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 405 ( 1252 - 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
ECR_DROME     (P34021)   1H1 Ecdysone                                     W650A        Cherbas L et al.,2003
ECR_DROME     (P34021)   1H1 Ecdysone                                     W650A        Hu X et al.,2003
NR1H3_HUMAN   (Q13133)   1H3 Oxysterol LXR alpha                          W443Y        Wang M et al.,2003
NR1I3_MOUSE   (O35627)   1I3 Constitutive Androstane alpha (CAR1)         C357A        Andersin T et al.,2003
NR1I3_MOUSE   (O35627)   1I3 Constitutive Androstane alpha (CAR1)         C357S        Andersin T et al.,2003
NR1I3_MOUSE   (O35627)   1I3 Constitutive Androstane alpha (CAR1)         C357Y        Andersin T et al.,2003
O77255_CHOFU  (O77255)   1H1 Ecdysone                                     W521A        Kumar MB et al.,2002
THB1_RAT      (P18113)   1A2 Thyroid hormone beta                         F459P        Kim HJ et al.,1998
VDR_HUMAN     (P11473)   1I1 Vitamin D3 (VDR)                             F422A        Nayeri S et al.,1996
VDR_HUMAN     (P11473)   1I1 Vitamin D3 (VDR)                             F422A        Nayeri S et al.,1997

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