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Sequence of EGLN2_MOUSE

EC Number:1.14.11.29

EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
hypoxia-inducible factor-proline dioxygenase
Q91YE2
Mus musculus
419
45109
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
show sequence in fasta format
  0 MDSPCQPQAL NQALPQLPGS VSESLESSRA RMGVESYLPC PLLPAYHRPG ASGEASAGNG
 60 TPRTTATATT TTASPLREGF GGQDGGELWP LQSEGAAALV TKECQRLAAQ GARPEAPKRK
120 WAKDGGDAPS PSKRPWARQE NQEAKGESGM GCDSGASNSS SSSSNTTSSS GEASARLREE
180 VQPSAPERLA LDYIVPCMRY YGICVKDNFL GAVLGGRVLA EVEALKWGGR LRDGQLVSQR
240 AIPPRSIRGD QIAWVEGHEP GCRSIGALMA HVDAVIRHCA GRLGNYVING RTKAMVACYP
300 GNGLGYVRHV DNPHGDGRCI TCIYYLNQNW DVKVHGGLLQ IFPEGRPVVA NIEPLFDRLL
360 IFWSDRRNPH EVKPAYATRY AITVWYFDAK ERAAARDKYQ LASGQKGVQV PVSQPTTPT
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Sequence related references
Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
29438
Taylor M.S.
Characterization and comparative analysis of the EGLN gene family.
Gene
275
125-132
2001
29439
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
29440
Erez N.,Milyavsky M.,Goldfinger N.,Peles E.,Gudkov A.V.,Rotter V.
Falkor, a novel cell growth regulator isolated by a functional genetic screen.
Oncogene
21
6713-6721
2002
29441
Carninci P.,Kasukawa T.,Katayama S.,Gough J.,Frith M.C.,Maeda N.,Oyama R.,Ravasi T.,Lenhard B.,Wells C.,Kodzius R.,Shimokawa K.,Bajic V.B.,Brenner S.E.,Batalov S.,Forrest A.R.,Zavolan M.,Davis M.J.,Wilming L.G.,Aidinis V.,Allen J.E.,Ambesi-Impiombato A.,Apweiler R.,Aturaliya R.N.,Bailey T.L.,Bansal M.,Baxter L.,Beisel K.W.,Bersano T.,Bono H.,Chalk A.M.,Chiu K.P.,Choudhary V.,Christoffels A.,Clutterbuck D.R.,Crowe M.L.,Dalla E.,Dalrymple B.P.,de Bono B.,Della Gatta G.,di Bernardo D.,Down T.,Engstrom P.,Fagiolini M.,Faulkner G.,Fletcher C.F.,Fukushima T.,Furuno M.,Futaki S.,Gariboldi M.,Georgii-Hemming P.,Gingeras T.R.,Gojobori T.,Green R.E.,Gustincich S.,Harbers M.,Hayashi Y.,Hensch T.K.,Hirokawa N.,Hill D.,Huminiecki L.,Iacono M.,Ikeo K.,Iwama A.,Ishikawa T.,Jakt M.,Kanapin A.,Katoh M.,Kawasawa Y.,Kelso J.,Kitamura H.,Kitano H.,Kollias G.,Krishnan S.P.,Kruger A.,Kummerfeld S.K.,Kurochkin I.V.,Lareau L.F.,Lazarevic D.,Lipovich L.,Liu J.,Liuni S.,McWilliam S.,Madan Babu M.,Madera M.,Marchionni L.,Matsuda H.,Matsuzawa S.,Miki H.,Mignone F.,Miyake S.,Morris K.,Mottagui-Tabar S.,Mulder N.,Nakano N.,Nakauchi H.,Ng P.,Nilsson R.,Nishiguchi S.,Nishikawa S.,Nori F.,Ohara O.,Okazaki Y.,Orlando V.,Pang K.C.,Pavan W.J.,Pavesi G.,Pesole G.,Petrovsky N.,Piazza S.,Reed J.,Reid J.F.,Ring B.Z.,Ringwald M.,Rost B.,Ruan Y.,Salzberg S.L.,Sandelin A.,Schneider C.,Schoenbach C.,Sekiguchi K.,Semple C.A.,Seno S.,Sessa L.,Sheng Y.,Shibata Y.,Shimada H.,Shimada K.,Silva D.,Sinclair B.,Sperling S.,Stupka E.,Sugiura K.,Sultana R.,Takenaka Y.,Taki K.,Tammoja K.,Tan S.L.,Tang S.,Taylor M.S.,Tegner J.,Teichmann S.A.,Ueda H.R.,van Nimwegen E.,Verardo R.,Wei C.L.,Yagi K.,Yamanishi H.,Zabarovsky E.,Zhu S.,Zimmer A.,Hide W.,Bult C.,Grimmond S.M.,Teasdale R.D.,Liu E.T.,Brusic V.,Quackenbush J.,Wahlestedt C.,Mattick J.S.,Hume D.A.,Kai C.,Sasaki D.,Tomaru Y.,Fukuda S.,Kanamori-Katayama M.,Suzuki M.,Aoki J.,Arakawa T.,Iida J.,Imamura K.,Itoh M.,Kato T.,Kawaji H.,Kawagashira N.,Kawashima T.,Kojima M.,Kondo S.,Konno H.,Nakano K.,Ninomiya N.,Nishio T.,Okada M.,Plessy C.,Shibata K.,Shiraki T.,Suzuki S.,Tagami M.,Waki K.,Watahiki A.,Okamura-Oho Y.,Suzuki H.,Kawai J.,Hayashizaki Y.
The transcriptional landscape of the mammalian genome.
Science
309
1559-1563
2005
29442
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Genome Res.
14
2121-2127
2004
29443
Aragones J.,Schneider M.,Van Geyte K.,Fraisl P.,Dresselaers T.,Mazzone M.,Dirkx R.,Zacchigna S.,Lemieux H.,Jeoung N.H.,Lambrechts D.,Bishop T.,Lafuste P.,Diez-Juan A.,Harten S.K.,Van Noten P.,De Bock K.,Willam C.,Tjwa M.,Grosfeld A.,Navet R.,Moons L.,Vandendriessche T.,Deroose C.,Wijeyekoon B.,Nuyts J.,Jordan B.,Silasi-Mansat R.,Lupu F.,Dewerchin M.,Pugh C.,Salmon P.,Mortelmans L.,Gallez B.,Gorus F.,Buyse J.,Sluse F.,Harris R.A.,Gnaiger E.,Hespel P.,Van Hecke P.,Schuit F.,Van Veldhoven P.,Ratcliffe P.,Baes M.,Maxwell P.,Carmeliet P.
Deficiency or inhibition of oxygen sensor Phd1 induces hypoxia tolerance by reprogramming basal metabolism.
Nat. Genet.
40
170-180
2008
29444
Siddiq A.,Aminova L.R.,Troy C.M.,Suh K.,Messer Z.,Semenza G.L.,Ratan R.R.
Selective inhibition of hypoxia-inducible factor (HIF) prolyl-hydroxylase 1 mediates neuroprotection against normoxic oxidative death via HIF- and CREB-independent pathways.
J. Neurosci.
29
8828-8838
2009
29445
Adluri R.S.,Thirunavukkarasu M.,Dunna N.R.,Zhan L.,Oriowo B.,Takeda K.,Sanchez J.A.,Otani H.,Maulik G.,Fong G.H.,Maulik N.
Disruption of hypoxia-inducible transcription factor-prolyl hydroxylase domain-1 (PHD-1-/-) attenuates ex vivo myocardial ischemia/reperfusion injury through hypoxia-inducible factor-1alpha transcription factor and its target genes in mice.
Antioxid. Redox Signal.
15
1789-1797
2011
29446
Scortegagna M.,Kim H.,Li J.L.,Yao H.,Brill L.M.,Han J.,Lau E.,Bowtell D.,Haddad G.,Kaufman R.J.,Ronai Z.A.
Fine tuning of the UPR by the ubiquitin ligases Siah1/2.
PLoS Genet.
10
0-0
2014