NucleaRDB: Extraction of mutation data from the literature

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This page lists the (extracted) point mutations found at one given position in one family multiple sequence alignment.

Point mutation(s) at position 398 ( 1245 - LBD HELIX 12 ) in 1 Thyroid hormone like (TR,RAR,ROR,PPAR,VDR family

See the multiple sequence alignment with the mutation data

Swiss-Prot ID   (AC)            Protein subfamily                    Point mutation
NR1I3_MOUSE   (O35627)   1I3 Constitutive Androstane alpha (CAR1)         T350A        Jyrkkarinne J et al.,2003
NR1I3_MOUSE   (O35627)   1I3 Constitutive Androstane alpha (CAR1)         T350M        Ueda A et al.,2002
NR1I3_MOUSE   (O35627)   1I3 Constitutive Androstane alpha (CAR1)         T350M        Jyrkkarinne J et al.,2003
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F.Horn (nucleardbcmbi.kun.nl), 21-Apr-2005