Target type: molecularfunction
Binding to syndecan, an integral membrane proteoglycan (250-300 kDa) associated largely with epithelial cells. [GOC:go_curators, PMID:9355727]
Syndecan binding is a molecular interaction that involves the binding of a protein or other molecule to a syndecan. Syndecans are a family of transmembrane proteins that play a critical role in cell signaling, adhesion, and migration. They are characterized by their extracellular domain, which contains a variable number of glycosaminoglycan (GAG) chains, typically heparan sulfate. These GAG chains are highly sulfated and can bind to a variety of ligands, including growth factors, chemokines, and extracellular matrix components.
Syndecan binding can be mediated by a variety of mechanisms, including direct interactions between the protein and the GAG chains, interactions with protein-binding domains in the syndecan core protein, or interactions with other molecules that are bound to the syndecan.
The molecular function of syndecan binding is diverse and depends on the specific ligand and context. In general, syndecan binding can:
* **Regulate cell signaling:** By binding to growth factors, chemokines, and other signaling molecules, syndecans can influence cell proliferation, differentiation, and migration.
* **Mediate cell adhesion:** Syndecans can interact with extracellular matrix components, such as collagen and fibronectin, to promote cell adhesion and anchorage.
* **Modulate inflammation:** Syndecans can bind to inflammatory mediators, such as cytokines and chemokines, and contribute to the regulation of inflammatory responses.
* **Promote angiogenesis:** Syndecans can bind to growth factors that stimulate blood vessel formation, contributing to angiogenesis.
* **Facilitate viral entry:** Some viruses, such as HIV, use syndecans as receptors for entry into cells.
The specific molecular function of syndecan binding is further determined by the type of syndecan involved, the specific ligand, and the cellular context. For example, syndecan-1 is known to bind to fibroblast growth factor (FGF) and promote FGF-mediated signaling. Syndecan-4, on the other hand, is involved in cell adhesion and migration through interactions with extracellular matrix components.
Overall, syndecan binding is a crucial molecular interaction that plays a central role in various cellular processes. By regulating cell signaling, adhesion, and migration, syndecan binding contributes to tissue development, wound healing, inflammation, and cancer progression.'
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Protein | Definition | Taxonomy |
---|---|---|
Heparanase | A heparanase that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q9Y251] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
astemizole | astemizole : A piperidine compound having a 2-(4-methoxyphenyl)ethyl group at the 1-position and an N-[(4-fluorobenzyl)benzimidazol-2-yl]amino group at the 4-position. Astemizole: Antihistamine drug now withdrawn from the market in many countries because of rare but potentially fatal side effects. | benzimidazoles; piperidines | anti-allergic agent; anticoronaviral agent; H1-receptor antagonist |
cisapride | cisapride : The amide resulting from formal condensation of 4-amino-5-chloro-2-methoxybenzoic acid with cis-1-[3-(4-fluorophenoxy)propyl]-3-methoxypiperidin-4-amine. It has been used (as its monohydrate or as its tartrate) for the treatment of gastro-oesophageal reflux disease and for non-ulcer dyspepsia, but its propensity to cause cardiac arrhythmias resulted in its complete withdrawal from many countries, including the U.K., and restrictions on its use elsewhere. Cisapride: A substituted benzamide used for its prokinetic properties. It is used in the management of gastroesophageal reflux disease, functional dyspepsia, and other disorders associated with impaired gastrointestinal motility. (Martindale The Extra Pharmacopoeia, 31st ed) | benzamides | |
labetalol | 2-hydroxy-5-{1-hydroxy-2-[(4-phenylbutan-2-yl)amino]ethyl}benzamide : A member of the class of benzamides that is benzamide substituted by a hydroxy group at position 2 and by a 1-hydroxy-2-[(4-phenylbutan-2-yl)amino]ethyl group at position 5. labetalol : A diastereoisomeric mixture of approximately equal amounts of all four possible stereoisomers ((R,S)-labetolol, (S,R)-labetolol, (S,S)-labetalol and (R,R)-labetalol). It is an adrenergic antagonist used to treat high blood pressure. Labetalol: A salicylamide derivative that is a non-cardioselective blocker of BETA-ADRENERGIC RECEPTORS and ALPHA-1 ADRENERGIC RECEPTORS. | benzamides; benzenes; phenols; primary carboxamide; salicylamides; secondary alcohol; secondary amino compound | |
hesperidin | hesperidin : A disaccharide derivative that consists of hesperetin substituted by a 6-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranosyl moiety at position 7 via a glycosidic linkage. Hesperidin: A flavanone glycoside found in CITRUS fruit peels. | 3'-hydroxyflavanones; 4'-methoxyflavanones; dihydroxyflavanone; disaccharide derivative; flavanone glycoside; monomethoxyflavanone; rutinoside | mutagen |
metergoline | metergoline : An ergoline alkaloid that is the N-benzyloxycarbonyl derivative of lysergamine. A 5-HT2 antagonist. Also 5-HT1 antagonist and 5-HT1D ligand. Has moderate affinity for 5-HT6 and high affinity for 5-HT7. Metergoline: A dopamine agonist and serotonin antagonist. It has been used similarly to BROMOCRIPTINE as a dopamine agonist and also for MIGRAINE DISORDERS therapy. | carbamate ester; ergoline alkaloid | dopamine agonist; geroprotector; serotonergic antagonist |
naringin | (2S)-flavan-4-one; 4'-hydroxyflavanones; dihydroxyflavanone; disaccharide derivative; neohesperidoside | anti-inflammatory agent; antineoplastic agent; metabolite | |
amodiaquine hydrochloride | |||
phosphomannopentaose sulfate | phosphomannopentaose sulfate: structure in first source | ||
rk 682 | |||
pg 545 | PG 545: an anti-angiogenesis agent with heparanase inhibitory activity; structure in first source |