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Sequence of TOMT_HUMAN

EC Number:2.1.1.6

EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
catechol O-methyltransferase
Q8WZ04
Homo sapiens
291
32155
Reaction
S-adenosyl-L-methionine + a catechol = S-adenosyl-L-homocysteine + a guaiacol
Other sequences found for EC No. 2.1.1.6

General information:

Sequence
show sequence in fasta format
  0 MGTPWRKRKG IAGPGLPDLS CALVLQPRAQ VGTMSPAIAL AFLPLVVTLL VRYRHYFRLL
 60 VRTVLLRSLR DCLSGLRIEE RAFSYVLTHA LPGDPGHILT TLDHWSSRCE YLSHMGPVKG
120 QILMRLVEEK APACVLELGT YCGYSTLLIA RALPPGGRLL TVERDPRTAA VAEKLIRLAG
180 FDEHMVELIV GSSEDVIPCL RTQYQLSRAD LVLLAHRPRC YLRDLQLLEA HALLPAGATV
240 LADHVLFPGA PRFLQYAKSC GRYRCRLHHT GLPDFPAIKD GIAQLTYAGP G
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Sequence related references
Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
747550
Ahmed Z.M.,Masmoudi S.,Kalay E.,Belyantseva I.A.,Mosrati M.A.,Collin R.W.J.,Riazuddin S.,Hmani-Aifa M.,Venselaar H.,Kawar M.N.,Tlili A.,van der Zwaag B.,Khan S.Y.,Ayadi L.,Riazuddin S.A.,Morell R.J.,Griffith A.J.,Charfedine I.,Caylan R.,Oostrik J.,Karaguzel A.,Ghorbel A.,Riazuddin S.,Friedman T.B.,Ayadi H.,Kremer H.
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
Nat. Genet.
40
1335-1340
2008
747551
Wan D.,Gong Y.,Qin W.,Zhang P.,Li J.,Wei L.,Zhou X.,Li H.,Qiu X.,Zhong F.,He L.,Yu J.,Yao G.,Jiang H.,Qian L.,Yu Y.,Shu H.,Chen X.,Xu H.,Guo M.,Pan Z.,Chen Y.,Ge C.,Yang S.,Gu J.
Large-scale cDNA transfection screening for genes related to cancer development and progression.
Proc. Natl. Acad. Sci. U.S.A.
101
15724-15729
2004
747552
Ota T.,Suzuki Y.,Nishikawa T.,Otsuki T.,Sugiyama T.,Irie R.,Wakamatsu A.,Hayashi K.,Sato H.,Nagai K.,Kimura K.,Makita H.,Sekine M.,Obayashi M.,Nishi T.,Shibahara T.,Tanaka T.,Ishii S.,Yamamoto J.,Saito K.,Kawai Y.,Isono Y.,Nakamura Y.,Nagahari K.,Murakami K.,Yasuda T.,Iwayanagi T.,Wagatsuma M.,Shiratori A.,Sudo H.,Hosoiri T.,Kaku Y.,Kodaira H.,Kondo H.,Sugawara M.,Takahashi M.,Kanda K.,Yokoi T.,Furuya T.,Kikkawa E.,Omura Y.,Abe K.,Kamihara K.,Katsuta N.,Sato K.,Tanikawa M.,Yamazaki M.,Ninomiya K.,Ishibashi T.,Yamashita H.,Murakawa K.,Fujimori K.,Tanai H.,Kimata M.,Watanabe M.,Hiraoka S.,Chiba Y.,Ishida S.,Ono Y.,Takiguchi S.,Watanabe S.,Yosida M.,Hotuta T.,Kusano J.,Kanehori K.,Takahashi-Fujii A.,Hara H.,Tanase T.-O.,Nomura Y.,Togiya S.,Komai F.,Hara R.,Takeuchi K.,Arita M.,Imose N.,Musashino K.,Yuuki H.,Oshima A.,Sasaki N.,Aotsuka S.,Yoshikawa Y.,Matsunawa H.,Ichihara T.,Shiohata N.,Sano S.,Moriya S.,Momiyama H.,Satoh N.,Takami S.,Terashima Y.,Suzuki O.,Nakagawa S.,Senoh A.,Mizoguchi H.,Goto Y.,Shimizu F.,Wakebe H.,Hishigaki H.,Watanabe T.,Sugiyama A.,Takemoto M.,Kawakami B.,Yamazaki M.,Watanabe K.,Kumagai A.,Itakura S.,Fukuzumi Y.,Fujimori Y.,Komiyama M.,Tashiro H.,Tanigami A.,Fujiwara T.,Ono T.,Yamada K.,Fujii Y.,Ozaki K.,Hirao M.,Ohmori Y.,Kawabata A.,Hikiji T.,Kobatake N.,Inagaki H.,Ikema Y.,Okamoto S.,Okitani R.,Kawakami T.,Noguchi S.,Itoh T.,Shigeta K.,Senba T.,Matsumura K.,Nakajima Y.,Mizuno T.,Morinaga M.,Sasaki M.,Togashi T.,Oyama M.,Hata H.,Watanabe M.,Komatsu T.,Mizushima-Sugano J.,Satoh T.,Shirai Y.,Takahashi Y.,Nakagawa K.,Okumura K.,Nagase T.,Nomura N.,Kikuchi H.,Masuho Y.,Yamashita R.,Nakai K.,Yada T.,Nakamura Y.,Ohara O.,Isogai T.,Sugano S.
Complete sequencing and characterization of 21,243 full-length human cDNAs.
Nat. Genet.
36
40-45
2004
747553
Taylor T.D.,Noguchi H.,Totoki Y.,Toyoda A.,Kuroki Y.,Dewar K.,Lloyd C.,Itoh T.,Takeda T.,Kim D.-W.,She X.,Barlow K.F.,Bloom T.,Bruford E.,Chang J.L.,Cuomo C.A.,Eichler E.,FitzGerald M.G.,Jaffe D.B.,LaButti K.,Nicol R.,Park H.-S.,Seaman C.,Sougnez C.,Yang X.,Zimmer A.R.,Zody M.C.,Birren B.W.,Nusbaum C.,Fujiyama A.,Hattori M.,Rogers J.,Lander E.S.,Sakaki Y.
Human chromosome 11 DNA sequence and analysis including novel gene identification.
Nature
440
497-500
2006
747554
Du X.,Schwander M.,Moresco E.M.Y.,Viviani P.,Haller C.,Hildebrand M.S.,Pak K.,Tarantino L.,Roberts A.,Richardson H.,Koob G.,Najmabadi H.,Ryan A.F.,Smith R.J.H.,Mueller U.,Beutler B.
A catechol-O-methyltransferase that is essential for auditory function in mice and humans.
Proc. Natl. Acad. Sci. U.S.A.
105
14609-14614
2008
747555
Cunningham C.L.,Wu Z.,Jafari A.,Zhao B.,Schrode K.,Harkins-Perry S.,Lauer A.,Mueller U.
The murine catecholamine methyltransferase mTOMT is essential for mechanotransduction by cochlear hair cells.
Elife
6
0-0
2017
747556
Wang R.,Han S.,Khan A.,Zhang X.
Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss.
Genet. Test. Mol. Biomarkers
21
316-321
2017