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Database: UniProt
Entry: W5K7W7_ASTMX
LinkDB: W5K7W7_ASTMX
Original site: W5K7W7_ASTMX 
ID   W5K7W7_ASTMX            Unreviewed;       676 AA.
AC   W5K7W7;
DT   16-APR-2014, integrated into UniProtKB/TrEMBL.
DT   05-DEC-2018, sequence version 2.
DT   27-MAR-2024, entry version 57.
DE   SubName: Full=Fragile X mental retardation syndrome-related protein 1 {ECO:0000313|Ensembl:ENSAMXP00000003678.2};
OS   Astyanax mexicanus (Blind cave fish) (Astyanax fasciatus mexicanus).
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
OC   Actinopterygii; Neopterygii; Teleostei; Ostariophysi; Characiformes;
OC   Characoidei; Characidae; Astyanax.
OX   NCBI_TaxID=7994 {ECO:0000313|Ensembl:ENSAMXP00000003678.2, ECO:0000313|Proteomes:UP000018467};
RN   [1] {ECO:0000313|Proteomes:UP000018467}
RP   NUCLEOTIDE SEQUENCE.
RC   STRAIN=female {ECO:0000313|Proteomes:UP000018467};
RA   Jeffery W., Warren W., Wilson R.K.;
RL   Submitted (MAR-2013) to the EMBL/GenBank/DDBJ databases.
RN   [2] {ECO:0000313|Proteomes:UP000018467}
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RC   STRAIN=female {ECO:0000313|Proteomes:UP000018467};
RX   PubMed=25329095; DOI=10.1038/ncomms6307;
RA   McGaugh S.E., Gross J.B., Aken B., Blin M., Borowsky R., Chalopin D.,
RA   Hinaux H., Jeffery W.R., Keene A., Ma L., Minx P., Murphy D., O'Quin K.E.,
RA   Retaux S., Rohner N., Searle S.M., Stahl B.A., Tabin C., Volff J.N.,
RA   Yoshizawa M., Warren W.C.;
RT   "The cavefish genome reveals candidate genes for eye loss.";
RL   Nat. Commun. 5:5307-5307(2014).
RN   [3] {ECO:0000313|Ensembl:ENSAMXP00000003678.2}
RP   IDENTIFICATION.
RG   Ensembl;
RL   Submitted (NOV-2023) to UniProtKB.
CC   -!- SUBCELLULAR LOCATION: Cytoplasm, Cytoplasmic ribonucleoprotein granule
CC       {ECO:0000256|ARBA:ARBA00004331}.
CC   -!- SIMILARITY: Belongs to the FMR1 family.
CC       {ECO:0000256|ARBA:ARBA00006633}.
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DR   AlphaFoldDB; W5K7W7; -.
DR   STRING; 7994.ENSAMXP00000003678; -.
DR   Ensembl; ENSAMXT00000003678.2; ENSAMXP00000003678.2; ENSAMXG00000003585.2.
DR   eggNOG; ENOG502QPKJ; Eukaryota.
DR   GeneTree; ENSGT00950000183189; -.
DR   HOGENOM; CLU_020699_3_0_1; -.
DR   InParanoid; W5K7W7; -.
DR   OrthoDB; 2995592at2759; -.
DR   Proteomes; UP000018467; Unassembled WGS sequence.
DR   Bgee; ENSAMXG00000003585; Expressed in heart and 14 other cell types or tissues.
DR   GO; GO:0036464; C:cytoplasmic ribonucleoprotein granule; IEA:UniProtKB-SubCell.
DR   GO; GO:0003729; F:mRNA binding; IEA:InterPro.
DR   GO; GO:0006417; P:regulation of translation; IEA:InterPro.
DR   CDD; cd20473; Tudor_Agenet_FXR2_rpt1; 1.
DR   CDD; cd20476; Tudor_Agenet_FXR2_rpt2; 1.
DR   Gene3D; 2.30.30.140; -; 2.
DR   Gene3D; 3.30.1370.10; K Homology domain, type 1; 2.
DR   InterPro; IPR008395; Agenet-like_dom.
DR   InterPro; IPR040148; FMR1.
DR   InterPro; IPR022034; FMR1-like_C_core.
DR   InterPro; IPR040472; FMRP_KH0.
DR   InterPro; IPR032172; FXR1_C1.
DR   InterPro; IPR004087; KH_dom.
DR   InterPro; IPR004088; KH_dom_type_1.
DR   InterPro; IPR036612; KH_dom_type_1_sf.
DR   InterPro; IPR047421; Tudor_Agenet_FXR2_rpt1.
DR   InterPro; IPR047420; Tudor_Agenet_FXR2_rpt2.
DR   InterPro; IPR041560; Tudor_FRM1.
DR   PANTHER; PTHR10603; FRAGILE X MENTAL RETARDATION SYNDROME-RELATED PROTEIN; 1.
DR   PANTHER; PTHR10603:SF3; FRAGILE X MENTAL RETARDATION SYNDROME-RELATED PROTEIN 2; 1.
DR   Pfam; PF05641; Agenet; 1.
DR   Pfam; PF12235; FXMRP1_C_core; 1.
DR   Pfam; PF16096; FXR_C1; 1.
DR   Pfam; PF00013; KH_1; 2.
DR   Pfam; PF17904; KH_9; 1.
DR   Pfam; PF18336; Tudor_FRX1; 1.
DR   SMART; SM00322; KH; 2.
DR   SUPFAM; SSF54791; Eukaryotic type KH-domain (KH-domain type I); 2.
DR   PROSITE; PS51641; AGENET_LIKE; 2.
DR   PROSITE; PS50084; KH_TYPE_1; 2.
PE   3: Inferred from homology;
KW   Cytoplasm {ECO:0000256|ARBA:ARBA00022490};
KW   Reference proteome {ECO:0000313|Proteomes:UP000018467};
KW   Repeat {ECO:0000256|ARBA:ARBA00022737};
KW   RNA-binding {ECO:0000256|PROSITE-ProRule:PRU00117}.
FT   DOMAIN          4..50
FT                   /note="Agenet-like"
FT                   /evidence="ECO:0000259|PROSITE:PS51641"
FT   DOMAIN          63..115
FT                   /note="Agenet-like"
FT                   /evidence="ECO:0000259|PROSITE:PS51641"
FT   REGION          397..676
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        458..483
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        495..513
FT                   /note="Polar residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        535..556
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        624..655
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        657..676
FT                   /note="Polar residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
SQ   SEQUENCE   676 AA;  74885 MW;  7D97911F75F92FED CRC64;
     MDGLAVEVRG SNGAFYKGFV KDVHEDSLTI VFENNWQPER QLPFSDVRLP PPSDYNKDIG
     EGEEVEVYSR ANEQEPCGWW LARVRMMKGE FYVIEYAACD ATYNEIVTAE RIRPVNPNSP
     ASRNTFYKVN VAVPEDLREI CLTENIHKDF RKAIGASCIF YNASIQELVV LSTTESTVKR
     AGLLSDMHFR SIRTKLMLMS RNEEATKHLE TSKQLASAYQ EEVRVREDLM GLAIGSHGAN
     IQQARKVPGV TAIELEEESC TFRIYGETPE AVKQARVYLE FKEDSFPVPR NLVGKVIGKS
     GKIIQEIVDK SGVVRVRIEG DNDKKLPREE VGWQASDSAD TVDGQEGMVP FIFVGTKENI
     SNAQALLEYH VAYLQEVEQL RLERLQIDEQ LRQIGVGYRA PPSRTGGPST GDRERGYLTD
     ESSNSLQTSR TYGGRGRGRK GNAYSGYGTN SEMSNASETE DLGEREPRPR GVGVDERGSR
     RGGRGRGSST GRGRGGPGPR NSNTISSVLR DPDSNPYSLL EGEGDLGGDT DASESMGGSD
     RRRRSRRRRN DQEPSVIDAD ANESDGQAAA SENGLDEDSK PQRRNRSRRR RNRGNRPEGG
     SASRDRQPVT VADLISRPES QSRQNLPVKK EDIQHASHPK ENGTSVKKEE RVPSKRSPSN
     GVATSGEALT LVNGVS
//
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