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Reviewed, UniProtKB/Swiss-Prot P26572 (MGAT1_HUMAN)

Last modified November 25, 2008. Version 79. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (6) | 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:
    Alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
    EC=2.4.1.101
Alternative name(s):
    N-glycosyl-oligosaccharide-glycoprotein N-acetylglucosaminyltransferase I
      Short name=GlcNAc-T I
      Short name=GNT-I
Gene names
Name: MGAT1
Synonyms: GGNT1, GLCT1, GLYT1, MGAT
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length445 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is not processed.
Protein existenceEvidence at transcript level.

General annotation (Comments)

Function

Initiates complex N-linked carbohydrate formation. Essential for the conversion of high-mannose to hybrid and complex N-glycans.

Catalytic activity

UDP-N-acetyl-D-glucosamine + 3-(alpha-D-mannosyl)-beta-D-mannosyl-R = UDP + 3-(2-(N-acetyl-beta-D-glucosaminyl)-alpha-D-mannosyl)-beta-D-mannosyl-R.

Pathway

Protein modification; protein glycosylation.

Subcellular location

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

Tissue specificity

Appears to be present in all tissues.

Sequence similarities

Belongs to the glycosyltransferase 13 family.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 445445Alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
PRO_0000191384

Regions

Topological domain1 – 66Cytoplasmic Potential
Transmembrane7 – 2923Signal-anchor for type II membrane protein Potential
Topological domain30 – 445416Lumenal Potential

Natural variations

Natural variant2231R → Q: dbSNP rs7726005.
VAR_028272
Natural variant4351P → L: dbSNP rs634501.
VAR_028273

Sequences

Sequence LengthMass (Da)Tools
P26572-1 [UniParc].

Last modified August 1, 1992. Version 1.
Checksum: 1340386EED69C302

FASTA44550,862
        10         20         30         40         50         60 
MLKKQSAGLV LWGAILFVAW NALLLLFFWT RPAPGRPPSV SALDGDPASL TREVIRLAQD 

        70         80         90        100        110        120 
AEVELERQRG LLQQIGDALS SQRGRVPTAA PPAQPRVPVT PAPAVIPILV IACDRSTVRR 

       130        140        150        160        170        180 
CLDKLLHYRP SAELFPIIVS QDCGHEETAQ AIASYGSAVT HIRQPDLSSI AVPPDHRKFQ 

       190        200        210        220        230        240 
GYYKIARHYR WALGQVFRQF RFPAAVVVED DLEVAPDFFE YFRATYPLLK ADPSLWCVSA 

       250        260        270        280        290        300 
WNDNGKEQMV DASRPELLYR TDFFPGLGWL LLAELWAELE PKWPKAFWDD WMRRPEQRQG 

       310        320        330        340        350        360 
RACIRPEISR TMTFGRKGVS HGQFFDQHLK FIKLNQQFVH FTQLDLSYLQ REAYDRDFLA 

       370        380        390        400        410        420 
RVYGAPQLQV EKVRTNDRKE LGEVRVQYTG RDSFKAFAKA LGVMDDLKSG VPRAGYRGIV 

       430        440 
TFQFRGRRVH LAPPPTWEGY DPSWN 

« Hide

References

« Hide 'large scale' references
[1]"Organization and localization to chromosome 5 of the human UDP-N-acetylglucosamine:alpha-3-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I gene."
Hull E., Sarkar M., Spruijt M.P.N., Hoeppener J.W.M., Dunn R., Schachter H.
Biochem. Biophys. Res. Commun. 176:608-615(1991) [PubMed: 1827260] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA].
Tissue: Myeloid leukemia cell.
[2]"Cloning and expression of N-acetylglucosaminyltransferase I, the medial Golgi transferase that initiates complex N-linked carbohydrate formation."
Kumar R., Yang J., Larsen R.D., Stanley P.
Proc. Natl. Acad. Sci. U.S.A. 87:9948-9952(1990) [PubMed: 1702225] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA], VARIANT LEU-435.
[3]"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: Kidney.
+Additional computationally mapped references.

Web resources

GGDB

GlycoGene database

Functional Glycomics Gateway - GTase

Alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase

Cross-references

Sequence databases

M61829 Genomic DNA. Translation: AAA75523.1.
M55621 mRNA. Translation: AAA52563.1.
BC003575 mRNA. Translation: AAH03575.1.
PIRXUHUMB. JH0397.
RefSeqNP_001108091.1.
NP_001108092.1.
NP_002397.2.
UniGeneHs.519818

3D structure databases

HSSPHSSP built from PDB template 1FO8 based on UniProtKB P27115.
SMRP26572. Positions 104-444.
ModBaseSearch...

PTM databases

PhosphoSiteP26572.

Genome annotation databases

EnsemblENSG00000131446. Homo sapiens. [Contig view]
GeneID4245.
KEGGhsa:4245.

Organism-specific databases

H-InvDBHIX0005500.
HGNCHGNC:7044. MGAT1.
MIM160995. gene.
PharmGKBPA30779.
GenAtlasSearch...
GeneCardsSearch...

Phylogenomic databases

HOVERGENP26572.

Gene expression databases

ArrayExpressP26572.
CleanExHS_MGAT1.
GermOnlineENSG00000131446. Homo sapiens.

Family and domain databases

InterProIPR004139. Glyco_trans_13.
[Graphical view]
PANTHERPTHR10468. Glyco_trans_13. 1 hit.
PfamPF03071. GNT-I. 1 hit.
[Graphical view]
ProtoNetSearch...

Other Resources

NextBio16733.
SOURCESearch...

Entry information

Entry nameMGAT1_HUMAN
AccessionPrimary (citable) accession number: P26572
Entry history
Integrated into UniProtKB/Swiss-Prot: August 1, 1992
Last sequence update: August 1, 1992
Last modified: November 25, 2008
This is version 79 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation projectHPI (Human Proteome Initiative)

Relevant documents

Human chromosome 5

Human chromosome 5: 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