Q9ZT82
Gene name |
CALS12 (GSL5, PMR4, At4g03550, F9H3.18, T5L23.4) |
Protein name |
Callose synthase 12 |
Names |
1,3-beta-glucan synthase, Protein GLUCAN SYNTHASE-LIKE 5, Protein POWDERY MILDEW RESISTANT 4 |
Species |
Arabidopsis thaliana (Mouse-ear cress) |
KEGG Pathway |
ath:AT4G03550 |
EC number |
2.4.1.34: Hexosyltransferases |
Protein Class |
|
Descriptions
The autoinhibited protein was predicted that may have potential autoinhibitory elements via cis-regPred.
Autoinhibitory domains (AIDs)
Target domain |
|
Relief mechanism |
|
Assay |
cis-regPred |
Accessory elements
No accessory elements
Autoinhibited structure
Activated structure
1 structures for Q9ZT82
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q9ZT82-F1 | Predicted | AlphaFoldDB |
57 variants for Q9ZT82
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| tmp_4_1573564_G_A | 18 | A>T | No | 1000Genomes | |
| tmp_4_1573570_G_T | 20 | A>S | No | 1000Genomes | |
| ENSVATH02633720 | 21 | V>A | No | 1000Genomes | |
| ENSVATH02633720 | 21 | V>G | No | 1000Genomes | |
| tmp_4_1573577_G_A | 22 | G>E | No | 1000Genomes | |
| tmp_4_1573592_C_T | 27 | P>L | No | 1000Genomes | |
| tmp_4_1573690_G_A | 60 | D>N | No | 1000Genomes | |
| tmp_4_1573699_C_T | 63 | R>C | No | 1000Genomes | |
| ENSVATH00458381 | 97 | M>V | No | 1000Genomes | |
| tmp_4_1573900_C_A | 130 | L>I | No | 1000Genomes | |
| ENSVATH00458382 | 132 | A>S | No | 1000Genomes | |
| ENSVATH06435387 | 136 | S>N | No | 1000Genomes | |
| tmp_4_1574213_C_G | 234 | A>G | No | 1000Genomes | |
| tmp_4_1574363_A_G | 284 | K>R | No | 1000Genomes | |
| ENSVATH06435392 | 350 | L>F | No | 1000Genomes | |
| tmp_4_1574593_C_T | 361 | L>F | No | 1000Genomes | |
| ENSVATH02633723 | 369 | A>T | No | 1000Genomes | |
| ENSVATH00458386 | 413 | Q>R | No | 1000Genomes | |
| tmp_4_1574777_C_G | 422 | T>R | No | 1000Genomes | |
| ENSVATH06435394 | 432 | V>M | No | 1000Genomes | |
| ENSVATH10575449 | 436 | L>V | No | 1000Genomes | |
| ENSVATH10575451 | 439 | E>K | No | 1000Genomes | |
| ENSVATH00458387 | 527 | D>E | No | 1000Genomes | |
| tmp_4_1575091_G_A | 527 | D>N | No | 1000Genomes | |
| tmp_4_1575221_C_T | 570 | A>V | No | 1000Genomes | |
| ENSVATH10575452 | 621 | G>S | No | 1000Genomes | |
| ENSVATH13895111 | 633 | R>K | No | 1000Genomes | |
| ENSVATH10575477 | 719 | C>R | No | 1000Genomes | |
| ENSVATH00458391 | 745 | V>I | No | 1000Genomes | |
| ENSVATH06435402 | 748 | E>D | No | 1000Genomes | |
| tmp_4_1575960_C_G | 763 | S>C | No | 1000Genomes | |
| ENSVATH02633733 | 765 | Q>H | No | 1000Genomes | |
| ENSVATH06435403 | 776 | D>E | No | 1000Genomes | |
| tmp_4_1576068_G_T | 799 | S>I | No | 1000Genomes | |
| tmp_4_1576176_G_A | 835 | R>Q | No | 1000Genomes | |
| ENSVATH06435405 | 869 | T>I | No | 1000Genomes | |
| tmp_4_1576395_T_C | 908 | M>T | No | 1000Genomes | |
| tmp_4_1576422_A_G | 917 | Y>C | No | 1000Genomes | |
| tmp_4_1576436_G_T | 922 | V>L | No | 1000Genomes | |
| ENSVATH13895125 | 1005 | A>T | No | 1000Genomes | |
| ENSVATH13895126 | 1045 | R>Q | No | 1000Genomes | |
| tmp_4_1576842_C_T | 1057 | T>M | No | 1000Genomes | |
| ENSVATH00458394 | 1099 | K>R | No | 1000Genomes | |
| ENSVATH02633736 | 1103 | A>G | No | 1000Genomes | |
| ENSVATH13895127 | 1106 | I>S | No | 1000Genomes | |
| tmp_4_1577166_G_A | 1165 | R>H | No | 1000Genomes | |
| ENSVATH00458396 | 1169 | V>I | No | 1000Genomes | |
| ENSVATH13895128 | 1170 | Q>K | No | 1000Genomes | |
| tmp_4_1577748_T_C | 1299 | V>A | No | 1000Genomes | |
| tmp_4_1577945_G_A | 1365 | A>T | No | 1000Genomes | |
| ENSVATH10575528 | 1384 | A>T | No | 1000Genomes | |
| ENSVATH06435416 | 1387 | T>M | No | 1000Genomes | |
| tmp_4_1578051_A_T | 1400 | Q>L | No | 1000Genomes | |
| tmp_4_1578595_C_A | 1581 | D>E | No | 1000Genomes | |
| ENSVATH06435420 | 1596 | I>L | No | 1000Genomes | |
| tmp_4_1578888_A_G | 1679 | H>R | No | 1000Genomes | |
| tmp_4_1579190_G_A | 1780 | V>I | No | 1000Genomes |
No associated diseases with Q9ZT82
3 regional properties for Q9ZT82
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| conserved_site | Cathelicidin, conserved site | 35 - 48 | IPR018216-1 |
| conserved_site | Cathelicidin, conserved site | 79 - 101 | IPR018216-2 |
| domain | Cathelicidin, antimicrobial peptide, C-terminal | 136 - 163 | IPR022746 |
Functions
| Description | ||
|---|---|---|
| EC Number | 2.4.1.34 | Hexosyltransferases |
| Subcellular Localization |
|
|
| PANTHER Family | ||
| PANTHER Subfamily | ||
| PANTHER Protein Class | ||
| PANTHER Pathway Category | No pathway information available | |
5 GO annotations of cellular component
| Name | Definition |
|---|---|
| 1,3-beta-D-glucan synthase complex | A protein complex that catalyzes the transfer of a glucose group from UDP-glucose to a (1->3)-beta-D-glucan chain. |
| Golgi apparatus | A membrane-bound cytoplasmic organelle of the endomembrane system that further processes the core oligosaccharides (e.g. N-glycans) added to proteins in the endoplasmic reticulum and packages them into membrane-bound vesicles. The Golgi apparatus operates at the intersection of the secretory, lysosomal, and endocytic pathways. |
| integral component of membrane | The component of a membrane consisting of the gene products and protein complexes having at least some part of their peptide sequence embedded in the hydrophobic region of the membrane. |
| plasma membrane | The membrane surrounding a cell that separates the cell from its external environment. It consists of a phospholipid bilayer and associated proteins. |
| plasmodesma | A fine cytoplasmic channel, found in all higher plants, that connects the cytoplasm of one cell to that of an adjacent cell. |
2 GO annotations of molecular function
| Name | Definition |
|---|---|
| 1,3-beta-D-glucan synthase activity | Catalysis of the reaction: UDP-glucose + [(1->3)-beta-D-glucosyl](n) = UDP + [(1->3)-beta-D-glucosyl](n+1). |
| glucosyltransferase activity | Catalysis of the transfer of a glucosyl group to an acceptor molecule, typically another carbohydrate or a lipid. |
14 GO annotations of biological process
| Name | Definition |
|---|---|
| (1->3)-beta-D-glucan biosynthetic process | The chemical reactions and pathways resulting in the formation of (1->3)-beta-D-glucans, compounds composed of glucose residues linked by (1->3)-beta-D-glucosidic bonds. |
| defense response | Reactions, triggered in response to the presence of a foreign body or the occurrence of an injury, which result in restriction of damage to the organism attacked or prevention/recovery from the infection caused by the attack. |
| defense response by callose deposition | Any process in which callose is transported to, and/or maintained in, a specific location during the defense response. Callose is a linear 1,3-beta-d-glucan formed from UDP-glucose and is found in certain plant cell walls. |
| defense response by callose deposition in cell wall | Any process in which callose is transported to, and/or maintained in, the cell wall during the defense response. Callose is a linear 1,3-beta-d-glucan formed from UDP-glucose and is found in certain plant cell walls. |
| defense response to bacterium | Reactions triggered in response to the presence of a bacterium that act to protect the cell or organism. |
| defense response to fungus | Reactions triggered in response to the presence of a fungus that act to protect the cell or organism. |
| innate immune response-activating signal transduction | The series of molecular signals generated as a consequence of a pathogen or microbial effector binding to a plant 'resistance-gene' receptor to activate a plant immune response, usually plant-type hypersensitive response. |
| leaf morphogenesis | The process in which the anatomical structures of the leaf are generated and organized. |
| leaf senescence | The last stage of leaf development during which programmed degradation of macromolecules and nutrient recycling take place. |
| pollen development | The process whose specific outcome is the progression of the pollen grain over time, from its formation to the mature structure. The process begins with the meiosis of the microsporocyte to form four haploid microspores. The nucleus of each microspore then divides by mitosis to form a two-celled organism, the pollen grain, that contains a tube cell as well as a smaller generative cell. The pollen grain is surrounded by an elaborate cell wall. In some species, the generative cell immediately divides again to give a pair of sperm cells. In most flowering plants, however this division takes place later, in the tube that develops when a pollen grain germinates. |
| regulation of cell shape | Any process that modulates the surface configuration of a cell. |
| reproduction | The production of new individuals that contain some portion of genetic material inherited from one or more parent organisms. |
| response to fungus | Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus from a fungus. |
| salicylic acid mediated signaling pathway | The series of molecular signals mediated by salicylic acid. |
3 homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| Q04952 | FKS3 | 1,3-beta-glucan synthase component FKS3 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) | PR |
| P38631 | FKS1 | 1,3-beta-glucan synthase component FKS1 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) | PR |
| P40989 | GSC2 | 1,3-beta-glucan synthase component GSC2 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) | PR |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MSLRHRTVPP | QTGRPLAAEA | VGIEEEPYNI | IPVNNLLADH | PSLRFPEVRA | AAAALKTVGD |
| 70 | 80 | 90 | 100 | 110 | 120 |
| LRRPPYVQWR | SHYDLLDWLA | LFFGFQKDNV | RNQREHMVLH | LANAQMRLSP | PPDNIDSLDS |
| 130 | 140 | 150 | 160 | 170 | 180 |
| AVVRRFRRKL | LANYSSWCSY | LGKKSNIWIS | DRNPDSRREL | LYVGLYLLIW | GEAANLRFMP |
| 190 | 200 | 210 | 220 | 230 | 240 |
| ECICYIFHNM | ASELNKILED | CLDENTGQPY | LPSLSGENAF | LTGVVKPIYD | TIQAEIDESK |
| 250 | 260 | 270 | 280 | 290 | 300 |
| NGTVAHCKWR | NYDDINEYFW | TDRCFSKLKW | PLDLGSNFFK | SRGKSVGKTG | FVERRTFFYL |
| 310 | 320 | 330 | 340 | 350 | 360 |
| YRSFDRLWVM | LALFLQAAII | VAWEEKPDTS | SVTRQLWNAL | KARDVQVRLL | TVFLTWSGMR |
| 370 | 380 | 390 | 400 | 410 | 420 |
| LLQAVLDAAS | QYPLVSRETK | RHFFRMLMKV | IAAAVWIVAF | TVLYTNIWKQ | KRQDRQWSNA |
| 430 | 440 | 450 | 460 | 470 | 480 |
| ATTKIYQFLY | AVGAFLVPEI | LALALFIIPW | MRNFLEETNW | KIFFALTWWF | QGKSFVGRGL |
| 490 | 500 | 510 | 520 | 530 | 540 |
| REGLVDNIKY | STFWIFVLAT | KFTFSYFLQV | KPMIKPSKLL | WNLKDVDYEW | HQFYGDSNRF |
| 550 | 560 | 570 | 580 | 590 | 600 |
| SVALLWLPVV | LIYLMDIQIW | YAIYSSIVGA | VVGLFDHLGE | IRDMGQLRLR | FQFFASAIQF |
| 610 | 620 | 630 | 640 | 650 | 660 |
| NLMPEEQLLN | ARGFGNKFKD | GIHRLKLRYG | FGRPFKKLES | NQVEANKFAL | IWNEIILAFR |
| 670 | 680 | 690 | 700 | 710 | 720 |
| EEDIVSDREV | ELLELPKNSW | DVTVIRWPCF | LLCNELLLAL | SQARELIDAP | DKWLWHKICK |
| 730 | 740 | 750 | 760 | 770 | 780 |
| NEYRRCAVVE | AYDSIKHLLL | SIIKVDTEEH | SIITVFFQII | NQSIQSEQFT | KTFRVDLLPK |
| 790 | 800 | 810 | 820 | 830 | 840 |
| IYETLQKLVG | LVNDEETDSG | RVVNVLQSLY | EIATRQFFIE | KKTTEQLSNE | GLTPRDPASK |
| 850 | 860 | 870 | 880 | 890 | 900 |
| LLFQNAIRLP | DASNEDFYRQ | VRRLHTILTS | RDSMHSVPVN | LEARRRIAFF | SNSLFMNMPH |
| 910 | 920 | 930 | 940 | 950 | 960 |
| APQVEKMMAF | SVLTPYYSEE | VVYSKEQLRN | ETEDGISTLY | YLQTIYADEW | KNFKERMHRE |
| 970 | 980 | 990 | 1000 | 1010 | 1020 |
| GIKTDSELWT | TKLRDLRLWA | SYRGQTLART | VRGMMYYYRA | LKMLAFLDSA | SEMDIREGAQ |
| 1030 | 1040 | 1050 | 1060 | 1070 | 1080 |
| ELGSVRNLQG | ELGGQSDGFV | SENDRSSLSR | ASSSVSTLYK | GHEYGTALMK | FTYVVACQIY |
| 1090 | 1100 | 1110 | 1120 | 1130 | 1140 |
| GSQKAKKEPQ | AEEILYLMKQ | NEALRIAYVD | EVPAGRGETD | YYSVLVKYDH | QLEKEVEIFR |
| 1150 | 1160 | 1170 | 1180 | 1190 | 1200 |
| VKLPGPVKLG | EGKPENQNHA | MIFTRGDAVQ | TIDMNQDSYF | EEALKMRNLL | QEYNHYHGIR |
| 1210 | 1220 | 1230 | 1240 | 1250 | 1260 |
| KPTILGVREH | IFTGSVSSLA | WFMSAQETSF | VTLGQRVLAN | PLKVRMHYGH | PDVFDRFWFL |
| 1270 | 1280 | 1290 | 1300 | 1310 | 1320 |
| SRGGISKASR | VINISEDIFA | GFNCTLRGGN | VTHHEYIQVG | KGRDVGLNQI | SMFEAKVASG |
| 1330 | 1340 | 1350 | 1360 | 1370 | 1380 |
| NGEQVLSRDV | YRLGHRLDFF | RMLSFFYTTV | GFFFNTMMVI | LTVYAFLWGR | VYLALSGVEK |
| 1390 | 1400 | 1410 | 1420 | 1430 | 1440 |
| SALADSTDTN | AALGVILNQQ | FIIQLGLFTA | LPMIVEWSLE | EGFLLAIWNF | IRMQIQLSAV |
| 1450 | 1460 | 1470 | 1480 | 1490 | 1500 |
| FYTFSMGTRA | HYFGRTILHG | GAKYRATGRG | FVVEHKGFTE | NYRLYARSHF | VKAIELGLIL |
| 1510 | 1520 | 1530 | 1540 | 1550 | 1560 |
| IVYASHSPIA | KDSLIYIAMT | ITSWFLVISW | IMAPFVFNPS | GFDWLKTVYD | FEDFMNWIWY |
| 1570 | 1580 | 1590 | 1600 | 1610 | 1620 |
| QGRISTKSEQ | SWEKWWYEEQ | DHLRNTGKAG | LFVEIILVLR | FFFFQYGIVY | QLKIANGSTS |
| 1630 | 1640 | 1650 | 1660 | 1670 | 1680 |
| LFVYLFSWIY | IFAIFVLFLV | IQYARDKYSA | KAHIRYRLVQ | FLLIVLAILV | IVALLEFTHF |
| 1690 | 1700 | 1710 | 1720 | 1730 | 1740 |
| SFIDIFTSLL | AFIPTGWGIL | LIAQTQRKWL | KNYTIFWNAV | VSVARMYDIL | FGILIMVPVA |
| 1750 | 1760 | 1770 | |||
| FLSWMPGFQS | MQTRILFNEA | FSRGLRIMQI | VTGKKSKGDV |