Page last updated: 2024-10-24

wide pore channel activity

Definition

Target type: molecularfunction

Enables the transport of a solute across a membrane via a large pore, un-gated channel. Examples include gap junctions, which transport substances from one cell to another; and porins which transport substances in and out of bacteria, mitochondria and chloroplasts. [GOC:mtg_transport, ISBN:0815340729]

Wide pore channel activity refers to the ability of a protein channel to allow the passage of large molecules or ions through a cellular membrane. This type of channel typically has a larger diameter than other types of channels, and it may be selective for specific molecules or ions. The molecular function of wide pore channels is complex and involves several key steps:

1. **Binding and Recognition:** The channel protein contains a binding site that specifically recognizes and binds to the target molecule or ion. This binding event is often triggered by a specific signal, such as a change in membrane potential or the presence of a ligand.
2. **Conformational Change:** Upon binding, the channel protein undergoes a conformational change that opens the pore, allowing the target molecule or ion to pass through. This change in conformation can be triggered by a variety of mechanisms, including the binding of a ligand, phosphorylation, or changes in the membrane environment.
3. **Passage Through the Pore:** Once the pore is open, the target molecule or ion can diffuse through the channel. The size and shape of the pore determine which molecules can pass through. Wide pore channels allow the passage of larger molecules than other types of channels, such as small ions or water molecules.
4. **Release and Reset:** After the target molecule or ion has passed through the pore, the channel protein returns to its closed conformation, preventing further passage. This reset step is essential for maintaining the integrity of the cell and for regulating the flow of molecules across the membrane.

Wide pore channels are involved in a wide variety of cellular processes, including:

* **Transport of macromolecules:** Wide pore channels are essential for the transport of large molecules, such as proteins, nucleic acids, and polysaccharides, across cell membranes. This transport is essential for processes such as protein synthesis, signaling, and cell-cell communication.
* **Nutrient uptake:** Wide pore channels can be involved in the uptake of nutrients, such as amino acids, sugars, and fatty acids, from the extracellular environment. This uptake is essential for cellular metabolism and growth.
* **Waste removal:** Wide pore channels can also be involved in the removal of waste products from the cell. This removal is essential for maintaining cellular homeostasis and preventing the accumulation of toxic substances.
* **Signaling:** Wide pore channels can be involved in signaling pathways by allowing the passage of signaling molecules across cell membranes. This signaling is important for a wide range of cellular processes, including cell growth, differentiation, and apoptosis.

In summary, wide pore channel activity is a complex molecular function that involves a series of steps, including binding, conformational change, passage, and release. These channels are essential for a wide range of cellular processes, including transport, signaling, and nutrient uptake.'
"

Proteins (3)

ProteinDefinitionTaxonomy
Pannexin-1A pannexin-1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q96RD7]Homo sapiens (human)
Macrophage-expressed gene 1 proteinA macrophage-expressed gene 1 protein that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q2M385]Homo sapiens (human)
Gasdermin-DA gasdermin-D that is encoded in the genome of human. [PRO:DNx, UniProtKB:P57764]Homo sapiens (human)

Compounds (7)

CompoundDefinitionClassesRoles
disulfiramorganic disulfide;
organosulfur acaricide
angiogenesis inhibitor;
antineoplastic agent;
apoptosis inducer;
EC 1.2.1.3 [aldehyde dehydrogenase (NAD(+))] inhibitor;
EC 3.1.1.1 (carboxylesterase) inhibitor;
EC 3.1.1.8 (cholinesterase) inhibitor;
EC 5.99.1.2 (DNA topoisomerase) inhibitor;
ferroptosis inducer;
fungicide;
NF-kappaB inhibitor
embelinembelin : A member of the class of dihydroxy-1,4-benzoquinones that is 2,5-dihydroxy-1,4-benzoquinone which is substituted by an undecyl group at position 3. Isolated from Lysimachia punctata and Embelia ribes, it exhibits antimicrobial, antineoplastic and inhibitory activity towards hepatitis C protease.

embelin: from Embelia fruit (Myrsinaceae)
dihydroxy-1,4-benzoquinonesantimicrobial agent;
antineoplastic agent;
hepatitis C protease inhibitor;
plant metabolite
probenecidprobenecid : A sulfonamide in which the nitrogen of 4-sulfamoylbenzoic acid is substituted with two propyl groups.

Probenecid: The prototypical uricosuric agent. It inhibits the renal excretion of organic anions and reduces tubular reabsorption of urate. Probenecid has also been used to treat patients with renal impairment, and, because it reduces the renal tubular excretion of other drugs, has been used as an adjunct to antibacterial therapy.
benzoic acids;
sulfonamide
uricosuric drug
ditiocarbdiethyldithiocarbamic acid : A member of the class of dithiocarbamic acids that is diethylcarbamic acid in which both of the oxygens are replaced by sulfur.

Ditiocarb: A chelating agent that has been used to mobilize toxic metals from the tissues of humans and experimental animals. It is the main metabolite of DISULFIRAM.
dithiocarbamic acidschelator;
copper chelator
rapanonerapanone: antiparasitic agent from Rapanea; structure similar to embelindihydroxy-1,4-benzoquinones
5-o-methylembelin5-O-methyl embelin : A member of the class of monohydroxy-1,4-benzoquinones that is embelin in which the hydroxy group at position 5 is replaced by a methoxy group. Isolated from Lysimachia punctata and Embelia ribes, it exhibits antileishmanial activity as well as inhibitory activity towards hepatitis C protease.

5-O-methylembelin: extracted from mangrove Aegiceras corniculatum; piscicide; see embelin
enol ether;
monohydroxy-1,4-benzoquinones
antileishmanial agent;
antineoplastic agent;
hepatitis C protease inhibitor;
metabolite
l 6635363-[3-(tert-butylsulfanyl)-1-(4-chlorobenzyl)-5-(propan-2-yl)-1H-indol-2-yl]-2,2-dimethylpropanoic acid : A member of the class of indoles that is 1H-indole substituted by a isopropyl group at position 5, a tert-butylsulfanediyl group at position 3, a 4-chlorobenzyl group at position 1 and a 2-carboxy-2-methylpropyl group at position 2. It acts as an inhibitor of arachidonate 5-lipoxygenase.

MK-886: orally active leukotriene biosynthesis inhibitor
aryl sulfide;
indoles;
monocarboxylic acid;
monochlorobenzenes
antineoplastic agent;
EC 1.13.11.34 (arachidonate 5-lipoxygenase) inhibitor;
leukotriene antagonist