NucleaRDB: Extraction of mutation data from the literature

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

Point mutation(s) at position 401 ( 1248 - 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
NR1H3_HUMAN   (Q13133)   1H3 Oxysterol LXR alpha                          L439A        Wang M et al.,2003
NR1I3_MOUSE   (O35627)   1I3 Constitutive Androstane alpha (CAR1)         L353A        Andersin T et al.,2003
O77255_CHOFU  (O77255)   1H1 Ecdysone                                     L517A        Kumar MB et al.,2002
PPAT_HUMAN    (P37231)   1C3 PPAR gamma                                   L497A        Chen S et al.,2000
VDR_HUMAN     (P11473)   1I1 Vitamin D3 (VDR)                             V418A        Kahlen JP et al.,1997
VDR_HUMAN     (P11473)   1I1 Vitamin D3 (VDR)                             V418A        Nayeri S et al.,1997
VDR_HUMAN     (P11473)   1I1 Vitamin D3 (VDR)                             V418S        Mohr SC et al.,2001

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