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Reviewed, UniProtKB/Swiss-Prot O43423 (AN32C_HUMAN)

Last modified November 24, 2009. Version 72. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (5) | 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:
    Acidic leucine-rich nuclear phosphoprotein 32 family member C
Alternative name(s):
    Phosphoprotein 32-related protein 1
    Tumorigenic protein pp32r1
Gene names
Name: ANP32C
Synonyms: PP32R1
OrganismHomo sapiens (Human) [Complete proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length234 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is not processed.
Protein existenceEvidence at transcript level.

General annotation (Comments)

Tissue specificity

Expressed in activated stem cells, such as mobilized CD34+ cells and cord blood CD34+ cells, but not in resting bone marrow CD34+ cells. Expressed in a variety of neoplastic cell lines, mainly in prostatic adenocarcinoma cell lines. Not expressed in normal protastic tissue. Ref.1 Ref.3

Sequence similarities

Belongs to the ANP32 family.

Contains 4 LRR (leucine-rich) repeats.

Caution

The His-140 polymorphism is uncertain. It has been found in prostatic cell line without corresponding normal tissue sample. Cells transfected with this variant expressed at least twice as much proteins than native cells.

Ontologies

Keywords
   Coding sequence diversityPolymorphism
   DomainLeucine-rich repeat
Repeat
   Technical termComplete proteome
Gene Ontology (GO)
   Molecular functionprotein binding

Inferred from electronic annotation. Source: InterPro

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 234234Acidic leucine-rich nuclear phosphoprotein 32 family member C
PRO_0000137597

Regions

Repeat44 – 6320LRR 1
Repeat64 – 8421LRR 2
Repeat85 – 10723LRR 3
Repeat111 – 13424LRR 4
Compositional bias157 – 22872Asp/Glu-rich (highly acidic)

Natural variations

Natural variant231A → V: dbSNP rs2288674.
VAR_026702
Natural variant711R → K: dbSNP rs2288675. Ref.3
VAR_020419
Natural variant1051L → P: dbSNP rs17008716.
VAR_048314
Natural variant1401Y → H
VAR_026703
Natural variant2041E → G: dbSNP rs2288676.
VAR_020420

Sequences

Sequence LengthMass (Da)Tools
O43423-1 [UniParc].

Last modified June 1, 1998. Version 1.
Checksum: 2515D9678EACC5C2

FASTA23426,762
        10         20         30         40         50         60 
MEMGRRIHSE LRNRAPSDVK ELALDNSRSN EGKLEALTDE FEELEFLSKI NGGLTSISDL 

        70         80         90        100        110        120 
PKLKLRKLEL RVSGGLEVLA EKCPNLTHLY LSGNKIKDLS TIEPLKQLEN LKSLDLFNCE 

       130        140        150        160        170        180 
VTNLNDYGEN VFKLLLQLTY LDSCYWDHKE APYSDIEDHV EGLDDEEEGE HEEEYDEDAQ 

       190        200        210        220        230 
VVEDEEGEEE EEEGEEEDVS GGDEEDEEGY NDGEVDGEED EEELGEEERG QKRK 

« Hide

References

[1]"Modulation of oncogenic potential by alternative gene use in human prostate cancer."
Kadkol S.S., Brody J.R., Pevsner J., Bai J., Pasternack G.R.
Nat. Med. 5:275-279(1999) [PubMed: 10086381] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA], TISSUE SPECIFICITY.
[2]Erratum
Kadkol S.S., Brody J.R., Pevsner J., Bai J., Pasternack G.R.
Nat. Med. 5:1087-1087(1999) [PubMed: 10471270] [Abstract]
[3]"Identification of a functional mutation in pp32r1 (ANP32C)."
Kochevar G.J., Brody J.R., Kadkol S.S., Murphy K.M., Pasternack G.R.
Hum. Mutat. 23:546-551(2004) [PubMed: 15146458] [Abstract]
Cited for: VARIANTS VAL-23; LYS-71 AND HIS-140, TISSUE SPECIFICITY.
[4]"The Anp32 family of proteins containing leucine-rich repeats."
Matilla A., Radrizzani M.
Cerebellum 4:7-18(2005) [PubMed: 15895553] [Abstract]
Cited for: GENE FAMILY, NOMENCLATURE.

Cross-references

Sequence databases

AF008216 Genomic DNA. Translation: AAD12746.1.
IPIIPI00018262.
RefSeqNP_036535.1.
UniGeneHs.661161

3D structure databases

ModBaseSearch...

Protein-protein interaction databases

STRINGO43423.

Proteomic databases

PRIDEO43423.

Genome annotation databases

EnsemblENST00000330241; ENSP00000329250; ENSG00000184701; Homo sapiens. [Genome view]
GeneID23520.
KEGGhsa:23520.
UCSCuc003iqt.1. human.

Organism-specific databases

CTD23520.
GeneCardsGC04M165337.
H-InvDBHIX0031531.
HGNCHGNC:16675. ANP32C.
MIM606877. gene.
PharmGKBPA24813.
GenAtlasSearch...

Phylogenomic databases

HOGENOMO43423.
HOVERGENO43423.
OMAGRRIHSE
OrthoDBEOG9GJ293

Gene expression databases

ArrayExpressO43423.
BgeeO43423.
CleanExHS_ANP32C.
GenevestigatorO43423.
GermOnlineENSG00000184701. Homo sapiens.

Family and domain databases

InterProIPR001611. Leu-rich_rpt.
[Graphical view]
PfamPF00560. LRR_1. 1 hit.
[Graphical view]
ProtoNetSearch...

Other Resources

NextBio45969.
SOURCESearch...

Entry information

Entry nameAN32C_HUMAN
AccessionPrimary (citable) accession number: O43423
Entry history
Integrated into UniProtKB/Swiss-Prot: December 6, 2002
Last sequence update: June 1, 1998
Last modified: November 24, 2009
This is version 72 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation projectHPI (Human Proteome Initiative)
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 4

Human chromosome 4: 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

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