GenomeNet

Database: UniProt
Entry: SAB_ARATH
LinkDB: SAB_ARATH
Original site: SAB_ARATH 
ID   SAB_ARATH               Reviewed;        2603 AA.
AC   Q6IMT1; F4I9T5; Q0WN66; Q38969; Q9C6Q6; Q9C727;
DT   01-APR-2015, integrated into UniProtKB/Swiss-Prot.
DT   05-JUL-2004, sequence version 1.
DT   24-JAN-2024, entry version 82.
DE   RecName: Full=Protein SABRE {ECO:0000303|PubMed:8275864};
DE   AltName: Full=Protein HYPERSENSITIVE TO PI STARVATION 4 {ECO:0000303|PubMed:22615140};
DE   Flags: Precursor;
GN   Name=SAB {ECO:0000303|PubMed:8275864};
GN   Synonyms=HPS4 {ECO:0000303|PubMed:22615140};
GN   OrderedLocusNames=At1g58250 {ECO:0000312|Araport:AT1G58250};
GN   ORFNames=F16M22.5 {ECO:0000312|EMBL:AAG50951.1},
GN   T18I24.18 {ECO:0000312|EMBL:AAG50770.1};
OS   Arabidopsis thaliana (Mouse-ear cress).
OC   Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;
OC   Spermatophyta; Magnoliopsida; eudicotyledons; Gunneridae; Pentapetalae;
OC   rosids; malvids; Brassicales; Brassicaceae; Camelineae; Arabidopsis.
OX   NCBI_TaxID=3702 {ECO:0000312|EMBL:DAA00365.1};
RN   [1]
RP   NUCLEOTIDE SEQUENCE [MRNA], FUNCTION, AND DISRUPTION PHENOTYPE.
RX   PubMed=14675453; DOI=10.1046/j.1365-313x.2003.01933.x;
RA   Procissi A., Guyon A., Pierson E.S., Giritch A., Knuiman B., Grandjean O.,
RA   Tonelli C., Derksen J., Pelletier G., Bonhomme S.;
RT   "KINKY POLLEN encodes a SABRE-like protein required for tip growth in
RT   Arabidopsis and conserved among eukaryotes.";
RL   Plant J. 36:894-904(2003).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RC   STRAIN=cv. Columbia;
RX   PubMed=11130712; DOI=10.1038/35048500;
RA   Theologis A., Ecker J.R., Palm C.J., Federspiel N.A., Kaul S., White O.,
RA   Alonso J., Altafi H., Araujo R., Bowman C.L., Brooks S.Y., Buehler E.,
RA   Chan A., Chao Q., Chen H., Cheuk R.F., Chin C.W., Chung M.K., Conn L.,
RA   Conway A.B., Conway A.R., Creasy T.H., Dewar K., Dunn P., Etgu P.,
RA   Feldblyum T.V., Feng J.-D., Fong B., Fujii C.Y., Gill J.E., Goldsmith A.D.,
RA   Haas B., Hansen N.F., Hughes B., Huizar L., Hunter J.L., Jenkins J.,
RA   Johnson-Hopson C., Khan S., Khaykin E., Kim C.J., Koo H.L.,
RA   Kremenetskaia I., Kurtz D.B., Kwan A., Lam B., Langin-Hooper S., Lee A.,
RA   Lee J.M., Lenz C.A., Li J.H., Li Y.-P., Lin X., Liu S.X., Liu Z.A.,
RA   Luros J.S., Maiti R., Marziali A., Militscher J., Miranda M., Nguyen M.,
RA   Nierman W.C., Osborne B.I., Pai G., Peterson J., Pham P.K., Rizzo M.,
RA   Rooney T., Rowley D., Sakano H., Salzberg S.L., Schwartz J.R., Shinn P.,
RA   Southwick A.M., Sun H., Tallon L.J., Tambunga G., Toriumi M.J., Town C.D.,
RA   Utterback T., Van Aken S., Vaysberg M., Vysotskaia V.S., Walker M., Wu D.,
RA   Yu G., Fraser C.M., Venter J.C., Davis R.W.;
RT   "Sequence and analysis of chromosome 1 of the plant Arabidopsis thaliana.";
RL   Nature 408:816-820(2000).
RN   [3]
RP   GENOME REANNOTATION, AND SEQUENCE REVISION.
RC   STRAIN=cv. Columbia;
RX   PubMed=27862469; DOI=10.1111/tpj.13415;
RA   Cheng C.Y., Krishnakumar V., Chan A.P., Thibaud-Nissen F., Schobel S.,
RA   Town C.D.;
RT   "Araport11: a complete reannotation of the Arabidopsis thaliana reference
RT   genome.";
RL   Plant J. 89:789-804(2017).
RN   [4]
RP   NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 1257-2603, FUNCTION, AND DISRUPTION
RP   PHENOTYPE.
RC   STRAIN=cv. Wassilewskija;
RX   PubMed=7867930; DOI=10.1101/gad.9.3.330;
RA   Aeschbacher R.A., Hauser M.-T., Feldmann K.A., Benfey P.N.;
RT   "The SABRE gene is required for normal cell expansion in Arabidopsis.";
RL   Genes Dev. 9:330-340(1995).
RN   [5]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 2051-2603.
RC   STRAIN=cv. Columbia;
RA   Totoki Y., Seki M., Ishida J., Nakajima M., Enju A., Kamiya A.,
RA   Narusaka M., Shin-i T., Nakagawa M., Sakamoto N., Oishi K., Kohara Y.,
RA   Kobayashi M., Toyoda A., Sakaki Y., Sakurai T., Iida K., Akiyama K.,
RA   Satou M., Toyoda T., Konagaya A., Carninci P., Kawai J., Hayashizaki Y.,
RA   Shinozaki K.;
RT   "Large-scale analysis of RIKEN Arabidopsis full-length (RAFL) cDNAs.";
RL   Submitted (JUL-2006) to the EMBL/GenBank/DDBJ databases.
RN   [6]
RP   FUNCTION, AND DISRUPTION PHENOTYPE.
RX   PubMed=8275864; DOI=10.1242/dev.119.supplement.57;
RA   Benfey P.N., Linstead P.J., Roberts K., Schiefelbein J.W., Hauser M.-T.,
RA   Aeschbacher R.A.;
RT   "Root development in Arabidopsis: four mutants with dramatically altered
RT   root morphogenesis.";
RL   Development 119:57-70(1993).
RN   [7]
RP   FUNCTION, MUTAGENESIS OF ALA-2118, DISRUPTION PHENOTYPE, AND TISSUE
RP   SPECIFICITY.
RC   STRAIN=cv. Columbia;
RX   PubMed=22615140; DOI=10.1093/jxb/ers131;
RA   Yu H., Luo N., Sun L., Liu D.;
RT   "HPS4/SABRE regulates plant responses to phosphate starvation through
RT   antagonistic interaction with ethylene signalling.";
RL   J. Exp. Bot. 63:4527-4538(2012).
CC   -!- FUNCTION: May be involved in membrane trafficking (By similarity).
CC       Required for cell expansion, especially in root cortex, probably by
CC       counteracting the action of ethylene in promoting cells radial
CC       expansion (PubMed:7867930, PubMed:8275864). Involved in female organ
CC       development (PubMed:14675453). Antagonistically interacts with ethylene
CC       signaling to regulate plant responses to Pi starvation
CC       (PubMed:22615140). {ECO:0000250|UniProtKB:K7VLR4,
CC       ECO:0000269|PubMed:14675453, ECO:0000269|PubMed:22615140,
CC       ECO:0000269|PubMed:7867930, ECO:0000269|PubMed:8275864}.
CC   -!- SUBCELLULAR LOCATION: Secreted {ECO:0000250|UniProtKB:Q6IMT0}. Golgi
CC       apparatus {ECO:0000250|UniProtKB:K7VLR4}.
CC   -!- ALTERNATIVE PRODUCTS:
CC       Event=Alternative splicing; Named isoforms=1;
CC         Comment=Additional isoforms seem to exist. {ECO:0000305};
CC       Name=1;
CC         IsoId=Q6IMT1-1; Sequence=Displayed;
CC   -!- TISSUE SPECIFICITY: Highest levels in leaves, also expressed in leaves,
CC       flowers, and siliques, and, to a lower extent, in roots and stems.
CC       {ECO:0000269|PubMed:22615140}.
CC   -!- DEVELOPMENTAL STAGE: In seedlings, expressed in hypocotyl and in the
CC       entire cotyledon. Observed in all types of cells in the root apex, but
CC       restricted to vascular tissue in the upper part of the root. Stronger
CC       expression in young leaves than in old leaves. Accumulates in all
CC       flower organs, including the sepal, petal, stamen, and gynoecium. In
CC       the silique, high levels at both ends but weak in the middle.
CC       {ECO:0000269|PubMed:22615140}.
CC   -!- DISRUPTION PHENOTYPE: Dwarf plants; smaller aerial organs and wider
CC       roots because of abnormal diffuse cell growth. Abnormal cell expansion
CC       that is greatest in the root cortex cell layer and is independent of
CC       the root growth rate, and that leads to a shift in the orientation of
CC       expansion (PubMed:7867930, PubMed:8275864). Sterility due to female
CC       organ anomalies (PubMed:8275864, PubMed:14675453). Enhanced responses
CC       to Pi starvation (PubMed:22615140). {ECO:0000269|PubMed:14675453,
CC       ECO:0000269|PubMed:22615140, ECO:0000269|PubMed:7867930,
CC       ECO:0000269|PubMed:8275864}.
CC   -!- MISCELLANEOUS: The sequence shown here is derived from an
CC       EMBL/GenBank/DDBJ third party annotation (TPA) entry.
CC   -!- SIMILARITY: Belongs to the SABRE family. {ECO:0000305}.
CC   -!- SEQUENCE CAUTION:
CC       Sequence=AAG50770.1; Type=Erroneous gene model prediction; Evidence={ECO:0000305};
CC       Sequence=AAG50951.1; Type=Erroneous gene model prediction; Evidence={ECO:0000305};
CC       Sequence=AEE33523.1; Type=Erroneous gene model prediction; Evidence={ECO:0000305};
CC       Sequence=BAF01434.1; Type=Frameshift; Evidence={ECO:0000305};
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DR   EMBL; BK000517; DAA00365.1; -; mRNA.
DR   EMBL; AC073943; AAG50951.1; ALT_SEQ; Genomic_DNA.
DR   EMBL; AC079131; AAG50770.1; ALT_SEQ; Genomic_DNA.
DR   EMBL; CP002684; AEE33523.1; ALT_SEQ; Genomic_DNA.
DR   EMBL; AH006602; AAC49734.1; -; Genomic_DNA.
DR   EMBL; AK229585; BAF01434.1; ALT_FRAME; mRNA.
DR   PIR; A96616; A96616.
DR   RefSeq; NP_176121.3; NM_104605.4.
DR   AlphaFoldDB; Q6IMT1; -.
DR   SMR; Q6IMT1; -.
DR   STRING; 3702.Q6IMT1; -.
DR   GlyCosmos; Q6IMT1; 15 sites, No reported glycans.
DR   PaxDb; 3702-AT1G58250-2; -.
DR   ProteomicsDB; 226682; -. [Q6IMT1-1]
DR   GeneID; 842193; -.
DR   KEGG; ath:AT1G58250; -.
DR   Araport; AT1G58250; -.
DR   TAIR; AT1G58250; SAB.
DR   eggNOG; KOG1910; Eukaryota.
DR   InParanoid; Q6IMT1; -.
DR   PRO; PR:Q6IMT1; -.
DR   Proteomes; UP000006548; Chromosome 1.
DR   ExpressionAtlas; Q6IMT1; baseline and differential.
DR   GO; GO:0005576; C:extracellular region; IEA:UniProtKB-SubCell.
DR   GO; GO:0005794; C:Golgi apparatus; IEA:UniProtKB-SubCell.
DR   GO; GO:0016036; P:cellular response to phosphate starvation; IMP:UniProtKB.
DR   GO; GO:0010105; P:negative regulation of ethylene-activated signaling pathway; IMP:UniProtKB.
DR   GO; GO:0030307; P:positive regulation of cell growth; IMP:UniProtKB.
DR   InterPro; IPR019443; BLTP2/FMP27/Hobbit_C.
DR   InterPro; IPR019441; FMP27/BLTP2/Hobbit_GFWDK_RBG.
DR   InterPro; IPR045167; Hobbit.
DR   PANTHER; PTHR15678; ANTIGEN MLAA-22-RELATED; 1.
DR   PANTHER; PTHR15678:SF6; PROTEIN KIAA0100; 1.
DR   Pfam; PF10351; FMP27-BLTP2_C; 1.
DR   Pfam; PF10347; Fmp27_GFWDK; 1.
DR   SMART; SM01214; Fmp27_GFWDK; 1.
PE   1: Evidence at protein level;
KW   Alternative splicing; Coiled coil; Developmental protein; Glycoprotein;
KW   Golgi apparatus; Reference proteome; Secreted; Signal.
FT   SIGNAL          1..35
FT                   /evidence="ECO:0000255"
FT   CHAIN           36..2603
FT                   /note="Protein SABRE"
FT                   /evidence="ECO:0000255"
FT                   /id="PRO_0000432482"
FT   REGION          259..287
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   REGION          786..814
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   REGION          1416..1436
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   REGION          1656..1676
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   REGION          1717..1777
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   REGION          2339..2380
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   REGION          2448..2479
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   REGION          2554..2603
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COILED          1995..2023
FT                   /evidence="ECO:0000255"
FT   COMPBIAS        259..283
FT                   /note="Polar residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        1658..1673
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        1727..1745
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        1746..1767
FT                   /note="Polar residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        2343..2380
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        2448..2466
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        2565..2596
FT                   /note="Polar residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   CARBOHYD        196
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00498"
FT   CARBOHYD        331
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00498"
FT   CARBOHYD        486
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00498"
FT   CARBOHYD        597
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00498"
FT   CARBOHYD        807
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00498"
FT   CARBOHYD        867
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00498"
FT   CARBOHYD        887
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00498"
FT   CARBOHYD        1154
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00498"
FT   CARBOHYD        1249
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00498"
FT   CARBOHYD        1280
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00498"
FT   CARBOHYD        1408
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00498"
FT   CARBOHYD        1492
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00498"
FT   CARBOHYD        1659
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00498"
FT   CARBOHYD        2333
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00498"
FT   CARBOHYD        2467
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00498"
FT   MUTAGEN         2118
FT                   /note="A->P: In hps4; enhanced responses to Pi starvation,
FT                   including increased inhibition of primary root growth,
FT                   probably due to an increased auxin accumulation in root
FT                   tips, enhanced expression of Pi starvation-induced genes,
FT                   and overproduction of root-associated acid phosphatases
FT                   (APase)."
FT                   /evidence="ECO:0000269|PubMed:22615140"
FT   CONFLICT        1898
FT                   /note="K -> N (in Ref. 4; AAC49734)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        2239
FT                   /note="A -> S (in Ref. 4; AAC49734)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        2464
FT                   /note="N -> D (in Ref. 5; BAF01434)"
FT                   /evidence="ECO:0000305"
SQ   SEQUENCE   2603 AA;  292913 MW;  509E210A22858ACF CRC64;
     MAASPAKFFF GFLIVSIVLW MIFMLFAWML SRVLGASVVF RVGGWKCLKD VVVKFKKGAI
     ESVSASEIKL SLRQSLVKLG VGFLSRDPKV QVLISDLEVV MRSSTSTTNL QKAKSHKPRT
     SGRGKWMVVA NVARFLSVSV ADMVVKTTKV IVEVKELKLD INKDGGTKPN LYVKLNVLPI
     LVHLCESRII SDQSSNVSFE CCPASQASSA SPDRSAATLF CDELSLSSEF GHDRAVGIVV
     RNVEVTSGDV ILNFDEDSFP KSKQSSASLR SDEVRTSATA ASSAKKPHKE HQLVAALAKY
     SSSFPEKVSF SLPKLDVRCV NREHDLLAEN NITGIQLRSV KSKSFEDTGE STRLDVQMEL
     SEIHVFREAD SSILEIMKVD VVSFIYIPVQ PVLPIRAEVD IKLGGTRCNL FISRLQPWLR
     LHFLKKKKLV LQEKTHNLEK TKAADMKAIM WTGTVSAPEM TVMLYGTEDI PLYHFCSQSS
     HVFANNVSSL GTAVHVELGE LNLHLADEYQ ECFREHLFGI EPNSGSLMHI AKVSLDWGRR
     DRTSSDEVGF RSKLVLSVDV TGMGIYFSFK RVQSLIINAL SFKALFKTLS VTGKKMNKTV
     SVQPSKGSGK GTRLVNINLE RCCVNFCDDT GLDNTVIDDP KSVNYGSQGG RVSFSSLADG
     TPRTASILST APEACKRLKY SVSLEISQFS FCLNKDKLST QMELGRAKSI YQEYLEEHTP
     CSNVILFDMH NAKLVRRSGG LNEIDVCSLF SATHISLGWE PDVHLSFYEL FLRLRSLVYA
     QRHKEPESGC NKGISSVKDG GPSEKINQSN SVNKQKKKES MFAIDVETLT ISAEVGDGVE
     VKLEAQSIFS ENACIGVLLE GLMLAFNGSR VFKTTRMQVS RIPTATNLSD AVPVMTDGPW
     DWVVQGLDVH ICMPYKLQLR AIDDSIEEML RGLKLISVAK GKHILSGKRE SSKPKKSSPK
     FGRIKFCIRR LTADIEEEPI QGWLDEHYQL VKKEACELAV RLKFLEDLIH KAGQSPKGAE
     TSAVLDERKM FFDGVEIDVE DPVAINKVKE EIHKRSFQSY YQACQGLAPS EGSGACREGF
     QAGFKPSAAR TSLLSVCATD FDLSLTAVHG GDAGLIEVLK KLDPICEEND IPFSRLYGSN
     VYLNTGSLVV QLRNYTLPLL SGTSGKCEGR IVLAQQATCF QPQISQDVFV GRWRKVKMFR
     SASGTTPPLK TYSDLRIHFE QGEVSFGVGY EPAFADISYA FTVALRRANL SHRNPDMVQV
     IKKERSLPWW DDMRNYVHGN ITLSFSESKW SVLATTDPYE SLDQLQIVSG PIELKQSDGR
     VFVSAKDFKI KLSSLESLIS RHSLKVPVRA SGAAFIEAPD FNLEVTMDWD CESGNSLNHY
     LYAFPAEGKP REKVFDPFRS TSLSLRWNFS LRPEKFHQSP SSTEHPTDVG TVYSSQDKPD
     SIPLASPTMN LGAHDLAWIL KFWGLNYYPP HKLRSFSRWP RFGVPRAARS GNLSLDKVMT
     EFMLRVDATP SLIKYMPWDS DDPAKGLTFN MAKLKYELCY SRGKQKYTFE CKRDALDLVY
     QGLDLHVPKA FINKDEHPCI PGSVQVLRKS TQDALIDRVP SGKDHKRYEK HRDEGFLLSS
     DYFTIRRQAP KADPERLLAW QEAGRRNLEM TYVRSEFENG SESDEHIRSD PSDDDGYNVV
     IADNCQRVFV YGLKLLWTIE NRDAVWSFVG GISKAFEPPK PSPSRQYTQR KIHEENQKES
     CPETHQGEMS RSSASPGRNL PSSPSHSIKI EKSDDIGTVE TIESEEEGTR HFMVNVIEPQ
     FNLHSEEANG RFLLAAVSGR VLARSFHSIM RVGVEVIEQA LGTGSVKIPE CSPEMTWTRM
     EVSVMLEHVQ AHVAPTDVDP GAGLQWLPKI RRNSPKVKRT GALLERVFMP CDMYFRYTRH
     KGGTPDLKVK PLKELTFNSH NIIATMTSRQ FQVMLDVLTN LLFARLPKPR KSSLQCPTED
     EDVEEEADEV VPYGVEEVEL AKINLEEKER ERKLLLDDIR KLSPCSDNMD DTHIEREGEL
     WMISTRRSIL VQGLKKELTY AQKSRKAASA SLRMALQKAA QLRIMEKEKN KSPSYAMCIS
     LQINKVVWSM LVDGKSFAEA EINDMIYDFD RDYKDIGVAR FTTKYFVVRN CLPNAKSDML
     LSAWNPPPEW GKKVMLRVDA KQGAPKDAHY PLELFHVEIY PLRIHLTETM YRMMWEYFFP
     EEEQDSQSRQ EVWKISTTAG SKRVKKGLVG HESSGHAIKD VEASRMSSSA LSASAAVQSQ
     SNDDSVQKSN VICLRSSTGA SAQELRRTSS FDREENVAEP IANELVLQAH SCNVSSSIEQ
     QEDFSKQKVK EIKPVKSGRS SHEEKKAGKS HEEKKSRPRK MMEFHNIKIS QVELLVTYEG
     SRFVVNDLKL LMDTFHRVEF TGTWRRLFSR VKKHIIWGVL KSVTGMQGKK FKDKSHNNRE
     STDNDLNLSD NDQTGKPDQQ QVTWFKRQSD GAGDGFVTSI RGLFNTQRRK AKAFVLRTMR
     GEAENDFHGD WSDSDVEFSP FARQLTITKA KRLIRRHTKK FRPRSQRGST SQQRESLPSS
     PIETTPFESG YSSGSSPYED FRE
//
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