Target type: molecularfunction
Binding to phosphatidylinositol-5-phosphate, a derivative of phosphatidylinositol in which the inositol ring is phosphorylated at the 5' position. [GOC:bf, GOC:tair_curators]
Phosphatidylinositol-5-phosphate (PIP5) binding is a crucial molecular function in cellular signaling and membrane dynamics. PIP5, a phospholipid located within the inner leaflet of the plasma membrane, acts as a signaling molecule, attracting proteins that possess PIP5-binding domains. These proteins, often referred to as PIP5 effectors, are involved in a wide range of cellular processes including:
- **Membrane trafficking:** PIP5 binding regulates the movement of vesicles and organelles within the cell. This includes endocytosis (internalization of molecules from the extracellular environment), exocytosis (release of molecules outside the cell), and protein sorting.
- **Signal transduction:** PIP5 acts as a signaling hub, recruiting and activating downstream signaling molecules. This leads to activation of various signaling pathways, such as the PI3K-AKT pathway, which plays a vital role in cell survival, growth, and proliferation.
- **Cytoskeletal organization:** PIP5 binding influences the organization and dynamics of the actin cytoskeleton, which provides structural support and mediates cell movement, adhesion, and division.
- **Enzyme activation:** PIP5 can directly activate certain enzymes by providing a binding site or by altering their conformation.
The interaction between PIP5 and its effectors is highly specific. These proteins contain specialized domains, such as PH (pleckstrin homology) domains, that bind to the 5-phosphate group of PIP5 with high affinity. The strength of this interaction can be modulated by factors such as the concentration of PIP5, the presence of other lipids, and the phosphorylation state of the effector protein.
Overall, phosphatidylinositol-5-phosphate binding is a multifaceted process that plays a critical role in regulating a diverse array of cellular processes. Its involvement in membrane trafficking, signal transduction, cytoskeletal organization, and enzyme activation underscores its importance in maintaining cellular homeostasis and function.'
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Protein | Definition | Taxonomy |
---|---|---|
Cytosolic phospholipase A2 | A cytosolic phospholipase A2 that is encoded in the genome of cow. [OMA:A4IFJ5, PRO:DNx] | Bos taurus (cattle) |
Cytosolic phospholipase A2 | A cytosolic phospholipase A2 that is encoded in the genome of human. [PRO:DNx, UniProtKB:P47712] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
ici 204,219 | zafirlukast: a leukotriene D4 receptor antagonist | carbamate ester; indoles; N-sulfonylcarboxamide | anti-asthmatic agent; leukotriene antagonist |
arachidonyltrifluoromethane | AACOCF3 : A fatty acid derivative that is arachidonic acid in which the OH part of the carboxy group has been replaced by a trifluoromethyl group arachidonyltrifluoromethane: structure given in first source; inhibits 85-kDa phospholipase A2 | fatty acid derivative; ketone; olefinic compound; organofluorine compound | EC 3.1.1.4 (phospholipase A2) inhibitor |
amentoflavone | biflavonoid; hydroxyflavone; ring assembly | angiogenesis inhibitor; antiviral agent; cathepsin B inhibitor; P450 inhibitor; plant metabolite | |
ochnaflavone | ochnaflavone : A biflavonoid with an ether linkage between the B-rings of the apigenin and luteolin subunits. It has been isolated from several members of the Ochnaceae plant family. ochnaflavone: from Lonicera japonica; structure given in first source | aromatic ether; biflavonoid; hydroxyflavone | anti-inflammatory agent; antiatherogenic agent; antibacterial agent; EC 3.1.1.4 (phospholipase A2) inhibitor; leukotriene antagonist; plant metabolite |
efipladib | efipladib: structure in first source | ||
methyl arachidonylfluorophosphonate | phosphonic ester | ||
pyrrophenone | pyrrophenone: structure in first source |