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Sep. 10, 2014:
A total of 174 experimentally verified S-nitrosylation sites on 94 S-nitrosylated proteins from individualized human colorectal cancer tissues using a label-free quantitation strategy.

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Protein Name: Stalled ribosome sensor GCN1

UniprotKB/SwissProt ID: Q92616 (Q92616)

Gene Name: GCN1

Organism: Homo sapiens (Human)

Function: Ribosome collision sensor that plays a key role in the RNF14-RNF25 translation quality control pathway, a pathway that takes place when a ribosome has stalled during translation, and which promotes ubiquitination and degradation of translation factors on stalled ribosomes (PubMed:32610081, PubMed:36638793, PubMed:37651229, PubMed:37951215, PubMed:37951216). Directly binds to the ribosome and acts as a sentinel for colliding ribosomes: activated following ribosome stalling and promotes recruitment of RNF14, which directly ubiquitinates EEF1A1/eEF1A, leading to its degradation (PubMed:36638793, PubMed:37951215, PubMed:37951216). In addition to EEF1A1/eEF1A, the RNF14-RNF25 translation quality control pathway mediates degradation of ETF1/eRF1 and ubiquitination of ribosomal protein (PubMed:36638793, PubMed:37651229). GCN1 also acts as a positive activator of the integrated stress response (ISR) by mediating activation of EIF2AK4/GCN2 in response to amino acid starvation (By similarity). Interaction with EIF2AK4/GCN2 on translating ribosomes stimulates EIF2AK4/GCN2 kinase activity, leading to phosphorylation of eukaryotic translation initiation factor 2 (eIF-2-alpha/EIF2S1) (By similarity). EIF2S1/eIF-2-alpha phosphorylation converts EIF2S1/eIF-2-alpha into a global protein synthesis inhibitor, leading to a global attenuation of cap-dependent translation, and thus to a reduced overall utilization of amino acids, while concomitantly initiating the preferential translation of ISR-specific mRNAs, such as the transcriptional activator ATF4, and hence allowing ATF4-mediated reprogramming of amino acid biosynthetic gene expression to alleviate nutrient depletion (By similarity)

Other Modifications: View all modification sites in dbPTM

Protein Subcellular Localization: Cytoplasm

Graphical Visualization of S-nitrosylation Sites:
InterPro ID Domain Name
IPR011989 ARM-like
IPR016024 ARM-type_fold
IPR021133 HEAT_type_2
IPR034085 TOG

The S-nitrosylation sites of Q92616

No. Position S-nitrosylated Peptide Secondary Structure of S-nitrosylated Peptide Solvent Accessibility of nitrosylated Site PubMed ID
1 1275 LNDRHPDVRK C MLDAALATLN  CCCHHHHHHH H HHHCCCCCCC 
2 1362 SQQVQESVAS C LPPLVPAIKE  CCCHHHHHHH H HHHCCCCCCC 
3 1482 NQYVREAADD C AKAVMSNLSA  CCCHHHHHHH H HHHCCCCCCC 
4 1527 SVELLGAMAY C APKQLSSCLP  CCCHHHHHHH H HHHCCCCCCC 
5 1535 AYCAPKQLSS C LPNIVPKLTE  CCCHHHHHHH H HHHCCCCCCC  19483679
6 1595 LTDPSRKTQK C LQTLLDTKFV  CCCHHHHHHH H HHHCCCCCCC 
7 2015 SLVPTARKAL C DPLEEVREAA  CCCHHHHHHH H HHHCCCCCCC 
8 2136 TPDEQLEMAN C QAVILSVEDD  CCCHHHHHHH H HHHCCCCCCC 
9 2179 QAAAIILNIY C SRSKADYTSH  CCCHHHHHHH H HHHCCCCCCC 
10 2255 ESKGEHVPGF C LPKKGVTSIL  CCCHHHHHHH H HHHCCCCCCC 
11 246 VKPPKYLLDS C APLLRYLSHS  CCCHHHHHHH H HHHCCCCCCC 
12 2558 PAKLSSLFVK C LQNPSSDIRL  CCCHHHHHHH H HHHCCCCCCC 
13 329 VLALRNLARQ C SDSSAMESLT  CCCHHHHHHH H HHHCCCCCCC 
14 939 KPECVLDKSW C QEELSVAVKR  CCCHHHHHHH H HHHCCCCCCC