Sequence of OSGEP_HUMAN
EC Number:2.3.1.234
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
Reaction
L-threonylcarbamoyladenylate + adenine37 in tRNA = AMP + N6-L-threonylcarbamoyladenine37 in tRNA
Other sequences found for EC No. 2.3.1.234
General information:
Sequence
0 MPAVLGFEGS ANKIGVGVVR DGKVLANPRR TYVTPPGTGF LPGDTARHHR AVILDLLQEA
60 LTESGLTSQD IDCIAYTKGP GMGAPLVSVA VVARTVAQLW NKPLVGVNHC IGHIEMGRLI
120 TGATSPTVLY VSGGNTQVIA YSEHRYRIFG ETIDIAVGNC LDRFARVLKI SNDPSPGYNI
180 EQMAKRGKKL VELPYTVKGM DVSFSGILSF IEDVAHRMLA TGECTPEDLC FSLQETVFAM
240 LVEITERAMA HCGSQEALIV GGVGCNVRLQ EMMATMCQER GARLFATDER FCIDNGAMIA
300 QAGWEMFRAG HRTPLSDSGV TQRYRTDEVE VTWRD
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Download all sequences for 2.3.1.234
Sequence related references
Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
70435
Seki Y.,Ikeda S.,Kiyohara H.,Ayabe H.,Seki T.,Matsui H.
Sequencing analysis of a putative human O-sialoglycoprotein endopeptidase gene (OSGEP) and analysis of a bidirectional promoter between the OSGEP and APEX genes.
Gene
285
101-108
2002
70437
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
70439
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Genome Res.
14
2121-2127
2004
70440
Burkard T.R.,Planyavsky M.,Kaupe I.,Breitwieser F.P.,Buerckstuemmer T.,Bennett K.L.,Superti-Furga G.,Colinge J.
Initial characterization of the human central proteome.
BMC Syst. Biol.
5
17-17
2011
70441
Costessi A.,Mahrour N.,Sharma V.,Stunnenberg R.,Stoel M.A.,Tijchon E.,Conaway J.W.,Conaway R.C.,Stunnenberg H.G.
The human EKC/KEOPS complex is recruited to Cullin2 ubiquitin ligases by the human tumour antigen PRAME.
PLoS ONE
7
0-0
2012
70442
Van Damme P.,Lasa M.,Polevoda B.,Gazquez C.,Elosegui-Artola A.,Kim D.S.,De Juan-Pardo E.,Demeyer K.,Hole K.,Larrea E.,Timmerman E.,Prieto J.,Arnesen T.,Sherman F.,Gevaert K.,Aldabe R.
N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB.
Proc. Natl. Acad. Sci. U.S.A.
109
12449-12454
2012
70443
Wan L.C.,Maisonneuve P.,Szilard R.K.,Lambert J.P.,Ng T.F.,Manczyk N.,Huang H.,Laister R.,Caudy A.A.,Gingras A.C.,Durocher D.,Sicheri F.
Proteomic analysis of the human KEOPS complex identifies C14ORF142 as a core subunit homologous to yeast Gon7.
Nucleic Acids Res.
45
805-817
2017
70444
Edvardson S.,Prunetti L.,Arraf A.,Haas D.,Bacusmo J.M.,Hu J.F.,Ta-Shma A.,Dedon P.C.,de Crecy-Lagard V.,Elpeleg O.
tRNA N6-adenosine threonylcarbamoyltransferase defect due to KAE1/TCS3 (OSGEP) mutation manifest by neurodegeneration and renal tubulopathy.
Eur. J. Hum. Genet.
25
545-551
2017
70445
Braun D.A.,Rao J.,Mollet G.,Schapiro D.,Daugeron M.C.,Tan W.,Gribouval O.,Boyer O.,Revy P.,Jobst-Schwan T.,Schmidt J.M.,Lawson J.A.,Schanze D.,Ashraf S.,Ullmann J.F.P.,Hoogstraten C.A.,Boddaert N.,Collinet B.,Martin G.,Liger D.,Lovric S.,Furlano M.,Guerrera I.C.,Sanchez-Ferras O.,Hu J.F.,Boschat A.C.,Sanquer S.,Menten B.,Vergult S.,De Rocker N.,Airik M.,Hermle T.,Shril S.,Widmeier E.,Gee H.Y.,Choi W.I.,Sadowski C.E.,Pabst W.L.,Warejko J.K.,Daga A.,Basta T.,Matejas V.,Scharmann K.,Kienast S.D.,Behnam B.,Beeson B.,Begtrup A.,Bruce M.,Ch'ng G.S.,Lin S.P.,Chang J.H.,Chen C.H.,Cho M.T.,Gaffney P.M.,Gipson P.E.,Hsu C.H.,Kari J.A.,Ke Y.Y.,Kiraly-Borri C.,Lai W.M.,Lemyre E.,Littlejohn R.O.,Masri A.,Moghtaderi M.,Nakamura K.,Ozaltin F.,Praet M.,Prasad C.,Prytula A.,Roeder E.R.,Rump P.,Schnur R.E.,Shiihara T.,Sinha M.D.,Soliman N.A.,Soulami K.,Sweetser D.A.,Tsai W.H.,Tsai J.D.,Topaloglu R.,Vester U.,Viskochil D.H.,Vatanavicharn N.,Waxler J.L.,Wierenga K.J.,Wolf M.T.F.,Wong S.N.,Leidel S.A.,Truglio G.,Dedon P.C.,Poduri A.,Mane S.,Lifton R.P.,Bouchard M.,Kannu P.,Chitayat D.,Magen D.,Callewaert B.,van Tilbeurgh H.,Zenker M.,Antignac C.,Hildebrandt F.
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.
Nat. Genet.
49
1529-1538
2017
70446
Arrondel C.,Missoury S.,Snoek R.,Patat J.,Menara G.,Collinet B.,Liger D.,Durand D.,Gribouval O.,Boyer O.,Buscara L.,Martin G.,Machuca E.,Nevo F.,Lescop E.,Braun D.A.,Boschat A.C.,Sanquer S.,Guerrera I.C.,Revy P.,Parisot M.,Masson C.,Boddaert N.,Charbit M.,Decramer S.,Novo R.,Macher M.A.,Ranchin B.,Bacchetta J.,Laurent A.,Collardeau-Frachon S.,van Eerde A.M.,Hildebrandt F.,Magen D.,Antignac C.,van Tilbeurgh H.,Mollet G.
Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome.
Nat. Commun.
10
3967-3967
2019