Descriptions

Nek6 is a NIMA-related kinase essential for proper mitotic spindle assembly and has a catalytic domain with a 30-40 amino acid N-terminal extension. Nek6 is subject to autoinhibition by the tyrosine motif, Tyr108. This is because the Y108A mutation is more active than wild-type Nek6. In addition, the activity of Nek6 is increased by interaction with the Nek9 noncatalytic C-terminal domain, which may release tyrosine from the autoinhibitory position.

Autoinhibitory domains (AIDs)

Target domain

31-41 (N-terminal extension of kinase domain)

Relief mechanism

Partner binding

Assay

Structural analysis, Mutagenesis experiment

Accessory elements

189-212 (Activation loop from InterPro)

Target domain

45-310 (Protein kinase domain)

Relief mechanism

Assay

Autoinhibited structure

Activated structure

1 structures for Q9HC98

Entry ID Method Resolution Chain Position Source
AF-Q9HC98-F1 Predicted AlphaFoldDB

202 variants for Q9HC98

Variant ID(s) Position Change Description Diseaes Association Provenance
CA374875763
rs1247048658
2 A>V No ClinGen
gnomAD
CA199686987
rs911139179
4 Q>E No ClinGen
TOPMed
CA5234091
rs779271535
4 Q>R No ClinGen
ExAC
gnomAD
CA374875781
rs1167516898
5 P>L No ClinGen
gnomAD
CA374875782
rs528727476
6 G>C No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA5234093
rs528727476
6 G>S No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1365078463
CA374875792
7 H>L No ClinGen
TOPMed
gnomAD
CA374875791
rs1365078463
7 H>R No ClinGen
TOPMed
gnomAD
CA374875801
rs1326135942
8 M>I No ClinGen
gnomAD
CA5234094
rs780230637
8 M>V No ClinGen
ExAC
gnomAD
CA374875807
rs1331996591
9 P>R No ClinGen
gnomAD
rs377403028
CA5234095
10 H>R No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs1366906036
CA374875816
11 G>R No ClinGen
gnomAD
rs1588482166
CA374875835
13 S>R No ClinGen
Ensembl
CA374875840
rs1465974668
14 S>C No ClinGen
gnomAD
CA374875846
rs1454488440
15 N>S No ClinGen
TOPMed
CA5234096
rs145488745
16 N>K No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA374875873
rs1290364170
18 C>Y No ClinGen
gnomAD
rs747894737
CA5234098
21 L>V No ClinGen
ExAC
gnomAD
CA374875936
rs867678055
22 G>R No ClinGen
TOPMed
CA199687059
rs867678055
22 G>W No ClinGen
TOPMed
CA374875951
rs1290547838
23 P>L No ClinGen
gnomAD
rs1446146786
CA374875953
24 V>M No ClinGen
gnomAD
CA5234099
rs769478376
25 H>R No ClinGen
ExAC
gnomAD
CA199687064
rs140978005
26 P>S No ClinGen
ESP
gnomAD
CA199687068
rs910941666
27 P>L No ClinGen
gnomAD
rs941098694
CA199687088
29 P>S No ClinGen
Ensembl
CA374876051
rs1384634882
30 Q>R No ClinGen
gnomAD
CA5234123
rs758964365
34 N>D No ClinGen
ExAC
gnomAD
CA374877205
rs1256928848
34 N>K No ClinGen
gnomAD
CA5234124
rs769243779
35 T>A No ClinGen
ExAC
gnomAD
CA5234125
rs774694008
35 T>M No ClinGen
ExAC
TOPMed
gnomAD
CA5234128
rs750746819
39 R>C No ClinGen
ExAC
gnomAD
rs1376354948
CA374877234
39 R>H No ClinGen
TOPMed
gnomAD
CA374877233
rs1376354948
39 R>L No ClinGen
TOPMed
gnomAD
CA374877238
rs1467238937
40 C>Y No ClinGen
TOPMed
gnomAD
rs763278157
CA5234129
41 S>L No ClinGen
ExAC
TOPMed
gnomAD
rs1409086630
CA374877248
42 L>M No ClinGen
TOPMed
gnomAD
CA374877252
rs1433128929
42 L>R No ClinGen
gnomAD
rs1409086630
CA374877249
42 L>V No ClinGen
TOPMed
gnomAD
CA5234131
rs183673274
43 A>V No ClinGen
1000Genomes
ExAC
gnomAD
rs148262318
CA5234134
48 E>K No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs755980284
CA5234135
49 K>N No ClinGen
ExAC
gnomAD
rs777558111
CA5234136
52 G>S No ClinGen
ExAC
gnomAD
CA5234137
rs749069904
53 R>* No ClinGen
ExAC
TOPMed
gnomAD
rs1341208772
CA374877344
56 F>Y No ClinGen
TOPMed
rs745431350
CA5234140
58 E>A No ClinGen
ExAC
gnomAD
CA5234139
rs778399540
58 E>K No ClinGen
ExAC
TOPMed
gnomAD
CA199696983
rs923279115
63 T>I No ClinGen
TOPMed
gnomAD
rs1588497542
CA374877391
63 T>P No ClinGen
Ensembl
CA374877409
rs1265646448
66 L>M No ClinGen
gnomAD
CA5234141
rs771504531
68 R>K No ClinGen
ExAC
TOPMed
gnomAD
CA374877426
rs1377794796
68 R>S No ClinGen
TOPMed
rs775022069
CA5234142
70 T>S No ClinGen
ExAC
TOPMed
gnomAD
CA374877478
rs1427488678
76 V>A No ClinGen
gnomAD
rs1372158895
CA374877475
76 V>L No ClinGen
TOPMed
gnomAD
CA374877474
rs1372158895
76 V>M No ClinGen
TOPMed
gnomAD
CA374877482
rs1370678576
77 Q>* No ClinGen
gnomAD
CA374877484
rs1429957019
77 Q>R No ClinGen
TOPMed
CA374877513
rs1386238966
79 F>L No ClinGen
TOPMed
gnomAD
rs1332109613
CA374877532
82 M>V No ClinGen
TOPMed
rs779439151
CA5234159
84 A>T No ClinGen
ExAC
gnomAD
rs1386167089
CA374877565
86 A>V No ClinGen
TOPMed
gnomAD
CA199698616
rs987052518
88 Q>R No ClinGen
Ensembl
CA374877581
rs1588499962
89 D>N No ClinGen
Ensembl
rs183711992
CA199698654
92 K>R No ClinGen
1000Genomes
gnomAD
rs183711992
CA374877606
92 K>T No ClinGen
1000Genomes
gnomAD
rs1463842648
CA374877612
93 E>* No ClinGen
gnomAD
rs774713096
CA5234165
95 G>D No ClinGen
ExAC
gnomAD
rs768754460
CA5234188
100 L>M No ClinGen
ExAC
gnomAD
CA374869994
rs1209363432
101 N>S No ClinGen
TOPMed
rs1271939785
CA374870054
109 L>W No ClinGen
gnomAD
CA199658042
rs1031164724
111 S>L No ClinGen
TOPMed
CA374870074
rs1182869786
112 F>C No ClinGen
gnomAD
CA374870080
rs1267853445
113 I>V No ClinGen
gnomAD
rs370008827
CA5234193
114 E>G No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs750249273
CA5234192
114 E>K No ClinGen
ExAC
TOPMed
gnomAD
rs370008827
CA374870088
114 E>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA374870093
rs1415316825
115 D>N No ClinGen
TOPMed
gnomAD
rs1168037323
CA374870100
116 N>D No ClinGen
gnomAD
CA5234195
rs143094065
117 E>K No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA5234197
rs780863742
119 N>S No ClinGen
ExAC
gnomAD
CA374870173
rs1417581726
127 A>T No ClinGen
TOPMed
CA5234204
rs747235761
132 Q>H No ClinGen
ExAC
gnomAD
rs780356311
CA5234203
132 Q>R No ClinGen
ExAC
TOPMed
gnomAD
CA374870223
rs1449600656
134 I>N No ClinGen
gnomAD
rs1223479281
CA374870228
135 K>E No ClinGen
gnomAD
rs868482996
CA199660864
136 Y>H No ClinGen
TOPMed
gnomAD
rs1472585159
CA374870530
138 K>R No ClinGen
gnomAD
rs1157394651
CA374870555
140 Q>R No ClinGen
gnomAD
CA199660870
rs759138170
142 R>Q No ClinGen
TOPMed
rs767329239
CA374870578
142 R>W No ClinGen
ExAC
gnomAD
rs775228582
CA5234232
143 L>V No ClinGen
ExAC
gnomAD
CA374870596
rs1454102379
144 I>V No ClinGen
TOPMed
CA5234233
rs368466543
145 P>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1395923597
CA374870621
146 E>Q No ClinGen
TOPMed
CA199660891
rs552985155
149 V>A No ClinGen
1000Genomes
TOPMed
rs1588517960
CA374870697
152 Y>D No ClinGen
Ensembl
CA374871106
rs1588517996
154 V>A No ClinGen
Ensembl
rs1407961158
CA374871100
154 V>L No ClinGen
gnomAD
CA374871099
rs1407961158
154 V>M No ClinGen
gnomAD
CA374871113
rs1289955664
155 Q>* No ClinGen
gnomAD
CA374871137
rs1483225181
157 C>Y No ClinGen
TOPMed
rs200565078
CA5234238
158 S>N No ClinGen
1000Genomes
ExAC
gnomAD
CA199660913
rs879292381
159 A>T No ClinGen
gnomAD
rs751958560
CA5234241
160 V>L No ClinGen
ExAC
TOPMed
gnomAD
CA5234240
rs751958560
160 V>M No ClinGen
ExAC
TOPMed
gnomAD
CA5234243
rs748409240
165 S>L No ClinGen
ExAC
TOPMed
gnomAD
rs369950028
CA5234244
166 R>C No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1420088183
CA374871249
166 R>H No ClinGen
gnomAD
CA374871244
rs369950028
166 R>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs777970915
CA5234245
167 R>Q No ClinGen
ExAC
TOPMed
gnomAD
rs1461941868
CA374871256
167 R>W No ClinGen
TOPMed
gnomAD
CA5234247
rs771033424
171 R>* No ClinGen
ExAC
gnomAD
CA374871305
rs1369451980
171 R>Q No ClinGen
gnomAD
CA5234282
rs760926146
175 P>A No ClinGen
ExAC
gnomAD
rs553709380
CA374871493
177 N>K No ClinGen
gnomAD
CA374871497
rs1482758201
178 V>M No ClinGen
gnomAD
rs1162626313
CA374871542
182 A>T No ClinGen
gnomAD
CA5234284
rs754146573
183 T>M No ClinGen
ExAC
TOPMed
gnomAD
CA5234286
rs779146612
185 V>I No ClinGen
ExAC
TOPMed
gnomAD
CA5234288
rs758428107
186 V>G No ClinGen
ExAC
gnomAD
CA5234287
rs775352569
186 V>M No ClinGen
ExAC
gnomAD
rs779821672
CA374871617
189 G>C No ClinGen
ExAC
TOPMed
gnomAD
rs779821672
CA5234289
189 G>S No ClinGen
ExAC
TOPMed
gnomAD
CA5234291
rs768356782
195 R>C No ClinGen
ExAC
gnomAD
CA374871678
rs768356782
195 R>S No ClinGen
ExAC
gnomAD
rs200086787
CA199661854
196 F>C No ClinGen
Ensembl
rs201207004
CA199661861
197 F>L No ClinGen
gnomAD
rs747816154
CA5234293
200 E>G No ClinGen
ExAC
gnomAD
rs1588519923
CA374871751
201 T>P No ClinGen
Ensembl
rs1588519942
CA374871761
202 T>P No ClinGen
Ensembl
rs772780677
CA5234296
203 A>V No ClinGen
ExAC
gnomAD
rs751648398
CA5234330
215 S>L No ClinGen
ExAC
gnomAD
CA5234331
rs555077914
216 P>A No ClinGen
1000Genomes
ExAC
gnomAD
CA5234332
rs767414917
216 P>L No ClinGen
ExAC
TOPMed
gnomAD
CA5234334
rs755926840
220 H>Y No ClinGen
ExAC
gnomAD
CA5234336
rs543844372
224 Y>* No ClinGen
1000Genomes
ExAC
gnomAD
CA199668393
rs201833354
230 I>M No ClinGen
ExAC
gnomAD
rs1042477188
CA199668386
230 I>V No ClinGen
TOPMed
gnomAD
CA5234339
rs779050538
232 S>A No ClinGen
ExAC
gnomAD
CA374873314
rs10760354
233 L>V No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA5234341
rs771906905
237 L>V No ClinGen
ExAC
gnomAD
CA374873377
rs1288821162
239 E>K No ClinGen
gnomAD
CA374874481
rs1190475979
242 A>T No ClinGen
gnomAD
rs1419093540
CA374874497
243 L>F No ClinGen
gnomAD
CA5234366
rs151138282
252 M>I No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs919717766
CA199675081
252 M>K No ClinGen
Ensembl
CA5234365
rs749637388
252 M>V No ClinGen
ExAC
gnomAD
rs1338625653
CA374874674
255 F>L No ClinGen
gnomAD
CA374874669
rs1588554508
255 F>S No ClinGen
Ensembl
rs774656051
CA5234367
256 S>C No ClinGen
ExAC
TOPMed
gnomAD
rs774656051
CA5234368
256 S>F No ClinGen
ExAC
TOPMed
gnomAD
rs772144294
CA5234369
259 Q>K No ClinGen
ExAC
gnomAD
CA5234372
rs764086271
262 E>K No ClinGen
ExAC
gnomAD
CA5234373
rs753614385
263 Q>E No ClinGen
ExAC
TOPMed
gnomAD
CA374874733
rs1315306769
264 C>F No ClinGen
TOPMed
CA5234374
rs761645776
264 C>R No ClinGen
ExAC
TOPMed
gnomAD
CA5234375
rs764888197
265 D>N No ClinGen
ExAC
gnomAD
CA5234376
rs750118016
266 Y>F No ClinGen
ExAC
CA374874746
rs750118016
266 Y>S No ClinGen
ExAC
rs779720887
CA5234379
267 P>H No ClinGen
ExAC
gnomAD
CA5234382
rs778322409
268 P>L No ClinGen
ExAC
gnomAD
rs1564666860
CA374874774
271 G>E No ClinGen
Ensembl
CA5234385
rs779084313
COSM1597960
271 G>R endometrium [Cosmic] No ClinGen
cosmic curated
ExAC
TOPMed
gnomAD
rs1564666865
CA374874777
272 E>K No ClinGen
Ensembl
CA374874794
rs1301876690
274 Y>H No ClinGen
TOPMed
CA5234386
rs746106299
275 S>Y No ClinGen
ExAC
gnomAD
rs144052872
CA5234388
276 E>K No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs144052872
CA374874806
276 E>Q No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs760711060
CA5234389
277 K>E No ClinGen
ExAC
gnomAD
rs768520677
CA5234390
277 K>M No ClinGen
ExAC
gnomAD
rs200398623
CA5234408
279 R>Q No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs1469571292
CA374874934
280 E>* No ClinGen
gnomAD
CA374874941
rs1193711970
281 L>V No ClinGen
gnomAD
rs758656747
CA5234409
283 S>G No ClinGen
ExAC
gnomAD
CA199677586
rs201113183
284 M>T No ClinGen
Ensembl
CA5234410
rs780223937
284 M>V No ClinGen
ExAC
CA5234411
rs747180914
285 C>S No ClinGen
ExAC
gnomAD
CA374874968
rs747180914
285 C>Y No ClinGen
ExAC
gnomAD
rs776507491
CA5234413
287 C>R No ClinGen
ExAC
gnomAD
rs748129024
CA5234415
289 D>E No ClinGen
ExAC
TOPMed
gnomAD
CA374875002
rs1248451252
290 P>A No ClinGen
TOPMed
CA5234417
rs146443565
291 H>D No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA5234418
rs762820475
292 Q>R No ClinGen
ExAC
gnomAD
rs1298408686
CA374875034
295 D>N No ClinGen
gnomAD
rs1271742411
CA374875053
297 G>A No ClinGen
gnomAD
rs774178334
CA5234420
297 G>R No ClinGen
ExAC
gnomAD
rs200235098
CA374875062
299 V>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA5234422
rs200235098
299 V>M No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs542509176
CA5234424
300 H>R No ClinGen
1000Genomes
ExAC
gnomAD
rs376476122
CA5234425
301 Q>K No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA374875084
rs1423213989
302 V>A No ClinGen
gnomAD
CA199677681
rs954971092
302 V>L No ClinGen
TOPMed
rs1414669747
CA374875122
307 H>R No ClinGen
TOPMed
CA199677696
rs915086313
309 W>* No ClinGen
Ensembl
rs1395201958
CA374875134
309 W>G No ClinGen
TOPMed
CA374875142
rs1165927187
310 M>L No ClinGen
gnomAD
CA374875162
rs1344640329
312 S>R No ClinGen
TOPMed
gnomAD
CA374875168
rs1451744753
313 T>I No ClinGen
gnomAD
rs1290755558
CA374875170
314 T>R No ClinGen
gnomAD
CA374875175
rs1363269245
314 T>W No ClinGen
gnomAD

No associated diseases with Q9HC98

6 regional properties for Q9HC98

Type Name Position InterPro Accession
domain Protein kinase domain 45 - 310 IPR000719
domain Serine-threonine/tyrosine-protein kinase, catalytic domain 122 - 135 IPR001245-1
domain Serine-threonine/tyrosine-protein kinase, catalytic domain 162 - 180 IPR001245-2
domain Serine-threonine/tyrosine-protein kinase, catalytic domain 228 - 250 IPR001245-3
domain Serine-threonine/tyrosine-protein kinase, catalytic domain 274 - 296 IPR001245-4
active_site Serine/threonine-protein kinase, active site 168 - 180 IPR008271

Functions

Description
EC Number 2.7.11.34 Protein-serine/threonine kinases
Subcellular Localization
  • Cytoplasm
  • Nucleus
  • Nucleus speckle
  • Cytoplasm, cytoskeleton, microtubule organizing center, centrosome
  • Cytoplasm, cytoskeleton, spindle pole
  • Colocalizes with APBB1 at the nuclear speckles
  • Colocalizes with PIN1 in the nucleus
  • Colocalizes with ATF4, CIR1, ARHGAP33, ANKRA2, CDC42, NEK9, RAD26L, RBBP6, RPS7, TRIP4, RELB and PHF1 in the centrosome
  • Localizes to spindle microtubules in metaphase and anaphase and to the midbody during cytokinesis
PANTHER Family PTHR43289 MITOGEN-ACTIVATED PROTEIN KINASE KINASE KINASE 20-RELATED
PANTHER Subfamily PTHR43289:SF13 SERINE_THREONINE-PROTEIN KINASE NEK6
PANTHER Protein Class non-receptor serine/threonine protein kinase
protein modifying enzyme
PANTHER Pathway Category No pathway information available

9 GO annotations of cellular component

Name Definition
centriolar satellite A small (70-100 nm) cytoplasmic granule that contains a number of centrosomal proteins; centriolar satellites traffic toward microtubule minus ends and are enriched near the centrosome.
cytoplasm The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures.
cytosol The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes.
microtubule Any of the long, generally straight, hollow tubes of internal diameter 12-15 nm and external diameter 24 nm found in a wide variety of eukaryotic cells; each consists (usually) of 13 protofilaments of polymeric tubulin, staggered in such a manner that the tubulin monomers are arranged in a helical pattern on the microtubular surface, and with the alpha/beta axes of the tubulin subunits parallel to the long axis of the tubule; exist in equilibrium with pool of tubulin monomers and can be rapidly assembled or disassembled in response to physiological stimuli; concerned with force generation, e.g. in the spindle.
nuclear speck A discrete extra-nucleolar subnuclear domain, 20-50 in number, in which splicing factors are seen to be localized by immunofluorescence microscopy.
nucleoplasm That part of the nuclear content other than the chromosomes or the nucleolus.
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.
protein-containing complex A stable assembly of two or more macromolecules, i.e. proteins, nucleic acids, carbohydrates or lipids, in which at least one component is a protein and the constituent parts function together.
spindle pole Either of the ends of a spindle, where spindle microtubules are organized; usually contains a microtubule organizing center and accessory molecules, spindle microtubules and astral microtubules.

10 GO annotations of molecular function

Name Definition
ATP binding Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator.
DNA-binding transcription factor binding Binding to a DNA-binding transcription factor, a protein that interacts with a specific DNA sequence (sometimes referred to as a motif) within the regulatory region of a gene to modulate transcription.
kinesin binding Interacting selectively and non-covalently and stoichiometrically with kinesin, a member of a superfamily of microtubule-based motor proteins that perform force-generating tasks such as organelle transport and chromosome segregation.
magnesium ion binding Binding to a magnesium (Mg) ion.
protein kinase binding Binding to a protein kinase, any enzyme that catalyzes the transfer of a phosphate group, usually from ATP, to a protein substrate.
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 serine/threonine/tyrosine kinase activity Catalysis of the reactions: ATP + a protein serine = ADP + protein serine phosphate; ATP + a protein threonine = ADP + protein threonine phosphate; and ATP + a protein tyrosine = ADP + protein tyrosine phosphate.
transcription corepressor binding Binding to a transcription corepressor, a protein involved in negative regulation of transcription via protein-protein interactions with transcription factors and other proteins that negatively regulate transcription. Transcription corepressors do not bind DNA directly, but rather mediate protein-protein interactions between repressing transcription factors and the basal transcription machinery.
ubiquitin protein ligase binding Binding to a ubiquitin protein ligase enzyme, any of the E3 proteins.

13 GO annotations of biological process

Name Definition
apoptotic process A programmed cell death process which begins when a cell receives an internal (e.g. DNA damage) or external signal (e.g. an extracellular death ligand), and proceeds through a series of biochemical events (signaling pathway phase) which trigger an execution phase. The execution phase is the last step of an apoptotic process, and is typically characterized by rounding-up of the cell, retraction of pseudopodes, reduction of cellular volume (pyknosis), chromatin condensation, nuclear fragmentation (karyorrhexis), plasma membrane blebbing and fragmentation of the cell into apoptotic bodies. When the execution phase is completed, the cell has died.
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.
mitotic nuclear membrane disassembly The mitotic cell cycle process in which the controlled partial or complete breakdown of the nuclear membranes during occurs during mitosis.
mitotic spindle organization A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of the microtubule spindle during a mitotic cell cycle.
peptidyl-serine phosphorylation The phosphorylation of peptidyl-serine to form peptidyl-O-phospho-L-serine.
positive regulation of I-kappaB kinase/NF-kappaB signaling Any process that activates or increases the frequency, rate or extent of I-kappaB kinase/NF-kappaB signaling.
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 phosphorylation The process of introducing a phosphate group on to a protein.
regulation of cellular senescence Any process that modulates the frequency, rate or extent of cellular senescence.
regulation of mitotic cell cycle Any process that modulates the rate or extent of progress through the mitotic cell cycle.
regulation of mitotic metaphase/anaphase transition Any process that modulates the frequency, rate or extent of the cell cycle process in which a cell progresses from metaphase to anaphase during mitosis, triggered by the activation of the anaphase promoting complex by Cdc20/Sleepy homolog which results in the degradation of Securin.
spindle assembly The aggregation, arrangement and bonding together of a set of components to form the spindle, the array of microtubules and associated molecules that serves to move duplicated chromosomes apart.

8 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
Q8TDX7 NEK7 Serine/threonine-protein kinase Nek7 Homo sapiens (Human) EV
Q00526 CDK3 Cyclin-dependent kinase 3 Homo sapiens (Human) PR
Q9ES74 Nek7 Serine/threonine-protein kinase Nek7 Mus musculus (Mouse) SS
Q9ES70 Nek6 Serine/threonine-protein kinase Nek6 Mus musculus (Mouse) SS
A2BD05 NEK6 Serine/threonine-protein kinase Nek6 Sus scrofa (Pig) SS
D3ZBE5 Nek7 Serine/threonine-protein kinase Nek7 Rattus norvegicus (Rat) SS
P59895 Nek6 Serine/threonine-protein kinase Nek6 Rattus norvegicus (Rat) SS
G5EFM9 nekl-3 Serine/threonine-protein kinase nekl-3 Caenorhabditis elegans PR
10 20 30 40 50 60
MAGQPGHMPH GGSSNNLCHT LGPVHPPDPQ RHPNTLSFRC SLADFQIEKK IGRGQFSEVY
70 80 90 100 110 120
KATCLLDRKT VALKKVQIFE MMDAKARQDC VKEIGLLKQL NHPNIIKYLD SFIEDNELNI
130 140 150 160 170 180
VLELADAGDL SQMIKYFKKQ KRLIPERTVW KYFVQLCSAV EHMHSRRVMH RDIKPANVFI
190 200 210 220 230 240
TATGVVKLGD LGLGRFFSSE TTAAHSLVGT PYYMSPERIH ENGYNFKSDI WSLGCLLYEM
250 260 270 280 290 300
AALQSPFYGD KMNLFSLCQK IEQCDYPPLP GEHYSEKLRE LVSMCICPDP HQRPDIGYVH
310
QVAKQMHIWM SST