Variant position: 353 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 410 The length of the canonical sequence.
Location on the sequence:
The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human TRGLKDPEHVEALQDQSQVM LSQHSKAHHPSQPVRFGKLLL
Mouse TRGLKDPEHVEALQDQSQVM LSQHSKAHHPSQPVRFGKLLL
Bovine TRGLKDPEHVEALQDQSQVM LSQHSKAHHPSQLVRFGKLLL
Sequence annotation in neighborhood: The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:
Type: the type of sequence feature. Positions: endpoints of the sequence feature. Description: contains additional information about the feature.
Type Positions Description
1 – 410 Photoreceptor-specific nuclear receptor
169 – 410 NR LBD
337 – 337 Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO)
372 – 372 L -> R. Reduces transcription repressor activity.
339 – 360
The crystal structure of the orphan nuclear receptor NR2E3/PNR ligand binding domain reveals a dimeric auto-repressed conformation.
Tan M.H.; Zhou X.E.; Soon F.F.; Li X.; Li J.; Yong E.L.; Melcher K.; Xu H.E.;
PLoS ONE 8:E74359-E74359(2013)
Cited for: X-RAY CRYSTALLOGRAPHY (2.7 ANGSTROMS) OF 217-410; SUBUNIT; MUTAGENESIS OF LEU-372 AND LEU-375; FUNCTION; CHARACTERIZATION OF VARIANT ASSOCIATED WITH ESCS GLY-334; CHARACTERIZATION OF VARIANTS ESCS PRO-263; GLY-309; GLN-311; PRO-336; VAL-353 AND LYS-407;
Mutation analysis of NR2E3 and NRL genes in enhanced S cone syndrome.
Wright A.F.; Reddick A.C.; Schwartz S.B.; Ferguson J.S.; Aleman T.S.; Kellner U.; Jurklies B.; Schuster A.; Zrenner E.; Wissinger B.; Lennon A.; Shu X.; Cideciyan A.V.; Stone E.M.; Jacobson S.G.; Swaroop A.;
Hum. Mutat. 24:439-439(2004)
Cited for: VARIANTS ESCS 67-CYS--GLY-69 DEL; VAL-88; HIS-97; TRP-104; SER-234; GLU-256; PRO-263; GLY-309; GLN-311; PRO-336; VAL-353 AND LYS-407;
Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.