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 I442A 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: | I442A | |
| Domain: | LBD HELIX 12 | |
| General numbering (NucleaRDB): | 1251 | |
| Protein: | NR1H3_HUMAN (NR1H3,LXR) | Swiss-Prot Cross-reference table Family page |
| Protein isoforms | 2 | |
| Other point mutations / same protein | List of mutations in NR1H3_HUMAN | |
| Family alignments |
1H3 Oxysterol LXR alpha 1H Ecdysone-like (ECR,LXR,FXR) 1 Thyroid hormone like (TR,RAR,ROR,PPAR,VDR | |
| Other point mutations / same position |
Position 404 in 1 Thyroid hormone like (TR,RAR,ROR,PPAR,VDR family | |
| Reference: | Molecular determinants of LXRalpha agonism. Wang M, Thomas J, Burris TP, Schkeryantz J, Michael LF J Mol Graph Model 2003 Nov;22(2):173-81. | Medline |
| Other point mutations / same article | List | |
| Text source | HTML full text | |
| Validation status | Not yet checked |
Relevant sentences:
I442A
cmbi.kun.nl), 21-Apr-2005