P32944
Gene name |
SWE1 (YJL187C, J0406) |
Protein name |
Mitosis inhibitor protein kinase SWE1 |
Names |
ICAM-3, CDw50, ICAM-R, Wee1 homolog |
Species |
Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) |
KEGG Pathway |
sce:YJL187C |
EC number |
2.7.11.1: Protein-serine/threonine kinases |
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
596-618 (Activation loop from InterPro)
Target domain |
443-791 (Catalytic domain of the Protein Tyrosine Kinases, Fungal Wee1 proteins) |
Relief mechanism |
|
Assay |
|
Autoinhibited structure

Activated structure

1 structures for P32944
Entry ID | Method | Resolution | Chain | Position | Source |
---|---|---|---|---|---|
AF-P32944-F1 | Predicted | AlphaFoldDB |
12 variants for P32944
Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
---|---|---|---|---|---|
s10-79173 | 30 | Q>R | No | SGRP | |
s10-79137 | 42 | G>E | No | SGRP | |
s10-78873 | 130 | K>R | No | SGRP | |
s10-78834 | 143 | R>Q | No | SGRP | |
s10-78632 | 210 | K>N | No | SGRP | |
s10-78536 | 242 | L>F | No | SGRP | |
s10-78405 | 286 | T>S | No | SGRP | |
s10-78214 | 350 | T>P | No | SGRP | |
s10-78067 | 399 | A>S | No | SGRP | |
s10-77202 | 687 | I>T | No | SGRP | |
s10-77139 | 708 | N>T | No | SGRP | |
s10-77127 | 712 | T>I | No | SGRP |
No associated diseases with P32944
Functions
Description | ||
---|---|---|
EC Number | 2.7.11.1 | Protein-serine/threonine kinases |
Subcellular Localization |
|
|
PANTHER Family | ||
PANTHER Subfamily | ||
PANTHER Protein Class | ||
PANTHER Pathway Category | No pathway information available |
2 GO annotations of cellular component
Name | Definition |
---|---|
cellular bud neck | The constriction between the mother cell and daughter cell (bud) in an organism that reproduces by budding. |
nucleus | A membrane-bounded organelle of eukaryotic cells in which chromosomes are housed and replicated. In most cells, the nucleus contains all of the cell's chromosomes except the organellar chromosomes, and is the site of RNA synthesis and processing. In some species, or in specialized cell types, RNA metabolism or DNA replication may be absent. |
6 GO annotations of molecular function
Name | Definition |
---|---|
ATP binding | Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator. |
metal ion binding | Binding to a metal ion. |
protein kinase activity | Catalysis of the phosphorylation of an amino acid residue in a protein, usually according to the reaction: a protein + ATP = a phosphoprotein + ADP. |
protein serine kinase activity | Catalysis of the reactions: ATP + protein serine = ADP + protein serine phosphate. |
protein serine/threonine kinase activity | Catalysis of the reactions: ATP + protein serine = ADP + protein serine phosphate, and ATP + protein threonine = ADP + protein threonine phosphate. |
protein tyrosine kinase activity | Catalysis of the reaction: ATP + a protein tyrosine = ADP + protein tyrosine phosphate. |
10 GO annotations of biological process
Name | Definition |
---|---|
cell division | The process resulting in division and partitioning of components of a cell to form more cells; may or may not be accompanied by the physical separation of a cell into distinct, individually membrane-bounded daughter cells. |
G2/M transition of mitotic cell cycle | The mitotic cell cycle transition by which a cell in G2 commits to M phase. The process begins when the kinase activity of M cyclin/CDK complex reaches a threshold high enough for the cell cycle to proceed. This is accomplished by activating a positive feedback loop that results in the accumulation of unphosphorylated and active M cyclin/CDK complex. |
meiotic cell cycle | Progression through the phases of the meiotic cell cycle, in which canonically a cell replicates to produce four offspring with half the chromosomal content of the progenitor cell via two nuclear divisions. |
mitotic morphogenesis checkpoint signaling | A signaling process that contributes to a mitotic cell cycle checkpoint which delays mitotic onset in response to perturbations that affect cell shape via the actin cytoskeleton, septin organization, small cell size, and/or the extent of membrane growth. |
negative regulation of mitotic spindle pole body separation | Any process that decreases the rate, frequency or extent of the process involving the release of duplicated mitotic spindle pole bodies (SPBs) and their migration away from each other within the nuclear membrane. |
positive regulation of sphingolipid biosynthetic process | Any process that increases the rate, frequency or extent of sphingolipid biosynthesis. Sphingolipid biosynthesis is the chemical reactions and pathways resulting in the formation of sphingolipids, any of a class of lipids containing the long-chain amine diol sphingosine or a closely related base (a sphingoid). |
re-entry into mitotic cell cycle | The resumption of the mitotic cell division cycle by cells that were in a quiescent or other non-dividing state. |
regulation of cell size | Any process that modulates the size of a cell. |
regulation of cyclin-dependent protein serine/threonine kinase activity | Any process that modulates the frequency, rate or extent of cyclin-dependent protein serine/threonine kinase activity. |
regulation of meiotic nuclear division | Any process that modulates the frequency, rate or extent of meiotic nuclear division, the process in which the nucleus of a diploid cell divides twice forming four haploid cells, one or more of which usually function as gametes. |
2 homologous proteins in AiPD
10 | 20 | 30 | 40 | 50 | 60 |
MSSLDEDEED | FEMLDTENLQ | FMGKKMFGKQ | AGEDESDDFA | IGGSTPTNKL | KFYPYSNNKL |
70 | 80 | 90 | 100 | 110 | 120 |
TRSTGTLNLS | LSNTALSEAN | SKFLGKIEEE | EEEEEEGKDE | ESVDSRIKRW | SPFHENESVT |
130 | 140 | 150 | 160 | 170 | 180 |
TPITKRSAEK | TNSPISLKQW | NQRWFPKNDA | RTENTSSSSS | YSVAKPNQSA | FTSSGLVSKM |
190 | 200 | 210 | 220 | 230 | 240 |
SMDTSLYPAK | LRIPETPVKK | SPLVEGRDHK | HVHLSSSKNA | SSSLSVSPLN | FVEDNNLQED |
250 | 260 | 270 | 280 | 290 | 300 |
LLFSDSPSSK | ALPSIHVPTI | DSSPLSEAKY | HAHDRHNNQT | NILSPTNSLV | TNSSPQTLHS |
310 | 320 | 330 | 340 | 350 | 360 |
NKFKKIKRAR | NSVILKNREL | TNSLQQFKDD | LYGTDENFPP | PIIISSHHST | RKNPQPYQFR |
370 | 380 | 390 | 400 | 410 | 420 |
GRYDNDTDEE | ISTPTRRKSI | IGATSQTHRE | SRPLSLSSAI | VTNTTSAETH | SISSTDSSPL |
430 | 440 | 450 | 460 | 470 | 480 |
NSKRRLISSN | KLSANPDSHL | FEKFTNVHSI | GKGQFSTVYQ | VTFAQTNKKY | AIKAIKPNKY |
490 | 500 | 510 | 520 | 530 | 540 |
NSLKRILLEI | KILNEVTNQI | TMDQEGKEYI | IDYISSWKFQ | NSYYIMTELC | ENGNLDGFLQ |
550 | 560 | 570 | 580 | 590 | 600 |
EQVIAKKKRL | EDWRIWKIIV | ELSLALRFIH | DSCHIVHLDL | KPANVMITFE | GNLKLGDFGM |
610 | 620 | 630 | 640 | 650 | 660 |
ATHLPLEDKS | FENEGDREYI | APEIISDCTY | DYKADIFSLG | LMIVEIAANV | VLPDNGNAWH |
670 | 680 | 690 | 700 | 710 | 720 |
KLRSGDLSDA | GRLSSTDIHS | ESLFSDITKV | DTNDLFDFER | DNISGNSNNA | GTSTVHNNSN |
730 | 740 | 750 | 760 | 770 | 780 |
INNPNMNNGN | DNNNVNTAAT | KNRLILHKSS | KIPAWVPKFL | IDGESLERIV | RWMIEPNYER |
790 | 800 | 810 | |||
RPTANQILQT | EECLYVEMTR | NAGAIIQEDD | FGPKPKFFI |