Page last updated: 2024-10-24

heparan sulfate binding

Definition

Target type: molecularfunction

Binding to heparan sulfate. [GO_REF:0000067, GOC:TermGenie, PMID:8567685]

Heparan sulfate (HS) binding is a crucial molecular interaction that plays a vital role in diverse biological processes, including cell signaling, adhesion, and development. HS is a highly sulfated glycosaminoglycan (GAG) found on the cell surface and in the extracellular matrix. The unique structural features of HS, including its variable sulfation patterns and chain length, enable it to bind to a wide array of proteins with high specificity.

The molecular function of HS binding can be summarized as follows:

1. **Ligand Binding and Recruitment:** HS acts as a docking site for a vast array of signaling molecules, growth factors, and extracellular matrix proteins. It binds to specific protein domains, such as the heparin-binding domain, present on these molecules, facilitating their recruitment to the cell surface or ECM.

2. **Signal Transduction and Regulation:** Upon ligand binding, HS can initiate or modulate signal transduction pathways. For example, HS can cluster growth factors, increasing their local concentration and enhancing their interaction with cell surface receptors. This can lead to the activation of downstream signaling cascades, ultimately influencing cell proliferation, migration, and differentiation.

3. **Cellular Adhesion and Migration:** HS contributes to cell-cell and cell-matrix interactions by binding to adhesion molecules like integrins and cadherins. This binding can stabilize cell-cell junctions, regulate cell migration, and promote tissue organization.

4. **Modulation of Protein Activity:** HS can influence the activity of proteins by binding to specific sites and altering their conformation or interactions with other molecules. For instance, HS can modulate the enzymatic activity of certain enzymes or inhibit protein-protein interactions.

5. **Extracellular Matrix Organization:** HS plays a critical role in the organization and function of the ECM. It interacts with various ECM components, such as collagens and laminins, contributing to tissue structure and stability.

6. **Viral and Bacterial Infection:** HS can serve as a receptor for viruses and bacteria, facilitating their attachment and entry into host cells. For example, some viruses use HS as a co-receptor for entry into cells.

Overall, heparan sulfate binding is a highly versatile and essential molecular interaction that governs a wide range of biological processes. Its ability to bind to numerous proteins with high specificity makes it a crucial player in cell signaling, adhesion, development, and many other cellular functions.
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Proteins (2)

ProteinDefinitionTaxonomy
Peptidyl-prolyl cis-trans isomerase A A peptidyl-prolyl cis-trans isomerase A that is encoded in the genome of human. [PRO:DNx, UniProtKB:P62937]Homo sapiens (human)
FurinA furin that is encoded in the genome of human. [PRO:CNA, UniProtKB:P09958]Homo sapiens (human)

Compounds (14)

CompoundDefinitionClassesRoles
diminazenediminazene : A triazene derivative that is triazene in which each of the terminal nitrogens is substituted by a 4-carbamimidoylphenyl group.

Diminazene: An effective trypanocidal agent.
carboxamidine;
triazene derivative
antiparasitic agent;
trypanocidal drug
camostatcamostat : A benzoate ester resulting from the formal condensation of the carboxy group of 4-guanidinobenzoic acid with the hydroxy group of 2-(dimethylamino)-2-oxoethyl (4-hydroxyphenyl)acetate. It is a potent inhibitor of the human transmembrane protease serine 2 (TMPRSS2) and its mesylate salt is currently under investigation for its effectiveness in COVID-19 patients.benzoate ester;
carboxylic ester;
diester;
guanidines;
tertiary carboxamide
anti-inflammatory agent;
anticoronaviral agent;
antifibrinolytic drug;
antihypertensive agent;
antineoplastic agent;
antiviral agent;
serine protease inhibitor
2,4-pyridinedicarboxylic acidlutidinic acid : A pyridinedicarboxylic acid carrying carboxy groups at positions 2 and 4.pyridinedicarboxylic acid
daminozidedaminozide: induces tumorsstraight-chain fatty acid
prolinalpyrrolidines
oxalylglycineN-oxalylglycine : An amino dicarboxylic acid that is iminodiacetic acid with an oxo substituent. It is used as an inhibitor of alpha-ketoglutarate dependent (EC 1.14.11.*) enzymes.

oxalylglycine: structure given in first source
amino dicarboxylic acid;
N-acylglycine
EC 1.14.11.* (oxidoreductase acting on paired donors, 2-oxoglutarate as one donor, incorporating 1 atom each of oxygen into both donors) inhibitor
cyclosporineramihyphin A: one of the metabolites produced by Fusarium sp. S-435; RN given refers to cpd with unknown MFhomodetic cyclic peptideanti-asthmatic drug;
anticoronaviral agent;
antifungal agent;
antirheumatic drug;
carcinogenic agent;
dermatologic drug;
EC 3.1.3.16 (phosphoprotein phosphatase) inhibitor;
geroprotector;
immunosuppressive agent;
metabolite
sanglifehrin asanglifehrin A: binds cyclophilin A; isolated from Streptomyces; structure in first source
(melle-4)cyclosporin(melle-4)cyclosporin: a non-immunosuppressive analog of cyclosporin A
cyclosporin gcyclosporin G: similar immunosuppressive actions as cyclosporin, but without nephrotoxic side effects; cyclosporin A analog; MW 1217
scy-635
n,n-(4-xylylidene)bisaminoguanidineN,N-(4-xylylidene)bisaminoguanidine: RN in Chemline for di-HCl: 7044-24-8; RN for unspecified HCl: 62580-72-7

N,N'-(p-xylylidene)bis(aminoguanidine) : A guanidine derivative comprised of two carbamimidamido (guanidino) groups, each linked via one of their amino nitrogens to the imino nitrogens of 1,4-phenylenedimethanimine.
alisporiviralisporivir: nonimmunosuppressive cyclosporin analog; structure/sequence in first sourcehomodetic cyclic peptideanticoronaviral agent
5-(5-nitrothiazol-2-ylthio)-1,3,4-thiadiazol-2-amine5-(5-nitrothiazol-2-ylthio)-1,3,4-thiadiazol-2-amine: structure in first source

halicin : A member of the class of thiadiazoles that is 1,3,4-thiadiazol-2-amine which is substituted by a (5-nitro-1,3-thiazol-2-yl)sulfanediyl group at position 5. It is a c-Jun N-terminal kinase inhibitor (IC50 = 0.7uM) and exhibits antibacterial properties.
1,3-thiazoles;
C-nitro compound;
organic sulfide;
primary amino compound;
thiadiazoles
antibacterial agent;
c-Jun N-terminal kinase inhibitor