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P78383 (S35B1_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified April 3, 2013. Version 89. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (5) | Third-party data text xml rdf/xml gff fasta
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Names and origin

Protein namesRecommended name:
Solute carrier family 35 member B1
Alternative name(s):
UDP-galactose transporter-related protein 1
Short name=UGTrel1
Short name=hUGTrel1
Gene names
Name:SLC35B1
Synonyms:UGTREL1
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length322 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

General annotation (Comments)

Function

Probable sugar transporter By similarity.

Subcellular location

Endoplasmic reticulum membrane; Multi-pass membrane protein Potential.

Domain

The di-lysine motif confers endoplasmic reticulum localization for type I membrane proteins By similarity.

Sequence similarities

Belongs to the nucleotide-sugar transporter family. SLC35B subfamily.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 322322Solute carrier family 35 member B1
PRO_0000213366

Regions

Transmembrane12 – 3221Helical; Potential
Transmembrane51 – 7121Helical; Potential
Transmembrane85 – 10521Helical; Potential
Transmembrane136 – 15621Helical; Potential
Transmembrane168 – 18821Helical; Potential
Transmembrane210 – 23021Helical; Potential
Transmembrane243 – 26321Helical; Potential
Transmembrane285 – 30521Helical; Potential
Motif318 – 3225Di-lysine motif

Natural variations

Natural variant811R → H. Ref.2
Corresponds to variant rs1135034 [ dbSNP | Ensembl ].
VAR_023778

Sequences

Sequence LengthMass (Da)Tools
P78383 [UniParc].

Last modified May 1, 1997. Version 1.
Checksum: 7B5124A4DEC23598

FASTA32235,760
        10         20         30         40         50         60 
MASSSSLVPD RLRLPLCFLG VFVCYFYYGI LQEKITRGKY GEGAKQETFT FALTLVFIQC 

        70         80         90        100        110        120 
VINAVFAKIL IQFFDTARVD RTRSWLYAAC SISYLGAMVS SNSALQFVNY PTQVLGKSCK 

       130        140        150        160        170        180 
PIPVMLLGVT LLKKKYPLAK YLCVLLIVAG VALFMYKPKK VVGIEEHTVG YGELLLLLSL 

       190        200        210        220        230        240 
TLDGLTGVSQ DHMRAHYQTG SNHMMLNINL WSTLLLGMGI LFTGELWEFL SFAERYPAII 

       250        260        270        280        290        300 
YNILLFGLTS ALGQSFIFMT VVYFGPLTCS IITTTRKFFT ILASVILFAN PISPMQWVGT 

       310        320 
VLVFLGLGLD AKFGKGAKKT SH 

« Hide

References

« Hide 'large scale' references
[1]"Molecular cloning and characterization of a novel isoform of the human UDP-galactose transporter, and of related complementary DNAs belonging to the nucleotide-sugar transporter gene family."
Ishida N., Miura N., Yoshioka S., Kawakita M.
J. Biochem. 120:1074-1078(1996) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA].
[2]"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] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT HIS-81.
Tissue: Skin.

Web resources

GGDB

GlycoGene database

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
D87989 mRNA. Translation: BAA13525.1.
BC011888 mRNA. Translation: AAH11888.1.
IPIIPI00940994.
PIRJC5024.
RefSeqNP_005818.1. NM_005827.1.
UniGeneHs.154073.

3D structure databases

ProteinModelPortalP78383.
ModBaseSearch...

Protein-protein interaction databases

STRING9606.ENSP00000240333.

Protein family/group databases

TCDB2.A.7.11.1. drug/metabolite transporter (DMT) superfamily.

Polymorphism databases

DMDM74735602.

Proteomic databases

PaxDbP78383.
PRIDEP78383.

Protocols and materials databases

DNASU10237.
StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000240333; ENSP00000240333; ENSG00000121073.
GeneID10237.
KEGGhsa:10237.
UCSCuc002iph.1. human.

Organism-specific databases

CTD10237.
GeneCardsGC17M047779.
HGNCHGNC:20798. SLC35B1.
MIM610790. gene.
neXtProtNX_P78383.
PharmGKBPA134864001.
GenAtlasSearch...

Phylogenomic databases

eggNOGCOG0697.
HOGENOMHOG000091197.
HOVERGENHBG083706.
InParanoidP78383.
KOK15275.
OrthoDBEOG4SN1P9.
PhylomeDBP78383.

Gene expression databases

ArrayExpressP78383.
BgeeP78383.
CleanExHS_SLC35B1.
GenevestigatorP78383.
GermOnlineENSG00000121073. Homo sapiens.

Family and domain databases

InterProIPR013657. UAA.
[Graphical view]
PfamPF08449. UAA. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

GenomeRNAi10237.
NextBio38780.
SOURCESearch...

Entry information

Entry nameS35B1_HUMAN
AccessionPrimary (citable) accession number: P78383
Secondary accession number(s): Q96EW7
Entry history
Integrated into UniProtKB/Swiss-Prot: November 22, 2005
Last sequence update: May 1, 1997
Last modified: April 3, 2013
This is version 89 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care.

Relevant documents

Human chromosome 17

Human chromosome 17: 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

SIMILARITY comments

Index of protein domains and families