Gene Ontology annotation through association of InterPro records with GO terms
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
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
Combined Automated Annotation using Multiple IEA Methods
An isoform-specific PDZ-binding motif targets type I PIP5 kinase beta to the uropod and controls polarization of neutrophil-like HL60 cells.
Type I phosphatidylinositol-4-phosphate 5-kinases are distinct members of this novel lipid kinase family.
Synthesis of PIPs at the plasma membrane
PI(3,4)P2 is phosphorylated to PI(3,4,5)P3 by PIP5K1A-C at the plasma membrane
PI is phosphorylated to PI5P by PIP5K1A/B at the plasma membrane
PI4P is phosphorylated to PI(4,5)P2 by PIP5K1A-C at the plasma membrane
PI3P is phosphorylated to PI(3,5)P2 by PIP5K1A/B at the plasma membrane
PI3P is phosphorylated to PI(3,4)P2 by PIP4K2/5K1 at the plasma membrane
Phosphorylated DVL recruits PIP5K1B to the plasma membrane
DVL-associated PIP5K1B phosphorylates PI4P to PI(4,5)P2
PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling
Clathrin and phosphatidylinositol-4,5-bisphosphate regulate autophagic lysosome reformation.
Clathrin and phosphatidylinositol-4,5-bisphosphate regulate autophagic lysosome reformation | Nature Cell Biology
Falcon deep research report for PIP5K1B
UniProt record for human PIP5K1B
Proteostasis Network autophagy-lysosome pathway mappings