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TLS Online TPP Program

#Id: 9302


11-cis-retinal covalently attached to the amino group of lysine residue 296 in the opsin protein

#XL - T Zoology #Visual Signaling #Part B Pointers
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TLS Online TPP Program

#Id: 7967

#XL - Q Biochemistry

Hydrolysis of the bound GTP accompanies disassembly of the SRP and SRP receptor and initiates transfer of the nascent chain and ribosome to a site on the ER membrane, where translocation can take place.

TLS Online TPP Program

#Id: 7966

#XL - Q Biochemistry

Binding of BiP to the luminal domain of monomeric Ire1 prevents formation of the Ire1 dimer.

TLS Online TPP Program

#Id: 7965

#XL - Q Biochemistry

Unassembled or misfolded proteins in the ER are often transported back to the cytosol, where they are degraded in the ubiquitin-proteasome pathway


TLS Online TPP Program

#Id: 7964

#XL - Q Biochemistry

Emphysema caused by a point mutation in -antitrypsin, which is normally secreted by hepatocytes and macrophages.

TLS Online TPP Program

#Id: 7963

#XL - Q Biochemistry

A hereditary form of emphysema illustrates the detrimental effects that can result from misfolding of proteins in the ER.

TLS Online TPP Program

#Id: 7962

#XL - Q Biochemistry

Hac1 activates transcription of genes encoding several protein-folding catalysts.

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