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 402 ( 1249 - 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)         G354A        Andersin T et al.,2003
NR1I3_MOUSE   (O35627)   1I3 Constitutive Androstane alpha (CAR1)         G354Q        Ueda A et al.,2002
PPAT_HUMAN    (P37231)   1C3 PPAR gamma                                   Q498A        Chen S et al.,2000
THB1_HUMAN    (P10828)   1A2 Thyroid hormone beta                         L456R        Ribeiro RC et al.,2001
THB1_HUMAN    (P10828)   1A2 Thyroid hormone beta                         L456R        Marimuthu A et al.,2002
VDR_HUMAN     (P11473)   1I1 Vitamin D3 (VDR)                             L419A        Kahlen JP et al.,1997
VDR_HUMAN     (P11473)   1I1 Vitamin D3 (VDR)                             L419A        Nayeri S et al.,1997

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