The distribution of somatic H1 subtypes is non-random on active vs. inactive chromatin: distribution in human fetal fibroblasts.
The human and mouse replication-dependent histone genes.
The DNA sequence and analysis of human chromosome 6.
Human SirT1 interacts with histone H1 and promotes formation of facultative heterochromatin.
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
H1 family histones in the nucleus. Control of binding and localization by the C-terminal domain.
HP1 binds specifically to Lys26-methylated histone H1.4, whereas simultaneous Ser27 phosphorylation blocks HP1 binding.
The consensus coding sequences of human breast and colorectal cancers.
Global, in vivo, and site-specific phosphorylation dynamics in signaling networks.
Systematic identification of SH3 domain-mediated human protein-protein interactions by peptide array target screening.
L3MBTL1, a histone-methylation-dependent chromatin lock.
A quantitative atlas of mitotic phosphorylation.
Kinase-selective enrichment enables quantitative phosphoproteomics of the kinome across the cell cycle.
Dynamic Histone H1 Isotype 4 Methylation and Demethylation by Histone Lysine Methyltransferase G9a/KMT1C and the Jumonji Domain-containing JMJD2/KDM4 Proteins.
Isolation and characterization of two human H1 histone genes within clusters of core histone genes.
Lys-N and trypsin cover complementary parts of the phosphoproteome in a refined SCX-based approach.
Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis.
Initial characterization of the human central proteome.
System-wide temporal characterization of the proteome and phosphoproteome of human embryonic stem cell differentiation.
Isoform-specific phosphorylation of human linker histone H1.4 in mitosis by the kinase Aurora B.
Protein kinase A-mediated serine 35 phosphorylation dissociates histone H1.4 from mitotic chromosome.
Comparative large scale characterization of plant versus mammal proteins reveals similar and idiosyncratic N-α-acetylation features.
A dual role of linker histone H1.4 Lys 34 acetylation in transcriptional activation.
The mRNA-bound proteome and its global occupancy profile on protein-coding transcripts.
N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB.
Toward a comprehensive characterization of a human cancer cell phosphoproteome.
An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.
N-terminome analysis of the human mitochondrial proteome.
Serine is a new target residue for endogenous ADP-ribosylation on histones.
Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability.
Architecture of the human interactome defines protein communities and disease networks.
Site-specific regulation of histone H1 phosphorylation in pluripotent cell differentiation.
Histone Interaction Landscapes Visualized by Crosslinking Mass Spectrometry in Intact Cell Nuclei.
Lysine benzoylation is a histone mark regulated by SIRT2.
Mechanistic and structural studies of KDM-catalysed demethylation of histone 1 isotype 4 at lysine 26.
Distinct Structures and Dynamics of Chromatosomes with Different Human Linker Histone Isoforms.
Site-Specific Phosphorylation of Histone H1.4 Is Associated with Transcription Activation.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Interactomes of SARS-CoV-2 and human coronaviruses reveal host factors potentially affecting pathogenesis.
Isonicotinylation is a histone mark induced by the anti-tuberculosis first-line drug isoniazid.
Mutations of the histone linker H1-4 in neurodevelopmental disorders and functional characterization of neurons expressing C-terminus frameshift mutant H1.4.
SARS-CoV-2 nucleocapsid protein binds host mRNAs and attenuates stress granules to impair host stress response.
Histone lysine methacrylation is a dynamic post-translational modification regulated by HAT1 and SIRT2.
OpenCell: Endogenous tagging for the cartography of human cellular organization.
Histone H1 binding to nucleosome arrays depends on linker DNA length and trajectory.
A comprehensive SARS-CoV-2-human protein-protein interactome reveals COVID-19 pathobiology and potential host therapeutic targets.
Protein interaction studies in human induced neurons indicate convergent biology underlying autism spectrum disorders.
Human spleen histone H1. Isolation and amino acid sequence of a main variant, H1b.
Imaging analysis of six human histone H1 variants reveals universal enrichment of H1.2, H1.3, and H1.5 at the nuclear periphery and nucleolar H1X presence.
Histone H1 deamidation facilitates chromatin relaxation for DNA repair.
CRAMP1 drives linker histone expression to enable Polycomb repression.
CRAMP1-dependent histone H1 biogenesis is essential for topoisomerase II inhibitor tolerance.
Gene Ontology annotation through association of InterPro records with GO terms
Annotation inferences using phylogenetic trees
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
Gene Ontology annotation based on curation of immunofluorescence data
Electronic Gene Ontology annotations created by ARBA machine learning models
Combined Automated Annotation using Multiple IEA Methods
H1-4 source evidence and context qualification