Sequence of MOCS1_MOUSE
EC Number:4.1.99.22
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
Reaction
GTP + S-adenosyl-L-methionine + reduced electron acceptor = (8S)-3',8-cyclo-7,8-dihydroguanosine 5'-triphosphate + 5'-deoxyadenosine + L-methionine + oxidized electron acceptor
Other sequences found for EC No. 4.1.99.22
General information:
Sequence
0 MAARPAFGIV RQLLRSNARG CSSGAPVTQP RPGEPSRPTR EGLSLRLQFL QEHAAPFSAF
60 LTDSFGRQHS YLRISLTEKC NLRCQYCMPE EGVPLTPKAD LLTTEEILTL ARLFVKEGVD
120 KIRLTGGEPL IRPDVVDIVA RLHGLEGLRT IGLTTNGINL ARLLPRLQQA GLNAVNISLD
180 TLVPAKFEFI VRRKGFHKVM EGIHKAIELG YKPVKVNCVV MRGLNEDELL DFVALTEGLP
240 LDVRFIEYMP FDGNKWNFKK MVSYKEMLDT IRQRWPGLEK LPEEDSSTAK AFKIPGFQGQ
300 ISFITSMSEH FCGTCNRLRI TADGNLKVCL FGNSEVSLRD HLRAGASEEE LLRIIGAAVG
360 RKKRQHAGMF NIAQMKNRPM ILIGVLLMLQ DSPPARWSNF SWDPLRVRNP SARQCLSDQM
420 ASLWKRHCIP KALPLSQQCL GSGSPQRHYS SYPDPDTHSK CLSTGSQAPD APSGPGPTSN
480 QLTHVDSAGR ASMVDVGGKP ETERVAVASA MVLLGPVAFK LVQQNQLKKG DALVVAQLAG
540 VQAAKLTSQL IPLCHHVALS HVQVHLELDS TRHAVLIQAS CRARGPTGVE MEALTSAAMA
600 ALTVYDMCKA VSRDIVVTEV KLISKTGGQR GDFHRA
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Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
189665
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
189666
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Genome Res.
14
2121-2127
2004
189667
Gray T.A.,Nicholls R.D.
Diverse splicing mechanisms fuse the evolutionarily conserved bicistronic MOCS1A and MOCS1B open reading frames.
RNA
6
928-936
2000
189668
Lee H.-J.,Adham I.M.,Schwarz G.,Kneussel M.,Sass J.O.,Engel W.,Reiss J.
Molybdenum cofactor-deficient mice resemble the phenotype of human patients.
Hum. Mol. Genet.
11
3309-3317
2002
189669
Reiss J.,Bonin M.,Schwegler H.,Sass J.O.,Garattini E.,Wagner S.,Lee H.-J.,Engel W.,Riess O.,Schwarz G.
The pathogenesis of molybdenum cofactor deficiency, its delay by maternal clearance, and its expression pattern in microarray analysis.
Mol. Genet. Metab.
85
12-20
2005
189670
Kuegler S.,Hahnewald R.,Garrido M.,Reiss J.
Long-term rescue of a lethal inherited disease by adeno-associated virus-mediated gene transfer in a mouse model of molybdenum-cofactor deficiency.
Am. J. Hum. Genet.
80
291-297
2007
189671
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
189672
Rardin M.J.,Newman J.C.,Held J.M.,Cusack M.P.,Sorensen D.J.,Li B.,Schilling B.,Mooney S.D.,Kahn C.R.,Verdin E.,Gibson B.W.
Label-free quantitative proteomics of the lysine acetylome in mitochondria identifies substrates of SIRT3 in metabolic pathways.
Proc. Natl. Acad. Sci. U.S.A.
110
6601-6606
2013
