NucleaRDB: Extraction of mutation data from the literature

logo    2005, NucleaRDB.


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 E318A 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 E318A in NR1I3_HUMAN

Point mutation:E318A
Cited point mutation:Glu318Ala,Glu318
Domain:LBD HELIX 10-11
General numbering (NucleaRDB): 1045
Protein:NR1I3_HUMAN (NR1I3,CA)Swiss-Prot
Cross-reference table
Family page
Protein isoforms2
Other point mutations / same proteinList of mutations in NR1I3_HUMAN
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 Position 380 in 1I Vitamin D3-like (VDR,PXR,CAR) family
Position 369 in 1 Thyroid hormone like (TR,RAR,ROR,PPAR,VDR family
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 full text
Validation statusNot yet checked

Relevant sentences:

Glu318


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