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An Open Library of Human Kinase Domain Constructs for Automated Bacterial Expression
- Authors
- Albanese, Steven KyleParton, Daniel LawrenceIsik, MehtapRodriguez-Laureano, Lucelenie7 more author(s)...
- Description
Source code, assay data, full expression results for all ABL1 constructs, wild-type kinases, and ABL1 and SRC mutants, plasmid libraries, and other supporting material for the generation of a library of human kinase domain constructs for automated bacterial expression. From the publication abstract, "Kinases play a critical role in cellular signaling and are dysregulated in a number of diseases,...
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Bacteria/metabolismBinding sitesEscherichia coli/metabolismPhosphorylationProtein Structure, SecondaryProtein-Tyrosine KinasesProto-Oncogene Proteins c-ablsrc-Family Kinases
- Access Rights
- Free to AllFee Required
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Binding Modes of Ligands Using Enhanced Sampling (BLUES): Rapid Decorrelation of Ligand Binding Modes via Nonequilibrium Candidate Monte Carlo
- Authors
- Gill, SamuelLim, NathanGrinaway, PatrickRustenburg, Ariën4 more author(s)...
- Description
Accurately predicting protein-ligand binding affinities and binding modes is a major goal in computational chemistry, but even the prediction of ligand binding modes in proteins poses major challenges. Here, we focus on solving the binding mode prediction problem for rigid fragments. That is, we focus on computing the dominant placement, conformation, and orientations of a relatively rigid, fragment-like...
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Binding sites
- Access Rights
- Free to All
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Cellular states, clonal dynamics, and evolution in Pearson syndrome revealed via single-cell multi-omics [Celline_scATAC]
- Authors
- Lareau, Caleb A.Ludwig, Leif S.
- Description
Summary from GEO: "Large deletions in mitochondrial DNA (mtDNA) have been linked to a variety of clinical pathologies, including somatic emergence in congenital disorders such as Pearson Syndrome (MIM:557000), a mitochondrial disease characterized by sideroblastic anemia and exocrine pancreas dysfunction. Here, we develop a multi-omics approach to quantify mtDNA deletion heteroplasmy and cell state...
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Anemia, SideroblasticBinding sitesFibroblastsGenomicsHeteroplasmy/geneticsMyelodysplastic SyndromesSingle-Cell Analysis
- Access Rights
- Free to All
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Cellular states, clonal dynamics, and evolution in Pearson syndrome revealed via single-cell multi-omics [PBMC_scATAC]
- Authors
- Lareau, Caleb A.Ludwig, Leif S.
- Description
Summary from GEO: "Large deletions in mitochondrial DNA (mtDNA) have been linked to a variety of clinical pathologies, including somatic emergence in congenital disorders such as Pearson Syndrome (MIM:557000), a mitochondrial disease characterized by sideroblastic anemia and exocrine pancreas dysfunction. Here, we develop a multi-omics approach to quantify mtDNA deletion heteroplasmy and cell state...
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Anemia, SideroblasticBinding sitesGenomicsHeteroplasmy/geneticsLeukocytes, MononuclearMyelodysplastic SyndromesSingle-Cell Analysis
- Access Rights
- Free to All
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A double negative post-transcriptional regulatory circuit mediates the virgin behavioral state
- Authors
- Garaulet, Daniel L.Moro, AlbertomariaLai, Eric C
- Description
Summary from GEO: "The survival and reproductive success of animals depends on the ability to harmonize their external behaviors with their internal states. For example, females conduct numerous social programs that are distinctive to virgins compared to post-mated and/or pregnant individuals. In Drosophila, the fact that the post-mating switch is initiated by seminal factors implies the default...
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Binding sitesMutationRNA-SeqSexual Behavior, AnimalTranscription Factors
- Access Rights
- Free to All
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STAT4 promotes Bhlhe40 induction to drive protective IFN-g from natural killer cells during viral infection [STAT4 CUT&RUN]
- Authors
- Kim, HyunuSun, Joseph C.
- Description
Summary from GEO: "NK cells represent a cellular component of the mammalian innate immune system, and mount rapid responses against viral infection, including the secretion of the potent anti-viral effector cytokine IFN-g. Following mouse cytomegalovirus (MCMV) infection, Bhlhe40 was the most highly induced transcription factor in NK cells among the basic helix-loop-helix family. Bhlhe40 upregulation...
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Basic Helix-Loop-Helix Transcription FactorsBinding sitesChromatin Immunoprecipitation SequencingInterferon-gammaInterleukin-12Interleukin-18Killer Cells, NaturalMouse CytomegalovirusSTAT4 Transcription Factor
- Access Rights
- Free to All
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STAT4 promotes Bhlhe40 induction to drive protective IFN-g from natural killer cells during viral infection [BHLHE40 CUT&RUN]
- Authors
- Kim, HyunuSun, Joseph C.
- Description
Summary from GEO: "NK cells represent a cellular component of the mammalian innate immune system, and mount rapid responses against viral infection, including the secretion of the potent anti-viral effector cytokine IFN-g. Following mouse cytomegalovirus (MCMV) infection, Bhlhe40 was the most highly induced transcription factor in NK cells among the basic helix-loop-helix family. Bhlhe40 upregulation...
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Basic Helix-Loop-Helix Transcription FactorsBinding sitesChromatin Immunoprecipitation SequencingInterferon-gammaInterleukin-12Interleukin-18Killer Cells, NaturalMouse CytomegalovirusSTAT4 Transcription Factor
- Access Rights
- Free to All
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RNA-seq identifies differential expressed genes upon YTHDC1 knockdown in MOLM13 human acute myeloid leukemia cells
- Authors
- Cheng, YuanmingChu, KarenKharas, Michael G.
- Description
Summary from GEO: "The goal of this study is to identify differential expressed genes upon YTHDC1 depletion in MOLM13 cells(AML)." Overall design from GEO: "RNAs were purified from MOLM13 cells transduced with control and YTHDC1 shRNAs and then used for RNA-seq."
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Binding sitesLeukemia, Myeloid, AcuteNuclear ProteinsRNA-Binding ProteinsRNA-Seq
- Access Rights
- Free to All
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YTHDC1-Hyper tribe uncover YTHDC1 binding sites in human leukemia cells
- Authors
- Cheng, YuanmingChu, KarenKharas, Michael G.
- Description
Summary from GEO: "The goal of this study is to identify YTHDC1 binding targets in MOLM13 cells(AML)." Overall design from GEO: "MOLM-13 cells overexpressing YTHDC1-ADAR fusion or empty vector for 48 hours were harvested for RNA-seq to look for A-G editing events."
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Adenosine DeaminaseBinding sitesLeukemia, Myeloid, AcuteNuclear ProteinsRNA-Binding ProteinsRNA-Seq
- Access Rights
- Free to All
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ChIP-Seq in DU-145 (ATCC HTB-81) Prostate Cancer Cells of FOSL1, TAZ, TEAD1, YAP
- Authors
- Chen, YuKhurana, EktaWong, Chen KhuanXu, Duo
- Description
Summary from GEO: "Genome-wide mapping of FOSL1, YAP, TAZ and TEAD1 binding sites in DU145 cells." Overall design from GEO: "Genome occupancy profiling of FOSL1, YAP, TAZ, and TEAD1 was performed in DU145 cells."
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Binding sitesChromatin Immunoprecipitation SequencingChromosome MappingProstatic Neoplasms
- Access Rights
- Free to All