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

Electronic Gene Ontology annotations created by ARBA machine learning models

Preso, a novel PSD-95-interacting FERM and PDZ domain protein that regulates dendritic spine morphogenesis.

Structural basis for interaction between the conserved cell polarity proteins Inscuteable and Leu-Gly-Asn repeat-enriched protein (LGN).

Large-scale interaction profiling of PDZ domains through proteomic peptide-phage display using human and viral phage peptidomes.

FRMPD4 mutations cause X-linked intellectual disability and disrupt dendritic spine morphogenesis.

Proteome-wide analysis of phospho-regulated PDZ domain interactions.

Host PDZ-containing proteins targeted by SARS-CoV-2.

Quantitative fragmentomics allow affinity mapping of interactomes.

Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro.

Complete sequencing and characterization of 21,243 full-length human cDNAs.

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

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

Preso1 dynamically regulates group I metabotropic glutamate receptors.

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.

Structural basis for the recognition of the scaffold protein Frmpd4/Preso1 by the TPR domain of the adaptor protein LGN.

FRMPD4 original annotation contexts, source measurements and genuine mapping

FRMPD4 quantitative fragment interaction audit