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- EMDB-51330: Structure of WT human mitochondrial DNA polymerase gamma -

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Basic information

Entry
Database: EMDB / ID: EMD-51330
TitleStructure of WT human mitochondrial DNA polymerase gamma
Map data
Sample
  • Complex: Structure of WT human mitochondrial DNA polymerase gamma
    • Protein or peptide: DNA polymerase subunit gamma-1
    • Protein or peptide: DNA polymerase subunit gamma-2
    • DNA: DNA (primer strand)
    • DNA: DNA (template strand)
  • Ligand: CALCIUM ION
  • Ligand: 2'-DEOXYCYTIDINE-5'-TRIPHOSPHATE
KeywordsMitochondrial DNA polymerase / activator / TRANSFERASE/DNA / TRANSFERASE-DNA complex
Function / homology
Function and homology information


gamma DNA polymerase complex / mitochondrial chromosome / mitochondrial DNA replication / Strand-asynchronous mitochondrial DNA replication / positive regulation of DNA-directed DNA polymerase activity / DNA replication proofreading / single-stranded DNA 3'-5' DNA exonuclease activity / Hydrolases; Acting on ester bonds; Exodeoxyribonucleases producing 5'-phosphomonoesters / DNA metabolic process / DNA polymerase processivity factor activity ...gamma DNA polymerase complex / mitochondrial chromosome / mitochondrial DNA replication / Strand-asynchronous mitochondrial DNA replication / positive regulation of DNA-directed DNA polymerase activity / DNA replication proofreading / single-stranded DNA 3'-5' DNA exonuclease activity / Hydrolases; Acting on ester bonds; Exodeoxyribonucleases producing 5'-phosphomonoesters / DNA metabolic process / DNA polymerase processivity factor activity / mitochondrial nucleoid / Lyases; Carbon-oxygen lyases; Other carbon-oxygen lyases / 5'-deoxyribose-5-phosphate lyase activity / base-excision repair, gap-filling / DNA polymerase binding / 3'-5' exonuclease activity / Transcriptional activation of mitochondrial biogenesis / base-excision repair / DNA-templated DNA replication / protease binding / double-stranded DNA binding / in utero embryonic development / DNA-directed DNA polymerase / DNA-directed DNA polymerase activity / mitochondrial matrix / intracellular membrane-bounded organelle / chromatin binding / protein-containing complex / mitochondrion / DNA binding / identical protein binding / cytoplasm
Similarity search - Function
DNA-directed DNA-polymerase, family A, mitochondria / DNA mitochondrial polymerase, exonuclease domain / POLG2, C-terminal / : / DNA mitochondrial polymerase exonuclease domain / Glycyl-tRNA synthetase/DNA polymerase subunit gamma-2 / Anticodon-binding / Anticodon binding domain / Anticodon-binding domain superfamily / DNA-directed DNA polymerase, family A, conserved site ...DNA-directed DNA-polymerase, family A, mitochondria / DNA mitochondrial polymerase, exonuclease domain / POLG2, C-terminal / : / DNA mitochondrial polymerase exonuclease domain / Glycyl-tRNA synthetase/DNA polymerase subunit gamma-2 / Anticodon-binding / Anticodon binding domain / Anticodon-binding domain superfamily / DNA-directed DNA polymerase, family A, conserved site / DNA polymerase family A signature. / DNA-directed DNA polymerase, family A, palm domain / DNA polymerase A domain / Class II Aminoacyl-tRNA synthetase/Biotinyl protein ligase (BPL) and lipoyl protein ligase (LPL) / Ribonuclease H-like superfamily / DNA/RNA polymerase superfamily
Similarity search - Domain/homology
DNA polymerase subunit gamma-1 / DNA polymerase subunit gamma-2
Similarity search - Component
Biological speciesHomo sapiens (human) / synthetic construct (others)
Methodsingle particle reconstruction / cryo EM / Resolution: 2.65 Å
AuthorsValenzuela S / Falkenberg M
Funding support Sweden, 3 items
OrganizationGrant numberCountry
Swedish Research Council Sweden
Knut and Alice Wallenberg Foundation Sweden
Cancerfonden Sweden
CitationJournal: Nature / Year: 2025
Title: Small molecules restore mutant mitochondrial DNA polymerase activity.
Authors: Sebastian Valenzuela / Xuefeng Zhu / Bertil Macao / Mattias Stamgren / Carol Geukens / Paul S Charifson / Gunther Kern / Emily Hoberg / Louise Jenninger / Anja V Gruszczyk / Seoeun Lee / ...Authors: Sebastian Valenzuela / Xuefeng Zhu / Bertil Macao / Mattias Stamgren / Carol Geukens / Paul S Charifson / Gunther Kern / Emily Hoberg / Louise Jenninger / Anja V Gruszczyk / Seoeun Lee / Katarina A S Johansson / Javier Miralles Fusté / Yonghong Shi / S Jordan Kerns / Laleh Arabanian / Gabriel Martinez Botella / Sofie Ekström / Jeremy Green / Andrew M Griffin / Carlos Pardo-Hernández / Thomas A Keating / Barbara Küppers-Munther / Nils-Göran Larsson / Cindy Phan / Viktor Posse / Juli E Jones / Xie Xie / Simon Giroux / Claes M Gustafsson / Maria Falkenberg /
Abstract: Mammalian mitochondrial DNA (mtDNA) is replicated by DNA polymerase γ (POLγ), a heterotrimeric complex consisting of a catalytic POLγA subunit and two accessory POLγB subunits. More than 300 ...Mammalian mitochondrial DNA (mtDNA) is replicated by DNA polymerase γ (POLγ), a heterotrimeric complex consisting of a catalytic POLγA subunit and two accessory POLγB subunits. More than 300 mutations in POLG, the gene encoding the catalytic subunit, have been linked to severe, progressive conditions with high rates of morbidity and mortality, for which no treatment exists. Here we report on the discovery and characterization of PZL-A, a first-in-class small-molecule activator of mtDNA synthesis that is capable of restoring function to the most common mutant variants of POLγ. PZL-A binds to an allosteric site at the interface between the catalytic POLγA subunit and the proximal POLγB subunit, a region that is unaffected by nearly all disease-causing mutations. The compound restores wild-type-like activity to mutant forms of POLγ in vitro and activates mtDNA synthesis in cells from paediatric patients with lethal POLG disease, thereby enhancing biogenesis of the oxidative phosphorylation machinery and cellular respiration. Our work demonstrates that a small molecule can restore function to mutant DNA polymerases, offering a promising avenue for treating POLG disorders and other severe conditions linked to depletion of mtDNA.
History
DepositionAug 13, 2024-
Header (metadata) releaseApr 16, 2025-
Map releaseApr 16, 2025-
UpdateApr 23, 2025-
Current statusApr 23, 2025Processing site: PDBe / Status: Released

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Structure visualization

Supplemental images

emd_51330.png

Downloads & links

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Map

FileDownload / File: emd_51330.map.gz / Format: CCP4 / Size: 125 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)
Projections & slices

Image control

Size
Brightness
Contrast
Others
AxesZ (Sec.)Y (Row.)X (Col.)
0.83 Å/pix.
x 320 pix.
= 264. Å		0.83 Å/pix.
x 320 pix.
= 264. Å		0.83 Å/pix.
x 320 pix.
= 264. Å

Surface

Projections

Slices (1/3)

Slices (1/2)

Slices (2/3)

Images are generated by Spider.

Voxel sizeX=Y=Z: 0.825 Å
Density

Histogram

Histogram (log scale)
Contour LevelBy AUTHOR: 3.5
Minimum - Maximum-28.956099999999999 - 47.320700000000002
Average (Standard dev.)0.0018176454 (±0.9749231)
SymmetrySpace group: 1
Details

EMDB XML:

Map geometry
Axis orderXYZ
Origin000
Dimensions320320320
Spacing320320320
CellA=B=C: 264.0 Å
α=β=γ: 90.0 °

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Supplemental data

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Mask #1

Fileemd_51330_msk_1.map
Projections & Slices
AxesZYX

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Slices (1/2)
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Histogram

Histogram (log scale)

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Additional map: DeepEMhancer map

Fileemd_51330_additional_1.map
AnnotationDeepEMhancer map
Projections & Slices
AxesZYX

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Histogram (log scale)

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Additional map: Unsharpened map

Fileemd_51330_additional_2.map
AnnotationUnsharpened map
Projections & Slices
AxesZYX

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Histogram

Histogram (log scale)

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Half map: cryoSPARC half map B

Fileemd_51330_half_map_1.map
AnnotationcryoSPARC half map B
Projections & Slices
AxesZYX

Projections

Slices (1/2)
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Histogram

Histogram (log scale)

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Half map: cryoSPARC half map A

Fileemd_51330_half_map_2.map
AnnotationcryoSPARC half map A
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AxesZYX

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Sample components

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Entire : Structure of WT human mitochondrial DNA polymerase gamma

EntireName: Structure of WT human mitochondrial DNA polymerase gamma
Components
  • Complex: Structure of WT human mitochondrial DNA polymerase gamma
    • Protein or peptide: DNA polymerase subunit gamma-1
    • Protein or peptide: DNA polymerase subunit gamma-2
    • DNA: DNA (primer strand)
    • DNA: DNA (template strand)
  • Ligand: CALCIUM ION
  • Ligand: 2'-DEOXYCYTIDINE-5'-TRIPHOSPHATE

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Supramolecule #1: Structure of WT human mitochondrial DNA polymerase gamma

SupramoleculeName: Structure of WT human mitochondrial DNA polymerase gamma
type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#4
Source (natural)Organism: Homo sapiens (human)

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Macromolecule #1: DNA polymerase subunit gamma-1

MacromoleculeName: DNA polymerase subunit gamma-1 / type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO / EC number: DNA-directed DNA polymerase
Source (natural)Organism: Homo sapiens (human)
Molecular weightTheoretical: 138.044641 KDa
Recombinant expressionOrganism: Spodoptera frugiperda (fall armyworm)
SequenceString: MHHHHHHVSS SVPASDPSDG QRRRQQQQQQ QQQQQQQPQQ PQVLSSEGGQ LRHNPLDIQM LSRGLHEQIF GQGGEMPGEA AVRRSVEHL QKHGLWGQPA VPLPDVELRL PPLYGDNLDQ HFRLLAQKQS LPYLEAANLL LQAQLPPKPP AWAWAEGWTR Y GPEGEAVP ...String:
MHHHHHHVSS SVPASDPSDG QRRRQQQQQQ QQQQQQQPQQ PQVLSSEGGQ LRHNPLDIQM LSRGLHEQIF GQGGEMPGEA AVRRSVEHL QKHGLWGQPA VPLPDVELRL PPLYGDNLDQ HFRLLAQKQS LPYLEAANLL LQAQLPPKPP AWAWAEGWTR Y GPEGEAVP VAIPEERALV FDVEVCLAEG TCPTLAVAIS PSAWYSWCSQ RLVEERYSWT SQLSPADLIP LEVPTGASSP TQ RDWQEQL VVGHNVSFDR AHIREQYLIQ GSRMRFLDTM SMHMAISGLS SFQRSLWIAA KQGKHKVQPP TKQGQKSQRK ARR GPAISS WDWLDISSVN SLAEVHRLYV GGPPLEKEPR ELFVKGTMKD IRENFQDLMQ YCAQDVWATH EVFQQQLPLF LERC PHPVT LAGMLEMGVS YLPVNQNWER YLAEAQGTYE ELQREMKKSL MDLANDACQL LSGERYKEDP WLWDLEWDLQ EFKQK KAKK VKKEPATASK LPIEGAGAPG DPMDQEDLGP CSEEEEFQQD VMARACLQKL KGTTELLPKR PQHLPGHPGW YRKLCP RLD DPAWTPGPSL LSLQMRVTPK LMALTWDGFP LHYSERHGWG YLVPGRRDNL AKLPTGTTLE SAGVVCPYRA IESLYRK HC LEQGKQQLMP QEAGLAEEFL LTDNSAIWQT VEELDYLEVE AEAKMENLRA AVPGQPLALT ARGGPKDTQP SYHHGNGP Y NDVDIPGCWF FKLPHKDGNS CNVGSPFAKD FLPKMEDGTL QAGPGGASGP RALEINKMIS FWRNAHKRIS SQMVVWLPR SALPRAVIRH PDYDEEGLYG AILPQVVTAG TITRRAVEPT WLTASNARPD RVGSELKAMV QAPPGYTLVG ADVDSQELWI AAVLGDAHF AGMHGCTAFG WMTLQGRKSR GTDLHSKTAT TVGISREHAK IFNYGRIYGA GQPFAERLLM QFNHRLTQQE A AEKAQQMY AATKGLRWYR LSDEGEWLVR ELNLPVDRTE GGWISLQDLR KVQRETARKS QWKKWEVVAE RAWKGGTESE MF NKLESIA TSDIPRTPVL GCCISRALEP SAVQEEFMTS RVNWVVQSSA VDYLHLMLVA MKWLFEEFAI DGRFCISIHD EVR YLVREE DRYRAALALQ ITNLLTRCMF AYKLGLNDLP QSVAFFSAVD IDRCLRKEVT MDCKTPSNPT GMERRYGIPQ GEAL DIYQI IELTKGSLEK RSQPGP

UniProtKB: DNA polymerase subunit gamma-1

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Macromolecule #2: DNA polymerase subunit gamma-2

MacromoleculeName: DNA polymerase subunit gamma-2 / type: protein_or_peptide / ID: 2 / Details: A169T (Single Nucleotide Polymorphism) / Number of copies: 2 / Enantiomer: LEVO
Source (natural)Organism: Homo sapiens (human)
Molecular weightTheoretical: 53.229684 KDa
Recombinant expressionOrganism: Spodoptera frugiperda (fall armyworm)
SequenceString: MDAGQPELLT ERSSPKGGHV KSHAELEGNG EHPEAPGSGE GSEALLEICQ RRHFLSGSKQ QLSRDSLLSG CHPGFGPLGV ELRKNLAAE WWTSVVVFRE QVFPVDALHH KPGPLLPGDS AFRLVSAETL REILQDKELS KEQLVTFLEN VLKTSGKLRE N LLHGALEH ...String:
MDAGQPELLT ERSSPKGGHV KSHAELEGNG EHPEAPGSGE GSEALLEICQ RRHFLSGSKQ QLSRDSLLSG CHPGFGPLGV ELRKNLAAE WWTSVVVFRE QVFPVDALHH KPGPLLPGDS AFRLVSAETL REILQDKELS KEQLVTFLEN VLKTSGKLRE N LLHGALEH YVNCLDLVNK RLPYGLAQIG VCFHPVFDTK QIRNGVKSIG EKTEASLVWF TPPRTSNQWL DFWLRHRLQW WR KFAMSPS NFSSSDCQDE EGRKGNKLYY NFPWGKELIE TLWNLGDHEL LHMYPGNVSK LHGRDGRKNV VPCVLSVNGD LDR GMLAYL YDSFQLTENS FTRKKNLHRK VLKLHPCLAP IKVALDVGRG PTLELRQVCQ GLFNELLENG ISVWPGYLET MQSS LEQLY SKYDEMSILF TVLVTETTLE NGLIHLRSRD TTMKEMMHIS KLKDFLIKYI SSAKNVHHHH HH

UniProtKB: DNA polymerase subunit gamma-2

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Macromolecule #3: DNA (primer strand)

MacromoleculeName: DNA (primer strand) / type: dna / ID: 3 / Number of copies: 1 / Classification: DNA
Source (natural)Organism: synthetic construct (others)
Molecular weightTheoretical: 7.764998 KDa
SequenceString:
(DG)(DC)(DA)(DT)(DG)(DC)(DG)(DG)(DT)(DC) (DG)(DA)(DG)(DT)(DC)(DT)(DA)(DG)(DA)(DG) (DG)(DA)(DG)(DC)(DC)

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Macromolecule #4: DNA (template strand)

MacromoleculeName: DNA (template strand) / type: dna / ID: 4 / Number of copies: 1 / Classification: DNA
Source (natural)Organism: synthetic construct (others)
Molecular weightTheoretical: 12.162783 KDa
SequenceString:
(DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT)(DT) (DA)(DT)(DC)(DC)(DG)(DG)(DG)(DC)(DT)(DC) (DC)(DT)(DC)(DT)(DA)(DG)(DA)(DC)(DT) (DC)(DG)(DA)(DC)(DC)(DG)(DC)(DA)(DT)(DG) (DC)

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Macromolecule #5: CALCIUM ION

MacromoleculeName: CALCIUM ION / type: ligand / ID: 5 / Number of copies: 1 / Formula: CA
Molecular weightTheoretical: 40.078 Da

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Macromolecule #6: 2'-DEOXYCYTIDINE-5'-TRIPHOSPHATE

MacromoleculeName: 2'-DEOXYCYTIDINE-5'-TRIPHOSPHATE / type: ligand / ID: 6 / Number of copies: 1 / Formula: DCP
Molecular weightTheoretical: 467.157 Da
Chemical component information

ChemComp-DCP:
2'-DEOXYCYTIDINE-5'-TRIPHOSPHATE

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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 / Instrument: FEI VITROBOT MARK IV

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Electron microscopy

MicroscopeTFS KRIOS
Image recordingFilm or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 40.0 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: 2.2 µm / Nominal defocus min: 0.8 µm / Nominal magnification: 105000
Experimental equipment
Model: Titan Krios / Image courtesy: FEI Company

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Image processing

Startup modelType of model: OTHER / Details: Ab-initio model
Final reconstructionApplied symmetry - Point group: C1 (asymmetric) / Resolution.type: BY AUTHOR / Resolution: 2.65 Å / Resolution method: FSC 0.143 CUT-OFF / Software - Name: cryoSPARC (ver. 4.3.1.) / Number images used: 821488
Initial angle assignmentType: MAXIMUM LIKELIHOOD / Software - Name: cryoSPARC (ver. 4.3.1.)
Final angle assignmentType: MAXIMUM LIKELIHOOD / Software - Name: cryoSPARC (ver. 4.3.1.)
FSC plot (resolution estimation)

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