<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Cohan MC</submitter><funding>NINDS NIH HHS</funding><funding>National Institutes of Health</funding><funding>National Science Foundation</funding><pagination>167373</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10178624</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>434(2)</volume><pubmed_abstract>Sequence-ensemble relationships of intrinsically disordered proteins (IDPs) are governed by binary patterns such as the linear clustering or mixing of specific residues or residue types with respect to one another. To enable the discovery of potentially important, shared patterns across sequence families, we describe a computational method referred to as NARDINI for Non-random Arrangement of Residues in Disordered Regions Inferred using Numerical Intermixing. This work was partially motivated by the observation that parameters that are currently in use for describing different binary patterns are not interoperable across IDPs of different amino acid compositions and lengths. In NARDINI, we generate an ensemble of scrambled sequences to set up a composition-specific null model for the patte</pubmed_abstract><journal>Journal of molecular biology</journal><pubmed_title>Uncovering Non-random Binary Patterns Within Sequences of Intrinsically Disordered Proteins.</pubmed_title><pmcid>PMC10178624</pmcid><funding_grant_id>R01 NS056114</funding_grant_id><funding_grant_id>R01 NS121114</funding_grant_id><pubmed_authors>Pappu RV</pubmed_authors><pubmed_authors>Shinn MK</pubmed_authors><pubmed_authors>Lalmansingh JM</pubmed_authors><pubmed_authors>Cohan MC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Uncovering Non-random Binary Patterns Within Sequences of Intrinsically Disordered Proteins.</name><description>Sequence-ensemble relationships of intrinsically disordered proteins (IDPs) are governed by binary patterns such as the linear clustering or mixing of specific residues or residue types with respect to one another. To enable the discovery of potentially important, shared patterns across sequence families, we describe a computational method referred to as NARDINI for Non-random Arrangement of Residues in Disordered Regions Inferred using Numerical Intermixing. This work was partially motivated by the observation that parameters that are currently in use for describing different binary patterns are not interoperable across IDPs of different amino acid compositions and lengths. In NARDINI, we generate an ensemble of scrambled sequences to set up a composition-specific null model for the patte</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2025-04-05T10:54:08.535Z</modification><creation>2025-04-05T10:54:08.535Z</creation></dates><accession>S-EPMC10178624</accession><cross_references><pubmed>34863777</pubmed><doi>10.1016/j.jmb.2021.167373</doi></cross_references></HashMap>