Basic Information
Gene Structure
Domain
Regulation&
Interaction
Annotation
Orthologus Group
Pathway
Basic Information
Gene ID
gene-IMY05_C4832000200
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Position
JAEQKX010001017.1:4923-6183 (-)
1260bp
Gene Type
gene
Gene Description (Protein Product)
Pleckstrin homology domain
Organism
Salix suchowensis
Also AS

Gene Structure

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Domain
Database EntryID E-Value Start end InterPro ID Description

Regulation&Interaction
Protein-protein interaction (PPI)
gene-IMY05_C4907000200 COG4 transport protein
gene-IMY05_C5091000300 The proteasome is a multicatalytic proteinase complex which is characterized by its ability to cleave peptides with Arg, Phe, Tyr, Leu, and Glu adjacent to the leaving group at neutral or slightly basic pH

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Annotation

Orthologous Group
Orthologous ID Species Number All hits in PereRegDB Hits of this species Orthologous Detail


Pathway
Go Pathway KEGG Pathway
GO Term Description GO Category
GO:0001558 regulation of cell growth BP
GO:0003674 molecular_function MF
GO:0005488 binding MF
GO:0005543 phospholipid binding MF
GO:0005547 phosphatidylinositol-3,4,5-trisphosphate binding MF
GO:0005575 cellular_component CC
GO:0005622 intracellular anatomical structure CC
GO:0005623 obsolete cell CC
GO:0005737 cytoplasm CC
GO:0005938 cell cortex CC
GO:0006810 transport BP
GO:0006886 intracellular protein transport BP
GO:0007163 establishment or maintenance of cell polarity BP
GO:0008104 protein localization BP
GO:0008150 biological_process BP
GO:0008289 lipid binding MF
GO:0008360 regulation of cell shape BP
GO:0009987 cellular process BP
GO:0015031 protein transport BP
GO:0015833 peptide transport BP
GO:0016192 vesicle-mediated transport BP
GO:0022603 regulation of anatomical structure morphogenesis BP
GO:0022604 regulation of cell morphogenesis BP
GO:0023052 signaling BP
GO:0030010 establishment of cell polarity BP
GO:0032153 cell division site CC
GO:0033036 macromolecule localization BP
GO:0034613 protein localization BP
GO:0035091 phosphatidylinositol binding MF
GO:0040008 regulation of growth BP
GO:0042886 amide transport BP
GO:0043167 ion binding MF
GO:0043168 anion binding MF
GO:0044424 obsolete intracellular part CC
GO:0044444 obsolete cytoplasmic part CC
GO:0044448 obsolete cell cortex part CC
GO:0044464 obsolete cell part CC
GO:0045184 establishment of protein localization BP
GO:0046907 intracellular transport BP
GO:0050789 regulation of biological process BP
GO:0050793 regulation of developmental process BP
GO:0050794 regulation of cellular process BP
GO:0051128 regulation of cellular component organization BP
GO:0051179 localization BP
GO:0051234 establishment of localization BP
GO:0051285 cell cortex of cell tip CC
GO:0051286 cell tip CC
GO:0051523 cell growth mode switching, monopolar to bipolar BP
GO:0051641 cellular localization BP
GO:0051649 establishment of localization in cell BP
GO:0061171 establishment of bipolar cell polarity BP
GO:0061389 regulation of direction of cell growth BP
GO:0065007 biological regulation BP
GO:0065008 regulation of biological quality BP
GO:0070727 cellular macromolecule localization BP
GO:0071702 organic substance transport BP
GO:0071705 nitrogen compound transport BP
GO:0071944 cell periphery CC
GO:0099568 cytoplasmic region CC
GO:0099738 cell cortex region CC
GO:1901981 phosphatidylinositol phosphate binding MF
KEGG Term Name Description
map04144 Endocytosis Endocytosis is a mechanism for cells to remove ligands, nutrients, and plasma membrane (PM) proteins, and lipids from the cell surface, bringing them into the cell interior. Transmembrane proteins entering through clathrin-dependent endocytosis (CDE) have sequences in their cytoplasmic domains that bind to the APs (adaptor-related protein complexes) and enable their rapid removal from the PM. In addition to APs and clathrin, there are numerous accessory proteins including dynamin. Depending on the various proteins that enter the endosome membrane, these cargoes are sorted to distinct destinations. Some cargoes, such as nutrient receptors, are recycled back to the PM. Ubiquitylated membrane proteins, such as activated growth-factor receptors, are sorted into intraluminal vesicles and eventually end up in the lysosome lumen via multivesicular endosomes (MVEs). There are distinct mechanisms of clathrin-independent endocytosis (CIE) depending upon the cargo and the cell type.