PARD3B

PARD3B
Par-3 partitioning defective 3 homolog B (C. elegans)

PDB rendering based on 1wg6.
Identifiers
Symbols PARD3B; ALS2CR19; FLJ92364; MGC16131; PAR3B; PAR3L; PAR3LC; PAR3beta; Par3Lb
External IDs MGI1919301 HomoloGene35389 GeneCards: PARD3B Gene
Orthologs
Species Human Mouse
Entrez 117583 72823
Ensembl ENSG00000116117 ENSMUSG00000052062
UniProt Q8TEW8 Q5SUH9
RefSeq (mRNA) NM_057177.6 NM_001081050.2
RefSeq (protein) NP_476518.4 NP_001074519.2
Location (UCSC) Chr 2:
205.41 – 206.48 Mb
Chr 1:
61.69 – 62.69 Mb
PubMed search [1] [2]

Partitioning defective 3 homolog B is a protein that in humans is encoded by the PARD3B gene.[1][2][3]


Interactions

PARD3B has been shown to interact with Mothers against decapentaplegic homolog 3.[4]

References

  1. ^ Hadano S, Hand CK, Osuga H, Yanagisawa Y, Otomo A, Devon RS, Miyamoto N, Showguchi-Miyata J, Okada Y, Singaraja R, Figlewicz DA, Kwiatkowski T, Hosler BA, Sagie T, Skaug J, Nasir J, Brown RH Jr, Scherer SW, Rouleau GA, Hayden MR, Ikeda JE (Oct 2001). "A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2". Nat Genet 29 (2): 166–73. doi:10.1038/ng1001-166. PMID 11586298. 
  2. ^ Kohjima M, Noda Y, Takeya R, Saito N, Takeuchi K, Sumimoto H (Dec 2002). "PAR3beta, a novel homologue of the cell polarity protein PAR3, localizes to tight junctions". Biochem Biophys Res Commun 299 (4): 641–6. doi:10.1016/S0006-291X(02)02698-0. PMID 12459187. 
  3. ^ "Entrez Gene: PARD3B par-3 partitioning defective 3 homolog B (C. elegans)". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=117583. 
  4. ^ Warner, Dennis R; Pisano M Michele, Roberts Emily A, Greene Robert M (Mar. 2003). "Identification of three novel Smad binding proteins involved in cell polarity". FEBS Lett. (Netherlands) 539 (1–3): 167–73. doi:10.1016/S0014-5793(03)00155-8. ISSN 0014-5793. PMID 12650946. 

Further reading




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