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Sequence of PGLT1_HUMAN

EC Number:2.4.1.376

EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
EGF-domain serine glucosyltransferase
Q8NBL1
Homo sapiens
392
46189
Reaction
UDP-alpha-D-glucose + [protein with EGF-like domain]-L-serine = UDP + [protein with EGF-like domain]-3-O-(beta-D-glucosyl)-L-serine
Other sequences found for EC No. 2.4.1.376

General information:

Sequence
show sequence in fasta format
  0 MEWWASSPLR LWLLLFLLPS AQGRQKESGS KWKVFIDQIN RSLENYEPCS SQNCSCYHGV
 60 IEEDLTPFRG GISRKMMAEV VRRKLGTHYQ ITKNRLYREN DCMFPSRCSG VEHFILEVIG
120 RLPDMEMVIN VRDYPQVPKW MEPAIPVFSF SKTSEYHDIM YPAWTFWEGG PAVWPIYPTG
180 LGRWDLFRED LVRSAAQWPW KKKNSTAYFR GSRTSPERDP LILLSRKNPK LVDAEYTKNQ
240 AWKSMKDTLG KPAAKDVHLV DHCKYKYLFN FRGVAASFRF KHLFLCGSLV FHVGDEWLEF
300 FYPQLKPWVH YIPVKTDLSN VQELLQFVKA NDDVAQEIAE RGSQFIRNHL QMDDITCYWE
360 NLLSEYSKFL SYNVTRRKGY DQIIPKMLKT EL
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Sequence related references
Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
712064
Teng Y.,Liu Q.,Ma J.,Liu F.,Han Z.,Wang Y.,Wang W.
Cloning, expression and characterization of a novel human CAP10-like gene hCLP46 from CD34+ stem/progenitor cells.
Gene
371
7-15
2006
712065
Clark H.F.,Gurney A.L.,Abaya E.,Baker K.,Baldwin D.T.,Brush J.,Chen J.,Chow B.,Chui C.,Crowley C.,Currell B.,Deuel B.,Dowd P.,Eaton D.,Foster J.S.,Grimaldi C.,Gu Q.,Hass P.E.,Heldens S.,Huang A.,Kim H.S.,Klimowski L.,Jin Y.,Johnson S.,Lee J.,Lewis L.,Liao D.,Mark M.R.,Robbie E.,Sanchez C.,Schoenfeld J.,Seshagiri S.,Simmons L.,Singh J.,Smith V.,Stinson J.,Vagts A.,Vandlen R.L.,Watanabe C.,Wieand D.,Woods K.,Xie M.-H.,Yansura D.G.,Yi S.,Yu G.,Yuan J.,Zhang M.,Zhang Z.,Goddard A.D.,Wood W.I.,Godowski P.J.,Gray A.M.
The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment.
Genome Res.
13
2265-2270
2003
712066
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
712067
Otsuki T.,Ota T.,Nishikawa T.,Hayashi K.,Suzuki Y.,Yamamoto J.,Wakamatsu A.,Kimura K.,Sakamoto K.,Hatano N.,Kawai Y.,Ishii S.,Saito K.,Kojima S.,Sugiyama T.,Ono T.,Okano K.,Yoshikawa Y.,Aotsuka S.,Sasaki N.,Hattori A.,Okumura K.,Nagai K.,Sugano S.,Isogai T.
Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries.
DNA Res.
12
117-126
2005
712069
Muzny D.M.,Scherer S.E.,Kaul R.,Wang J.,Yu J.,Sudbrak R.,Buhay C.J.,Chen R.,Cree A.,Ding Y.,Dugan-Rocha S.,Gill R.,Gunaratne P.,Harris R.A.,Hawes A.C.,Hernandez J.,Hodgson A.V.,Hume J.,Jackson A.,Khan Z.M.,Kovar-Smith C.,Lewis L.R.,Lozado R.J.,Metzker M.L.,Milosavljevic A.,Miner G.R.,Morgan M.B.,Nazareth L.V.,Scott G.,Sodergren E.,Song X.-Z.,Steffen D.,Wei S.,Wheeler D.A.,Wright M.W.,Worley K.C.,Yuan Y.,Zhang Z.,Adams C.Q.,Ansari-Lari M.A.,Ayele M.,Brown M.J.,Chen G.,Chen Z.,Clendenning J.,Clerc-Blankenburg K.P.,Chen R.,Chen Z.,Davis C.,Delgado O.,Dinh H.H.,Dong W.,Draper H.,Ernst S.,Fu G.,Gonzalez-Garay M.L.,Garcia D.K.,Gillett W.,Gu J.,Hao B.,Haugen E.,Havlak P.,He X.,Hennig S.,Hu S.,Huang W.,Jackson L.R.,Jacob L.S.,Kelly S.H.,Kube M.,Levy R.,Li Z.,Liu B.,Liu J.,Liu W.,Lu J.,Maheshwari M.,Nguyen B.-V.,Okwuonu G.O.,Palmeiri A.,Pasternak S.,Perez L.M.,Phelps K.A.,Plopper F.J.,Qiang B.,Raymond C.,Rodriguez R.,Saenphimmachak C.,Santibanez J.,Shen H.,Shen Y.,Subramanian S.,Tabor P.E.,Verduzco D.,Waldron L.,Wang J.,Wang J.,Wang Q.,Williams G.A.,Wong G.K.-S.,Yao Z.,Zhang J.,Zhang X.,Zhao G.,Zhou J.,Zhou Y.,Nelson D.,Lehrach H.,Reinhardt R.,Naylor S.L.,Yang H.,Olson M.,Weinstock G.,Gibbs R.A.
The DNA sequence, annotation and analysis of human chromosome 3.
Nature
440
1194-1198
2006
712071
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Genome Res.
14
2121-2127
2004
712072
Zhang Z.,Henzel W.J.
Signal peptide prediction based on analysis of experimentally verified cleavage sites.
Protein Sci.
13
2819-2824
2004
712073
Fernandez-Valdivia R.,Takeuchi H.,Samarghandi A.,Lopez M.,Leonardi J.,Haltiwanger R.S.,Jafar-Nejad H.
Regulation of mammalian Notch signaling and embryonic development by the protein O-glucosyltransferase Rumi.
Development
138
1925-1934
2011
712074
Wu Z.L.,Ethen C.M.,Prather B.,Machacek M.,Jiang W.
Universal phosphatase-coupled glycosyltransferase assay.
Glycobiology
21
727-733
2011
712075
Takeuchi H.,Fernandez-Valdivia R.C.,Caswell D.S.,Nita-Lazar A.,Rana N.A.,Garner T.P.,Weldeghiorghis T.K.,Macnaughtan M.A.,Jafar-Nejad H.,Haltiwanger R.S.
Rumi functions as both a protein O-glucosyltransferase and a protein O-xylosyltransferase.
Proc. Natl. Acad. Sci. U.S.A.
108
16600-16605
2011
712076
Basmanav F.B.,Oprisoreanu A.M.,Pasternack S.M.,Thiele H.,Fritz G.,Wenzel J.,Grosser L.,Wehner M.,Wolf S.,Fagerberg C.,Bygum A.,Altmuller J.,Rutten A.,Parmentier L.,El Shabrawi-Caelen L.,Hafner C.,Nurnberg P.,Kruse R.,Schoch S.,Hanneken S.,Betz R.C.
Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease.
Am. J. Hum. Genet.
94
135-143
2014
712077
Servian-Morilla E.,Takeuchi H.,Lee T.V.,Clarimon J.,Mavillard F.,Area-Gomez E.,Rivas E.,Nieto-Gonzalez J.L.,Rivero M.C.,Cabrera-Serrano M.,Gomez-Sanchez L.,Martinez-Lopez J.A.,Estrada B.,Marquez C.,Morgado Y.,Suarez-Calvet X.,Pita G.,Bigot A.,Gallardo E.,Fernandez-Chacon R.,Hirano M.,Haltiwanger R.S.,Jafar-Nejad H.,Paradas C.
A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss.
EMBO Mol. Med.
8
1289-1309
2016
712078
Li Z.,Fischer M.,Satkunarajah M.,Zhou D.,Withers S.G.,Rini J.M.
Structural basis of Notch O-glucosylation and O-xylosylation by mammalian protein-O-glucosyltransferase 1 (POGLUT1).
Nat. Commun.
8
185-185
2017
712079
Wilson N.J.,Cole C.,Kroboth K.,Hunter W.N.,Mann J.A.,McLean W.H.,Kernland Lang K.,Beltraminelli H.,Sabroe R.A.,Tiffin N.,Sobey G.J.,Borradori L.,Simpson E.,Smith F.J.
Mutations in POGLUT1 in Galli-Galli/Dowling-Degos disease.
Br. J. Dermatol.
176
270-274
2017