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Sequence of KDSR_HUMAN

EC Number:1.1.1.102

EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
3-dehydrosphinganine reductase
Q06136
Homo sapiens
332
36187
Reaction
sphinganine + NADP+ = 3-dehydrosphinganine + NADPH + H+
Other sequences found for EC No. 1.1.1.102

General information:

Sequence
show sequence in fasta format
  0 MLLLAAAFLV AFVLLLYMVS PLISPKPLAL PGAHVVVTGG SSGIGKCIAI ECYKQGAFIT
 60 LVARNEDKLL QAKKEIEMHS INDKQVVLCI SVDVSQDYNQ VENVIKQAQE KLGPVDMLVN
120 CAGMAVSGKF EDLEVSTFER LMSINYLGSV YPSRAVITTM KERRVGRIVF VSSQAGQLGL
180 FGFTAYSASK FAIRGLAEAL QMEVKPYNVY ITVAYPPDTD TPGFAEENRT KPLETRLISE
240 TTSVCKPEQV AKQIVKDAIQ GNFNSSLGSD GYMLSALTCG MAPVTSITEG LQQVVTMGLF
300 RTIALFYLGS FDSIVRRCMM QREKSENADK TA
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Sequence related references
Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
179662
Rimokh R.,Gadoux M.,Bertheas M.-F.,Berger F.,Garoscio M.,Deleage G.,Germain D.,Magaud J.-P.
FVT-1, a novel human transcription unit affected by variant translocation t(2;18)(p11;q21) of follicular lymphoma.
Blood
81
136-142
1993
179664
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
179665
Nusbaum C.,Zody M.C.,Borowsky M.L.,Kamal M.,Kodira C.D.,Taylor T.D.,Whittaker C.A.,Chang J.L.,Cuomo C.A.,Dewar K.,FitzGerald M.G.,Yang X.,Abouelleil A.,Allen N.R.,Anderson S.,Bloom T.,Bugalter B.,Butler J.,Cook A.,DeCaprio D.,Engels R.,Garber M.,Gnirke A.,Hafez N.,Hall J.L.,Norman C.H.,Itoh T.,Jaffe D.B.,Kuroki Y.,Lehoczky J.,Lui A.,Macdonald P.,Mauceli E.,Mikkelsen T.S.,Naylor J.W.,Nicol R.,Nguyen C.,Noguchi H.,O'Leary S.B.,Piqani B.,Smith C.L.,Talamas J.A.,Topham K.,Totoki Y.,Toyoda A.,Wain H.M.,Young S.K.,Zeng Q.,Zimmer A.R.,Fujiyama A.,Hattori M.,Birren B.W.,Sakaki Y.,Lander E.S.
DNA sequence and analysis of human chromosome 18.
Nature
437
551-555
2005
179667
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Genome Res.
14
2121-2127
2004
179668
Kihara A.,Igarashi Y.
FVT-1 is a mammalian 3-ketodihydrosphingosine reductase with an active site that faces the cytosolic side of the endoplasmic reticulum membrane.
J. Biol. Chem.
279
49243-49250
2004
179669
Boyden L.M.,Vincent N.G.,Zhou J.,Hu R.,Craiglow B.G.,Bayliss S.J.,Rosman I.S.,Lucky A.W.,Diaz L.A.,Goldsmith L.A.,Paller A.S.,Lifton R.P.,Baserga S.J.,Choate K.A.
Mutations in KDSR cause recessive progressive symmetric erythrokeratoderma.
Am. J. Hum. Genet.
100
978-984
2017