NucleaRDB: Extraction of mutation data from the literature

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This data was extracted from Medline abstracts and full texts (when available) in an automated manner.

The table below describes the selected point mutation and provides links to other documents. The sentence(s) where the point mutation L326A was found are listed after the table.

The mutated residues are also indicated in the family sequence alignments and hyperlinked to the corresponding mutation pages.


Point mutation L326A in NR1I3_MOUSE

Point mutation:L326A
Cited point mutation:Leu326Ala,Leu326
Domain:LBD HELIX 10-11
General numbering (NucleaRDB): 1047
Protein:NR1I3_MOUSE (Nr1i3,Ca)Swiss-Prot
Cross-reference table
Family page
Protein isoforms2
Other point mutations / same proteinList of mutations in NR1I3_MOUSE
Family alignments 1I3 Constitutive Androstane alpha (CAR1)
1I Vitamin D3-like (VDR,PXR,CAR)
1 Thyroid hormone like (TR,RAR,ROR,PPAR,VDR
Other point mutations / same position
Reference:The peptide near the C terminus regulates receptor CAR nuclear translocation induced by xenochemicals in mouse liver.
Zelko I, Sueyoshi T, Kawamoto T, Moore R, Negishi M
Mol Cell Biol 2001 Apr;21(8):2838-46.
Medline
Other point mutations / same articleList
Text sourceHTML and PDF full texts
Validation statusTrue positive

Relevant sentences:

Leu326


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F.Horn (nucleardbcmbi.kun.nl), 21-Apr-2005