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Reviewed, UniProtKB/Swiss-Prot Q9NQS1 (AVEN_HUMAN)

Last modified July 22, 2008. Version 50. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (4) | 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 · Cross-references · Entry information · Relevant documents

Names and origin

Protein namesRecommended name:
    Cell death regulator Aven
Gene names
Name: AVEN
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length362 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is not processed.
Protein existenceEvidence at protein level.

General annotation (Comments)

Function

Protects against apoptosis mediated by Apaf-1.

Subunit structure

Binds Apaf-1, BCL-2 and BAD (Bcl-xl).

Subcellular location

Membrane; Peripheral membrane protein. Note= Associated with intracellular membranes.

Tissue specificity

Highly expressed in testis, ovary, thymus, prostate, spleen, small intestine, colon, heart, skeletal muscle, liver, kidney and pancreas.

Ontologies

Keywords

   Biological processApoptosis
   Cellular componentMembrane
   Coding sequence diversityPolymorphism
   PTMPhosphoprotein

Gene Ontology (GO)

   Biological processanti-apoptosis Ref.1

Inferred from direct assay. Source: UniProtKB

   Cellular componentintracellular Ref.1

Inferred from direct assay. Source: UniProtKB

membrane fraction Ref.1

Inferred from direct assay. Source: UniProtKB

   Molecular functionprotein binding Ref.1

Inferred from physical interaction. Source: UniProtKB

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical view

Molecule processing

Chain1 – 362362Cell death regulator Aven

Regions

Compositional bias5 – 8581Ala/Gly-rich

Amino acid modifications

Modified residue941Phosphoserine By similarity

Natural variations

Natural variant2281Q → R: dbSNP rs2241647.

Sequences

Sequence LengthMass (Da)Tools
Q9NQS1-1 [UniParc].

Last modified October 1, 2000. Version 1.
Checksum: D86517BA087232D4

FASTA36238,506
        10         20         30         40         50         60 
MQAERGARGG RGRRPGRGRP GGDRHSERPG AAAAVARGGG GGGGGDGGGR RGRGRGRGFR 

        70         80         90        100        110        120 
GARGGRGGGG APRGSRREPG GWGAGASAPV EDDSDAETYG EENDEQGNYS KRKIVSNWDR 

       130        140        150        160        170        180 
YQDIEKEVNN ESGESQRGTD FSVLLSSAGD SFSQFRFAEE KEWDSEASCP KQNSAFYVDS 

       190        200        210        220        230        240 
ELLVRALQEL PLCLRLNVAA ELVQGTVPLE VPQVKPKRTD DGKGLGMQLK GPLGPGGRGP 

       250        260        270        280        290        300 
IFELKSVAAG CPVLLGKDNP SPGPSRDSQK PTSPLQSAGD HLEEELDLLL NLDAPIKEGD 

       310        320        330        340        350        360 
NILPDQTSQD LKSKEDGEVV QEEEVCAKPS VTEEKNMEPE QPSTSKNVTE EELEDWLDSM 


IS 

« Hide

References

« Hide 'large scale' references
[1]"Aven, a novel inhibitor of caspase activation, binds Bcl-xL and Apaf-1."
Chau B.N., Cheng E.H.-Y., Kerr D.A., Hardwick J.M.
Mol. Cell 6:31-40(2000) [PubMed: 10949025] [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: 15489334] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
Tissue: Kidney and Placenta.
+Additional computationally mapped references.

Cross-references

Sequence databases

AF283508 mRNA. Translation: AAF91470.1.
BC010488 mRNA. Translation: AAH10488.1.
BC063533 mRNA. Translation: AAH63533.1.
RefSeqNP_065104.1.
UniGeneHs.555966

3D structure databases

ModBaseSearch...

PTM databases

PhosphoSiteQ9NQS1.

Proteomic databases

PeptideAtlasQ9NQS1.

Genome annotation databases

EnsemblENSG00000169857. Homo sapiens. [Contig view]
GeneID57099.
KEGGhsa:57099.

Organism-specific databases

H-InvDBHIX0012083.
HGNCHGNC:13509. AVEN.
MIM605265. gene.
PharmGKBPA134874337.
GenAtlasSearch...
GeneCardsSearch...

Phylogenomic databases

HOGENOMQ9NQS1.
HOVERGENQ9NQS1.

Gene expression databases

CleanExHS_AVEN.
GermOnlineENSG00000169857. Homo sapiens.

Family and domain databases

ProDomQ9NQS1.
[Graphical view] [Entries sharing at least one domain]
BLOCKSSearch...

Other Resources

SOURCESearch...
ProtoNetSearch...

Entry information

Entry nameAVEN_HUMAN
AccessionPrimary (citable) accession number: Q9NQS1
Entry history
Integrated into UniProtKB/Swiss-Prot: May 2, 2002
Last sequence update: October 1, 2000
Last modified: July 22, 2008
This is version 50 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 15

Human chromosome 15: 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

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