Target type: molecularfunction
Binding to suramin, a naphthalenesulfonic acid compound which is used in the treatment of diseases caused by trypanosomes and worms. [GOC:jl, Wikipedia:Suramin]
Suramin is a polysulfonated naphthylurea derivative that acts as a potent inhibitor of a variety of biological processes, including enzyme activity, signal transduction, and cell growth. Its molecular function primarily revolves around its ability to bind to and interfere with the activity of various protein targets.
One of the key mechanisms of suramin binding is its interaction with negatively charged molecules and sites, such as sulfates, phosphates, and carboxylates. This characteristic allows it to bind to a wide range of protein targets, including growth factors, enzymes, and receptors.
For instance, suramin has been shown to bind to and inhibit the activity of several kinases, such as the epidermal growth factor receptor (EGFR) and the platelet-derived growth factor receptor (PDGFR). This inhibition occurs through competitive binding to the ATP-binding site of these kinases, thereby preventing their phosphorylation activity and downstream signaling pathways.
Furthermore, suramin can bind to and interfere with the function of other important proteins involved in cell growth and proliferation. For example, it can bind to and inhibit the activity of the fibroblast growth factor receptor (FGFR) and the vascular endothelial growth factor receptor (VEGFR), which are critical for angiogenesis and tumor growth.
Beyond its interaction with receptor tyrosine kinases, suramin can also bind to and inhibit the activity of other enzymes, including trypanosome enzymes like trypanothione reductase and trypanosome RNA polymerase. This inhibitory action is attributed to its binding to the active site of these enzymes, effectively blocking their catalytic activity.
In addition to its direct binding to protein targets, suramin can also form complexes with other molecules, such as heparin, which enhances its affinity and specificity for certain proteins.
In summary, the molecular function of suramin binding is multifaceted and involves its interaction with various protein targets, including kinases, growth factor receptors, and other enzymes. This interaction disrupts their activity, leading to the inhibition of cell growth, signaling pathways, and other biological processes. The binding mechanisms involve electrostatic interactions with negatively charged residues on protein targets, as well as the formation of complexes with other molecules.'
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Protein | Definition | Taxonomy |
---|---|---|
Ryanodine receptor 2 | A ryanodine receptor 2 that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q92736] | Homo sapiens (human) |
P2X purinoceptor 1 | A P2X purinoceptor 1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:P51575] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
pyridoxal phosphate | pyridoxal 5'-phosphate : The monophosphate ester obtained by condensation of phosphoric acid with the primary hydroxy group of pyridoxal. Pyridoxal Phosphate: This is the active form of VITAMIN B 6 serving as a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. During transamination of amino acids, pyridoxal phosphate is transiently converted into pyridoxamine phosphate (PYRIDOXAMINE). | methylpyridines; monohydroxypyridine; pyridinecarbaldehyde; vitamin B6 phosphate | coenzyme; cofactor; EC 2.7.7.7 (DNA-directed DNA polymerase) inhibitor; Escherichia coli metabolite; human metabolite; mouse metabolite; Saccharomyces cerevisiae metabolite |
adenosine diphosphate | Adenosine Diphosphate: Adenosine 5'-(trihydrogen diphosphate). An adenine nucleotide containing two phosphate groups esterified to the sugar moiety at the 5'-position. | adenosine 5'-phosphate; purine ribonucleoside 5'-diphosphate | fundamental metabolite; human metabolite |
diadenosine tetraphosphate | P(1),P(4)-bis(5'-adenosyl) tetraphosphate : A diadenosyl tetraphosphate compound having the two 5'-adenosyl residues attached at the P(1)- and P(4)-positions. | diadenosyl tetraphosphate | Escherichia coli metabolite; mouse metabolite |
arylid | |||
5'-adenylyl (beta,gamma-methylene)diphosphonate | 5'-adenylyl (beta,gamma-methylene)diphosphonate: do not confuse with alpha,beta-methyleneadenosine 5'-triphosphate | nucleoside triphosphate analogue | |
alpha,beta-methyleneadenosine 5'-triphosphate | alpha,beta-methyleneadenosine 5'-triphosphate: do not confuse with beta,gamma-methylene ATP; RN given refers to parent cpd | nucleoside triphosphate analogue | |
adenosine 5'-o-(3-thiotriphosphate) | adenosine 5'-[gamma-thio]triphosphate : A nucleoside triphosphate analogue that is ATP in which one of the oxygens attached to 3-phosphate group is replaced by sulfur. adenosine 5'-O-(3-thiotriphosphate): RN given refers to cpd with unspecified locant for thio group; see also records for 1-thio & 2-thio-isomers | nucleoside triphosphate analogue | |
8-azidoadenosine 5'-triphosphate | |||
6-thioinosine-5'-triphosphate | organic molecule | ||
imd 0354 | N-(3,5-bis(trifluoromethyl)phenyl)-5-chloro-2-hydroxybenzamide: a cardioprotective agent that inhibits IkappaB kinase beta (IKKbeta); structure in first source | benzamides | |
2-methylthio-atp | 2-methylthio-ATP: purinergic receptors agonist; relaxes mammalian gut preparations; structure given in first source | ||
adp beta s | adenosine 5'-O-(2-thiodiphosphate): partial agonist toward platelet aggregation; see also record for 1-thiodiphosphate cpd | ||
nf023 | |||
nf 449 | |||
chlorantranilipole | chlorantranilipole: anthranilic diamide insecticide.that disrupts mating in codling moth (Lepidoptera: Tortricidae) chlorantraniliprole : A carboxamide resulting from the formal condensation of the carboxylic acid group of 3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylic acid with the primary amino group of 2-amino-5-chloro-N,3-dimethylbenzamide. The first of the anthranilic diamide insecticides, it is a ryanodine receptor activator and is used to protect a wide variety of crops, including corn, cotton, grapes, rice and potatoes. | monochlorobenzenes; organobromine compound; pyrazole insecticide; pyrazoles; pyridines; secondary carboxamide | ryanodine receptor agonist |
af 353 | 5-(5-iodo-2-isopropyl-4-methoxyphenoxy)pyrimidine-2,4-diamine: a P2X3 and P2X2/3 receptor antagonist; structure in first source |