875 - 1158.,Construct shown is the N-terminally tagged TNKS2 SAM-PARP (amino acids 850 - 1166). The N-terminal tag is twin-strep fused to maltose-binding protein. The modelled structure features residues 875 - 1158.,Construct shown is the N-terminally tagged TNKS2 SAM-PARP (amino acids 850 - 1166). The N-terminal tag is twin-strep fused to maltose-binding protein. The modelled structure features residues 875 - 1158.,Construct shown is the N-terminally tagged TNKS2 SAM-PARP (amino acids 850 - 1166). The N-terminal tag is twin-strep fused to maltose-binding protein. The modelled structure features residues 875 - 1158.,Construct shown is the N-terminally tagged TNKS2 SAM-PARP (amino acids 850 - 1166). The N-terminal tag is twin-strep fused to maltose-binding protein. The modelled structure features residues 875 - 1158.,Construct shown is the N-terminally tagged TNKS2 SAM-PARP (amino acids 850 - 1166). The N-terminal tag is twin-strep fused to maltose-binding protein. The modelled structure features residues 875 - 1158.,Construct shown is the N-terminally tagged TNKS2 SAM-PARP (amino acids 850 - 1166). The N-terminal tag is twin-strep fused to maltose-binding protein. The modelled structure features residues 875 - 1158.,Construct shown is the N-terminally tagged TNKS2 SAM-PARP (amino acids 850 - 1166). The N-terminal tag is twin-strep fused to maltose-binding protein. The modelled structure features residues 875 - 1158.
Number of copies: 20 / Enantiomer: LEVO / EC number: NAD+ ADP-ribosyltransferase
Source (natural)Organism: Homo sapiens (human)
Molecular weightTheoretical: 80.614008 KDa
Recombinant expressionOrganism: Spodoptera frugiperda (fall armyworm)
SequenceString: MSAWSHPQFE KGGGSGGGSG GSAWSHPQFE KTGSMGIEEG KLVIWINGDK GYNGLAEVGK KFEKDTGIKV TVEHPDKLEE KFPQVAATG DGPDIIFWAH DRFGGYAQSG LLAEITPDKA FQDKLYPFTW DAVRYNGKLI AYPIAVEALS LIYNKDLLPN P PKTWEEIP ...String:
MSAWSHPQFE KGGGSGGGSG GSAWSHPQFE KTGSMGIEEG KLVIWINGDK GYNGLAEVGK KFEKDTGIKV TVEHPDKLEE KFPQVAATG DGPDIIFWAH DRFGGYAQSG LLAEITPDKA FQDKLYPFTW DAVRYNGKLI AYPIAVEALS LIYNKDLLPN P PKTWEEIP ALDKELKAKG KSALMFNLQE PYFTWPLIAA DGGYAFKYEN GKYDIKDVGV DNAGAKAGLT FLVDLIKNKH MN ADTDYSI AEAAFNKGET AMTINGPWAW SNIDTSKVNY GVTVLPTFKG QPSKPFVGVL SAGINAASPN KELAKEFLEN YLL TDEGLE AVNKDKPLGA VALKSYEEEL AKDPRIAATM ENAQKGEIMP NIPQMSAFWY AVRTAVINAA SGRQTVDEAL KDAQ TELEL EVLFQGPELS SVVSSSGTEG ASSLEKKEVP GVDFSITQFV RNLGLEHLMD IFEREQITLD VLVEMGHKEL KEIGI NAYG HRHKLIKGVE RLISGQQGLN PYLTLNTSGS GTILIDLSPD DKEFQSVEEE MQSTVREHRD GGHAGGIFNR YNILKI QKV CNKKLWERYT HRRKEVSEEN HNHANERMLF HGSPFVNAII HKGFDERHAY IGGMFGAGIY FAENSSKSNQ YVYGIGG GT GCPVHKDRSC YICHRQLLFC RVTLGKSFLQ FSAMKMAHSP PGHHSVTGRP SVNGLALAEY VIYRGEQAYP EYLITYQI M RPEGMVDG

UniProtKB: Maltose/maltodextrin-binding periplasmic protein, Poly [ADP-ribose] polymerase tankyrase-2

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Macromolecule #2: ZINC ION

MacromoleculeName: ZINC ION / type: ligand / ID: 2 / Number of copies: 20 / Formula: ZN
Molecular weightTheoretical: 65.409 Da

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Macromolecule #3: N-{2-[4-(2-hydroxypropan-2-yl)phenyl]-4-oxo-1,4-dihydroquinazolin...

MacromoleculeName: N-{2-[4-(2-hydroxypropan-2-yl)phenyl]-4-oxo-1,4-dihydroquinazolin-7-yl}-4-methoxy-6-phenylpyridine-3-carboxamide
type: ligand / ID: 3 / Number of copies: 20 / Formula: A1AE4
Molecular weightTheoretical: 506.552 Da

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Experimental details

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Structure determination

Methodcryo EM
Processingsingle particle reconstruction
Aggregation statefilament

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Sample preparation

Concentration1.3 mg/mL
BufferpH: 7.5
Component:
ConcentrationFormulaName
500.0 millimolarNaClSodium Chloride
20.0 millimolarHEPES
5.0 % v/vGlycerol
2.0 millimolar2-mercaptoethanol
0.05 % v/vTween-20

Details: Sample was purified and concentrated in the above buffer but exchanged prior to vitrification to a low-salt (minimal) buffer composed of 20 millimolar HEPES pH 7.5. Sample buffer was ...Details: Sample was purified and concentrated in the above buffer but exchanged prior to vitrification to a low-salt (minimal) buffer composed of 20 millimolar HEPES pH 7.5. Sample buffer was exchanged on grid via manual side-blotting.
GridModel: Quantifoil R1.2/1.3 / Material: GRAPHENE OXIDE / Mesh: 400
VitrificationCryogen name: ETHANE / Chamber humidity: 95 % / Chamber temperature: 283 K / Instrument: FEI VITROBOT MARK IV

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Electron microscopy

MicroscopeTFS KRIOS
Image recordingFilm or detector model: GATAN K3 (6k x 4k) / Average electron dose: 55.7 e/Å2
Electron beamAcceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN
Electron opticsIllumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 3.0 µm / Nominal defocus min: 0.8 µm / Nominal magnification: 29000
Sample stageSpecimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN
Experimental equipment
Model: Titan Krios / Image courtesy: FEI Company

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Image processing

CTF correctionSoftware - Name: cryoSPARC / Type: PHASE FLIPPING AND AMPLITUDE CORRECTION
Startup modelType of model: INSILICO MODEL / In silico model: Ab-initio reconstruction in cryosparc
Final reconstructionResolution.type: BY AUTHOR / Resolution: 2.28 Å / Resolution method: FSC 0.143 CUT-OFF / Software - Name: cryoSPARC / Number images used: 1310954
Initial angle assignmentType: MAXIMUM LIKELIHOOD / Software - Name: cryoSPARC
Final angle assignmentType: MAXIMUM LIKELIHOOD / Software - Name: cryoSPARC
FSC plot (resolution estimation)

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Atomic model buiding 1

Initial modelPDB ID:

8aly


Chain - Source name: PDB / Chain - Initial model type: experimental model
Output model

PDB-8w23:
Cryo-EM structure of human tankyrase 2 SAM-PARP filament bound to compound, TDI-2804 (consensus map).

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