P40527
Gene name |
NEO1 (YIL048W) |
Protein name |
Probable phospholipid-transporting ATPase NEO1 |
Names |
|
Species |
Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) |
KEGG Pathway |
sce:YIL048W |
EC number |
7.6.2.1: Linked to the hydrolysis of a nucleoside triphosphate |
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

4 structures for P40527
Entry ID | Method | Resolution | Chain | Position | Source |
---|---|---|---|---|---|
7RD6 | EM | 325 A | A | 1-1151 | PDB |
7RD7 | EM | 308 A | A | 1-1151 | PDB |
7RD8 | EM | 564 A | A | 1-1151 | PDB |
AF-P40527-F1 | Predicted | AlphaFoldDB |
5 variants for P40527
Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
---|---|---|---|---|---|
s09-261703 | 90 | T>A | No | SGRP | |
s09-262568 | 378 | G>A | No | SGRP | |
s09-262705 | 424 | A>T | No | SGRP | |
s09-263836 | 801 | T>P | No | SGRP | |
s09-264598 | 1055 | A>T | No | SGRP |
No associated diseases with P40527
4 regional properties for P40527
Functions
Description | ||
---|---|---|
EC Number | 7.6.2.1 | Linked to the hydrolysis of a nucleoside triphosphate |
Subcellular Localization |
|
|
PANTHER Family | ||
PANTHER Subfamily | ||
PANTHER Protein Class | ||
PANTHER Pathway Category | No pathway information available |
8 GO annotations of cellular component
Name | Definition |
---|---|
endosome | A vacuole to which materials ingested by endocytosis are delivered. |
endosome membrane | The lipid bilayer surrounding an endosome. |
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. |
late endosome | A prelysosomal endocytic organelle differentiated from early endosomes by lower lumenal pH and different protein composition. Late endosomes are more spherical than early endosomes and are mostly juxtanuclear, being concentrated near the microtubule organizing center. |
plasma membrane | The membrane surrounding a cell that separates the cell from its external environment. It consists of a phospholipid bilayer and associated proteins. |
trans-Golgi network | The network of interconnected tubular and cisternal structures located within the Golgi apparatus on the side distal to the endoplasmic reticulum, from which secretory vesicles emerge. The trans-Golgi network is important in the later stages of protein secretion where it is thought to play a key role in the sorting and targeting of secreted proteins to the correct destination. |
4 GO annotations of molecular function
Name | Definition |
---|---|
ATP binding | Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator. |
ATP hydrolysis activity | Catalysis of the reaction: ATP + H2O = ADP + H+ phosphate. ATP hydrolysis is used in some reactions as an energy source, for example to catalyze a reaction or drive transport against a concentration gradient. |
ATPase-coupled intramembrane lipid transporter activity | Catalysis of the movement of lipids from one membrane leaflet to the other, driven by ATP hydrolysis. This includes flippases and floppases. |
magnesium ion binding | Binding to a magnesium (Mg) ion. |
6 GO annotations of biological process
Name | Definition |
---|---|
endocytosis | A vesicle-mediated transport process in which cells take up external materials or membrane constituents by the invagination of a small region of the plasma membrane to form a new membrane-bounded vesicle. |
phospholipid translocation | The movement of a phospholipid molecule from one leaflet of a membrane bilayer to the opposite leaflet. |
protein transport | The directed movement of proteins into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. |
retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum | The directed movement of substances from the Golgi back to the endoplasmic reticulum, mediated by vesicles bearing specific protein coats such as COPI or COG. |
trans-Golgi network membrane organization | A process which results in the assembly, arrangement of constituent parts, or disassembly of a trans-Golgi network membrane. |
vacuole organization | A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of a vacuole. |
4 homologous proteins in AiPD
UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
---|---|---|---|---|
P39524 | DRS2 | Phospholipid-transporting ATPase DRS2 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) | EV |
P32660 | DNF1 | Phospholipid-transporting ATPase DNF1 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) | PR |
O43861 | ATP9B | Probable phospholipid-transporting ATPase IIB | Homo sapiens (Human) | PR |
F1Q4S1 | atp9b | Probable phospholipid-transporting ATPase IIB | Danio rerio (Zebrafish) (Brachydanio rerio) | PR |
10 | 20 | 30 | 40 | 50 | 60 |
MPNPPSFKSH | KQNLFNSNNN | QHANSVDSFD | LHLDDSFDAA | LDSLQINNNP | EPLSKHNTVG |
70 | 80 | 90 | 100 | 110 | 120 |
DRESFEMRTV | DDLDNFSNHS | SDSHRKSSNT | DTHPLMYDNR | LSQDDNFKFT | NIASSPPSSS |
130 | 140 | 150 | 160 | 170 | 180 |
NNIFSKALSY | LKVSNTKNWS | KFGSPIELSD | QHIEREIHPD | TTPVYDRNRY | VSNELSNAKY |
190 | 200 | 210 | 220 | 230 | 240 |
NAVTFVPTLL | YEQFKFFYNL | YFLVVALSQA | VPALRIGYLS | SYIVPLAFVL | TVTMAKEAID |
250 | 260 | 270 | 280 | 290 | 300 |
DIQRRRRDRE | SNNELYHVIT | RNRSIPSKDL | KVGDLIKVHK | GDRIPADLVL | LQSSEPSGES |
310 | 320 | 330 | 340 | 350 | 360 |
FIKTDQLDGE | TDWKLRVACP | LTQNLSENDL | INRISITASA | PEKSIHKFLG | KVTYKDSTSN |
370 | 380 | 390 | 400 | 410 | 420 |
PLSVDNTLWA | NTVLASSGFC | IACVVYTGRD | TRQAMNTTTA | KVKTGLLELE | INSISKILCA |
430 | 440 | 450 | 460 | 470 | 480 |
CVFALSILLV | AFAGFHNDDW | YIDILRYLIL | FSTIIPVSLR | VNLDLAKSVY | AHQIEHDKTI |
490 | 500 | 510 | 520 | 530 | 540 |
PETIVRTSTI | PEDLGRIEYL | LSDKTGTLTQ | NDMQLKKIHL | GTVSYTSETL | DIVSDYVQSL |
550 | 560 | 570 | 580 | 590 | 600 |
VSSKNDSLNN | SKVALSTTRK | DMSFRVRDMI | LTLAICHNVT | PTFEDDELTY | QAASPDEIAI |
610 | 620 | 630 | 640 | 650 | 660 |
VKFTESVGLS | LFKRDRHSIS | LLHEHSGKTL | NYEILQVFPF | NSDSKRMGII | VRDEQLDEYW |
670 | 680 | 690 | 700 | 710 | 720 |
FMQKGADTVM | SKIVESNDWL | EEETGNMARE | GLRTLVIGRK | KLNKKIYEQF | QKEYNDASLS |
730 | 740 | 750 | 760 | 770 | 780 |
MLNRDQQMSQ | VITKYLEHDL | ELLGLTGVED | KLQKDVKSSI | ELLRNAGIKI | WMLTGDKVET |
790 | 800 | 810 | 820 | 830 | 840 |
ARCVSISAKL | ISRGQYVHTI | TKVTRPEGAF | NQLEYLKINR | NACLLIDGES | LGMFLKHYEQ |
850 | 860 | 870 | 880 | 890 | 900 |
EFFDVVVHLP | TVIACRCTPQ | QKADVALVIR | KMTGKRVCCI | GDGGNDVSMI | QCADVGVGIV |
910 | 920 | 930 | 940 | 950 | 960 |
GKEGKQASLA | ADFSITQFCH | LTELLLWHGR | NSYKRSAKLA | QFVMHRGLII | AICQAVYSIC |
970 | 980 | 990 | 1000 | 1010 | 1020 |
SLFEPIALYQ | GWLMVGYATC | YTMAPVFSLT | LDHDIEESLT | KIYPELYKEL | TEGKSLSYKT |
1030 | 1040 | 1050 | 1060 | 1070 | 1080 |
FFVWVLLSLF | QGSVIQLFSQ | AFTSLLDTDF | TRMVAISFTA | LVVNELIMVA | LEIYTWNKTM |
1090 | 1100 | 1110 | 1120 | 1130 | 1140 |
LVTEIATLLF | YIVSVPFLGD | YFDLGYMTTV | NYYAGLLVIL | LISIFPVWTA | KAIYRRLHPP |
1150 | |||||
SYAKVQEFAT | P |