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A common mechanism of Sec61 translocon inhibition by small molecules
by
Itskanov, Samuel
, Blanchard, Nicolas
, Wang, Laurie
, Spiess, Martin
, Sherriff, Rumi
, Hoepfner, Dominic
, Shi, Wei Q.
, Forsyth, Craig
, Junne, Tina
, Xiao, Li
, Park, Eunyong
in
631/45/612/1237
/ 631/535
/ 631/92/609
/ Binding sites
/ Biochemical Engineering
/ Biochemistry
/ Biochemistry, Molecular Biology
/ Biology
/ Bioorganic Chemistry
/ Cell Biology
/ Chemical Sciences
/ Chemistry
/ Chemistry and Materials Science
/ Chemistry/Food Science
/ Depsipeptides - pharmacology
/ Drug development
/ Endoplasmic reticulum
/ Endoplasmic Reticulum - metabolism
/ Humans
/ Inhibitors
/ Life Sciences
/ Lipids
/ Medicinal Chemistry
/ Membrane proteins
/ Membrane Proteins - metabolism
/ Membranes
/ Molecular interactions
/ Plugs
/ Polypeptides
/ Protein transport
/ Protein Transport - physiology
/ Proteins
/ SEC Translocation Channels - antagonists & inhibitors
/ SEC Translocation Channels - chemistry
/ SEC Translocation Channels - metabolism
/ Sulfonamides - pharmacology
/ Therapeutic applications
/ Translocation
/ Triazoles - pharmacology
/ Yeast
2023
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A common mechanism of Sec61 translocon inhibition by small molecules
by
Itskanov, Samuel
, Blanchard, Nicolas
, Wang, Laurie
, Spiess, Martin
, Sherriff, Rumi
, Hoepfner, Dominic
, Shi, Wei Q.
, Forsyth, Craig
, Junne, Tina
, Xiao, Li
, Park, Eunyong
in
631/45/612/1237
/ 631/535
/ 631/92/609
/ Binding sites
/ Biochemical Engineering
/ Biochemistry
/ Biochemistry, Molecular Biology
/ Biology
/ Bioorganic Chemistry
/ Cell Biology
/ Chemical Sciences
/ Chemistry
/ Chemistry and Materials Science
/ Chemistry/Food Science
/ Depsipeptides - pharmacology
/ Drug development
/ Endoplasmic reticulum
/ Endoplasmic Reticulum - metabolism
/ Humans
/ Inhibitors
/ Life Sciences
/ Lipids
/ Medicinal Chemistry
/ Membrane proteins
/ Membrane Proteins - metabolism
/ Membranes
/ Molecular interactions
/ Plugs
/ Polypeptides
/ Protein transport
/ Protein Transport - physiology
/ Proteins
/ SEC Translocation Channels - antagonists & inhibitors
/ SEC Translocation Channels - chemistry
/ SEC Translocation Channels - metabolism
/ Sulfonamides - pharmacology
/ Therapeutic applications
/ Translocation
/ Triazoles - pharmacology
/ Yeast
2023
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A common mechanism of Sec61 translocon inhibition by small molecules
by
Itskanov, Samuel
, Blanchard, Nicolas
, Wang, Laurie
, Spiess, Martin
, Sherriff, Rumi
, Hoepfner, Dominic
, Shi, Wei Q.
, Forsyth, Craig
, Junne, Tina
, Xiao, Li
, Park, Eunyong
in
631/45/612/1237
/ 631/535
/ 631/92/609
/ Binding sites
/ Biochemical Engineering
/ Biochemistry
/ Biochemistry, Molecular Biology
/ Biology
/ Bioorganic Chemistry
/ Cell Biology
/ Chemical Sciences
/ Chemistry
/ Chemistry and Materials Science
/ Chemistry/Food Science
/ Depsipeptides - pharmacology
/ Drug development
/ Endoplasmic reticulum
/ Endoplasmic Reticulum - metabolism
/ Humans
/ Inhibitors
/ Life Sciences
/ Lipids
/ Medicinal Chemistry
/ Membrane proteins
/ Membrane Proteins - metabolism
/ Membranes
/ Molecular interactions
/ Plugs
/ Polypeptides
/ Protein transport
/ Protein Transport - physiology
/ Proteins
/ SEC Translocation Channels - antagonists & inhibitors
/ SEC Translocation Channels - chemistry
/ SEC Translocation Channels - metabolism
/ Sulfonamides - pharmacology
/ Therapeutic applications
/ Translocation
/ Triazoles - pharmacology
/ Yeast
2023
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A common mechanism of Sec61 translocon inhibition by small molecules
Journal Article
A common mechanism of Sec61 translocon inhibition by small molecules
2023
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Overview
The Sec61 complex forms a protein-conducting channel in the endoplasmic reticulum membrane that is required for secretion of soluble proteins and production of many membrane proteins. Several natural and synthetic small molecules specifically inhibit Sec61, generating cellular effects that are useful for therapeutic purposes, but their inhibitory mechanisms remain unclear. Here we present near-atomic-resolution structures of human Sec61 inhibited by a comprehensive panel of structurally distinct small molecules—cotransin, decatransin, apratoxin, ipomoeassin, mycolactone, cyclotriazadisulfonamide and eeyarestatin. All inhibitors bind to a common lipid-exposed pocket formed by the partially open lateral gate and plug domain of Sec61. Mutations conferring resistance to the inhibitors are clustered at this binding pocket. The structures indicate that Sec61 inhibitors stabilize the plug domain in a closed state, thereby preventing the protein-translocation pore from opening. Our study provides the atomic details of Sec61–inhibitor interactions and the structural framework for further pharmacological studies and drug design.
Itskanov and Wang et al. determined high-resolution structures of the human Sec61 channel inhibited by several structurally distinct small molecules and revealed the common inhibitor-binding site in Sec61 and molecular interactions in atomic detail.
Publisher
Nature Publishing Group US,Nature Publishing Group
Subject
/ 631/535
/ Biochemistry, Molecular Biology
/ Biology
/ Chemistry and Materials Science
/ Depsipeptides - pharmacology
/ Endoplasmic Reticulum - metabolism
/ Humans
/ Lipids
/ Membrane Proteins - metabolism
/ Plugs
/ Protein Transport - physiology
/ Proteins
/ SEC Translocation Channels - antagonists & inhibitors
/ SEC Translocation Channels - chemistry
/ SEC Translocation Channels - metabolism
/ Yeast
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