Sequence of NEUR1_MOUSE
EC Number:3.2.1.18
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
Reaction
colominic acid + H2O = sialic acid + lactose
Other sequences found for EC No. 3.2.1.18
General information:
Sequence
0 MVGADPTRPR GPLSYWAGRR GQGLAAIFLL LVSAAESEAR AEDDFSLVQP LVTMEQLLWV
60 SGKQIGSVDT FRIPLITATP RGTLLAFAEA RKKSASDEGA KFIAMRRSTD QGSTWSSTAF
120 IVDDGEASDG LNLGAVVNDV DTGIVFLIYT LCAHKVNCQV ASTMLVWSKD DGISWSPPRN
180 LSVDIGTEMF APGPGSGIQK QREPGKGRLI VCGHGTLERD GVFCLLSDDH GASWHYGTGV
240 SGIPFGQPKH DHDFNPDECQ PYELPDGSVI INARNQNNYH CRCRIVLRSY DACDTLRPRD
300 VTFDPELVDP VVAAGALATS SGIVFFSNPA HPEFRVNLTL RWSFSNGTSW QKERVQVWPG
360 PSGYSSLTAL ENSTDGKKQP PQLFVLYEKG LNRYTESISM VKISVYGTL
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Sequence related references
Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
65682
Carrillo M.B.,Milner C.M.,Ball S.T.,Snoek M.,Campbell R.D.
Cloning and characterization of a sialidase from the murine histocompatibility-2 complex: low levels of mRNA and a single amino acid mutation are responsible for reduced sialidase activity in mice carrying the Neu1a allele.
Glycobiology
7
975-986
1997
65683
Igdoura S.A.,Gafuik C.,Mertineit C.,Saberi F.,Pshezhetsky A.V.,Potier M.,Trasler J.M.,Gravel R.A.
Cloning of the cDNA and gene encoding mouse lysosomal sialidase and correction of sialidase deficiency in human sialidosis and mouse SM/J fibroblasts.
Hum. Mol. Genet.
7
115-121
1998
65684
Xie T.,Rowen L.,Aguado B.,Ahearn M.E.,Madan A.,Qin S.,Campbell R.D.,Hood L.
Analysis of the gene-dense major histocompatibility complex class III region and its comparison to mouse.
Genome Res.
13
2621-2636
2003
65685
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Genome Res.
14
2121-2127
2004
65686
Huttlin E.L.,Jedrychowski M.P.,Elias J.E.,Goswami T.,Rad R.,Beausoleil S.A.,Villen J.,Haas W.,Sowa M.E.,Gygi S.P.
A tissue-specific atlas of mouse protein phosphorylation and expression.
Cell
143
1174-1189
2010
65687
Rottier R.J.,Bonten E.J.,d'Azzo A.
A point mutation in the neu-1 locus causes the neuraminidase defect in the SM/J mouse.
Hum. Mol. Genet.
7
313-321
1998