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 F171A 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: | F171A | |
| Cited point mutation: | Phe171Ala,Phe171 | |
| Domain: | LBD HELIX 3 | |
| General numbering (NucleaRDB): | 335 | |
| Protein: | NR1I3_MOUSE (Nr1i3,Ca) | Swiss-Prot Cross-reference table Family page |
| Protein isoforms | 2 | |
| Other point mutations / same protein / same position | Point mutations at position 171 in NR1I3_MOUSE | |
| Other point mutations / same protein | List 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 |
Position 171 in 1I3 Constitutive Androstane alpha (CAR1) family Position 225 in 1I Vitamin D3-like (VDR,PXR,CAR) family Position 218 in 1 Thyroid hormone like (TR,RAR,ROR,PPAR,VDR family | |
| Reference: | Molecular determinants of steroid inhibition for the mouse constitutive androstane receptor. Jyrkkarinne J, Makinen J, Gynther J, Savolainen H, Poso A, Honkakoski P J Med Chem 2003 Oct 23;46(22):4687-95. | Medline |
| Other point mutations / same article | List | |
| Text source | HTML full text | |
| Validation status | Not yet checked |
Relevant sentences:
Phe171
cmbi.kun.nl), 21-Apr-2005