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Q969T3 (SNX21_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified May 29, 2013. Version 98. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (4) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Sorting nexin-21
Alternative name(s):
Sorting nexin L
Short name=SNX-L
Gene names
Name:SNX21
Synonyms:C20orf161, SNXL
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length373 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

General annotation (Comments)

Function

May be involved in several stages of intracellular trafficking By similarity.

Subcellular location

Cytoplasmic vesicle membrane; Peripheral membrane protein; Cytoplasmic side By similarity.

Tissue specificity

Highly expressed in fetus liver, but only weakly expressed in brain, skeleton muscle, smooth muscle, and cardiac muscle, kidney, and adrenal gland. Ref.2

Domain

The PX domain mediates specific binding to membranes enriched in phosphatidylinositol 3-phosphate (PtdIns(P3)) By similarity.

Sequence similarities

Belongs to the sorting nexin family.

Contains 1 PX (phox homology) domain.

Ontologies

Keywords
   Biological processProtein transport
Transport
   Cellular componentCytoplasmic vesicle
Membrane
   Coding sequence diversityAlternative splicing
Polymorphism
   LigandLipid-binding
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Biological_processcell communication

Inferred from electronic annotation. Source: InterPro

protein transport

Inferred from electronic annotation. Source: UniProtKB-KW

   Cellular_componentcytoplasmic vesicle membrane

Inferred from electronic annotation. Source: UniProtKB-SubCell

   Molecular_functionphosphatidylinositol binding

Inferred from electronic annotation. Source: InterPro

Complete GO annotation...

Alternative products

This entry describes 2 isoforms produced by alternative splicing. [Align] [Select]
Isoform 1 (identifier: Q969T3-1)

This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry.
Isoform 2 (identifier: Q969T3-2)

The sequence of this isoform differs from the canonical sequence as follows:
     197-199: RKR → QSH
     200-373: Missing.
Note: No experimental confirmation available.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 373373Sorting nexin-21
PRO_0000213870

Regions

Domain129 – 246118PX

Sites

Binding site1711Phosphatidylinositol 3-phosphate By similarity
Binding site1731Phosphatidylinositol 3-phosphate; via amide nitrogen and carbonyl oxygen By similarity
Binding site1981Phosphatidylinositol 3-phosphate By similarity
Binding site2121Phosphatidylinositol 3-phosphate By similarity

Natural variations

Alternative sequence197 – 1993RKR → QSH in isoform 2.
VSP_045048
Alternative sequence200 – 373174Missing in isoform 2.
VSP_045049
Natural variant1541A → T. Ref.5
Corresponds to variant rs4638862 [ dbSNP | Ensembl ].
VAR_052482

Sequences

Sequence LengthMass (Da)Tools
Isoform 1 [UniParc].

Last modified December 1, 2001. Version 1.
Checksum: 83E4A752BAAEA7B5

FASTA37341,365
        10         20         30         40         50         60 
MHRGTQEGAM ASRLLHRLRH ALAGDGPGEA AASPEAEQFP ESSELEDDDA EGLSSRLSGT 

        70         80         90        100        110        120 
LSFTSAEDDE DDEDEDDEEA GPDQLPLGDG TSGEDAERSP PPDGQWGSQL LARQLQDFWK 

       130        140        150        160        170        180 
KSRNTLAPQR LLFEVTSANV VKDPPSKYVL YTLAVIGPGP PDCQPAQISR RYSDFERLHR 

       190        200        210        220        230        240 
NLQRQFRGPM AAISFPRKRL RRNFTAETIA RRSRAFEQFL GHLQAVPELR HAPDLQDFFV 

       250        260        270        280        290        300 
LPELRRAQSL TCTGLYREAL ALWANAWQLQ AQLGTPSGPD RPLLTLAGLA VCHQELEDPG 

       310        320        330        340        350        360 
EARACCEKAL QLLGDKSLHP LLAPFLEAHV RLSWRLGLDK RQSEARLQAL QEAGLTPTPP 

       370 
PSLKELLIKE VLD 

« Hide

Isoform 2 [UniParc].

Checksum: CEDD7CD4B0C771C0
Show »

FASTA19921,842

References

« Hide 'large scale' references
[1]"A new member (SNX21) of the sorting nexin protein family."
Hong W.
Submitted (JUN-2001) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1).
[2]"Expression of a novel member of sorting nexin gene family, SNX-L, in human liver development."
Zeng W., Yuan W., Wang Y., Jiao W., Zhu Y., Huang C., Li D., Li Y., Zhu C., Wu X., Liu M.
Biochem. Biophys. Res. Commun. 299:542-548(2002) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1), TISSUE SPECIFICITY.
[3]Stavrides G.S., Huckle E.J., Deloukas P.
Submitted (MAY-2001) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1).
[4]"The DNA sequence and comparative analysis of human chromosome 20."
Deloukas P., Matthews L.H., Ashurst J.L., Burton J., Gilbert J.G.R., Jones M., Stavrides G., Almeida J.P., Babbage A.K., Bagguley C.L., Bailey J., Barlow K.F., Bates K.N., Beard L.M., Beare D.M., Beasley O.P., Bird C.P., Blakey S.E. expand/collapse author list , Bridgeman A.M., Brown A.J., Buck D., Burrill W.D., Butler A.P., Carder C., Carter N.P., Chapman J.C., Clamp M., Clark G., Clark L.N., Clark S.Y., Clee C.M., Clegg S., Cobley V.E., Collier R.E., Connor R.E., Corby N.R., Coulson A., Coville G.J., Deadman R., Dhami P.D., Dunn M., Ellington A.G., Frankland J.A., Fraser A., French L., Garner P., Grafham D.V., Griffiths C., Griffiths M.N.D., Gwilliam R., Hall R.E., Hammond S., Harley J.L., Heath P.D., Ho S., Holden J.L., Howden P.J., Huckle E., Hunt A.R., Hunt S.E., Jekosch K., Johnson C.M., Johnson D., Kay M.P., Kimberley A.M., King A., Knights A., Laird G.K., Lawlor S., Lehvaeslaiho M.H., Leversha M.A., Lloyd C., Lloyd D.M., Lovell J.D., Marsh V.L., Martin S.L., McConnachie L.J., McLay K., McMurray A.A., Milne S.A., Mistry D., Moore M.J.F., Mullikin J.C., Nickerson T., Oliver K., Parker A., Patel R., Pearce T.A.V., Peck A.I., Phillimore B.J.C.T., Prathalingam S.R., Plumb R.W., Ramsay H., Rice C.M., Ross M.T., Scott C.E., Sehra H.K., Shownkeen R., Sims S., Skuce C.D., Smith M.L., Soderlund C., Steward C.A., Sulston J.E., Swann R.M., Sycamore N., Taylor R., Tee L., Thomas D.W., Thorpe A., Tracey A., Tromans A.C., Vaudin M., Wall M., Wallis J.M., Whitehead S.L., Whittaker P., Willey D.L., Williams L., Williams S.A., Wilming L., Wray P.W., Hubbard T., Durbin R.M., Bentley D.R., Beck S., Rogers J.
Nature 414:865-871(2001) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[5]"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] (ISOFORM 2), VARIANT THR-154.
Tissue: Kidney.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AF395845 mRNA. Translation: AAK73126.1.
AF523834 mRNA. Translation: AAM77915.1.
AL591562 mRNA. Translation: CAC39140.1.
AL008726 Genomic DNA. Translation: CAI20243.1.
AL008726 Genomic DNA. Translation: CAI20244.1.
BC019823 mRNA. Translation: AAH19823.1.
IPIIPI00056503.
IPI00335868.
RefSeqNP_219489.1. NM_033421.2.
NP_690857.1. NM_152897.1.
UniGeneHs.472854.

3D structure databases

ProteinModelPortalQ969T3.
ModBaseSearch...

Protein-protein interaction databases

IntActQ969T3. 1 interaction.
STRING9606.ENSP00000418593.

PTM databases

PhosphoSiteQ969T3.

Polymorphism databases

DMDM20140138.

Proteomic databases

PaxDbQ969T3.
PRIDEQ969T3.

Protocols and materials databases

DNASU90203.
StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000342644; ENSP00000344586; ENSG00000124104.
ENST00000491381; ENSP00000418593; ENSG00000124104.
GeneID90203.
KEGGhsa:90203.
UCSCuc002xps.1. human.
uc002xpv.1. human.

Organism-specific databases

CTD90203.
GeneCardsGC20P044462.
HGNCHGNC:16154. SNX21.
HPAHPA046359.
neXtProtNX_Q969T3.
PharmGKBPA25703.
GenAtlasSearch...

Phylogenomic databases

eggNOGNOG299779.
HOGENOMHOG000118351.
HOVERGENHBG056464.
InParanoidQ969T3.
OMARRNFTAE.
PhylomeDBQ969T3.

Enzyme and pathway databases

SignaLinkQ969T3.

Gene expression databases

ArrayExpressQ969T3.
BgeeQ969T3.
CleanExHS_SNX21.
GenevestigatorQ969T3.
GermOnlineENSG00000124104. Homo sapiens.

Family and domain databases

Gene3D1.25.40.10. 1 hit.
3.30.1520.10. 1 hit.
InterProIPR001683. Phox.
IPR011990. TPR-like_helical.
[Graphical view]
PfamPF00787. PX. 1 hit.
[Graphical view]
SMARTSM00312. PX. 1 hit.
[Graphical view]
SUPFAMSSF64268. PX. 1 hit.
PROSITEPS50195. PX. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

GenomeRNAi90203.
NextBio76589.

Entry information

Entry nameSNX21_HUMAN
AccessionPrimary (citable) accession number: Q969T3
Secondary accession number(s): Q5JZH5 expand/collapse secondary AC list , Q5JZH6, Q8WUR6, Q9BR16
Entry history
Integrated into UniProtKB/Swiss-Prot: March 27, 2002
Last sequence update: December 1, 2001
Last modified: May 29, 2013
This is version 98 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 20

Human chromosome 20: 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

SIMILARITY comments

Index of protein domains and families