O48626
Gene name |
ZW10 (MIP1) |
Protein name |
Centromere/kinetochore protein zw10 homolog |
Names |
AtZW10, MAG2-interacting protein 1 |
Species |
Arabidopsis thaliana (Mouse-ear cress) |
KEGG Pathway |
ath:AT2G32900 |
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 O48626
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-O48626-F1 | Predicted | AlphaFoldDB |
62 variants for O48626
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| tmp_2_13953816_A_G | 4 | I>V | No | 1000Genomes | |
| tmp_2_13953821_C_G | 5 | D>E | No | 1000Genomes | |
| ENSVATH00257674 | 12 | N>T | No | 1000Genomes | |
| ENSVATH05646755 | 13 | V>F | No | 1000Genomes | |
| ENSVATH13511838 | 15 | D>E | No | 1000Genomes | |
| tmp_2_13953909_C_A | 35 | R>S | No | 1000Genomes | |
| ENSVATH14579685 | 39 | N>K | No | 1000Genomes | |
| tmp_2_13953936_C_T | 44 | H>Y | No | 1000Genomes | |
| ENSVATH05646756 | 68 | S>F | No | 1000Genomes | |
| tmp_2_13954008_T_A | 68 | S>T | No | 1000Genomes | |
| ENSVATH13511841 | 81 | S>F | No | 1000Genomes | |
| ENSVATH13511842 | 89 | Q>K | No | 1000Genomes | |
| ENSVATH05646759 | 100 | I>L | No | 1000Genomes | |
| tmp_2_13954116_G_T | 104 | V>L | No | 1000Genomes | |
| tmp_2_13954129_C_A | 108 | T>K | No | 1000Genomes | |
| tmp_2_13954136_G_T | 110 | K>N | No | 1000Genomes | |
| ENSVATH13511843 | 113 | E>K | No | 1000Genomes | |
| ENSVATH01941760 | 142 | K>N | No | 1000Genomes | |
| ENSVATH01941759 | 142 | K>T | No | 1000Genomes | |
| ENSVATH14579686 | 149 | A>P | No | 1000Genomes | |
| tmp_2_13954259_G_T | 151 | E>D | No | 1000Genomes | |
| tmp_2_13954261_G_A | 152 | R>K | No | 1000Genomes | |
| ENSVATH01941764 | 174 | A>V | No | 1000Genomes | |
| ENSVATH13511844 | 198 | A>V | No | 1000Genomes | |
| ENSVATH00257681 | 208 | I>L | No | 1000Genomes | |
| tmp_2_13954598_G_A | 232 | E>K | No | 1000Genomes | |
| tmp_2_13954715_G_A | 235 | G>E | No | 1000Genomes | |
| tmp_2_13954714_G_A | 235 | G>R | No | 1000Genomes | |
| ENSVATH05646763 | 241 | L>F | No | 1000Genomes | |
| ENSVATH00257682 | 249 | F>V | No | 1000Genomes | |
| tmp_2_13954783_A_G | 258 | T>A | No | 1000Genomes | |
| tmp_2_13954820_G_T | 270 | C>F | No | 1000Genomes | |
| tmp_2_13955056_T_G | 304 | L>R | No | 1000Genomes | |
| ENSVATH01941772 | 325 | F>L | No | 1000Genomes | |
| ENSVATH00257685 | 362 | R>Q | No | 1000Genomes | |
| tmp_2_13955384_G_A | 372 | E>K | No | 1000Genomes | |
| ENSVATH00257686 | 375 | F>V | No | 1000Genomes | |
| ENSVATH05646767 | 389 | A>V | No | 1000Genomes | |
| tmp_2_13955465_A_G | 399 | R>G | No | 1000Genomes | |
| tmp_2_13955466_G_A | 399 | R>K | No | 1000Genomes | |
| ENSVATH13511887 | 400 | K>E | No | 1000Genomes | |
| ENSVATH13511888 | 404 | I>T | No | 1000Genomes | |
| ENSVATH05646768 | 414 | Q>L | No | 1000Genomes | |
| tmp_2_13955629_T_G | 423 | I>M | No | 1000Genomes | |
| tmp_2_13955631_C_A | 424 | A>D | No | 1000Genomes | |
| ENSVATH13511889 | 442 | V>L | No | 1000Genomes | |
| tmp_2_13955841_G_C | 468 | V>L | No | 1000Genomes | |
| tmp_2_13955845_C_G | 469 | A>G | No | 1000Genomes | |
| ENSVATH05646770 | 474 | N>D | No | 1000Genomes | |
| tmp_2_13955895_G_A | 486 | V>I | No | 1000Genomes | |
| tmp_2_13956057_G_A | 496 | D>N | No | 1000Genomes | |
| tmp_2_13956097_G_A | 509 | C>Y | No | 1000Genomes | |
| tmp_2_13956116_G_T | 515 | E>D | No | 1000Genomes | |
| tmp_2_13956126_C_G | 519 | L>V | No | 1000Genomes | |
| tmp_2_13956136_A_T | 522 | E>V | No | 1000Genomes | |
| tmp_2_13956397_G_C | 559 | V>L | No | 1000Genomes | |
| ENSVATH01941780 | 661 | D>N | No | 1000Genomes | |
| tmp_2_13957031_C_T | 681 | R>C | No | 1000Genomes | |
| tmp_2_13957183_C_G | 694 | L>V | No | 1000Genomes | |
| tmp_2_13957423_C_T | 728 | P>S | No | 1000Genomes | |
| ENSVATH05646780 | 738 | D>E | No | 1000Genomes | |
| ENSVATH00257696 | 741 | N>S | No | 1000Genomes |
No associated diseases with O48626
No regional properties for O48626
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| No domain, repeats, and functional sites for O48626 | |||
Functions
4 GO annotations of cellular component
| Name | Definition |
|---|---|
| endoplasmic reticulum membrane | The lipid bilayer surrounding the endoplasmic reticulum. |
| 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. |
| RZZ complex | A kinetochore component required for both meiotic and mitotic spindle assembly checkpoints. |
| spindle | The array of microtubules and associated molecules that forms between opposite poles of a eukaryotic cell during mitosis or meiosis and serves to move the duplicated chromosomes apart. |
No GO annotations of molecular function
| Name | Definition |
|---|---|
| No GO annotations for molecular function |
6 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. |
| 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. |
| endoplasmic reticulum to Golgi vesicle-mediated transport | The directed movement of substances from the endoplasmic reticulum (ER) to the Golgi, mediated by COP II vesicles. Small COP II coated vesicles form from the ER and then fuse directly with the cis-Golgi. Larger structures are transported along microtubules to the cis-Golgi. |
| mitotic spindle assembly checkpoint signaling | A signal transduction process that contributes to a mitotic cell cycle spindle assembly checkpoint, that delays the metaphase/anaphase transition of a mitotic nuclear division until the spindle is correctly assembled and chromosomes are attached to the spindle. |
| protein exit from endoplasmic reticulum | The directed movement of proteins from the endoplasmic reticulum. |
| 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. |
No homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| No homologous proteins | ||||
| 10 | 20 | 30 | 40 | 50 | 60 |
| MPEIDALFES | INVRDLLAGH | DLNDPTTPLS | APDLRLLINR | LESHSLRIKS | KVQSYLVAHH |
| 70 | 80 | 90 | 100 | 110 | 120 |
| SDFSELFSLC | QDTVSRTRLI | SDDVSDVLQL | VSDRPIDVEI | RSVVDEITEK | TKEVKLKRES |
| 130 | 140 | 150 | 160 | 170 | 180 |
| LDLVNAIVGI | CEALQETKEA | LKNGRFRFAA | ERIRELKVVL | RIGEEEDGEP | VAYALLRKEW |
| 190 | 200 | 210 | 220 | 230 | 240 |
| SNCFDEIQEV | LAKFMENAVR | FELDSSRIRI | KYQLSVGETA | GIALSTVLEA | MEVIGILDYG |
| 250 | 260 | 270 | 280 | 290 | 300 |
| LAKAADSIFK | HVITPAVTHA | STFAAVEDLC | KSAGEVTEAT | LRLEQSSDHK | FEDVDGDAMY |
| 310 | 320 | 330 | 340 | 350 | 360 |
| SGILKVVKFI | CSSLCFGNVT | WIHSFGRLTW | PRISELIISK | FLSKVVPEDA | SKLADFQKII |
| 370 | 380 | 390 | 400 | 410 | 420 |
| ERTSQFEAAL | KELNFVSSSD | AESRLSKYAE | DVEVHFASRK | KIEILAKARN | LLLQCNFTIP |
| 430 | 440 | 450 | 460 | 470 | 480 |
| QDIAMRNAKH | IVCLLFSSER | CVVSEAASQL | MNLVHKTLED | VCVSSARVAS | EFYNAARDSI |
| 490 | 500 | 510 | 520 | 530 | 540 |
| LLYEAVVPVK | LEKQLDGLNE | AAVLLHNDCL | YLFEEILGLA | FEYRASFPSS | IKEYAVFADI |
| 550 | 560 | 570 | 580 | 590 | 600 |
| APRFKLMAEE | VLQKQVHLVI | SSLREAIDSA | DGFQNTHQIK | QFKSAEFSID | QVVFSLKNVH |
| 610 | 620 | 630 | 640 | 650 | 660 |
| MIWEPVLRPK | TYKQSMCAVL | ESVFRRIARD | ILLLDDMAAD | ETFELQKLIY | LMLKNLSSVL |
| 670 | 680 | 690 | 700 | 710 | 720 |
| DSVRSADETS | RPLDDIIPSL | RKTRKLAELL | DMPLMSITSA | WESGELFRCN | FTRTEVQDFI |
| 730 | 740 | ||||
| KAIFTDSPLR | KECLWRIDEV | NQ |