Evidence map›Paper›PMID 32914530›Full record

ArticleProtein science : a publication of the Protein Society2020

Structural characterization and computational analysis of PDZ domains in Monosiga brevicollis.

Melody Gao, Iain G P Mackley, Samaneh Mesbahi-Vasey, Haley A Bamonte, Sarah A Struyvenberg, Louisa Landolt, Nick J Pederson, Lucy I Williams, Christopher D Bahl, Lionel Brooks and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Protein science : a publication of the Protein Society, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.4field-weighted citation impact, top 40% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 11 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Melody GaoDepartment of Chemistry, Western Washington University, Bellingham, Washington, USA.
Iain G P MackleyDepartment of Chemistry, Western Washington University, Bellingham, Washington, USA.
Samaneh Mesbahi-VaseyInstitute for Protein Innovation, Boston, Massachusetts, USA.
Haley A BamonteDepartment of Chemistry, Western Washington University, Bellingham, Washington, USA.
Sarah A StruyvenbergDepartment of Chemistry, Western Washington University, Bellingham, Washington, USA.
Louisa LandoltDepartment of Chemistry, Western Washington University, Bellingham, Washington, USA.
Nick J PedersonDepartment of Chemistry, Western Washington University, Bellingham, Washington, USA.
Lucy I WilliamsDepartment of Chemistry, Western Washington University, Bellingham, Washington, USA.
Christopher D BahlInstitute for Protein Innovation, Boston, Massachusetts, USA.ORCID 0000-0002-3652-3693
Lionel BrooksDepartment of Biology, Western Washington University, Bellingham, Washington, USA.
Jeanine F AmacherDepartment of Chemistry, Western Washington University, Bellingham, Washington, USA.ORCID 0000-0002-3646-7521
Western Washington University · USBoston Children's Hospital · US

Funding

Pilatus 6mS10OD021832 · OD · UNIVERSITY OF CALIFORNIA BERKELEY · PI ADAMS, PAUL DAVID · 2016 to 2016
$980k
Howard Hughes Medical InstituteNIH HHS S10 OD021832NIH HHS S10OD021832
6 · The paper itself

Abstract

Identification of the molecular networks that facilitated the evolution of multicellular animals from their unicellular ancestors is a fundamental problem in evolutionary cellular biology. Choanoflagellates are recognized as the closest extant nonmetazoan ancestors to animals. These unicellular eukaryotes can adopt a multicellular-like "rosette" state. Therefore, they are compelling models for the study of early multicellularity. Comparative studies revealed that a number of putative human orthologs are present in choanoflagellate genomes, suggesting that a subset of these genes were necessary for the emergence of multicellularity. However, previous work is largely based on sequence alignments alone, which does not confirm structural nor functional similarity. Here, we focus on the PDZ domain, a peptide-binding domain which plays critical roles in myriad cellular signaling networks and which underwent a gene family expansion in metazoan lineages. Using a customized sequence similarity search algorithm, we identified 178 PDZ domains in the Monosiga brevicollis proteome. This includes 11 previously unidentified sequences, which we analyzed using Rosetta and homology modeling. To assess conservation of protein structure, we solved high-resolution crystal structures of representative M. brevicollis PDZ domains that are homologous to human Dlg1 PDZ2, Dlg1 PDZ3, GIPC, and SHANK1 PDZ domains. To assess functional conservation, we calculated binding affinities for mbGIPC, mbSHANK1, mbSNX27, and mbDLG-3 PDZ domains from M. brevicollis. Overall, we find that peptide selectivity is generally conserved between these two disparate organisms, with one possible exception, mbDLG-3. Overall, our results provide novel insight into signaling pathways in a choanoflagellate model of primitive multicellularity.

Indexed as

AlgorithmsModels, MolecularPDZ DomainsSequence Analysis, ProteinChoanoflagellataCrystallography, X-RayDatabases, ProteinProtozoan ProteinsProtozoan Proteinsbinding affinitieschoanoflagellatesevolutionmotifsPDZpeptide-binding domainsprotein-protein interactionsselectivity determinantsX-ray crystallography

Identifiers

PMID32914530
PMCPMC7586902
OpenAlexW3085292324

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.