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

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

MOS2, a protein containing G-patch and KOW motifs, is essential for innate immunity in Arabidopsis thaliana.

Smad6 is a protein kinase X phosphorylation substrate and is required for HL-60 cell differentiation.

Global, in vivo, and site-specific phosphorylation dynamics in signaling networks.

Combining protein-based IMAC, peptide-based IMAC, and MudPIT for efficient phosphoproteomic analysis.

A quantitative atlas of mitotic phosphorylation.

Lys-N and trypsin cover complementary parts of the phosphoproteome in a refined SCX-based approach.

Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions.

Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis.

Genome-wide YFP fluorescence complementation screen identifies new regulators for telomere signaling in human cells.

Initial characterization of the human central proteome.

Next-generation sequencing to generate interactome datasets.

G-patch domain and KOW motifs-containing protein, GPKOW; a nuclear RNA-binding protein regulated by protein kinase A.

Dynamic protein-protein interaction wiring of the human spliceosome.

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.

GPKOW is essential for pre-mRNA splicing in vitro and suppresses splicing defect caused by dominant-negative DHX16 mutation in vivo.

A proteome-scale map of the human interactome network.

Site-specific mapping of the human SUMO proteome reveals co-modification with phosphorylation.

Architecture of the human interactome defines protein communities and disease networks.

Variant in the X-chromosome spliceosomal gene GPKOW causes male-lethal microcephaly with intrauterine growth restriction.

Histone Interaction Landscapes Visualized by Crosslinking Mass Spectrometry in Intact Cell Nuclei.

Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations.

A reference map of the human binary protein interactome.

Structure of the activated human minor spliceosome.

Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.

Systematic identification of post-transcriptional regulatory modules.

Multimodal cell maps as a foundation for structural and functional genomics.

C-terminal frameshift variants in GPKOW are associated with a multisystemic X-linked disorder.

Long-range map of a 3.5-Mb region in Xp11.23-22 with a sequence-ready map from a 1.1-Mb gene-rich interval.

Formation of the Spliceosomal B* complex

Formation of the Spliceosomal Bact complex

NS5 interacts with Spliceosome

UniProtKB Q92917 GPKOW_HUMAN

GPKOW source access and interpretation guide

GPKOW incoming contexts and original source joins

GPKOW UniProt record: Q92917