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 E542A 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 E542A in RORA_HUMAN

Point mutation:E542A
Cited point mutation:E509A
Domain:C-term
General numbering (NucleaRDB): -
Protein:RORA_HUMAN (RORA,NR1F1, RZR)Swiss-Prot
Cross-reference table
Family page
Protein isoforms4
Other point mutations / same proteinList of mutations in RORA_HUMAN
Family alignments 1F1 ROR alpha
1F RAR-related orphan receptor (ROR,HR3)
1 Thyroid hormone like (TR,RAR,ROR,PPAR,VDR
Other point mutations / same position Position 403 in 1 Thyroid hormone like (TR,RAR,ROR,PPAR,VDR family
Reference:Crystal structure of the human RORalpha Ligand binding domain in complex with cholesterol sulfate at 2.2 A.
Kallen J, Schlaeppi JM, Bitsch F, Delhon I, Fournier B
J Biol Chem 2004 Apr 2;279(14):14033-8. Epub 2004 Jan 13.
Medline
Other point mutations / same articleList
Text sourceHTML full text
Validation statusNot yet checked

Relevant sentences:

E509A


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