Sequence of EGLN1_MOUSE
EC Number:1.14.11.29
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
Reaction
hypoxia-inducible factor-L-proline + 2-oxoglutarate + O2 = hypoxia-inducible factor-(4R)-4-hydroxy-L-proline + succinate + CO2
Other sequences found for EC No. 1.14.11.29
General information:
Sequence
0 MASDSGGPGV LSASERDRQY CELCGKMENL LRCGRCRSSF YCCKEHQRQD WKKHKLVCQG
60 GEAPRAQPAP AQPRVAPPPG GAPGAARAGG AARRGDSAAA SRVPGPEDAA QARSGPGPAE
120 PGSEDPPLSR SPGPERASLC PAGGGPGEAL SPGGGLRPNG QTKPLPALKL ALEYIVPCMN
180 KHGICVVDDF LGRETGQQIG DEVRALHDTG KFTDGQLVSQ KSDSSKDIRG DQITWIEGKE
240 PGCETIGLLM SSMDDLIRHC SGKLGNYRIN GRTKAMVACY PGNGTGYVRH VDNPNGDGRC
300 VTCIYYLNKD WDAKVSGGIL RIFPEGKAQF ADIEPKFDRL LFFWSDRRNP HEVQPAYATR
360 YAITVWYFDA DERARAKVKY LTGEKGVRVE LKPNSVSKDV
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Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
29399
Church D.M.,Goodstadt L.,Hillier L.W.,Zody M.C.,Goldstein S.,She X.,Bult C.J.,Agarwala R.,Cherry J.L.,DiCuccio M.,Hlavina W.,Kapustin Y.,Meric P.,Maglott D.,Birtle Z.,Marques A.C.,Graves T.,Zhou S.,Teague B.,Potamousis K.,Churas C.,Place M.,Herschleb J.,Runnheim R.,Forrest D.,Amos-Landgraf J.,Schwartz D.C.,Cheng Z.,Lindblad-Toh K.,Eichler E.E.,Ponting C.P.
Lineage-specific biology revealed by a finished genome assembly of the mouse.
PLoS Biol.
7
0-0
2009
29400
Taylor M.S.
Characterization and comparative analysis of the EGLN gene family.
Gene
275
125-132
2001
29401
Lieb M.E.,Menzies K.,Moschella M.C.,Ni R.,Taubman M.B.
Mammalian EGLN genes have distinct patterns of mRNA expression and regulation.
Biochem. Cell Biol.
80
421-426
2002
29402
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Genome Res.
14
2121-2127
2004
29403
Moschella M.C.,Menzies K.,Tsao L.,Lieb M.A.,Kohtz J.D.,Kohtz D.S.,Taubman M.B.
SM-20 is a novel growth factor-responsive gene regulated during skeletal muscle development and differentiation.
Gene Expr.
8
59-66
1999
29404
Minamishima Y.A.,Moslehi J.,Bardeesy N.,Cullen D.,Bronson R.T.,Kaelin W.G. Jr.
Somatic inactivation of the PHD2 prolyl hydroxylase causes polycythemia and congestive heart failure.
Blood
111
3236-3244
2008
29405
Wu S.,Nishiyama N.,Kano M.R.,Morishita Y.,Miyazono K.,Itaka K.,Chung U.I.,Kataoka K.
Enhancement of angiogenesis through stabilization of hypoxia-inducible factor-1 by silencing prolyl hydroxylase domain-2 gene.
Mol. Ther.
16
1227-1234
2008
29406
Huttlin E.L.,Jedrychowski M.P.,Elias J.E.,Goswami T.,Rad R.,Beausoleil S.A.,Villen J.,Haas W.,Sowa M.E.,Gygi S.P.
A tissue-specific atlas of mouse protein phosphorylation and expression.
Cell
143
1174-1189
2010
29407
Duan L.J.,Takeda K.,Fong G.H.
Prolyl hydroxylase domain protein 2 (PHD2) mediates oxygen-induced retinopathy in neonatal mice.
Am. J. Pathol.
178
1881-1890
2011
