Q6L538
Gene name |
CSLC7 (Os05g0510800, LOC_Os05g43530, OJ1005_B11.7) |
Protein name |
Probable xyloglucan glycosyltransferase 7 |
Names |
Cellulose synthase-like protein C7, OsCslC7 |
Species |
Oryza sativa subsp japonica (Rice) |
KEGG Pathway |
osa:4339283 |
EC number |
|
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 Q6L538
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q6L538-F1 | Predicted | AlphaFoldDB |
No variants for Q6L538
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| No variants for Q6L538 | |||||
No associated diseases with Q6L538
1 regional properties for Q6L538
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | Glycosyltransferase 2-like | 324 - 518 | IPR001173 |
3 GO annotations of cellular component
| Name | Definition |
|---|---|
| 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. |
| Golgi membrane | The lipid bilayer surrounding any of the compartments of the Golgi apparatus. |
| 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. |
1 GO annotations of molecular function
| Name | Definition |
|---|---|
| glycosyltransferase activity | Catalysis of the transfer of a glycosyl group from one compound (donor) to another (acceptor). |
1 GO annotations of biological process
| Name | Definition |
|---|---|
| cell wall organization | A process that results in the assembly, arrangement of constituent parts, or disassembly of the cell wall, the rigid or semi-rigid envelope lying outside the cell membrane of plant, fungal and most prokaryotic cells, maintaining their shape and protecting them from osmotic lysis. |
10 homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| Q7XIF5 | CSLA7 | Probable glucomannan 4-beta-mannosyltransferase 7 | Oryza sativa subsp japonica (Rice) | PR |
| Q69L19 | CSLC2 | Probable xyloglucan glycosyltransferase 2 | Oryza sativa subsp japonica (Rice) | PR |
| Q6AU53 | CSLC9 | Probable xyloglucan glycosyltransferase 9 | Oryza sativa subsp japonica (Rice) | PR |
| Q7PC69 | CSLC3 | Probable xyloglucan glycosyltransferase 3 | Oryza sativa subsp japonica (Rice) | PR |
| Q6YWK8 | CSLA11 | Probable glucomannan 4-beta-mannosyltransferase 11 | Oryza sativa subsp japonica (Rice) | PR |
| Q8LIY0 | CSLC1 | Probable xyloglucan glycosyltransferase 1 | Oryza sativa subsp japonica (Rice) | PR |
| Q9SJA2 | CSLC8 | Probable xyloglucan glycosyltransferase 8 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| Q9SRT3 | CSLC6 | Probable xyloglucan glycosyltransferase 6 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| Q9LJP4 | CSLC4 | Xyloglucan glycosyltransferase 4 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| Q9ZQB9 | CSLC12 | Probable xyloglucan glycosyltransferase 12 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MAPSWWGRSG | GGGVGNGGGT | PVVVKMENPN | WSISEVEAAE | VAPGSPAGAG | KAGRGKNARQ |
| 70 | 80 | 90 | 100 | 110 | 120 |
| ITWVLLLKAH | RAAGRLTGAA | SAALAVASAA | RRRVASGRTD | ADAAPGESTA | LRARSYGCIR |
| 130 | 140 | 150 | 160 | 170 | 180 |
| VSLVLSLLLL | AVEVAAYLQG | WHLEEVASLL | AVDGLFAASY | AGWMRLRLDY | LAPPLQFLTN |
| 190 | 200 | 210 | 220 | 230 | 240 |
| ACVALFMVQS | IDRLVLCLGC | FWIRFKGIKP | VPQAAAAGKP | DVEAGAGDYP | MVLVQMPMCN |
| 250 | 260 | 270 | 280 | 290 | 300 |
| EREVYQQSIG | AVCNLDWPKS | NFLVQVLDDS | DDATTSALIK | EEVEKWQREG | VRIIYRHRVI |
| 310 | 320 | 330 | 340 | 350 | 360 |
| RDGYKAGNLK | SAMNCSYVKD | YEFVVIFDAD | FQPQADFLKR | TVPHFKGKDD | VGLVQARWSF |
| 370 | 380 | 390 | 400 | 410 | 420 |
| VNKDENLLTR | LQNVNLCFHF | EVEQQVNGAF | LNFFGFNGTA | GVWRIKALED | SGGWMERTTV |
| 430 | 440 | 450 | 460 | 470 | 480 |
| EDMDIAVRAH | LKGWKFVFLN | DVECQCELPE | SYEAYRKQQH | RWHSGPMQLF | RLCFVDIIKS |
| 490 | 500 | 510 | 520 | 530 | 540 |
| KIGFWKKFNL | IFLFFLLRKL | ILPFYSFTLF | CVILPMTMFV | PEAELPAWVV | CYIPATMSIL |
| 550 | 560 | 570 | 580 | 590 | 600 |
| NILPAPKSFP | FIVPYLLFEN | TMSVTKFNAM | ISGLFQLGSA | YEWVVTKKSG | RSSEGDLVGL |
| 610 | 620 | 630 | 640 | 650 | 660 |
| VEKHSKQQRV | GSAPNLDALT | KEESNPKKDS | KKKKHNRIYR | KELALSFLLL | TAAARSLLSA |
| 670 | 680 | ||||
| QGIHFYFLLF | QGVSFLVVGL | DLIGEQVE |