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Ask your administrator if you think this is wrong. ======= PPBP ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: PPBP * **<color #00a2e8>Official Name</color>**: pro-platelet basic protein * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=5473|5473]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/P02775|P02775]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=PPBP&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20PPBP|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/121010|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: N/A * **<color #00a2e8>UniProt Summary</color>**: LA-PF4 stimulates DNA synthesis, mitosis, glycolysis, intracellular cAMP accumulation, prostaglandin E2 secretion, and synthesis of hyaluronic acid and sulfated glycosaminoglycan. It also stimulates the formation and secretion of plasminogen activator by human synovial cells. NAP-2 is a ligand for CXCR1 and CXCR2, and NAP-2, NAP-2(73), NAP-2(74), NAP-2(1-66), and most potent NAP-2(1-63) are chemoattractants and activators for neutrophils. TC-1 and TC-2 are antibacterial proteins, in vitro released from activated platelet alpha-granules. CTAP-III(1-81) is more potent than CTAP-III desensitize chemokine-induced neutrophil activation. {ECO:0000269|PubMed:10877842, ECO:0000269|PubMed:7890771, ECO:0000269|PubMed:8950790, ECO:0000269|PubMed:9794434}. <button type='primary' size='sm' modal='Pfam_Domains'>Pfam Domains</button> <button type='primary' size='sm' modal='GO_terms'>GO Terms</button> <modal id='Pfam_Domains' size='lg' title='Pfam Domains'> |IL8| </modal> <modal id='GO_terms' size='lg' title='GO Terms'> |glucose transmembrane transporter activity| |glucose transmembrane transport| |hexose transmembrane transport| |monosaccharide transmembrane transport| |carbohydrate transmembrane transport| |chemokine activity| |tertiary granule lumen| |antimicrobial humoral immune response mediated by antimicrobial peptide| |platelet alpha granule lumen| |carbohydrate transport| |chemokine-mediated signaling pathway| |neutrophil chemotaxis| |positive regulation of cell division| |granulocyte chemotaxis| |cellular response to chemokine| |response to chemokine| |neutrophil migration| |granulocyte migration| |antimicrobial humoral response| |myeloid leukocyte migration| |platelet degranulation| |leukocyte chemotaxis| |growth factor activity| |regulation of cell division| |cellular response to lipopolysaccharide| |cellular response to molecule of bacterial origin| |cell chemotaxis| |cellular response to biotic stimulus| |response to lipopolysaccharide| |response to molecule of bacterial origin| |defense response to bacterium| |humoral immune response| |leukocyte migration| |neutrophil degranulation| |neutrophil activation involved in immune response| |neutrophil mediated immunity| |inflammatory response| |neutrophil activation| |granulocyte activation| |leukocyte degranulation| |myeloid leukocyte mediated immunity| |cellular response to lipid| |myeloid cell activation involved in immune response| |chemotaxis| |taxis| |myeloid leukocyte activation| |leukocyte activation involved in immune response| |cell activation involved in immune response| |cytokine-mediated signaling pathway| |response to bacterium| |regulated exocytosis| |leukocyte mediated immunity| |exocytosis| |response to lipid| |leukocyte activation| |defense response to other organism| |cell migration| |secretion by cell| |cellular response to cytokine stimulus| |export from cell| |cellular response to oxygen-containing compound| |cell activation| |localization of cell| |cell motility| |immune effector process| |response to cytokine| |secretion| |transmembrane transport| |response to other organism| |response to external biotic stimulus| |locomotion| |G protein-coupled receptor signaling pathway| |response to biotic stimulus| |defense response| |movement of cell or subcellular component| |response to oxygen-containing compound| |extracellular space| |immune response| |extracellular region| |vesicle-mediated transport| </modal> \\ === CRISPR Data === <button type='primary' size='small' modal='Compound_Hit'>Compound Hit</button> <button type='default' size='small' modal='Most_Correlated_Genes'>Most Correlated Genes in Chemogenomics</button> <button type='primary' size='small' modal='Essential_Avana'>Tissues where Essential in the Avana Dataset (DepMap 20Q1)</button> <modal id='Compound_Hit' size='lg' title='Compound Hit'> ^Screen^Score^ |[[:results:exp502|Milciclib 2μM R08 exp502]]|-1.78| |[[:results:exp246|UM0011500 10μM R05 exp246]]|1.77| </modal> <modal id='Most_Correlated_Genes' size='lg' title='Most Correlated Genes in Chemogenomics'> No correlation found to any other genes in chemogenomics. </modal> <modal id='Essential_Avana' size='lg' title='Tissues where Essential in the Avana Dataset (DepMap 20Q1)'> Global Fraction of Cell Lines Where Essential: 0/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/26| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/16| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| </modal> == Essentiality in NALM6 == * **<color #00a2e8>Essentiality Rank</color>**: 17477 * **<color #00a2e8>Expression level (log2 read counts)</color>**: -7.68 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='PPBP Expression in NALM6 Cells: -7.68'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2026/01/07 22:36by 127.0.0.1