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- EMDB-42131: Komagataella pastoris Cytochrome c oxidase in complex with human ... -

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Entry
Database: EMDB / ID: EMD-42131
TitleKomagataella pastoris Cytochrome c oxidase in complex with human VMAT2 and Reserpine
Map data3.14A DEEPEMhancer cryoEM map of Komagataella pastoris Cytochrome c oxidase in complex with human VMAT2 and Reserpine
Sample
  • Complex: Cytochrome c oxidase-VMAT2-Reserpine PARTICLE
    • Protein or peptide: x 10 types
  • Ligand: x 6 types
KeywordsVMAT / SLC18 / vascular monoamine transporter / Cytochrome c oxidase-VMAT2 complex / Neurotransmitters / Reserpine / MEMBRANE PROTEIN
Function / homology
Function and homology information


serotonin secretion by mast cell / somato-dendritic dopamine secretion / histamine uptake / aminergic neurotransmitter loading into synaptic vesicle / neurotransmitter loading into synaptic vesicle / monoamine:proton antiporter activity / clathrin-sculpted monoamine transport vesicle membrane / Serotonin Neurotransmitter Release Cycle / serotonin:sodium:chloride symporter activity / Dopamine Neurotransmitter Release Cycle ...serotonin secretion by mast cell / somato-dendritic dopamine secretion / histamine uptake / aminergic neurotransmitter loading into synaptic vesicle / neurotransmitter loading into synaptic vesicle / monoamine:proton antiporter activity / clathrin-sculpted monoamine transport vesicle membrane / Serotonin Neurotransmitter Release Cycle / serotonin:sodium:chloride symporter activity / Dopamine Neurotransmitter Release Cycle / Norepinephrine Neurotransmitter Release Cycle / serotonin uptake / dopamine transport / monoamine transmembrane transporter activity / histamine secretion by mast cell / monoamine transport / dopaminergic synapse / respiratory chain complex IV / mitochondrial envelope / Na+/Cl- dependent neurotransmitter transporters / cytochrome-c oxidase / mitochondrial electron transport, cytochrome c to oxygen / cytochrome-c oxidase activity / neurotransmitter transport / electron transport coupled proton transport / negative regulation of reactive oxygen species biosynthetic process / secretory granule membrane / response to amphetamine / post-embryonic development / locomotory behavior / response to toxic substance / terminal bouton / synaptic vesicle / synaptic vesicle membrane / chemical synaptic transmission / oxidoreductase activity / mitochondrial inner membrane / axon / intracellular membrane-bounded organelle / heme binding / dendrite / centrosome / mitochondrion / metal ion binding / membrane / plasma membrane
Similarity search - Function
Cytochrome c oxidase, subunit VIIa, fungal / : / Cytochrome c oxidase subunit VIIc / Cytochrome c oxidase subunit IV family / Cytochrome c oxidase subunit VIIc superfamily / Cytochrome c oxidase subunit IV superfamily / Cytochrome c oxidase subunit VIIc / Cytochrome c oxidase subunit IV / Cytochrome c oxidase, subunit Va/VI / Cytochrome c oxidase, subunit Va/VI superfamily ...Cytochrome c oxidase, subunit VIIa, fungal / : / Cytochrome c oxidase subunit VIIc / Cytochrome c oxidase subunit IV family / Cytochrome c oxidase subunit VIIc superfamily / Cytochrome c oxidase subunit IV superfamily / Cytochrome c oxidase subunit VIIc / Cytochrome c oxidase subunit IV / Cytochrome c oxidase, subunit Va/VI / Cytochrome c oxidase, subunit Va/VI superfamily / Cytochrome c oxidase subunit Va / Cytochrome c oxidase subunit VII / Cytochrome c oxidase subunit VII / Cytochrome c oxidase, subunit Vb / Cytochrome c oxidase subunit III domain / Cytochrome c oxidase subunit Vb / Cytochrome c oxidase subunit Vb, zinc binding domain profile. / Cytochrome c oxidase, subunit Vb superfamily / Cytochrome c oxidase subunit I domain / Cytochrome c oxidase subunit III / Cytochrome c oxidase subunit III-like / Cytochrome c oxidase, subunit III, 4-helical bundle / Cytochrome c oxidase subunit III / Heme-copper oxidase subunit III family profile. / Cytochrome c oxidase subunit III-like superfamily / Cytochrome c oxidase, subunit I, copper-binding site / Heme-copper oxidase catalytic subunit, copper B binding region signature. / Cytochrome c oxidase-like, subunit I domain / Cytochrome oxidase subunit I profile. / Cytochrome c oxidase subunit I / Cytochrome c oxidase-like, subunit I superfamily / Cytochrome C and Quinol oxidase polypeptide I / Major facilitator superfamily / Major Facilitator Superfamily / Major facilitator superfamily domain / Major facilitator superfamily (MFS) profile. / MFS transporter superfamily
Similarity search - Domain/homology
Cytochrome c oxidase subunit 9, mitochondrial / Cytochrome c oxidase subunit 8, mitochondrial / Cytochrome c oxidase subunit 7 / Cytochrome c oxidase subunit 4, mitochondrial / Cytochrome c oxidase subunit 6, mitochondrial / Cytochrome c oxidase subunit 5B / Cytochrome c oxidase subunit 3 / Cytochrome c oxidase subunit 1 / Synaptic vesicular amine transporter
Similarity search - Component
Biological speciesHomo sapiens (human) / Komagataella pastoris (fungus)
Methodsingle particle reconstruction / cryo EM / Resolution: 3.14 Å
AuthorsYe J / Liu B / Li W
Funding support United States, 1 items
OrganizationGrant numberCountry
American Heart AssociationEstablished Investigator Award United States
CitationJournal: To Be Published
Title: Komagataella pastoris Cytochrome c oxidase in complex with human VMAT2 and Reserpine
Authors: Ye J / Liu B / Li W
History
DepositionSep 26, 2023-
Header (metadata) releaseOct 9, 2024-
Map releaseOct 9, 2024-
UpdateOct 9, 2024-
Current statusOct 9, 2024Processing site: RCSB / Status: Released

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Structure visualization

Downloads & links

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Map

FileDownload / File: emd_42131.map.gz / Format: CCP4 / Size: 421.9 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)
Annotation3.14A DEEPEMhancer cryoEM map of Komagataella pastoris Cytochrome c oxidase in complex with human VMAT2 and Reserpine
Voxel sizeX=Y=Z: 0.664 Å
Density
Contour LevelBy AUTHOR: 0.07
Minimum - Maximum-0.0017636068 - 1.7126286
Average (Standard dev.)0.0010411734 (±0.023896998)
SymmetrySpace group: 1
Details

EMDB XML:

Map geometry
Axis orderXYZ
Origin000
Dimensions480480480
Spacing480480480
CellA=B=C: 318.72 Å
α=β=γ: 90.0 °

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Supplemental data

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Sample components

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Entire : Cytochrome c oxidase-VMAT2-Reserpine PARTICLE

EntireName: Cytochrome c oxidase-VMAT2-Reserpine PARTICLE
Components
  • Complex: Cytochrome c oxidase-VMAT2-Reserpine PARTICLE
    • Protein or peptide: Synaptic vesicular amine transporter
    • Protein or peptide: Cytochrome c oxidase subunit 1
    • Protein or peptide: Cytochrome c oxidase subunit 2
    • Protein or peptide: Cytochrome c oxidase subunit 3
    • Protein or peptide: Cytochrome c oxidase subunit 4
    • Protein or peptide: Cytochrome c oxidase subunit 5
    • Protein or peptide: Cytochrome c oxidase subunit 6
    • Protein or peptide: Cytochrome c oxidase subunit 7
    • Protein or peptide: Cytochrome c oxidase subunit 8
    • Protein or peptide: Cytochrome c oxidase subunit 9
  • Ligand: reserpine
  • Ligand: COPPER (II) ION
  • Ligand: HEME-A
  • Ligand: DINUCLEAR COPPER ION
  • Ligand: PHOSPHATIDYLETHANOLAMINE
  • Ligand: ZINC ION

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Supramolecule #1: Cytochrome c oxidase-VMAT2-Reserpine PARTICLE

SupramoleculeName: Cytochrome c oxidase-VMAT2-Reserpine PARTICLE / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#10
Source (natural)Organism: Homo sapiens (human)
Molecular weightTheoretical: 225 KDa

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Macromolecule #1: Synaptic vesicular amine transporter

MacromoleculeName: Synaptic vesicular amine transporter / type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO
Source (natural)Organism: Homo sapiens (human)
Molecular weightTheoretical: 55.749352 KDa
Recombinant expressionOrganism: Komagataella pastoris (fungus)
SequenceString: MALSELALVR WLQESRRSRK LILFIVFLAL LLDNMLLTVV VPIIPSYLYS IKHEKNATEI QTARPVHTAS ISDSFQSIFS YYDNSTMVT GNATRDLTLH QTATQHMVTN ASAVPSDCPS EDKDLLNENV QVGLLFASKA TVQLITNPFI GLLTNRIGYP I PIFAGFCI ...String:
MALSELALVR WLQESRRSRK LILFIVFLAL LLDNMLLTVV VPIIPSYLYS IKHEKNATEI QTARPVHTAS ISDSFQSIFS YYDNSTMVT GNATRDLTLH QTATQHMVTN ASAVPSDCPS EDKDLLNENV QVGLLFASKA TVQLITNPFI GLLTNRIGYP I PIFAGFCI MFVSTIMFAF SSSYAFLLIA RSLQGIGSSC SSVAGMGMLA SVYTDDEERG NVMGIALGGL AMGVLVGPPF GS VLYEFVG KTAPFLVLAA LVLLDGAIQL FVLQPSRVQP ESQKGTPLTT LLKDPYILIA AGSICFANMG IAMLEPALPI WMM ETMCSR KWQLGVAFLP ASISYLIGTN IFGILAHKMG RWLCALLGMI IVGVSILCIP FAKNIYGLIA PNFGVGFAIG MVDS SMMPI MGYLVDLRHV SVYGSVYAIA DVAFCMGYAI GPSAGGAIAK AIGFPWLMTI IGIIDILFAP LCFFLRSPPA KEEKM AILM DHNCPIKTKM YTQNNIQSYP IGEDEESESD

UniProtKB: Synaptic vesicular amine transporter

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Macromolecule #2: Cytochrome c oxidase subunit 1

MacromoleculeName: Cytochrome c oxidase subunit 1 / type: protein_or_peptide / ID: 2 / Number of copies: 1 / Enantiomer: LEVO
Source (natural)Organism: Komagataella pastoris (fungus)
Molecular weightTheoretical: 58.857352 KDa
SequenceString: MNYINRWLFS TNAKDIAVLY FIFALFCGLL GSIMSLILRL ELSAPGNQIL MGNHQLFNVV ATAHAVLMVF FLVMPAAIGF FGNYLLPLM IGASDMSFAR LNNISFWLLP PALVSLLASA LIENGAGTGW TVYPPLAGVQ SHSGPSVDLA IFALHLTSIS S LLGAINFI ...String:
MNYINRWLFS TNAKDIAVLY FIFALFCGLL GSIMSLILRL ELSAPGNQIL MGNHQLFNVV ATAHAVLMVF FLVMPAAIGF FGNYLLPLM IGASDMSFAR LNNISFWLLP PALVSLLASA LIENGAGTGW TVYPPLAGVQ SHSGPSVDLA IFALHLTSIS S LLGAINFI TTTLNMRTIG MTMSKLPLFV WAVVFTSILL LLSLPVLSAG VTLLLLDRNF NTSFFEPAGG GDPILYQHLF WF FGHPEVY ILIIPGFGII SHIVSTYSKK PVFGAIGMVY AMGSIGFLGL LVWSHHMYTV GLDVDSRAYF TSATMVIAVP TGI KIFSWL ATLYGGSIRY TTPMLYAFAF LFLFTVGGLS GVVLSNASLD IAFHDTYYVI GHFHYVLSLG AVFSLFAGYY YWSP LITGL YYNNNLANIQ FWLLFIGTNV TFFPMHFLGL NGMPRRIPDY PDAFAGWNAI SSFGSLISII SVILFAYVIY DQLVN GLTN KQLSTNSLFK NPDFIESNII FNDNSIKSSS IDFLLTSPPL PHTFNTPAIQ S

UniProtKB: Cytochrome c oxidase subunit 1

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Macromolecule #3: Cytochrome c oxidase subunit 2

MacromoleculeName: Cytochrome c oxidase subunit 2 / type: protein_or_peptide / ID: 3 / Number of copies: 1 / Enantiomer: LEVO
Source (natural)Organism: Komagataella pastoris (fungus)
Molecular weightTheoretical: 26.886889 KDa
SequenceString: DVPTPWGIFF QDSATPNMEG IIELHNNIMF YLVLILTFVS YILYTIIYNY SNATIVHKYM NHGQLIEIVW TTLPAVILLI IAFPSFILL YLCDEVISPA MTIKAIGLQW YWKYEYSDFI NDDGEIVEFE SYVIPEELLE DGQLRLLDVD ASVVVPVDTH I RFIVSSAD ...String:
DVPTPWGIFF QDSATPNMEG IIELHNNIMF YLVLILTFVS YILYTIIYNY SNATIVHKYM NHGQLIEIVW TTLPAVILLI IAFPSFILL YLCDEVISPA MTIKAIGLQW YWKYEYSDFI NDDGEIVEFE SYVIPEELLE DGQLRLLDVD ASVVVPVDTH I RFIVSSAD VIHDFCVPAL GVKVDASPGR LNQTSALIQR EGVYYGQCSE LCGVMHSAMP IKIEAVSLYE FINWLDEQ

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Macromolecule #4: Cytochrome c oxidase subunit 3

MacromoleculeName: Cytochrome c oxidase subunit 3 / type: protein_or_peptide / ID: 4 / Number of copies: 1 / Enantiomer: LEVO
Source (natural)Organism: Komagataella pastoris (fungus)
Molecular weightTheoretical: 30.561145 KDa
SequenceString: MRIQNRENLQ LFPFHLVTNS PWPLTTSLAL MSLALTLGLT MHGYIGNHLW LFLAISLVLS SIFLWVRDVV IEGTYLGDHT IAVRKGLNI GFMLFVLSEI LIFAALFWSY FHSAMGPTIE IGCQWPPVGI TSIKPTELPL LNTIILLASG ATVTWAHHSI L YKDRQGTL ...String:
MRIQNRENLQ LFPFHLVTNS PWPLTTSLAL MSLALTLGLT MHGYIGNHLW LFLAISLVLS SIFLWVRDVV IEGTYLGDHT IAVRKGLNI GFMLFVLSEI LIFAALFWSY FHSAMGPTIE IGCQWPPVGI TSIKPTELPL LNTIILLASG ATVTWAHHSI L YKDRQGTL VGLFITTLLI ILFVGCQVLE YTWATFTIAD SVFGSIFYAG TGLHFIHMVM LIVMLAICYA RMYFYHFTSN HH LGLETTI LYLHVLDIIW LFLYIVFYWW G

UniProtKB: Cytochrome c oxidase subunit 3

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Macromolecule #5: Cytochrome c oxidase subunit 4

MacromoleculeName: Cytochrome c oxidase subunit 4 / type: protein_or_peptide / ID: 5 / Number of copies: 1 / Enantiomer: LEVO
Source (natural)Organism: Komagataella pastoris (fungus)
Molecular weightTheoretical: 12.970557 KDa
SequenceString:
QFKTATSIAE VEGLENLVGP GAKTGTVPTD LEQATGLERY ELLGKLEGIE VFDETPLEAV RKGTMKDPIL IDSYDDYRYV GCTGVPADS HNIEWLKPTT EKNARCWECG SVYKLNFL

UniProtKB: Cytochrome c oxidase subunit 4, mitochondrial

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Macromolecule #6: Cytochrome c oxidase subunit 5

MacromoleculeName: Cytochrome c oxidase subunit 5 / type: protein_or_peptide / ID: 6 / Number of copies: 1 / Enantiomer: LEVO
Source (natural)Organism: Komagataella pastoris (fungus)
Molecular weightTheoretical: 14.51934 KDa
SequenceString:
NATVTNLEKR WEDLPETDQK DIISQLSERQ KLPWKDLTLS EKKAAWYISF GEWGPRRPVH TKEDKLYIFW GTVIGIVISA TIFGAFRYN RNVPKTMNRE WQAASDEYLK SKNAEPFTGY SQIQS

UniProtKB: Cytochrome c oxidase subunit 5B

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Macromolecule #7: Cytochrome c oxidase subunit 6

MacromoleculeName: Cytochrome c oxidase subunit 6 / type: protein_or_peptide / ID: 7 / Number of copies: 1 / Enantiomer: LEVO
Source (natural)Organism: Komagataella pastoris (fungus)
Molecular weightTheoretical: 11.851136 KDa
SequenceString:
EETYEEFSQR YEKEFDEAYD LFEVQRVLNN CFSYDIVPSP AVIGKALNAC RRVNDYATAV RVFEGLKHKV ETKEQYDAYL EELKDVREE LGIDLKEELF P

UniProtKB: Cytochrome c oxidase subunit 6, mitochondrial

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Macromolecule #8: Cytochrome c oxidase subunit 7

MacromoleculeName: Cytochrome c oxidase subunit 7 / type: protein_or_peptide / ID: 8 / Number of copies: 1 / Enantiomer: LEVO
Source (natural)Organism: Komagataella pastoris (fungus)
Molecular weightTheoretical: 6.573613 KDa
SequenceString:
TATEKIIELQ KFYQSTNKPI YAAHPRSKYY LIPYFGLLGV SVAATLFYTG RACFGIKD

UniProtKB: Cytochrome c oxidase subunit 7

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Macromolecule #9: Cytochrome c oxidase subunit 8

MacromoleculeName: Cytochrome c oxidase subunit 8 / type: protein_or_peptide / ID: 9 / Number of copies: 1 / Enantiomer: LEVO
Source (natural)Organism: Komagataella pastoris (fungus)
Molecular weightTheoretical: 5.456455 KDa
SequenceString:
DVGPYSNLPF KVKNRRVPYA VPHFLFFAIG MGIPFFACYV QLKRSGSI

UniProtKB: Cytochrome c oxidase subunit 8, mitochondrial

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Macromolecule #10: Cytochrome c oxidase subunit 9

MacromoleculeName: Cytochrome c oxidase subunit 9 / type: protein_or_peptide / ID: 10 / Number of copies: 1 / Enantiomer: LEVO
Source (natural)Organism: Komagataella pastoris (fungus)
Molecular weightTheoretical: 6.490561 KDa
SequenceString:
SLTRIQGSVK RRILTDISVG LTLGFGFASY WWWGVHKPTV AHRENYYIEL AKKKKA

UniProtKB: Cytochrome c oxidase subunit 9, mitochondrial

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Macromolecule #11: reserpine

MacromoleculeName: reserpine / type: ligand / ID: 11 / Number of copies: 1 / Formula: YHR
Molecular weightTheoretical: 608.679 Da
Chemical component information

ChemComp-YHR:
reserpine

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Macromolecule #12: COPPER (II) ION

MacromoleculeName: COPPER (II) ION / type: ligand / ID: 12 / Number of copies: 1 / Formula: CU
Molecular weightTheoretical: 63.546 Da
Chemical component information

ChemComp-CU:
COPPER (II) ION

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Macromolecule #13: HEME-A

MacromoleculeName: HEME-A / type: ligand / ID: 13 / Number of copies: 2 / Formula: HEA
Molecular weightTheoretical: 852.837 Da
Chemical component information

ChemComp-HEA:
HEME-A

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Macromolecule #14: DINUCLEAR COPPER ION

MacromoleculeName: DINUCLEAR COPPER ION / type: ligand / ID: 14 / Number of copies: 1 / Formula: CUA
Molecular weightTheoretical: 127.092 Da
Chemical component information

ChemComp-CUA:
DINUCLEAR COPPER ION

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Macromolecule #15: PHOSPHATIDYLETHANOLAMINE

MacromoleculeName: PHOSPHATIDYLETHANOLAMINE / type: ligand / ID: 15 / Number of copies: 4 / Formula: PTY
Molecular weightTheoretical: 734.039 Da
Chemical component information

ChemComp-PTY:
PHOSPHATIDYLETHANOLAMINE / phospholipid*YM

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Macromolecule #16: ZINC ION

MacromoleculeName: ZINC ION / type: ligand / ID: 16 / Number of copies: 1 / Formula: ZN
Molecular weightTheoretical: 65.409 Da

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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

Concentration5 mg/mL
BufferpH: 8
GridModel: Quantifoil R1.2/1.3 / Material: COPPER / Mesh: 300 / Support film - Material: CARBON / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 60 sec.
VitrificationCryogen name: ETHANE / Chamber humidity: 90 % / Chamber temperature: 281 K / Instrument: LEICA EM GP

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Electron microscopy

MicroscopeFEI TITAN KRIOS
TemperatureMin: 63.0 K / Max: 77.0 K
Specialist opticsEnergy filter - Name: GIF Bioquantum / Energy filter - Slit width: 20 eV
Image recordingFilm or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Digitization - Dimensions - Width: 5760 pixel / Digitization - Dimensions - Height: 4092 pixel / Number grids imaged: 1 / Average exposure time: 2.0 sec. / Average electron dose: 50.0 e/Å2
Electron beamAcceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN
Electron opticsC2 aperture diameter: 50.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.0 µm / Nominal defocus min: 1.0 µm / Nominal magnification: 130000
Sample stageSpecimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER
Experimental equipment
Model: Titan Krios / Image courtesy: FEI Company

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Image processing

Startup modelType of model: NONE
Final reconstructionApplied symmetry - Point group: C1 (asymmetric) / Algorithm: SIMULTANEOUS ITERATIVE (SIRT) / Resolution.type: BY AUTHOR / Resolution: 3.14 Å / Resolution method: FSC 0.143 CUT-OFF / Software - Name: cryoSPARC / Number images used: 61624
Initial angle assignmentType: MAXIMUM LIKELIHOOD / Software - Name: cryoSPARC
Final angle assignmentType: MAXIMUM LIKELIHOOD / Software - Name: cryoSPARC

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