| Tag |
Content |
LipidDB ID |
LipidDB-3702-01401 |
Entry Name |
|
UniProt Accession |
|
Theoretical PI |
8.71 |
Molecular Weight |
217087.23 |
Genbank Protein ID |
|
Genbank Nucleotide ID |
|
Protein Name |
Callose synthase 9 |
Protein Synonyms/Alias |
2.4.1.34; 1,3-beta-glucan synthase; Protein GLUCAN SYNTHASE-LIKE 10; |
Gene Name |
CALS9 |
Gene Synonyms/Alias |
GSL10; At3g07160; T1B9.18; |
Created Date |
20-MAY-2008 |
| Lipid Modification Sites |
|---|
| Position |
Sequence Form |
Peptide |
References |
Modification Type |
1799 | Canonical | SVTDIFACVLAFIPT | [1] | S-Palmitoylation | 1852 | Canonical | IFLPVALCSWFPFVS | [1] | S-Palmitoylation |
|
Organism |
Arabidopsis thaliana (Mouse-ear cress) |
NCBI Taxa ID |
3702 |
Reference |
[1] Predicted from GPS-Lipid
|
Functional Description |
Involved in sporophytic and gametophytic development. Required for normal plant development. During pollen formation, required for the entry of microspores into mitosis and microspore symmetric division. May be required for correct temporal and spatial control of callose deposition during pollen mitosis. 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. |
Sequence Annotation |
Topological domain: 1 489 Cytoplasmic.
Transmembrane: 490 510 Helical.
Topological domain: 511 523 Extracellular.
Transmembrane: 524 544 Helical.
Topological domain: 545 560 Cytoplasmic.
Transmembrane: 561 581 Helical.
Topological domain: 582 591 Extracellular.
Transmembrane: 592 612 Helical.
Topological domain: 613 658 Cytoplasmic.
Transmembrane: 659 679 Helical.
Topological domain: 680 722 Extracellular.
Transmembrane: 723 743 Helical.
Topological domain: 744 1457 Cytoplasmic.
Transmembrane: 1458 1478 Helical.
Topological domain: 1479 1512 Extracellular.
Transmembrane: 1513 1533 Helical.
Topological domain: 1534 1539 Cytoplasmic.
Transmembrane: 1540 1560 Helical.
Topological domain: 1561 1609 Extracellular.
Transmembrane: 1610 1630 Helical.
Transmembrane: 1631 1651 Helical.
Topological domain: 1652 1703 Extracellular.
Transmembrane: 1704 1724 Helical.
Topological domain: 1725 1732 Cytoplasmic.
Transmembrane: 1733 1753 Helical.
Topological domain: 1754 1768 Extracellular.
Transmembrane: 1769 1789 Helical.
Topological domain: 1790 1795 Cytoplasmic.
Transmembrane: 1796 1816 Helical.
Topological domain: 1817 1838 Extracellular.
Transmembrane: 1839 1859 Helical.
Topological domain: 1860 1890 Cytoplasmic.
|
Protein Length |
1890 AA. |
Protein Sequence
(Canonical) |
MSRAESSWER LVNAALRRDR TGGVAGGNQS SIVGYVPSSL SNNRDIDAIL RAADEIQDED 60
PNIARILCEH GYSLAQNLDP NSEGRGVLQF KTGLMSVIKQ KLAKREVGTI DRSQDILRLQ 120
EFYRLYREKN NVDTLKEEEK QLRESGAFTD ELERKTVKRK RVFATLKVLG SVLEQLAKEI 180
PEELKHVIDS DAAMSEDTIA YNIIPLDAPV TTNATTTFPE VQAAVAALKY FPGLPKLPPD 240
FPIPATRTAD MLDFLHYIFG FQKDSVSNQR EHIVLLLANE QSRLNIPEET EPKLDDAAVR 300
KVFLKSLENY IKWCDYLCIQ PAWSNLEAIN GDKKLLFLSL YFLIWGEAAN IRFLPECLCY 360
IFHHMVREMD EILRQQVARP AESCMPVDSR GSDDGVSFLD HVIAPLYGVV SAEAFNNDNG 420
RAPHSAWRNY DDFNEYFWSL HSFELGWPWR TSSSFFQKPI PRKKLKTGRA KHRGKTSFVE 480
HRTFLHLYHS FHRLWIFLAM MFQALAIIAF NKDDLTSRKT LLQILSLGPT FVVMKFSESV 540
LEVIMMYGAY STTRRLAVSR IFLRFIWFGL ASVFISFLYV KSLKAPNSDS PIVQLYLIVI 600
AIYGGVQFFF SILMRIPTCH NIANKCDRWP VIRFFKWMRQ ERHYVGRGMY ERTSDFIKYL 660
LFWLVVLSAK FSFAYFLQIK PLVGPTRMIV KQNNIPYSWH DFVSRKNYNA LTVASLWAPV 720
VAIYLLDIHI FYTIFSAFLG FLLGARDRLG EIRSLEAIHK LFEEFPGAFM RALHVPLTNR 780
TSDTSHQTVD KKNKVDAAHF APFWNQIIKS LREEDYITDF EMELLLMPKN SGRLELVQWP 840
LFLLSSKILL AKEIAAESNS QEEILERIER DDYMKYAVEE VYHTLKLVLT ETLEAEGRLW 900
VERIYEDIQT SLKERNIHHD FQLNKLSLVI TRVTALLGIL KENETPEHAK GAIKALQDLY 960
DVMRLDILTF NMRGHYETWN LLTQAWNEGR LFTKLKWPKD PELKALVKRL YSLFTIKDSA 1020
AHVPRNLEAR RRLQFFTNSL FMDVPPPKSV RKMLSFSVFT PYYSEVVLYS MAELTKRNED 1080
GISILFYLQK IYPDEWKNFL ARIGRDENAL EGDLDNERDI LELRFWASYR GQTLARTVRG 1140
MMYYRKALML QSYLERKAGN DATDAEGFEL SPEARAQADL KFTYVVTCQI YGRQKEDQKP 1200
EAVDIALLMQ RNEALRIAYI DVVDSPKEGK SHTEYYSKLV KADISGKDKE IYSIKLPGDP 1260
KLGEGKPENQ NHAIVFTRGN AIQTIDMNQD NYFEEALKMR NLLEEFDRDH GIRPPTILGV 1320
REHVFTGSVS SLASFMSNQE TSFVTLGQRV LAKPLKIRMH YGHPDVFDRV FHITRGGISK 1380
ASRVINISED IFAGFNTTLR QGNVTHHEYI QVGKGRDVGL NQIALFEGKV AGGNGEQVLS 1440
RDVYRLGQLL DFFRMMSFFF TTVGFYLCTM LTVLTVYIFL YGRAYLALSG VGATIRERAI 1500
LLDDTALSAA LNAQFLFQIG VFTAVPMVLG FILEQGFLQA IVSFITMQFQ LCTVFFTFSL 1560
GTRTHYFGRT ILHGGARYQA TGRGFVVKHI KFSENYRLYS RSHFVKAMEV ILLLVVYLAY 1620
GNDEAGAVSY ILLTVSSWFL AVSWLFAPYL FNPAGFEWQK VVEDFKEWTN WLFYRGGIGV 1680
KGAESWEAWW EEELSHIRTL SGRIMETILS LRFFIFQYGI VYKLKLQGSD TSFAVYGWSW 1740
VAFAMIIVLF KVFTFSQKIS VNFQLLLRFI QGLSLLMALA GIIVAVVLTP LSVTDIFACV 1800
LAFIPTGWGI LSIACAWKPV LKRMGMWKSI RSLARLYDAL MGMLIFLPVA LCSWFPFVST 1860
FQTRMMFNQA FSRGLEISLI LAGDNPNSGL 1890
|
FASTA
(Canonical) |
>LipidDB-3702-01401|Q9SFU6
MSRAESSWERLVNAALRRDRTGGVAGGNQSSIVGYVPSSLSNNRDIDAILRAADEIQDED
PNIARILCEHGYSLAQNLDPNSEGRGVLQFKTGLMSVIKQKLAKREVGTIDRSQDILRLQ
EFYRLYREKNNVDTLKEEEKQLRESGAFTDELERKTVKRKRVFATLKVLGSVLEQLAKEI
PEELKHVIDSDAAMSEDTIAYNIIPLDAPVTTNATTTFPEVQAAVAALKYFPGLPKLPPD
FPIPATRTADMLDFLHYIFGFQKDSVSNQREHIVLLLANEQSRLNIPEETEPKLDDAAVR
KVFLKSLENYIKWCDYLCIQPAWSNLEAINGDKKLLFLSLYFLIWGEAANIRFLPECLCY
IFHHMVREMDEILRQQVARPAESCMPVDSRGSDDGVSFLDHVIAPLYGVVSAEAFNNDNG
RAPHSAWRNYDDFNEYFWSLHSFELGWPWRTSSSFFQKPIPRKKLKTGRAKHRGKTSFVE
HRTFLHLYHSFHRLWIFLAMMFQALAIIAFNKDDLTSRKTLLQILSLGPTFVVMKFSESV
LEVIMMYGAYSTTRRLAVSRIFLRFIWFGLASVFISFLYVKSLKAPNSDSPIVQLYLIVI
AIYGGVQFFFSILMRIPTCHNIANKCDRWPVIRFFKWMRQERHYVGRGMYERTSDFIKYL
LFWLVVLSAKFSFAYFLQIKPLVGPTRMIVKQNNIPYSWHDFVSRKNYNALTVASLWAPV
VAIYLLDIHIFYTIFSAFLGFLLGARDRLGEIRSLEAIHKLFEEFPGAFMRALHVPLTNR
TSDTSHQTVDKKNKVDAAHFAPFWNQIIKSLREEDYITDFEMELLLMPKNSGRLELVQWP
LFLLSSKILLAKEIAAESNSQEEILERIERDDYMKYAVEEVYHTLKLVLTETLEAEGRLW
VERIYEDIQTSLKERNIHHDFQLNKLSLVITRVTALLGILKENETPEHAKGAIKALQDLY
DVMRLDILTFNMRGHYETWNLLTQAWNEGRLFTKLKWPKDPELKALVKRLYSLFTIKDSA
AHVPRNLEARRRLQFFTNSLFMDVPPPKSVRKMLSFSVFTPYYSEVVLYSMAELTKRNED
GISILFYLQKIYPDEWKNFLARIGRDENALEGDLDNERDILELRFWASYRGQTLARTVRG
MMYYRKALMLQSYLERKAGNDATDAEGFELSPEARAQADLKFTYVVTCQIYGRQKEDQKP
EAVDIALLMQRNEALRIAYIDVVDSPKEGKSHTEYYSKLVKADISGKDKEIYSIKLPGDP
KLGEGKPENQNHAIVFTRGNAIQTIDMNQDNYFEEALKMRNLLEEFDRDHGIRPPTILGV
REHVFTGSVSSLASFMSNQETSFVTLGQRVLAKPLKIRMHYGHPDVFDRVFHITRGGISK
ASRVINISEDIFAGFNTTLRQGNVTHHEYIQVGKGRDVGLNQIALFEGKVAGGNGEQVLS
RDVYRLGQLLDFFRMMSFFFTTVGFYLCTMLTVLTVYIFLYGRAYLALSGVGATIRERAI
LLDDTALSAALNAQFLFQIGVFTAVPMVLGFILEQGFLQAIVSFITMQFQLCTVFFTFSL
GTRTHYFGRTILHGGARYQATGRGFVVKHIKFSENYRLYSRSHFVKAMEVILLLVVYLAY
GNDEAGAVSYILLTVSSWFLAVSWLFAPYLFNPAGFEWQKVVEDFKEWTNWLFYRGGIGV
KGAESWEAWWEEELSHIRTLSGRIMETILSLRFFIFQYGIVYKLKLQGSDTSFAVYGWSW
VAFAMIIVLFKVFTFSQKISVNFQLLLRFIQGLSLLMALAGIIVAVVLTPLSVTDIFACV
LAFIPTGWGILSIACAWKPVLKRMGMWKSIRSLARLYDALMGMLIFLPVALCSWFPFVST
FQTRMMFNQAFSRGLEISLILAGDNPNSGL
|
Gene Ontology |
GO:0000148; C:1,3-beta-D-glucan synthase complex; IEA:InterPro GO:0016021; C:integral component of membrane; IEA:UniProtKB-KW GO:0003843; F:1,3-beta-D-glucan synthase activity; IEA:UniProtKB-EC GO:0006075; P:(1->3)-beta-D-glucan biosynthetic process; IEA:InterPro GO:0071555; P:cell wall organization; IEA:UniProtKB-KW GO:0008360; P:regulation of cell shape; IEA:UniProtKB-KW |
Interpro |
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Pfam |
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SMART |
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PROSITE |
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PRINTS |
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