Q9LNJ9
Gene name |
FKGP (At1g01220, F6F3.3) |
Protein name |
Bifunctional fucokinase/fucose pyrophosphorylase |
Names |
AtFKGP |
Species |
Arabidopsis thaliana (Mouse-ear cress) |
KEGG Pathway |
ath:AT1G01220 |
EC number |
2.7.1.52: Phosphotransferases with an alcohol group as acceptor |
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 Q9LNJ9
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q9LNJ9-F1 | Predicted | AlphaFoldDB |
45 variants for Q9LNJ9
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| tmp_1_91792_C_T | 15 | R>C | No | 1000Genomes | |
| tmp_1_91944_C_G | 65 | S>R | No | 1000Genomes | |
| ENSVATH04501376 | 108 | M>V | No | 1000Genomes | |
| ENSVATH01001033 | 109 | E>K | No | 1000Genomes | |
| ENSVATH10440474 | 177 | A>G | No | 1000Genomes | |
| ENSVATH09375261 | 182 | Q>K | No | 1000Genomes | |
| tmp_1_92640_G_T | 209 | A>S | No | 1000Genomes | |
| ENSVATH04501382 | 212 | I>V | No | 1000Genomes | |
| tmp_1_92808_C_T | 265 | H>Y | No | 1000Genomes | |
| ENSVATH00000355 | 284 | S>L | No | 1000Genomes | |
| ENSVATH13847976 | 287 | V>I | No | 1000Genomes | |
| tmp_1_92877_G_A | 288 | A>T | No | 1000Genomes | |
| tmp_1_92887_G_A | 291 | C>Y | No | 1000Genomes | |
| ENSVATH10440476 | 294 | Q>K | No | 1000Genomes | |
| ENSVATH04501386 | 298 | L>V | No | 1000Genomes | |
| ENSVATH04501392 | 317 | W>L | No | 1000Genomes | |
| tmp_1_93095_T_A | 323 | D>E | No | 1000Genomes | |
| tmp_1_93114_T_G | 330 | L>V | No | 1000Genomes | |
| tmp_1_93152_G_C | 342 | K>N | No | 1000Genomes | |
| ENSVATH10440480 | 430 | V>L | No | 1000Genomes | |
| ENSVATH04501402 | 436 | P>L | No | 1000Genomes | |
| tmp_1_93542_T_G | 439 | D>E | No | 1000Genomes | |
| ENSVATH10440481 | 444 | E>K | No | 1000Genomes | |
| ENSVATH00000358 | 446 | F>C | No | 1000Genomes | |
| ENSVATH04501405 | 501 | G>S | No | 1000Genomes | |
| tmp_1_93730_T_G | 502 | I>S | No | 1000Genomes | |
| tmp_1_93866_C_A | 547 | N>K | No | 1000Genomes | |
| ENSVATH00000363 | 587 | G>A | No | 1000Genomes | |
| ENSVATH00000364 | 629 | P>H | No | 1000Genomes | |
| ENSVATH04501411 | 662 | I>V | No | 1000Genomes | |
| ENSVATH13847980 | 712 | R>M | No | 1000Genomes | |
| tmp_1_94584_A_T | 762 | N>Y | No | 1000Genomes | |
| tmp_1_94727_A_T | 809 | E>D | No | 1000Genomes | |
| ENSVATH10440484 | 814 | S>C | No | 1000Genomes | |
| ENSVATH01001046 | 847 | Q>K | No | 1000Genomes | |
| tmp_1_94873_T_C | 858 | I>T | No | 1000Genomes | |
| ENSVATH04501415 | 858 | I>V | No | 1000Genomes | |
| ENSVATH04501416 | 905 | L>I | No | 1000Genomes | |
| ENSVATH04501417 | 916 | Q>H | No | 1000Genomes | |
| ENSVATH10440486 | 969 | E>D | No | 1000Genomes | |
| ENSVATH04501421 | 972 | E>Q | No | 1000Genomes | |
| ENSVATH00000371 | 973 | V>I | No | 1000Genomes | |
| ENSVATH00000372 | 1001 | E>A | No | 1000Genomes | |
| ENSVATH00000372 | 1001 | E>V | No | 1000Genomes | |
| ENSVATH10440487 | 1005 | P>R | No | 1000Genomes |
No associated diseases with Q9LNJ9
1 regional properties for Q9LNJ9
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | GRAM domain | 138 - 259 | IPR004182 |
Functions
| Description | ||
|---|---|---|
| EC Number | 2.7.1.52 | Phosphotransferases with an alcohol group as acceptor |
| Subcellular Localization |
|
|
| PANTHER Family | ||
| PANTHER Subfamily | ||
| PANTHER Protein Class | ||
| PANTHER Pathway Category | No pathway information available | |
No GO annotations of cellular component
| Name | Definition |
|---|---|
| No GO annotations for cellular component |
4 GO annotations of molecular function
| Name | Definition |
|---|---|
| ATP binding | Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator. |
| fucokinase activity | Catalysis of the reaction: L-fucose + ATP = beta-L-fucose 1-phosphate + ADP + 2 H(+). |
| fucose-1-phosphate guanylyltransferase activity | Catalysis of the reaction: beta-L-fucose 1-phosphate + GTP + H+ = diphosphate + GDP-beta-L-fucose. |
| metal ion binding | Binding to a metal ion. |
3 GO annotations of biological process
| Name | Definition |
|---|---|
| carbohydrate metabolic process | The chemical reactions and pathways involving carbohydrates, any of a group of organic compounds based of the general formula Cx(H2O)y. |
| GDP-L-fucose salvage | The formation of GDP-L-fucose from L-fucose, without de novo synthesis. L-fucose is phosphorylated by fucokinase and then converted by fucose-1-phosphate guanylyltransferase (EC:2.7.7.30). |
| phosphorylation | The process of introducing a phosphate group into a molecule, usually with the formation of a phosphoric ester, a phosphoric anhydride or a phosphoric amide. |
1 homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| Q8N0W3 | FCSK | L-fucose kinase | Homo sapiens (Human) | PR |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MSKQRKKADL | ATVLRKSWYH | LRLSVRHPTR | VPTWDAIVLT | AASPEQAELY | DWQLRRAKRM |
| 70 | 80 | 90 | 100 | 110 | 120 |
| GRIASSTVTL | AVPDPDGKRI | GSGAATLNAI | YALARHYEKL | GFDLGPEMEV | ANGACKWVRF |
| 130 | 140 | 150 | 160 | 170 | 180 |
| ISAKHVLMLH | AGGDSKRVPW | ANPMGKVFLP | LPYLAADDPD | GPVPLLFDHI | LAIASCARQA |
| 190 | 200 | 210 | 220 | 230 | 240 |
| FQDQGGLFIM | TGDVLPCFDA | FKMTLPEDAA | SIVTVPITLD | IASNHGVIVT | SKSESLAESY |
| 250 | 260 | 270 | 280 | 290 | 300 |
| TVSLVNDLLQ | KPTVEDLVKK | DAILHDGRTL | LDTGIISARG | RAWSDLVALG | CSCQPMILEL |
| 310 | 320 | 330 | 340 | 350 | 360 |
| IGSKKEMSLY | EDLVAAWVPS | RHDWLRTRPL | GELLVNSLGR | QKMYSYCTYD | LQFLHFGTSS |
| 370 | 380 | 390 | 400 | 410 | 420 |
| EVLDHLSGDA | SGIVGRRHLC | SIPATTVSDI | AASSVILSSE | IAPGVSIGED | SLIYDSTVSG |
| 430 | 440 | 450 | 460 | 470 | 480 |
| AVQIGSQSIV | VGIHIPSEDL | GTPESFRFML | PDRHCLWEVP | LVGHKGRVIV | YCGLHDNPKN |
| 490 | 500 | 510 | 520 | 530 | 540 |
| SIHKDGTFCG | KPLEKVLFDL | GIEESDLWSS | YVAQDRCLWN | AKLFPILTYS | EMLKLASWLM |
| 550 | 560 | 570 | 580 | 590 | 600 |
| GLDDSRNKEK | IKLWRSSQRV | SLEELHGSIN | FPEMCNGSSN | HQADLAGGIA | KACMNYGMLG |
| 610 | 620 | 630 | 640 | 650 | 660 |
| RNLSQLCHEI | LQKESLGLEI | CKNFLDQCPK | FQEQNSKILP | KSRAYQVEVD | LLRACGDEAK |
| 670 | 680 | 690 | 700 | 710 | 720 |
| AIELEHKVWG | AVAEETASAV | RYGFREHLLE | SSGKSHSENH | ISHPDRVFQP | RRTKVELPVR |
| 730 | 740 | 750 | 760 | 770 | 780 |
| VDFVGGWSDT | PPWSLERAGY | VLNMAITLEG | SLPIGTIIET | TNQMGISIQD | DAGNELHIED |
| 790 | 800 | 810 | 820 | 830 | 840 |
| PISIKTPFEV | NDPFRLVKSA | LLVTGIVQEN | FVDSTGLAIK | TWANVPRGSG | LGTSSILAAA |
| 850 | 860 | 870 | 880 | 890 | 900 |
| VVKGLLQISN | GDESNENIAR | LVLVLEQLMG | TGGGWQDQIG | GLYPGIKFTS | SFPGIPMRLQ |
| 910 | 920 | 930 | 940 | 950 | 960 |
| VVPLLASPQL | ISELEQRLLV | VFTGQVRLAH | QVLHKVVTRY | LQRDNLLISS | IKRLTELAKS |
| 970 | 980 | 990 | 1000 | 1010 | 1020 |
| GREALMNCEV | DEVGDIMSEA | WRLHQELDPY | CSNEFVDKLF | EFSQPYSSGF | KLVGAGGGGF |
| 1030 | 1040 | 1050 | |||
| SLILAKDAEK | AKELRQRLEE | HAEFDVKVYN | WSICI |