P40433
Gene name |
PFK26 (YIL107C) |
Protein name |
6-phosphofructo-2-kinase 1 |
Names |
6PF-2-K 1, Phosphofructokinase 2 I |
Species |
Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) |
KEGG Pathway |
sce:YIL107C |
EC number |
2.7.1.105: 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 P40433
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-P40433-F1 | Predicted | AlphaFoldDB |
17 variants for P40433
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| s09-165407 | 118 | K>E | No | SGRP | |
| s09-165400 | 120 | P>L | No | SGRP | |
| s09-165068 | 231 | G>R | No | SGRP | |
| s09-165036 | 241 | E>D | No | SGRP | |
| s09-164519 | 414 | R>C | No | SGRP | |
| s09-164501 | 420 | H>N | No | SGRP | |
| s09-164329 | 477 | G>E | No | SGRP | |
| s09-164057 | 568 | V>L | No | SGRP | |
| s09-164014 | 582 | G>D | No | SGRP | |
| s09-163790 | 657 | F>L | No | SGRP | |
| s09-163499 | 754 | L>F | No | SGRP | |
| s09-163471 | 763 | S>F | No | SGRP | |
| s09-163458 | 767 | N>K | No | SGRP | |
| s09-163424 | 779 | F>I | No | SGRP | |
| s09-163405 | 785 | D>G | No | SGRP | |
| s09-163336 | 808 | D>G | No | SGRP | |
| s09-163276 | 828 | V>L | No | SGRP |
No associated diseases with P40433
1 regional properties for P40433
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | 6-phosphofructo-2-kinase | 174 - 395 | IPR013079 |
Functions
| Description | ||
|---|---|---|
| EC Number | 2.7.1.105 | Phosphotransferases with an alcohol group as acceptor |
| Subcellular Localization |
|
|
| PANTHER Family | ||
| PANTHER Subfamily | ||
| PANTHER Protein Class | ||
| PANTHER Pathway Category | No pathway information available | |
2 GO annotations of cellular component
2 GO annotations of molecular function
| Name | Definition |
|---|---|
| 6-phosphofructo-2-kinase activity | Catalysis of the reaction: beta-D-fructose 6-phosphate + ATP = beta-D-fructose 2,6-bisphosphate + ADP + 2 H(+). |
| ATP binding | Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator. |
2 GO annotations of biological process
| Name | Definition |
|---|---|
| fructose 2,6-bisphosphate metabolic process | The chemical reactions and pathways involving fructose 2,6-bisphosphate. The D enantiomer is an important regulator of the glycolytic and gluconeogenic pathways. It inhibits fructose 1,6-bisphosphatase and activates phosphofructokinase. |
| fructose metabolic process | The chemical reactions and pathways involving fructose, the ketohexose arabino-2-hexulose. Fructose exists in a open chain form or as a ring compound. D-fructose is the sweetest of the sugars and is found free in a large number of fruits and honey. |
1 homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| P32604 | FBP26 | Fructose-2,6-bisphosphatase | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) | PR |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MFKPVDFSET | SPVPPDIDLA | PTQSPHHVAP | SQDSSYDLLS | RSSDDKIDAE | KGPHDELSKH |
| 70 | 80 | 90 | 100 | 110 | 120 |
| LPLFQKRPLS | DTPISSNWNS | PGITEENTPS | DSPENSATNL | KSLHRLHIND | ETQLKNAKIP |
| 130 | 140 | 150 | 160 | 170 | 180 |
| TNDTTDYMPP | SDGANEVTRI | DLKDIKSPTR | HHKRRPTTID | VPGLTKSKTS | PDGLISKEDS |
| 190 | 200 | 210 | 220 | 230 | 240 |
| GSKLVIVMVG | LPATGKSFIT | NKLSRFLNYS | LYYCKVFNVG | NTRRKFAKEH | GLKDQDSKFF |
| 250 | 260 | 270 | 280 | 290 | 300 |
| EPKNADSTRL | RDKWAMDTLD | ELLDYLLEGS | GSVGIFDATN | TSRERRKNVL | ARIRKRSPHL |
| 310 | 320 | 330 | 340 | 350 | 360 |
| KVLFLESVCS | DHALVQKNIR | LKLFGPDYKG | KDPESSLKDF | KSRLANYLKA | YEPIEDDENL |
| 370 | 380 | 390 | 400 | 410 | 420 |
| QYIKMIDVGK | KVIAYNIQGF | LASQTVYYLL | NFNLADRQIW | ITRSGESEDN | VSGRIGGNSH |
| 430 | 440 | 450 | 460 | 470 | 480 |
| LTPRGLRFAK | SLPKFIARQR | EIFYQNLMQQ | KKNNENTDGN | IYNDFFVWTS | MRARTIGTAQ |
| 490 | 500 | 510 | 520 | 530 | 540 |
| YFNEDDYPIK | QMKMLDELSA | GDYDGMTYPE | IKNNFPEEFE | KRQKDKLRYR | YPGIGGESYM |
| 550 | 560 | 570 | 580 | 590 | 600 |
| DVINRLRPVI | TELERIEDNV | LIITHRVVAR | ALLGYFMNLS | MGIIANLDVP | LHCVYCLEPK |
| 610 | 620 | 630 | 640 | 650 | 660 |
| PYGITWSLWE | YDEASDSFSK | VPQTDLNTTR | VKEVGLVYNE | RRYSVIPTAP | PSARSSFASD |
| 670 | 680 | 690 | 700 | 710 | 720 |
| FLSRKRSNPT | SASSSQSELS | EQPKNSVSAQ | TGSNNTTLIG | SNFNIKNENG | DSRIPLSAPL |
| 730 | 740 | 750 | 760 | 770 | 780 |
| MATNTSNNIL | DGGGTSISIH | RPRVVPNQNN | VNPLLANNNK | AASNVPNVKK | SAATPRQIFE |
| 790 | 800 | 810 | 820 | ||
| IDKVDEKLSM | LKNKSFLLHG | KDYPNNADNN | DNEDIRAKTM | NRSQSHV |