P39535
Gene name |
PHO90 (YJL198W, J0336) |
Protein name |
Low-affinity phosphate transporter PHO90 |
Names |
|
Species |
Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) |
KEGG Pathway |
sce:YJL198W |
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 P39535
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-P39535-F1 | Predicted | AlphaFoldDB |
11 variants for P39535
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| s10-60958 | 39 | V>A | No | SGRP | |
| s10-60978 | 46 | F>I | No | SGRP | |
| s10-61390 | 183 | D>G | No | SGRP | |
| s10-61544 | 234 | I>M | No | SGRP | |
| s10-61707 | 289 | S>T | No | SGRP | |
| s10-61735 | 298 | A>V | No | SGRP | |
| s10-61813 | 324 | R>Q | No | SGRP | |
| s10-62043 | 401 | N>Y | No | SGRP | |
| s10-62856 | 672 | T>A | No | SGRP | |
| s10-62901 | 687 | I>V | No | SGRP | |
| s10-63278 | 812 | L>F | No | SGRP |
No associated diseases with P39535
3 GO annotations of cellular component
| Name | Definition |
|---|---|
| cell periphery | The part of a cell encompassing the cell cortex, the plasma membrane, and any external encapsulating structures. |
| 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. |
1 GO annotations of molecular function
| Name | Definition |
|---|---|
| inorganic phosphate transmembrane transporter activity | Enables the transfer of a inorganic phosphate from one side of a membrane to the other, up its concentration gradient. The transporter binds the solute and undergoes a series of conformational changes. Transport works equally well in either direction and is driven by a chemiosmotic source of energy. Secondary active transporters include symporters and antiporters. |
4 GO annotations of biological process
| Name | Definition |
|---|---|
| anion transmembrane transport | The process in which an anion is transported across a membrane. |
| phosphate ion transport | The directed movement of phosphate into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. |
| polyphosphate metabolic process | The chemical reactions and pathways involving a polyphosphate, the anion or salt of polyphosphoric acid. |
| regulation of phosphate transmembrane transport | Any process that modulates the frequency, rate or extent of phosphate transmembrane transport. |
2 homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| P25360 | PHO87 | Inorganic phosphate transporter PHO87 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) | PR |
| P27514 | PHO91 | Low-affinity phosphate transporter PHO91 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) | PR |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MRFSHFLKYN | AVPEWQNHYM | DYSELKNLIY | TLQTDELQVG | DNEEGFGAGK | SSNITDRFKN |
| 70 | 80 | 90 | 100 | 110 | 120 |
| KFSFKNAKED | TSSGMNKDAG | IVEETIELRE | LPTAQTVAAK | PSPFRRMKEK | IFYKRRSSSA |
| 130 | 140 | 150 | 160 | 170 | 180 |
| SSVSSTANEN | LQLDTYDTFV | GDLTAEKQKV | DDFYKRTEAK | FYDKFDALVK | DLKKIGVIEY |
| 190 | 200 | 210 | 220 | 230 | 240 |
| DIDDDTLFNE | PIASTNDEVP | PLDLDDDEDD | DEFYDDQSNI | EDNTALLHHS | QYNIKSQKKS |
| 250 | 260 | 270 | 280 | 290 | 300 |
| LLKKSIVNLY | IDLCQLKSFI | ELNRIGFAKI | TKKSDKVLHL | NTRTELIESE | QFFKDTYAFQ |
| 310 | 320 | 330 | 340 | 350 | 360 |
| AETIELLNSK | ISQLVTFYAR | ITDRPHNISH | SKQELKSYLH | DHIVWERSNT | WKDMLGLLSQ |
| 370 | 380 | 390 | 400 | 410 | 420 |
| ADELTPKETE | YNANKLVGKL | DLEYYRWPLP | RPINLKFTSI | NNVALPKLFF | TKKAYKIYFI |
| 430 | 440 | 450 | 460 | 470 | 480 |
| ILVTGLLLGI | KTFNDAAQHR | CMALVECVAF | LWASEAIPLH | ITAFLVPLLV | VLFKVLKTSD |
| 490 | 500 | 510 | 520 | 530 | 540 |
| GAIMSAASAS | SEILAAMWSS | TIMILLAGFT | LGEVLAQYNI | AKVLASWLLA | FAGCKPRNVL |
| 550 | 560 | 570 | 580 | 590 | 600 |
| LMAMCVVFFL | SMWISNVAAP | VLTYSLLSPL | LDAMDADSPF | AQALVLGVAL | AANIGGMSSP |
| 610 | 620 | 630 | 640 | 650 | 660 |
| ISSPQNIISM | SYLKPYGIGW | GQFFAVALPS | GILAMLLVWI | LLFTTFKMNK | TKLEKFKPIK |
| 670 | 680 | 690 | 700 | 710 | 720 |
| TKFTVKQYYI | ITVTVATILL | WCVESQIEGA | FGSSGQIAII | PIVLFFGTGL | LSTQDLNAFP |
| 730 | 740 | 750 | 760 | 770 | 780 |
| WSIVILAMGG | IALGKAVSSS | GLLSTIAKAL | QKKIENDGVF | AILCIFGILM | LVVGTFVSHT |
| 790 | 800 | 810 | 820 | 830 | 840 |
| VSAIIIIPLV | QEVGDKLGNP | KAAPILVFGC | ALLSSCGMGL | ASSGFPNVTA | ISKVDRKGDR |
| 850 | 860 | 870 | 880 | ||
| YLSVMTFLTR | GVPASILAFL | CVITLGYGIM | ASVVKGNATS | A |