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Reviewed, UniProtKB/Swiss-Prot Q9LYS6 (CALS6_ARATH)

Last modified June 16, 2009. Version 29. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (2) | Third-party data | Customize display text xml rdf/xml gff fasta
Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents

Names and origin

Protein namesRecommended name:
    Putative callose synthase 6
    EC=2.4.1.34
Alternative name(s):
    1,3-beta-glucan synthase
    Protein GLUCAN SYNTHASE-LIKE 11
Gene names
Name: CALS6
Synonyms: GSL11
Ordered Locus Names: At3g59100
ORF Names: F17J16.150
OrganismArabidopsis thaliana (Mouse-ear cress) [Complete proteome]
Taxonomic identifier3702 [NCBI]
Taxonomic lineageEukaryotaViridiplantaeStreptophytaEmbryophytaTracheophytaSpermatophytaMagnoliophytaeudicotyledonscore eudicotyledonsrosidseurosids IIBrassicalesBrassicaceaeArabidopsis

Protein attributes

Sequence length1921 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is not processed.
Protein existenceInferred from homology.

General annotation (Comments)

Function

Probably involved in callose synthesis, but not required for callose formation after wounding or pathogen attack. During plant growth and development, callose is found as a transitory component of the cell plate in dividing cells, is a major component of pollen mother cell walls and pollen tubes, and is found as a structural component of plasmodesmatal canals. Ref.3

Catalytic activity

UDP-glucose + ((1->3)-beta-D-glucosyl)(n) = UDP + ((1->3)-beta-D-glucosyl)(n+1).

Subcellular location

Cell membrane; Multi-pass membrane protein Probable.

Sequence similarities

Belongs to the glycosyltransferase 48 family.

Sequence caution

The sequence CAB86938.1 differs from that shown. Reason: Erroneous gene model prediction.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 19211921Putative callose synthase 6
PRO_0000334578

Regions

Topological domain1 – 492492Cytoplasmic Potential
Transmembrane493 – 51321 Potential
Topological domain514 – 52613Extracellular Potential
Transmembrane527 – 54721 Potential
Topological domain548 – 56013Cytoplasmic Potential
Transmembrane561 – 58121 Potential
Topological domain582 – 61130Extracellular Potential
Transmembrane612 – 63221 Potential
Topological domain633 – 67442Cytoplasmic Potential
Transmembrane675 – 69521 Potential
Topological domain696 – 72126Extracellular Potential
Transmembrane722 – 74221 Potential
Topological domain743 – 1484742Cytoplasmic Potential
Transmembrane1485 – 150521 Potential
Topological domain1506 – 154035Extracellular Potential
Transmembrane1541 – 156121 Potential
Topological domain1562 – 15643Cytoplasmic Potential
Transmembrane1565 – 158521 Potential
Topological domain1586 – 162843Extracellular Potential
Transmembrane1629 – 164921 Potential
Topological domain1650 – 16556Cytoplasmic Potential
Transmembrane1656 – 167621 Potential
Topological domain1677 – 173054Extracellular Potential
Transmembrane1731 – 175121 Potential
Topological domain1752 – 17598Cytoplasmic Potential
Transmembrane1760 – 178021 Potential
Topological domain1781 – 179616Extracellular Potential
Transmembrane1797 – 181721 Potential
Topological domain1818 – 18236Cytoplasmic Potential
Transmembrane1824 – 184421 Potential
Topological domain1845 – 186723Extracellular Potential
Transmembrane1868 – 188821 Potential
Topological domain1889 – 192133Cytoplasmic Potential
Compositional bias103 – 1086Poly-Glu
Compositional bias1633 – 16397Poly-Leu

Sequences

Sequence LengthMass (Da)Tools
Q9LYS6-1 [UniParc].

Last modified May 20, 2008. Version 2.
Checksum: F2CC970B984F9710

FASTA1,921223,514
        10         20         30         40         50         60 
MEASSSGTAE LPRSLSRRAP SRATTMMIDR PNEDASAMDS ELVPSSLASI APILRVANEI 

        70         80         90        100        110        120 
EKDNPRVAYL CRFHAFEKAH RMDATSSGRG VRQFKTYLLH RLEKEEEETK PQLAKNDPRE 

       130        140        150        160        170        180 
IQAYYQNFYE KYIKEGETSR KPEEMARLYQ IASVLYDVLK TVVPSPKVDY ETRRYAEEVE 

       190        200        210        220        230        240 
RKRDRYEHYN ILPLYAVGTK PAIVELPEVK AAFSAVRNVR NLPRRRIHLP SNTPNEMRKA 

       250        260        270        280        290        300 
RTKLNDILEW LASEFGFQRG NVANQREHII LLLANADIRK RNDEEYDELK PSTVTELMDK 

       310        320        330        340        350        360 
TFKSYYSWCK YLHSTSNLKF PDDCDKQQLQ LIYISLYLLI WGEASNVRFM PECICYIFHN 

       370        380        390        400        410        420 
MANDVYGILF SNVEAVSGET YETEEVIDEE SFLRTVITPI YQVIRNEAKR NKGGTASHSQ 

       430        440        450        460        470        480 
WRNYDDLNEY FWSKKCFKIG WPLDLKADFF LNSDEITPQD ERLNQVTYGK SKPKTNFVEV 

       490        500        510        520        530        540 
RTFWNLFRDF DRMWIFLVMA FQAMVIVGWH GSGSLGDIFD KDVFKTVLTI FITSAYLTLL 

       550        560        570        580        590        600 
QAALDIILNF NAWKNFKFSQ ILRYLLKFAV AFMWAVLLPI AYSKSVQRPT GVVKFFSTWT 

       610        620        630        640        650        660 
GDWKDQSFYT YAVSFYVLPN ILAALLFLVP PFRRAMECSD MRPIKVIMWW AQPKLYVGRG 

       670        680        690        700        710        720 
MHEDMFSLFK YTTFWIMLLI SKLAFNYYVE ILPLITPTKM IMNLHIGHYQ WHEFFPHATN 

       730        740        750        760        770        780 
NIGVVIAIWA PIVLVYLMDT QIWYAIFSTL FGGIHGAFSH LGEIRTLGML RSRFESIPIA 

       790        800        810        820        830        840 
FSRTLMPSED AKRKHADDYV DQKNITNFSQ VWNEFIYSMR SEDKISDRDR DLLLVPSSSG 

       850        860        870        880        890        900 
DVSVIQWPPF LLASKIPIAV DMAKDFKGKE DAELFRKIKS DSYMYYAVIE SYETLKKIIY 

       910        920        930        940        950        960 
ALLEDEADRR VMNQVFLEVD MSMQQQRFIY EFRMSGLPLL SDKLEKFLSI LLSDYEDQGT 

       970        980        990       1000       1010       1020 
YKSQLINVFQ DVIEIITQDL LVNGHEILER ARVHSPDIKN EKKEQRFEKI NIHLVRDRCW 

      1030       1040       1050       1060       1070       1080 
REKVIRLHLL LSVKESAINV PQNLEARRRI TFFANSLFMN MPSAPRIRDM LSFSVLTPYY 

      1090       1100       1110       1120       1130       1140 
KEDVLYSEED LNKENEDGIS ILFYLQKIYP DEWTNYLDRL KDPKLPEKDK SEFLREWVSY 

      1150       1160       1170       1180       1190       1200 
RGQTLARTVR GMMYYRQALE LQCYQEVAGE QAEFSVFRAM ASNDENQKAF LERARALADL 

      1210       1220       1230       1240       1250       1260 
KFTYVVSCQV YGNQKKSGDI HNRSCYTNIL QLMLKYPSLR VAYVDEREET ADAKSPKVFY 

      1270       1280       1290       1300       1310       1320 
SVLLKGGDKF DEEIYRIKLP GPPAEIGEGK PENQNHAIIF TRGEALQTID MNQDNYFEEA 

      1330       1340       1350       1360       1370       1380 
FKLRNVLEEF NKERVGRRKP TILGLREHIF TGSVSSLAWF MSNQESSFVT IGQRILANPL 

      1390       1400       1410       1420       1430       1440 
RVRFHYGHPD IFDRIFHITR GGVSKASKVI NLSEDIFGGF NSTLRGGYVT HHEYIQVGKG 

      1450       1460       1470       1480       1490       1500 
RDVGLNPISI FEAKVANGNG EQTLSRDVYR LGHRFDFYRM LSFYFTTIGF YFSSMLTVLT 

      1510       1520       1530       1540       1550       1560 
VYAFLYGRMY MVMSGLEKEI LRLASPNQLE ALEQALATQS IFQLGFLMVL PMVMEIGLEH 

      1570       1580       1590       1600       1610       1620 
GFRSAIVDFF IMQLQLASVF FTFQLGTKSH YYGRTILHGG SKYRPTGRGF VVFHAKFAEN 

      1630       1640       1650       1660       1670       1680 
YRLYSRSHFV KGLELLLLLV VYQIYGHSYR SSNLYLYITV SMWFMVGSWL FAPFIFNPSG 

      1690       1700       1710       1720       1730       1740 
FEWQKTVDDW TDWKRWLGDR GGIGIPVEKS WESWWNVEQE HLKHTSIRGR ILEITLALRF 

      1750       1760       1770       1780       1790       1800 
FIYQYGIVYQ LNISQRSKSF LVYGLSWVVL LTSLLVLKMV SMGRRRFGTD FQLMFRILKA 

      1810       1820       1830       1840       1850       1860 
LLFLGFLSVM TILFVVFKLT LTDLSASVLA FLPTGWAILL IGQVLRSPIK ALGVWDSVKE 

      1870       1880       1890       1900       1910       1920 
LGRAYENIMG LVIFAPIAVL SWFPIVSEFQ ARLLFNQAFS RGLQISMILA GRKDKATSSH 


K 

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References

« Hide 'large scale' references
[1]"Sequence and analysis of chromosome 3 of the plant Arabidopsis thaliana."
Salanoubat M., Lemcke K., Rieger M., Ansorge W., Unseld M., Fartmann B., Valle G., Bloecker H., Perez-Alonso M., Obermaier B., Delseny M., Boutry M., Grivell L.A., Mache R., Puigdomenech P., De Simone V., Choisne N., Artiguenave F. expand/collapse author list , Robert C., Brottier P., Wincker P., Cattolico L., Weissenbach J., Saurin W., Quetier F., Schaefer M., Mueller-Auer S., Gabel C., Fuchs M., Benes V., Wurmbach E., Drzonek H., Erfle H., Jordan N., Bangert S., Wiedelmann R., Kranz H., Voss H., Holland R., Brandt P., Nyakatura G., Vezzi A., D'Angelo M., Pallavicini A., Toppo S., Simionati B., Conrad A., Hornischer K., Kauer G., Loehnert T.-H., Nordsiek G., Reichelt J., Scharfe M., Schoen O., Bargues M., Terol J., Climent J., Navarro P., Collado C., Perez-Perez A., Ottenwaelder B., Duchemin D., Cooke R., Laudie M., Berger-Llauro C., Purnelle B., Masuy D., de Haan M., Maarse A.C., Alcaraz J.-P., Cottet A., Casacuberta E., Monfort A., Argiriou A., Flores M., Liguori R., Vitale D., Mannhaupt G., Haase D., Schoof H., Rudd S., Zaccaria P., Mewes H.-W., Mayer K.F.X., Kaul S., Town C.D., Koo H.L., Tallon L.J., Jenkins J., Rooney T., Rizzo M., Walts A., Utterback T., Fujii C.Y., Shea T.P., Creasy T.H., Haas B., Maiti R., Wu D., Peterson J., Van Aken S., Pai G., Militscher J., Sellers P., Gill J.E., Feldblyum T.V., Preuss D., Lin X., Nierman W.C., Salzberg S.L., White O., Venter J.C., Fraser C.M., Kaneko T., Nakamura Y., Sato S., Kato T., Asamizu E., Sasamoto S., Kimura T., Idesawa K., Kawashima K., Kishida Y., Kiyokawa C., Kohara M., Matsumoto M., Matsuno A., Muraki A., Nakayama S., Nakazaki N., Shinpo S., Takeuchi C., Wada T., Watanabe A., Yamada M., Yasuda M., Tabata S.
Nature 408:820-822(2000) [PubMed: 11130713] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
Strain: cv. Columbia.
[2]"A cell plate-specific callose synthase and its interaction with phragmoplastin."
Hong Z., Delauney A.J., Verma D.P.S.
Plant Cell 13:755-768(2001) [PubMed: 11283334] [Abstract]
Cited for: GENE FAMILY AND NOMENCLATURE.
[3]"An Arabidopsis callose synthase, GSL5, is required for wound and papillary callose formation."
Jacobs A.K., Lipka V., Burton R.A., Panstruga R., Strizhov N., Schulze-Lefert P., Fincher G.B.
Plant Cell 15:2503-2513(2003) [PubMed: 14555698] [Abstract]
Cited for: FUNCTION.
[4]"Two callose synthases, GSL1 and GSL5, play an essential and redundant role in plant and pollen development and in fertility."
Enns L.C., Kanaoka M.M., Torii K.U., Comai L., Okada K., Cleland R.E.
Plant Mol. Biol. 58:333-349(2005) [PubMed: 16021399] [Abstract]
Cited for: NOMENCLATURE.

Cross-references

Sequence databases

AL163527 Genomic DNA. Translation: CAB86938.1. Sequence problems.
IPIIPI00530564.
PIRT47792.

3D structure databases

ModBaseSearch...

Protein family/group databases

CAZyGT48. Glycosyltransferase Family 48.

Genome annotation databases

GenomeReviewsGene locus AT3G59100 in contig BA000014_GR.

Organism-specific databases

TAIRAt3g59100.

Family and domain databases

InterProIPR003440. Glyco_trans_48.
[Graphical view]
PfamPF02364. Glucan_synthase. 1 hit.
[Graphical view]
ProtoNetSearch...

Entry information

Entry nameCALS6_ARATH
AccessionPrimary (citable) accession number: Q9LYS6
Entry history
Integrated into UniProtKB/Swiss-Prot: May 20, 2008
Last sequence update: May 20, 2008
Last modified: June 16, 2009
This is version 29 of the entry and version 2 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation projectPPAP (Plant Proteome Annotation Project)

Relevant documents

Arabidopsis thaliana

Arabidopsis thaliana: entries and gene names

SIMILARITY comments

Index of protein domains and families

Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents