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Reviewed, UniProtKB/Swiss-Prot O75752 (B3GL1_HUMAN)

Last modified December 16, 2008. Version 67. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (7) | Third-party data | Customize display text xml rdf/xml gff fasta
Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Sequence annotation (Features) · Sequences · References · Web resources · Cross-references · Entry information · Relevant documents

Names and origin

Protein namesRecommended name:
    UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 1
    EC=2.4.1.79
Alternative name(s):
    Beta-3-GalNAc-T1
    Beta-1,3-galactosyltransferase 3
      Short name=Beta-1,3-GalTase 3
      Short name=Beta3Gal-T3
      Short name=b3Gal-T3
    Beta-3-Gx-T3
    Galactosylgalactosylglucosylceramide beta-D-acetyl-galactosaminyltransferase
    UDP-N-acetylgalactosamine:globotriaosylceramide beta-1,3-N-acetylgalactosaminyltransferase
    Globoside synthase
Gene names
Name: B3GALNT1
Synonyms: B3GALT3
ORF Names: UNQ531/PRO1074
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length331 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is not processed.
Protein existenceEvidence at protein level.

General annotation (Comments)

Function

Transfers N-acetylgalactosamine onto globotriaosylceramide. Ref.2

Catalytic activity

UDP-N-acetyl-D-galactosamine + alpha-D-galactosyl-(1->4)-beta-D-galactosyl-(1->4)-beta-D-glucosyl-(1<->1)-ceramide = UDP + N-acetyl-beta-D-galactosaminyl-(1->3)-alpha-D-galactosyl-(1->4)-beta-D-galactosyl-(1->4)-beta-D-glucosyl-(1<->1)-ceramide.

Cofactor

Magnesium. Ref.2 Ref.1

Pathway

Protein modification; protein glycosylation.

Subcellular location

Golgi apparatus membrane; Single-pass type II membrane protein.

Tissue specificity

Higher expression in heart and brain, and to a lesser extent in lung, placenta, kidney and testis. Lower expression in liver, spleen and stomach. No expression in skeletal muscle. Ref.2 Ref.1

Polymorphism

Different combinations or absence of the P blood group system antigens define 5 different phenotypes: P1, P2, P1(k), P2(k), and P. Genetic variation in B3GALT3 determines the P1(k) and P2(k) phenotype, which is rare and lack the capability to synthesize P antigen identified as globoside.

Sequence similarities

Belongs to the glycosyltransferase 31 family.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 331331UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 1
PRO_0000219153

Regions

Topological domain1 – 2020Cytoplasmic Potential
Transmembrane21 – 4323Signal-anchor for type II membrane protein Potential
Topological domain44 – 331288Lumenal Potential

Amino acid modifications

Modified residue1401Phosphotyrosine Ref.10
Modified residue1521Phosphotyrosine Ref.10
Glycosylation721N-linked (GlcNAc...) Potential
Glycosylation1541N-linked (GlcNAc...) Potential
Glycosylation1981N-linked (GlcNAc...) Potential
Glycosylation2121N-linked (GlcNAc...) Potential
Glycosylation3261N-linked (GlcNAc...) Potential

Natural variations

Natural variant1261D → N: dbSNP rs2231257. Ref.8
VAR_025091
Natural variant2661E → A in an French with P2(k) phenotype. Ref.5
VAR_019646
Natural variant2711G → R in an English with P1(k) phenotype.
VAR_019647

Sequences

Sequence LengthMass (Da)Tools
O75752-1 [UniParc].

Last modified November 1, 1998. Version 1.
Checksum: 3556BCAF1646F702

FASTA33139,512
        10         20         30         40         50         60 
MASALWTVLP SRMSLRSLKW SLLLLSLLSF FVMWYLSLPH YNVIERVNWM YFYEYEPIYR 

        70         80         90        100        110        120 
QDFHFTLREH SNCSHQNPFL VILVTSHPSD VKARQAIRVT WGEKKSWWGY EVLTFFLLGQ 

       130        140        150        160        170        180 
EAEKEDKMLA LSLEDEHLLY GDIIRQDFLD TYNNLTLKTI MAFRWVTEFC PNAKYVMKTD 

       190        200        210        220        230        240 
TDVFINTGNL VKYLLNLNHS EKFFTGYPLI DNYSYRGFYQ KTHISYQEYP FKVFPPYCSG 

       250        260        270        280        290        300 
LGYIMSRDLV PRIYEMMGHV KPIKFEDVYV GICLNLLKVN IHIPEDTNLF FLYRIHLDVC 

       310        320        330 
QLRRVIAAHG FSSKEIITFW QVMLRNTTCH Y 

« Hide

References

« Hide 'large scale' references
[1]"A family of human beta3-galactosyltransferases. Characterization of four members of a UDP-galactose:beta-N-acetyl-glucosamine/beta-nacetyl-galactosamine beta-1,3-galactosyltransferase family."
Amado M., Almeida R., Carneiro F., Levery S.B., Holmes E.H., Nomoto M., Hollingsworth M.A., Hassan H., Schwientek T., Nielsen P.A., Bennett E.P., Clausen H.
J. Biol. Chem. 273:12770-12778(1998) [PubMed: 9582303] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA], COFACTOR, TISSUE SPECIFICITY.
[2]"Expression cloning of human globoside synthase cDNAs. Identification of beta3Gal-T3 as UDP-N-acetylgalactosamine:globotriaosylceramide beta1,3-N-acetylgalactosaminyltransferase."
Okajima T., Nakamura Y., Uchikawa M., Haslam D.B., Numata S., Furukawa K., Urano T., Furukawa K.
J. Biol. Chem. 275:40498-40503(2000) [PubMed: 10993897] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA], FUNCTION, COFACTOR, TISSUE SPECIFICITY.
Tissue: Kidney.
[3]Luo W.Q., Chen J.H., Huang X.W., Zhou Y., Zhou H.J., Hu S.N., Yuan J.G.
Submitted (MAR-1999) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [MRNA].
[4]Zhou H.J., Huang X.W., Zhou Y., Hu S.L., Yuan J.G., Qiang B.Q.
Submitted (MAY-1999) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [MRNA].
[5]"Molecular basis of the globoside-deficient P(k) blood group phenotype. Identification of four inactivating mutations in the UDP-N-acetylgalactosamine: globotriaosylceramide 3-beta-N-acetylgalactosaminyltransferase gene."
Hellberg A., Poole J., Olsson M.L.
J. Biol. Chem. 277:29455-29459(2002) [PubMed: 12023287] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA], VARIANT ALA-266.
[6]"The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment."
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. expand/collapse author list , 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.
Genome Res. 13:2265-2270(2003) [PubMed: 12975309] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
[7]"Cloning of human full open reading frames in Gateway(TM) system entry vector (pDONR201)."
Ebert L., Schick M., Neubert P., Schatten R., Henze S., Korn B.
Submitted (JUN-2004) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
[8]SeattleSNPs program for genomic applications
Submitted (AUG-2005) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA], VARIANT ASN-126.
[9]"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res. 14:2121-2127(2004) [PubMed: 15489334] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
Tissue: Brain.
[10]"Tyrosine phosphorylated Par3 regulates epithelial tight junction assembly promoted by EGFR signaling."
Wang Y., Du D., Fang L., Yang G., Zhang C., Zeng R., Ullrich A., Lottspeich F., Chen Z.
EMBO J. 25:5058-5070(2006) [PubMed: 17053785] [Abstract]
Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT TYR-140 AND TYR-152, MASS SPECTROMETRY.

Web resources

BGMUT

Blood group antigen gene mutation database"

GGDB

GlycoGene database

SeattleSNPs
Functional Glycomics Gateway - GTase

Beta-1,3-galactosyltransferase 3

Cross-references

Sequence databases

Y15062 mRNA. Translation: CAA75346.1.
AB050855 mRNA. Translation: BAB17690.1.
AB050856 mRNA. Translation: BAB17691.1.
AF132731 mRNA. Translation: AAF66442.1.
AF154848 mRNA. Translation: AAF72106.1.
AF494106 Genomic DNA. Translation: AAM96012.1.
AY359049 mRNA. Translation: AAQ89408.1.
CR457170 mRNA. Translation: CAG33451.1.
DQ158095 Genomic DNA. Translation: AAZ67917.1.
BC047618 mRNA. Translation: AAH47618.1.
RefSeqNP_001033717.1.
NP_003772.1.
NP_149357.1.
NP_149358.1.
NP_149359.1.
UniGeneHs.418062

3D structure databases

ModBaseSearch...

PTM databases

PhosphoSiteO75752.

Proteomic databases

PRIDEO75752.

Genome annotation databases

EnsemblENSG00000169255. Homo sapiens. [Contig view]
GeneID8706.
KEGGhsa:8706.

Organism-specific databases

GeneCardsGC03M162285.
H-InvDBHIX0003823.
HGNCHGNC:918. B3GALNT1.
MIM111400. phenotype.
603094. gene.
GenAtlasSearch...

Phylogenomic databases

HOGENOMO75752.
HOVERGENO75752.

Gene expression databases

ArrayExpressO75752.
CleanExHS_B3GALNT1.
GermOnlineENSG00000169255. Homo sapiens.

Family and domain databases

InterProIPR002659. Glyco_trans_31.
[Graphical view]
PANTHERPTHR11214. Glyco_trans_31. 1 hit.
PfamPF01762. Galactosyl_T. 1 hit.
[Graphical view]
ProtoNetSearch...

Other Resources

LinkHubO75752.
NextBio32645.
SOURCESearch...

Entry information

Entry nameB3GL1_HUMAN
AccessionPrimary (citable) accession number: O75752
Secondary accession number(s): Q3Y531 expand/collapse secondary AC list , Q6IAI5, Q8NFM8, Q9HA06
Entry history
Integrated into UniProtKB/Swiss-Prot: August 16, 2004
Last sequence update: November 1, 1998
Last modified: December 16, 2008
This is version 67 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation projectHPI (Human Proteome Initiative)

Relevant documents

Blood group antigen proteins

Nomenclature of blood group antigens and list of entries

Human chromosome 3

Human chromosome 3: entries, gene names and cross-references to MIM

Human entries with polymorphisms or disease mutations

List of human entries with polymorphisms or disease mutations

Human polymorphisms and disease mutations

Index of human polymorphisms and disease mutations

MIM cross-references

Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot

PATHWAY comments

Index of metabolic and biosynthesis pathways

SIMILARITY comments

Index of protein domains and families

Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Sequence annotation (Features) · Sequences · References · Web resources · Cross-references · Entry information · Relevant documents