Q84VX4
Gene name |
MPS1 (PPK1, At1g77720, T32E8.5) |
Protein name |
Serine/threonine-protein kinase MPS1 |
Names |
EC 2.7.12.2 , Monopolar spindle protein 1 homolog |
Species |
Arabidopsis thaliana (Mouse-ear cress) |
KEGG Pathway |
ath:AT1G77720 |
EC number |
2.7.12.2: Dual-specificity kinases (those acting on Ser/Thr and Tyr residues) |
Protein Class |
|

Descriptions
Autoinhibitory domains (AIDs)
Target domain |
400-693 (Protein kinase domain) |
Relief mechanism |
PTM |
Assay |
|
Accessory elements
567-592 (Activation loop from InterPro)
Target domain |
400-693 (Protein kinase domain) |
Relief mechanism |
|
Assay |
|
References
Autoinhibited structure

Activated structure

1 structures for Q84VX4
Entry ID | Method | Resolution | Chain | Position | Source |
---|---|---|---|---|---|
AF-Q84VX4-F1 | Predicted | AlphaFoldDB |
58 variants for Q84VX4
Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
---|---|---|---|---|---|
ENSVATH05162937 | 2 | D>N | No | 1000Genomes | |
ENSVATH14488774 | 15 | P>T | No | 1000Genomes | |
tmp_1_29210796_T_G | 23 | L>V | No | 1000Genomes | |
ENSVATH13828170 | 68 | S>T | No | 1000Genomes | |
tmp_1_29211277_G_T | 75 | A>S | No | 1000Genomes | |
tmp_1_29211284_G_A | 77 | R>K | No | 1000Genomes | |
ENSVATH05162948 | 86 | G>R | No | 1000Genomes | |
ENSVATH05162948 | 86 | G>W | No | 1000Genomes | |
tmp_1_29211368_C_T | 105 | T>I | No | 1000Genomes | |
ENSVATH00146568 | 116 | S>F | No | 1000Genomes | |
tmp_1_29211419_C_T | 122 | A>V | No | 1000Genomes | |
ENSVATH05162949 | 128 | T>A | No | 1000Genomes | |
tmp_1_29211486_A_C | 144 | K>N | No | 1000Genomes | |
ENSVATH13828171 | 149 | S>N | No | 1000Genomes | |
ENSVATH01550455 | 159 | K>T | No | 1000Genomes | |
tmp_1_29211551_C_A | 166 | T>K | No | 1000Genomes | |
tmp_1_29211709_G_C | 172 | W>C | No | 1000Genomes | |
ENSVATH05162956 | 174 | A>P | No | 1000Genomes | |
tmp_1_29211734_T_A | 181 | S>T | No | 1000Genomes | |
ENSVATH05162957 | 183 | L>I | No | 1000Genomes | |
ENSVATH00146569 | 198 | D>N | No | 1000Genomes | |
tmp_1_29211795_T_G | 201 | V>G | No | 1000Genomes | |
tmp_1_29211830_C_G | 213 | L>V | No | 1000Genomes | |
tmp_1_29211843_A_T | 217 | Q>L | No | 1000Genomes | |
tmp_1_29211864_C_G | 224 | P>R | No | 1000Genomes | |
tmp_1_29211945_C_T | 251 | S>L | No | 1000Genomes | |
ENSVATH05162958 | 267 | E>K | No | 1000Genomes | |
tmp_1_29212005_A_G | 271 | N>S | No | 1000Genomes | |
tmp_1_29212053_G_A | 287 | C>Y | No | 1000Genomes | |
ENSVATH05162959 | 302 | A>D | No | 1000Genomes | |
ENSVATH01550458 | 316 | V>L | No | 1000Genomes | |
ENSVATH13828174 | 322 | D>Y | No | 1000Genomes | |
ENSVATH00146570 | 323 | T>M | No | 1000Genomes | |
tmp_1_29212184_A_T | 331 | T>S | No | 1000Genomes | |
tmp_1_29212233_A_G | 347 | Q>R | No | 1000Genomes | |
tmp_1_29212326_G_C | 378 | G>A | No | 1000Genomes | |
ENSVATH05162962 | 423 | T>I | No | 1000Genomes | |
ENSVATH13828176 | 436 | D>E | No | 1000Genomes | |
ENSVATH05162963 | 438 | A>G | No | 1000Genomes | |
tmp_1_29212545_A_G | 451 | K>R | No | 1000Genomes | |
tmp_1_29212548_A_G | 452 | K>R | No | 1000Genomes | |
tmp_1_29212756_A_G | 482 | S>G | No | 1000Genomes | |
tmp_1_29212779_G_C | 489 | K>N | No | 1000Genomes | |
tmp_1_29212884_T_G | 524 | D>E | No | 1000Genomes | |
tmp_1_29213355_C_A | 604 | S>R | No | 1000Genomes | |
tmp_1_29213457_T_G | 638 | D>E | No | 1000Genomes | |
ENSVATH05162972 | 638 | D>N | No | 1000Genomes | |
ENSVATH05162973 | 654 | H>N | No | 1000Genomes | |
ENSVATH05162974 | 654 | H>P | No | 1000Genomes | |
ENSVATH01550462 | 660 | Q>E | No | 1000Genomes | |
ENSVATH00146575 | 700 | E>K | No | 1000Genomes | |
ENSVATH05162975 | 739 | P>A | No | 1000Genomes | |
ENSVATH05162975 | 739 | P>T | No | 1000Genomes | |
ENSVATH00146577 | 740 | L>R | No | 1000Genomes | |
tmp_1_29213774_A_T | 744 | D>V | No | 1000Genomes | |
ENSVATH05162976 | 750 | D>V | No | 1000Genomes | |
tmp_1_29213807_T_G | 755 | L>R | No | 1000Genomes | |
ENSVATH05162977 | 755 | L>V | No | 1000Genomes |
No associated diseases with Q84VX4
4 regional properties for Q84VX4
Type | Name | Position | InterPro Accession |
---|---|---|---|
domain | Protein kinase domain | 400 - 693 | IPR000719 |
active_site | Serine/threonine-protein kinase, active site | 547 - 559 | IPR008271 |
binding_site | Protein kinase, ATP binding site | 406 - 428 | IPR017441 |
domain | Protein kinase Mps1 family, catalytic domain | 398 - 693 | IPR027084 |
Functions
Description | ||
---|---|---|
EC Number | 2.7.12.2 | Dual-specificity kinases (those acting on Ser/Thr and Tyr residues) |
Subcellular Localization |
|
|
PANTHER Family | ||
PANTHER Subfamily | ||
PANTHER Protein Class | ||
PANTHER Pathway Category | No pathway information available |
2 GO annotations of cellular component
Name | Definition |
---|---|
kinetochore | A multisubunit complex that is located at the centromeric region of DNA and provides an attachment point for the spindle microtubules. |
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. |
5 GO annotations of molecular function
Name | Definition |
---|---|
ATP binding | Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator. |
MAP kinase kinase activity | Catalysis of the concomitant phosphorylation of threonine (T) and tyrosine (Y) residues in a Thr-Glu-Tyr (TEY) thiolester sequence in a MAP kinase (MAPK) substrate. |
protein serine kinase activity | Catalysis of the reactions |
protein serine/threonine kinase activity | Catalysis of the reactions |
protein tyrosine kinase activity | Catalysis of the reaction |
6 GO annotations of biological process
Name | Definition |
---|---|
chromosome segregation | The process in which genetic material, in the form of chromosomes, is organized into specific structures and then physically separated and apportioned to two or more sets. In eukaryotes, chromosome segregation begins with the condensation of chromosomes, includes chromosome separation, and ends when chromosomes have completed movement to the spindle poles. |
meiotic spindle assembly checkpoint signaling | A signal transduction process that contributes to a meiotic spindle assembly checkpoint, that delays the metaphase/anaphase transition of a meiotic cell cycle until the spindle is correctly assembled and chromosomes are attached to the spindle. |
mitotic spindle assembly checkpoint signaling | A mitotic cell cycle checkpoint that delays mitotic sister chromatid separation and consequently the mitotic metaphase/anaphase transition until the spindle is correctly assembled and chromosomes are attached to the spindle. Spindle assembly checkpoint signalling begins with the activated Mph family kinase, and results in the inhibition of the Anaphase Promoting Complex and its activator Sleepy/Cdc20 by the mitotic checkpoint complex (MCC). |
organelle organization | A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of an organelle within a cell. An organelle is an organized structure of distinctive morphology and function. Includes the nucleus, mitochondria, plastids, vacuoles, vesicles, ribosomes and the cytoskeleton. Excludes the plasma membrane. |
protein autophosphorylation | The phosphorylation by a protein of one or more of its own amino acid residues (cis-autophosphorylation), or residues on an identical protein (trans-autophosphorylation). |
protein localization to kinetochore | Any process in which a protein is transported to, or maintained at, the kinetochore. |
3 homologous proteins in AiPD
10 | 20 | 30 | 40 | 50 | 60 |
MDREDNLPVQ | PDKPPKSLVR | PILNLETTSS | SSSSSSSSPE | LLRHLQAAFK | RHRPLSKMQT |
70 | 80 | 90 | 100 | 110 | 120 |
TSIGPRRSVA | PQRQASRNTR | LVTAEGQRSQ | DVVTLSQSLA | ANTLTQDTTN | NLAITSVAGE |
130 | 140 | 150 | 160 | 170 | 180 |
SASITQPTVS | EHFNPSDRQM | DFGKSAVTSL | ESNLDVQRKS | QSLIGTSQDM | EWDATNQAEA |
190 | 200 | 210 | 220 | 230 | 240 |
SHLDACIGSK | HQNLPSVDSE | VSLKSEYKDS | SSLAKIQGQL | GEFPNFLNQP | RTRCSAVGSS |
250 | 260 | 270 | 280 | 290 | 300 |
WATTTLIHSS | SAPMLNATTH | VSRSYVEADS | NANPHAVQSQ | GNLPSCCPSS | KVSNILHPNK |
310 | 320 | 330 | 340 | 350 | 360 |
DATASEMPAS | TNDPEVRVKE | TDTSKQQQIT | TGLEAPVGSS | IYGSDGQANA | RLPEELHTSV |
370 | 380 | 390 | 400 | 410 | 420 |
SSQPQKSDKH | EKVASSKGPS | APRKRNYDPD | LFFKVNGKLY | QRLGKIGSGG | SSEVHKVISS |
430 | 440 | 450 | 460 | 470 | 480 |
DCTIYALKKI | KLKGRDYATA | YGFCQEIGYL | KKLKGKTNII | QLIDYEVTDK | TLLQEVLNGT |
490 | 500 | 510 | 520 | 530 | 540 |
MSNKDGRVKE | DGFIYMVLEY | GEIDLAHMLS | QKWREIEGSD | RTIDENWLRF | YWQQILQAVN |
550 | 560 | 570 | 580 | 590 | 600 |
TIHEERIVHS | DLKPANFLLV | RGFLKLIDFG | IAKAINSDTT | NIQRDSQVGT | LSYMSPEAFM |
610 | 620 | 630 | 640 | 650 | 660 |
CNESDENGNT | IKCGRPSDIW | SLGCILYQMV | YGRTPFADYK | TFWAKFKVIT | DPNHEITYNQ |
670 | 680 | 690 | 700 | 710 | 720 |
LSNPWLIDLM | KKCLAWDRNQ | RWRIPELLQH | PFLAPPIPHE | PQVKTIKLFS | LIAESCGSDD |
730 | 740 | 750 | 760 | 770 | |
DKANSMISQL | EQLLSNPAPL | PRNDVLDSRD | QNQQLLSRVS | ELCIQLQDRL | QGLEGEN |