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Sequence of PLOD3_HUMAN

EC Number:2.4.1.66

EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
procollagen glucosyltransferase
O60568
Homo sapiens
738
84785
Reaction
UDP-alpha-D-glucose + [procollagen]-(5R)-5-O-(beta-D-galactosyl)-5-hydroxy-L-lysine = UDP + [procollagen]-(5R)-5-O-[alpha-D-glucosyl-(1->2)-beta-D-galactosyl]-5-hydroxy-L-lysine
Other sequences found for EC No. 2.4.1.66

General information:

Sequence
show sequence in fasta format
  0 MTSSGPGPRF LLLLPLLLPP AASASDRPRG RDPVNPEKLL VITVATAETE GYLRFLRSAE
 60 FFNYTVRTLG LGEEWRGGDV ARTVGGGQKV RWLKKEMEKY ADREDMIIMF VDSYDVILAG
120 SPTELLKKFV QSGSRLLFSA ESFCWPEWGL AEQYPEVGTG KRFLNSGGFI GFATTIHQIV
180 RQWKYKDDDD DQLFYTRLYL DPGLREKLSL NLDHKSRIFQ NLNGALDEVV LKFDRNRVRI
240 RNVAYDTLPI VVHGNGPTKL QLNYLGNYVP NGWTPEGGCG FCNQDRRTLP GGQPPPRVFL
300 AVFVEQPTPF LPRFLQRLLL LDYPPDRVTL FLHNNEVFHE PHIADSWPQL QDHFSAVKLV
360 GPEEALSPGE ARDMAMDLCR QDPECEFYFS LDADAVLTNL QTLRILIEEN RKVIAPMLSR
420 HGKLWSNFWG ALSPDEYYAR SEDYVELVQR KRVGVWNVPY ISQAYVIRGD TLRMELPQRD
480 VFSGSDTDPD MAFCKSFRDK GIFLHLSNQH EFGRLLATSR YDTEHLHPDL WQIFDNPVDW
540 KEQYIHENYS RALEGEGIVE QPCPDVYWFP LLSEQMCDEL VAEMEHYGQW SGGRHEDSRL
600 AGGYENVPTV DIHMKQVGYE DQWLQLLRTY VGPMTESLFP GYHTKARAVM NFVVRYRPDE
660 QPSLRPHHDS STFTLNVALN HKGLDYEGGG CRFLRYDCVI SSPRKGWALL HPGRLTHYHE
720 GLPTTWGTRY IMVSFVDP
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Sequence related references
Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
75954
Valtavaara M.,Szpirer C.,Szpirer J.,Myllylae R.
Primary structure, tissue distribution, and chromosomal localization of a novel isoform of lysyl hydroxylase (lysyl hydroxylase 3).
J. Biol. Chem.
273
12881-12886
1998
75955
Passoja K.,Rautavuoma K.,Ala-Kokko L.,Kosonen T.,Kivirikko K.I.
Cloning and characterization of a third human lysyl hydroxylase isoform.
Proc. Natl. Acad. Sci. U.S.A.
95
10482-10486
1998
75956
Rautavuoma K.,Passoja K.,Helaakoski T.,Kivirikko K.I.
Complete exon-intron organization of the gene for human lysyl hydroxylase 3 (LH3).
Matrix Biol.
19
73-79
2000
75958
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
75959
Hillier L.W.,Fulton R.S.,Fulton L.A.,Graves T.A.,Pepin K.H.,Wagner-McPherson C.,Layman D.,Maas J.,Jaeger S.,Walker R.,Wylie K.,Sekhon M.,Becker M.C.,O'Laughlin M.D.,Schaller M.E.,Fewell G.A.,Delehaunty K.D.,Miner T.L.,Nash W.E.,Cordes M.,Du H.,Sun H.,Edwards J.,Bradshaw-Cordum H.,Ali J.,Andrews S.,Isak A.,Vanbrunt A.,Nguyen C.,Du F.,Lamar B.,Courtney L.,Kalicki J.,Ozersky P.,Bielicki L.,Scott K.,Holmes A.,Harkins R.,Harris A.,Strong C.M.,Hou S.,Tomlinson C.,Dauphin-Kohlberg S.,Kozlowicz-Reilly A.,Leonard S.,Rohlfing T.,Rock S.M.,Tin-Wollam A.-M.,Abbott A.,Minx P.,Maupin R.,Strowmatt C.,Latreille P.,Miller N.,Johnson D.,Murray J.,Woessner J.P.,Wendl M.C.,Yang S.-P.,Schultz B.R.,Wallis J.W.,Spieth J.,Bieri T.A.,Nelson J.O.,Berkowicz N.,Wohldmann P.E.,Cook L.L.,Hickenbotham M.T.,Eldred J.,Williams D.,Bedell J.A.,Mardis E.R.,Clifton S.W.,Chissoe S.L.,Marra M.A.,Raymond C.,Haugen E.,Gillett W.,Zhou Y.,James R.,Phelps K.,Iadanoto S.,Bubb K.,Simms E.,Levy R.,Clendenning J.,Kaul R.,Kent W.J.,Furey T.S.,Baertsch R.A.,Brent M.R.,Keibler E.,Flicek P.,Bork P.,Suyama M.,Bailey J.A.,Portnoy M.E.,Torrents D.,Chinwalla A.T.,Gish W.R.,Eddy S.R.,McPherson J.D.,Olson M.V.,Eichler E.E.,Green E.D.,Waterston R.H.,Wilson R.K.
The DNA sequence of human chromosome 7.
Nature
424
157-164
2003
75961
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Genome Res.
14
2121-2127
2004
75962
Heikkinen J.,Risteli M.,Wang C.,Latvala J.,Rossi M.,Valtavaara M.,Myllylae R.
Lysyl hydroxylase 3 is a multifunctional protein possessing collagen glucosyltransferase activity.
J. Biol. Chem.
275
36158-36163
2000
75963
Wang C.,Risteli M.,Heikkinen J.,Hussa A.K.,Uitto L.,Myllyla R.
Identification of amino acids important for the catalytic activity of the collagen glucosyltransferase associated with the multifunctional lysyl hydroxylase 3 (LH3).
J. Biol. Chem.
277
18568-18573
2002
75964
Rautavuoma K.,Takaluoma K.,Passoja K.,Pirskanen A.,Kvist A.P.,Kivirikko K.I.,Myllyharju J.
Characterization of three fragments that constitute the monomers of the human lysyl hydroxylase isoenzymes 1-3. The 30-kDa N-terminal fragment is not required for lysyl hydroxylase activity.
J. Biol. Chem.
277
23084-23091
2002
75965
Wang C.,Luosujaervi H.,Heikkinen J.,Risteli M.,Uitto L.,Myllylae R.
The third activity for lysyl hydroxylase 3: galactosylation of hydroxylysyl residues in collagens in vitro.
Matrix Biol.
21
559-566
2002
75966
Wang C.,Kovanen V.,Raudasoja P.,Eskelinen S.,Pospiech H.,Myllylae R.
The glycosyltransferase activities of lysyl hydroxylase 3 (LH3) in the extracellular space are important for cell growth and viability.
J. Cell. Mol. Med.
13
508-521
2009
75967
Liefhebber J.M.,Punt S.,Spaan W.J.,van Leeuwen H.C.
The human collagen beta(1-O)galactosyltransferase, GLT25D1, is a soluble endoplasmic reticulum localized protein.
BMC Cell Biol.
11
33-33
2010
75968
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
75969
Wang C.,Ristiluoma M.M.,Salo A.M.,Eskelinen S.,Myllylae R.
Lysyl hydroxylase 3 is secreted from cells by two pathways.
J. Cell. Physiol.
227
668-675
2012
75970
Risteli M.,Ruotsalainen H.,Bergmann U.,Venkatraman Girija U.,Wallis R.,Myllylae R.
Lysyl hydroxylase 3 modifies lysine residues to facilitate oligomerization of mannan-binding lectin.
PLoS ONE
9
0-0
2014
75971
Vaca Jacome A.S.,Rabilloud T.,Schaeffer-Reiss C.,Rompais M.,Ayoub D.,Lane L.,Bairoch A.,Van Dorsselaer A.,Carapito C.
N-terminome analysis of the human mitochondrial proteome.
Proteomics
15
2519-2524
2015
75972
Scietti L.,Chiapparino A.,De Giorgi F.,Fumagalli M.,Khoriauli L.,Nergadze S.,Basu S.,Olieric V.,Cucca L.,Banushi B.,Profumo A.,Giulotto E.,Gissen P.,Forneris F.
Molecular architecture of the multifunctional collagen lysyl hydroxylase and glycosyltransferase LH3.
Nat. Commun.
9
3163-3163
2018
75973
Salo A.M.,Cox H.,Farndon P.,Moss C.,Grindulis H.,Risteli M.,Robins S.P.,Myllylae R.
A connective tissue disorder caused by mutations of the lysyl hydroxylase 3 gene.
Am. J. Hum. Genet.
83
495-503
2008
75974
Maddirevula S.,Alzahrani F.,Al-Owain M.,Al Muhaizea M.A.,Kayyali H.R.,AlHashem A.,Rahbeeni Z.,Al-Otaibi M.,Alzaidan H.I.,Balobaid A.,El Khashab H.Y.,Bubshait D.K.,Faden M.,Yamani S.A.,Dabbagh O.,Al-Mureikhi M.,Jasser A.A.,Alsaif H.S.,Alluhaydan I.,Seidahmed M.Z.,Alabbasi B.H.,Almogarri I.,Kurdi W.,Akleh H.,Qari A.,Al Tala S.M.,Alhomaidi S.,Kentab A.Y.,Salih M.A.,Chedrawi A.,Alameer S.,Tabarki B.,Shamseldin H.E.,Patel N.,Ibrahim N.,Abdulwahab F.,Samira M.,Goljan E.,Abouelhoda M.,Meyer B.F.,Hashem M.,Shaheen R.,AlShahwan S.,Alfadhel M.,Ben-Omran T.,Al-Qattan M.M.,Monies D.,Alkuraya F.S.
Autozygome and high throughput confirmation of disease genes candidacy.
Genet. Med.
21
736-742
2019