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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: Egl nine homolog 1

UniprotKB/SwissProt ID: P59722 (P59722)

Gene Name: Egln1

Organism: Rattus norvegicus (Rat)

Function: Cellular oxygen sensor that catalyzes, under normoxic conditions, the post-translational formation of 4-hydroxyproline in hypoxia-inducible factor (HIF) alpha proteins. Hydroxylates a specific proline found in each of the oxygen-dependent degradation (ODD) domains (N-terminal, NODD, and C-terminal, CODD) of HIF1A. Also hydroxylates HIF2A. Has a preference for the CODD site for both HIF1A and HIF1B. Hydroxylated HIFs are then targeted for proteasomal degradation via the von Hippel-Lindau ubiquitination complex. Under hypoxic conditions, the hydroxylation reaction is attenuated allowing HIFs to escape degradation resulting in their translocation to the nucleus, heterodimerization with HIF1B, and increased expression of hypoxy-inducible genes. EGLN1 is the most important isozyme under normoxia and, through regulating the stability of HIF1, involved in various hypoxia-influenced processes such as angiogenesis in retinal and cardiac functionality. Target proteins are preferentially recognized via a LXXLAP motif

Other Modifications: View all modification sites in dbPTM

Protein Subcellular Localization: Cytoplasm. Nucleus

Graphical Visualization of S-nitrosylation Sites:
InterPro ID Domain Name
IPR051559 HIF_prolyl_hydroxylases
IPR005123 Oxoglu/Fe-dep_dioxygenase_dom
IPR006620 Pro_4_hyd_alph
IPR044862 Pro_4_hyd_alph_FE2OG_OXY

The S-nitrosylation sites of P59722

No. Position S-nitrosylated Peptide Secondary Structure of S-nitrosylated Peptide Solvent Accessibility of nitrosylated Site PubMed ID
1 116 LKLALEYIVP C MNKHGICVVD  CCCCCCCCCC C CCCCCCCCCC  41.54%
2 123 IVPCMNKHGI C VVDDFLGRET  CCCCCCCCCC C CCCCCCCCCC  4.75%
3 217 INGRTKAMVA C YPGNGTGYVR  CCCCCCCCCC C CCCCCCCCCC  35.97%
4 238 HVDNPNGDGR C VTCIYYLNKD  CCCCCCCCCC C CCCCCCCCCC 
5 241 NPNGDGRCVT C IYYLNKDWDA  CCCCCCCCCC C CCCCCCCCCC