Mus musculus Protein: Egln2
Summary
InnateDB Protein IDBP-264658.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Egln2
Protein Name EGL nine homolog 2 (C. elegans)
Synonyms 0610011A13Rik; C85656; Hif-p4h-1; Ier4; Phd1; SM-20;
Species Mus musculus
Ensembl Protein ENSMUSP00000104019
InnateDB Gene IDBG-159886 (Egln2)
Protein Structure
UniProt Annotation
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 HIF2A. 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. EGLN2 is involved in regulating hypoxia tolerance and apoptosis in cardiac and skeletal muscle. Also regulates susceptibility to normoxic oxidative neuronal death. Links oxygen sensing to cell cycle and primary cilia formation by hydroxylating the critical centrosome component CEP192 which promotes its ubiquitination and subsequent proteasomal degradation. Hydroxylates IKBKB, mediating NF-kappaB activation in hypoxic conditions. Target proteins are preferencially recognized via a LXXLAP motif. {ECO:0000269PubMed:18176562, ECO:0000269PubMed:19587290, ECO:0000269PubMed:21083501}.
Subcellular Localization Nucleus {ECO:0000269PubMed:12360397}.
Disease Associations
Tissue Specificity Highly expressed in testis, expression was also detected in the heart brain, liver kidney and lung. Expression was lowest in spleen and skeletal muscle. Constitutively expressed during differentiation of C2C12 skeletal myocytes. {ECO:0000269PubMed:12234095}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
They are also associated with 2 interaction(s) predicted by orthology.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 2 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005506 iron ion binding
GO:0016491 oxidoreductase activity
GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
GO:0016706 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, 2-oxoglutarate as one donor, and incorporation of one atom each of oxygen into both donors
GO:0019826 oxygen sensor activity
GO:0031418 L-ascorbic acid binding
GO:0031545 peptidyl-proline 4-dioxygenase activity
Biological Process
GO:0001666 response to hypoxia
GO:0018401 peptidyl-proline hydroxylation to 4-hydroxy-L-proline
GO:0043523 regulation of neuron apoptotic process
GO:0045454 cell redox homeostasis
GO:0045732 positive regulation of protein catabolic process
GO:0055114 oxidation-reduction process
Cellular Component
GO:0005634 nucleus
GO:0005829 cytosol
Protein Structure and Domains
PDB ID MGI:1932287
InterPro IPR005123 Oxoglutarate/iron-dependent dioxygenase
IPR006620 Prolyl 4-hydroxylase, alpha subunit
PFAM PF03171
PF13640
PRINTS
PIRSF
SMART SM00702
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q91YE2
PhosphoSite PhosphoSite-Q91YE2
TrEMBL Q80X29
UniProt Splice Variant
Entrez Gene 112406
UniGene Mm.29978
RefSeq XP_006539536
MGI ID
MGI Symbol Egln2
OMIM
CCDS CCDS21011
HPRD
IMGT
EMBL AF340231 AF453879 AJ310547 AK075582 AK152223 BC023299 BC051436 BC086764 CH466593
GenPept AAH23299 AAH51436 AAH86764 AAK37525 AAL65166 BAC35835 BAE31050 CAC42516 EDL24202 EDL24203