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ZENODO
Dataset . 2024
License: CC BY
Data sources: ZENODO
image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
ZENODO
Dataset . 2024
License: CC BY
Data sources: ZENODO
ZENODO
Dataset . 2024
License: CC BY
Data sources: Datacite
ZENODO
Dataset . 2024
License: CC BY
Data sources: Datacite
ZENODO
Dataset . 2024
License: CC BY
Data sources: Datacite
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CB2 Receptor Signaling Complexes with Beta-Arrestin-2 and Gi Protein

Authors: Abrol, Ravinder; Heo, Eun Ha;

CB2 Receptor Signaling Complexes with Beta-Arrestin-2 and Gi Protein

Abstract

CB2 receptor signaling complexes with beta-arrestin-2 and Gi proteinEun Ha Heo and Ravinder Abrol (CSUN)11/27/2024 (Zenodo) System names as filename prefixes: CB2R-WT-NoPhosphoC_BARR2_*: wildtype CB2 receptor without phosphorylated C-terminus bound to beta-arrestin-2. CB2R-WT-NoPhosphoC_Gi-Empty_*: wildtype CB2 receptor without phosphorylated C-terminus bound to nucleotide-free Gi protein (no GDP). CB2R-WT-NoPhosphoC_Gi-GDP_*: wildtype CB2 receptor without phosphorylated C-terminus bound to Gi-GDP. CB2R-WT-PhosphoC_BARR2_*: wildtype CB2 receptor with a phosphorylated C-terminus bound to beta-arrestin-2. CB2R-Q63R-NoPhosphoC_BARR2_*: CB2 receptor mutant Q63R without phosphorylated C-terminus bound to beta-arrestin-2. CB2R-Q63R-NoPhosphoC_Gi-Empty_*: CB2 receptor mutant Q63R without phosphorylated C-terminus bound to nucleotide-free Gi protein (no GDP). CB2R-Q63R-NoPhosphoC_Gi-GDP_*: CB2 receptor mutant Q63R without phosphorylated C-terminus bound to Gi-GDP. CB2R-Q63R-PhosphoC_BARR2_*: CB2 receptor mutant Q63R with a phosphorylated C-terminus bound to beta-arrestin-2. CB2R-L133I-NoPhosphoC_BARR2_*: CB2 receptor mutant L133I without phosphorylated C-terminus bound to beta-arrestin-2. CB2R-L133I-NoPhosphoC_Gi-Empty_*: CB2 receptor mutant L133I without phosphorylated C-terminus bound to nucleotide-free Gi protein (no GDP). CB2R-L133I-NoPhosphoC_Gi-GDP_*: CB2 receptor mutant L133I without phosphorylated C-terminus bound to Gi-GDP. CB2R-L133I-PhosphoC_BARR2_*: CB2 receptor L133I mutant with a phosphorylated C-terminus bound to beta-arrestin-2. Different file types in following folders when uncompressed: Folder: PDB files for signaling complex starting and average structures*_md.pdb: Solvated complex structures used as starting geometries.*_avgframe#.pdb: PDB file of average frame given by #. Folder: MD simulation input files for Amber MD*_md.inpcrd: input coordinates file for MD job*_md.prmtop: parameter and topology file for MD jobStep1_mini_solv.in: mdin file for energy minimization of solvent keeping protein fixed.Step2_equi_solv.in: mdin file for NPT equilibration of solvent while keeping protein fixed.Step3_mini_full.in: mdin file for energy minimization of whole system.Step4_heat_full.in: mdin file for heating system under NPT of whole system.Step5_equi_full.in: mdin file for NPT equilibration of whole system.Step6_prod_full.in: mdin file for 100ns production NPT equilibration of whole system. Step7a_prod_full.in: mdin file for 500ns production NPT equilibration of whole system.Step7b_prod_full.in: mdin file for 500ns production NPT equilibration of whole system.Step7c_prod_full.in: mdin file for 500ns production NPT equilibration of whole system.Step7d_prod_full.in: mdin file for 500ns production NPT equilibration of whole system. Folder: MD trajectories*_step7_ai_stride10.xtc: Trajectory file in Gromacs xtc format.

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
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