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- EMDB-44945: 5HT2AR-miniGq heterotrimer in complex with a novel agonist obtain... -

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Basic information

Entry
Database: EMDB / ID: EMD-44945
Title5HT2AR-miniGq heterotrimer in complex with a novel agonist obtained from large scale docking local map
Map data
Sample
  • Complex: Active state complex of 5HT2AR with mini-Gq heterotrimer stabilized by scFv16
Keywordsactive state GPCR / heterotrimer / complex / serotonin / MEMBRANE PROTEIN
Biological speciesHomo sapiens (human)
Methodsingle particle reconstruction / cryo EM / Resolution: 2.9 Å
AuthorsGumpper RH / Wang L / Kapolka N / Skiniotis G / Roth BL
Funding support United States, 1 items
OrganizationGrant numberCountry
Defense Advanced Research Projects Agency (DARPA)HR0011-20-2-0029 United States
CitationJournal: Science / Year: 2024
Title: AlphaFold2 structures guide prospective ligand discovery.
Authors: Jiankun Lyu / Nicholas Kapolka / Ryan Gumpper / Assaf Alon / Liang Wang / Manish K Jain / Ximena Barros-Álvarez / Kensuke Sakamoto / Yoojoong Kim / Jeffrey DiBerto / Kuglae Kim / Isabella S ...Authors: Jiankun Lyu / Nicholas Kapolka / Ryan Gumpper / Assaf Alon / Liang Wang / Manish K Jain / Ximena Barros-Álvarez / Kensuke Sakamoto / Yoojoong Kim / Jeffrey DiBerto / Kuglae Kim / Isabella S Glenn / Tia A Tummino / Sijie Huang / John J Irwin / Olga O Tarkhanova / Yurii Moroz / Georgios Skiniotis / Andrew C Kruse / Brian K Shoichet / Bryan L Roth /
Abstract: AlphaFold2 (AF2) models have had wide impact but mixed success in retrospective ligand recognition. We prospectively docked large libraries against unrefined AF2 models of the σ and serotonin 2A (5- ...AlphaFold2 (AF2) models have had wide impact but mixed success in retrospective ligand recognition. We prospectively docked large libraries against unrefined AF2 models of the σ and serotonin 2A (5-HT2A) receptors, testing hundreds of new molecules and comparing results with those obtained from docking against the experimental structures. Hit rates were high and similar for the experimental and AF2 structures, as were affinities. Success in docking against the AF2 models was achieved despite differences between orthosteric residue conformations in the AF2 models and the experimental structures. Determination of the cryo-electron microscopy structure for one of the more potent 5-HT2A ligands from the AF2 docking revealed residue accommodations that resembled the AF2 prediction. AF2 models may sample conformations that differ from experimental structures but remain low energy and relevant for ligand discovery, extending the domain of structure-based drug design.
History
DepositionMay 20, 2024-
Header (metadata) releaseMay 21, 2025-
Map releaseMay 21, 2025-
UpdateMay 21, 2025-
Current statusMay 21, 2025Processing site: RCSB / Status: Released

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Structure visualization

Supplemental images

Downloads & links

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Map

FileDownload / File: emd_44945.map.gz / Format: CCP4 / Size: 244.1 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.)
0.87 Å/pix.
x 400 pix.
= 347.2 Å
0.87 Å/pix.
x 400 pix.
= 347.2 Å
0.87 Å/pix.
x 400 pix.
= 347.2 Å

Surface

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Images are generated by Spider.

Voxel sizeX=Y=Z: 0.868 Å
Density
Contour LevelBy AUTHOR: 0.293
Minimum - Maximum-2.4140933 - 3.6886513
Average (Standard dev.)-0.00019558248 (±0.034038994)
SymmetrySpace group: 1
Details

EMDB XML:

Map geometry
Axis orderXYZ
Origin000
Dimensions400400400
Spacing400400400
CellA=B=C: 347.19998 Å
α=β=γ: 90.0 °

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Supplemental data

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Half map: #1

Fileemd_44945_half_map_1.map
Projections & Slices
AxesZYX

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Half map: #2

Fileemd_44945_half_map_2.map
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Sample components

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Entire : Active state complex of 5HT2AR with mini-Gq heterotrimer stabiliz...

EntireName: Active state complex of 5HT2AR with mini-Gq heterotrimer stabilized by scFv16
Components
  • Complex: Active state complex of 5HT2AR with mini-Gq heterotrimer stabilized by scFv16

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Supramolecule #1: Active state complex of 5HT2AR with mini-Gq heterotrimer stabiliz...

SupramoleculeName: Active state complex of 5HT2AR with mini-Gq heterotrimer stabilized by scFv16
type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#5
Source (natural)Organism: Homo sapiens (human)

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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: 7.4
VitrificationCryogen name: ETHANE-PROPANE

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Electron microscopy

MicroscopeFEI TITAN KRIOS
Image recordingFilm or detector model: GATAN K3 (6k x 4k) / Average electron dose: 50.0 e/Å2
Electron beamAcceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN
Electron opticsIllumination mode: OTHER / Imaging mode: OTHER / Nominal defocus max: 20.0 µm / Nominal defocus min: 5.0 µm
Experimental equipment
Model: Titan Krios / Image courtesy: FEI Company

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Image processing

CTF correctionType: PHASE FLIPPING AND AMPLITUDE CORRECTION
Startup modelType of model: PDB ENTRY
PDB model - PDB ID:
Final reconstructionResolution.type: BY AUTHOR / Resolution: 2.9 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 220509
Initial angle assignmentType: MAXIMUM LIKELIHOOD
Final angle assignmentType: MAXIMUM LIKELIHOOD

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