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

175-197 (Activation loop from InterPro)

Target domain

40-325 (Protein kinase domain)

Relief mechanism

Assay

Autoinhibited structure

Activated structure

33 structures for P19784

Entry ID Method Resolution Chain Position Source
3E3B X-ray 320 A X 1-334 PDB
3OFM X-ray 200 A A 1-350 PDB
3U87 X-ray 290 A A/B 327-350 PDB
5M4U X-ray 219 A A 1-350 PDB
5M56 X-ray 224 A A/B 1-350 PDB
5OOI X-ray 200 A A/B 1-350 PDB
5Y9M X-ray 201 A A/X 1-334 PDB
5YF9 X-ray 189 A B/X 1-334 PDB
5YWM X-ray 194 A X 1-334 PDB
6HMB X-ray 104 A A 1-350 PDB
6HMC X-ray 103 A A 1-350 PDB
6HMD X-ray 100 A A 1-350 PDB
6HMQ X-ray 097 A A 1-346 PDB
6L20 X-ray 309 A A/D/G/J 1-333 PDB
6QY8 X-ray 170 A A/B/C/D 1-335 PDB
6QY9 X-ray 150 A A 1-335 PDB
6TE2 X-ray 092 A A 1-350 PDB
6TEW X-ray 108 A A 1-350 PDB
6TGU X-ray 083 A A 1-350 PDB
7A1B X-ray 129 A A 1-350 PDB
7A1Z X-ray 102 A A 1-350 PDB
7A22 X-ray 101 A A 1-350 PDB
7A2H X-ray 101 A A 1-350 PDB
7AT9 X-ray 105 A A 1-350 PDB
7ATV X-ray 098 A A 1-350 PDB
7XYH X-ray 204 A A/B 1-334 PDB
8Q77 X-ray 125 A A 1-350 PDB
8Q9S X-ray 135 A A 1-350 PDB
8QBU X-ray 109 A A 1-350 PDB
8QCD X-ray 103 A A 1-350 PDB
8QCG X-ray 104 A A/B 1-350 PDB
8QF1 X-ray 132 A A/B 1-350 PDB
AF-P19784-F1 Predicted AlphaFoldDB

138 variants for P19784

Variant ID(s) Position Change Description Diseaes Association Provenance
rs1276382492
CA396143262
2 P>A No ClinGen
TOPMed
gnomAD
rs1276382492
CA396143259
2 P>S No ClinGen
TOPMed
gnomAD
CA8086212
rs761960574
3 G>D No ClinGen
ExAC
TOPMed
gnomAD
CA396143228
rs1327124704
4 P>L No ClinGen
gnomAD
CA396143222
rs1385598542
5 A>G No ClinGen
gnomAD
CA8086211
rs774365294
5 A>T No ClinGen
ExAC
TOPMed
gnomAD
rs1396273832
CA396143149
11 R>Q No ClinGen
gnomAD
rs763134466
CA8086209
12 V>I No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 14 A>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA396143058
rs1474767631
18 S>G No ClinGen
gnomAD
rs576968089
CA8086208
18 S>R No ClinGen
1000Genomes
ExAC
gnomAD
rs1195162965
CA396143034
20 R>K No ClinGen
gnomAD
rs1165057931
CA396143005
22 R>C No ClinGen
gnomAD
rs1597130691
CA396142982
23 E>D No ClinGen
Ensembl
CA281656792
rs867887217
COSM1189284
25 W>C lung [Cosmic] No ClinGen
cosmic curated
Ensembl
CA8086206
rs745740318
26 D>Y No ClinGen
ExAC
gnomAD
CA396142902
rs1256338649
29 A>G No ClinGen
gnomAD
rs1304897203
CA396142866
32 P>S No ClinGen
TOPMed
rs747744716
CA8086178
36 N>D No ClinGen
ExAC
gnomAD
TCGA novel 38 D>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA396142676
rs1489690587
40 Y>* No ClinGen
TOPMed
rs1470616474
CA396142622
46 L>F No ClinGen
gnomAD
rs113595783
CA281656414
48 R>W No ClinGen
Ensembl
rs746222418
CA8086175
50 K>R No ClinGen
ExAC
gnomAD
CA396142543
rs1434461489
53 E>D No ClinGen
TOPMed
CA281656409
rs755082916
55 F>L No ClinGen
Ensembl
TCGA novel 56 E>* Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA281656404
rs749158672
59 N>S No ClinGen
TOPMed
gnomAD
rs757751451
CA8086173
60 I>T No ClinGen
ExAC
gnomAD
rs752039831
CA8086172
62 N>S No ClinGen
ExAC
gnomAD
rs141110736
CA8086171
63 N>T No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs758554247
CA8086169
64 E>D No ClinGen
ExAC
gnomAD
TCGA novel 66 V>E Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA8086145
rs766137540
79 I>K No ClinGen
ExAC
gnomAD
rs922058971
CA281649217
81 R>Q No ClinGen
Ensembl
CA396139703
rs1321409878
83 V>F No ClinGen
gnomAD
CA396139668
rs1461119155
84 K>N No ClinGen
gnomAD
rs1395549018
CA396139654
85 I>V No ClinGen
gnomAD
CA396139608
rs1187368784
87 E>G No ClinGen
TOPMed
rs1431525244
CA396139511
90 R>C Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
CA8086143
rs750301809
90 R>H No ClinGen
ExAC
TOPMed
gnomAD
CA396139502
rs750301809
90 R>L No ClinGen
ExAC
TOPMed
gnomAD
rs1395763592
CA396139406
94 N>S No ClinGen
TOPMed
rs1437189490
CA396139390
95 I>V No ClinGen
TOPMed
CA396139315
rs1187552611
98 L>M No ClinGen
gnomAD
CA396139190
rs1597122741
101 T>I No ClinGen
Ensembl
rs968510502
CA281649203
106 V>M No ClinGen
TOPMed
gnomAD
TCGA novel 108 K>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs750167395
CA8086125
114 F>L No ClinGen
ExAC
TOPMed
gnomAD
CA8086124
rs138081655
115 E>D No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs547345655
CA281646826
116 Y>C No ClinGen
1000Genomes
CA8086122
rs751520619
117 I>F No ClinGen
ExAC
gnomAD
CA396138174
rs1305423634
118 N>S No ClinGen
gnomAD
CA396138138
rs1389880598
120 T>R No ClinGen
gnomAD
rs1433940583
CA396135488
124 Q>H No ClinGen
gnomAD
rs769274520
CA8086112
125 L>F No ClinGen
ExAC
gnomAD
rs749317833
CA8086111
128 I>F No ClinGen
ExAC
TOPMed
gnomAD
rs749317833
CA396135424
128 I>V No ClinGen
ExAC
TOPMed
gnomAD
CA8086110
rs780233214
131 D>A No ClinGen
ExAC
gnomAD
CA8086109
rs769880764
132 F>L No ClinGen
ExAC
gnomAD
CA8086108
rs144995982
132 F>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA396135333
rs1377840811
133 D>G No ClinGen
gnomAD
rs1336128000
CA396135319
134 I>T No ClinGen
TOPMed
CA8086107
rs780916581
135 R>Q No ClinGen
ExAC
gnomAD
CA396135235
rs1453441068
139 Y>C No ClinGen
gnomAD
rs746032185
CA8086091
146 D>H No ClinGen
ExAC
gnomAD
rs879123154
CA281633510
151 K>Q No ClinGen
Ensembl
CA8086090
rs781398318
153 I>V No ClinGen
ExAC
gnomAD
TCGA novel 164 M>I Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA396134241
rs1419394704
170 K>R No ClinGen
gnomAD
TCGA novel 171 K>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 172 L>A Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA396134104
rs1351945441
178 G>V No ClinGen
gnomAD
VAR_040416
rs55911801
CA281632955
188 E>A No ClinGen
UniProt
dbSNP
gnomAD
TCGA novel 188 E>K Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1195346315
CA396133844
196 R>G No ClinGen
gnomAD
TCGA novel 203 L>F Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA281632938
rs964390881
206 D>E No ClinGen
Ensembl
rs974586708
CA281632680
213 S>N No ClinGen
Ensembl
CA396132825
rs1374823589
219 L>F No ClinGen
gnomAD
CA281632672
rs914498045
219 L>V No ClinGen
Ensembl
CA8086046
rs150003385
219 L>W No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA396132764
rs1174571175
224 A>G No ClinGen
TOPMed
rs201815819
CA281632638
229 R>Q No ClinGen
TOPMed
gnomAD
rs1486182360
CA396132698
230 R>K No ClinGen
gnomAD
CA396132634
rs1158151383
235 H>R No ClinGen
gnomAD
TCGA novel 236 G>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs755699042
CA8086043
238 D>N No ClinGen
ExAC
TOPMed
gnomAD
CA8086042
rs527723255
240 Y>C No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1214155978
CA396132581
240 Y>H No ClinGen
TOPMed
gnomAD
rs1367136506
CA396132469
246 I>V No ClinGen
gnomAD
rs371309575
CA8086020
248 K>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1567463706
CA396132430
252 T>K No ClinGen
Ensembl
CA8086018
rs754263768
257 G>V No ClinGen
ExAC
gnomAD
rs1419361114
CA396132289
264 I>V No ClinGen
gnomAD
COSM386740
CA396132250
rs1451645931
267 D>N lung [Cosmic] No ClinGen
cosmic curated
gnomAD
rs756627324
CA396132212
269 H>Q No ClinGen
ExAC
TOPMed
gnomAD
CA396132218
rs1251533091
269 H>R Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA281632177
rs760578490
270 F>L No ClinGen
gnomAD
rs375864630
CA8086015
271 N>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1435591271
CA396132178
272 D>G No ClinGen
gnomAD
CA281631618
rs998635769
278 S>L No ClinGen
Ensembl
rs752511537
CA8085985
279 R>Q No ClinGen
ExAC
gnomAD
rs1289137648
CA396132051
279 R>W No ClinGen
gnomAD
CA396132030
rs1374223667
281 R>C Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA396132027
rs1465113121
281 R>H Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
rs951500034
CA281631594
289 E>D No ClinGen
TOPMed
rs1398029204
CA396131880
294 V>I No ClinGen
TOPMed
rs1243143862
CA396131865
295 S>T No ClinGen
TOPMed
gnomAD
CA8085983
rs759457020
296 P>L Variant assessed as Somatic; 9.24e-05 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs201664709
CA8085982
298 A>S No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs550840644
CA281631588
305 L>P No ClinGen
1000Genomes
TCGA novel 305 L>R Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA396131753
rs1597109046
307 R>* No ClinGen
Ensembl
CA8085981
rs755124535
307 R>Q No ClinGen
ExAC
TOPMed
gnomAD
rs1310591338
CA396131726
309 D>N No ClinGen
TOPMed
rs772756341
CA8085979
311 Q>R No ClinGen
ExAC
gnomAD
CA396131580
rs1255264484
315 T>A No ClinGen
gnomAD
CA396131579
rs1255264484
315 T>S No ClinGen
gnomAD
rs747830904
CA8085977
317 K>R No ClinGen
ExAC
TOPMed
gnomAD
rs775784514
CA8085976
322 H>Q No ClinGen
ExAC
gnomAD
TCGA novel 326 Y>= Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs965309455
CA281630731
327 P>R No ClinGen
Ensembl
rs539754676
CA8085955
327 P>S Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
ExAC
NCI-TCGA
TOPMed
gnomAD
CA396131318
rs1351765884
329 V>L No ClinGen
TOPMed
gnomAD
CA8085953
rs747552329
332 Q>H No ClinGen
ExAC
gnomAD
CA396131287
rs1162169662
333 S>A Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA8085952
rs777939766
335 P>S No ClinGen
ExAC
gnomAD
rs1370067990
CA396131268
336 C>R No ClinGen
gnomAD
CA8085951
rs772280375
336 C>Y No ClinGen
ExAC
gnomAD
CA8085950
rs748302134
338 D>Y No ClinGen
ExAC
gnomAD
rs1006567762
CA281630712
339 N>S No ClinGen
TOPMed
CA396131243
rs1390575356
340 A>T No ClinGen
gnomAD
rs755276523
CA8085948
344 S>T No ClinGen
ExAC
gnomAD
CA396131185
rs1409707784
346 L>F No ClinGen
gnomAD
CA396131173
rs753544192
347 T>K No ClinGen
ExAC
gnomAD
CA8085947
rs753544192
347 T>M No ClinGen
ExAC
gnomAD
CA396131135
rs1250089462
351 R>R No ClinGen
gnomAD

No associated diseases with P19784

1 regional properties for P19784

Type Name Position InterPro Accession
conserved_site UDP-glycosyltransferase family, conserved site 347 - 390 IPR035595

Functions

Description
EC Number 2.7.11.1 Protein-serine/threonine kinases
Subcellular Localization
  • Nucleus
  • Cytoplasm
  • Interaction with SIRT6 prevents translocation into the nucleus
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

7 GO annotations of cellular component

Name Definition
acrosomal vesicle A structure in the head of a spermatozoon that contains acid hydrolases, and is concerned with the breakdown of the outer membrane of the ovum during fertilization. It lies just beneath the plasma membrane and is derived from the lysosome.
chromatin The ordered and organized complex of DNA, protein, and sometimes RNA, that forms the chromosome.
cytosol The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes.
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.
plasma membrane The membrane surrounding a cell that separates the cell from its external environment. It consists of a phospholipid bilayer and associated proteins.
protein kinase CK2 complex A protein complex that possesses protein serine/threonine kinase activity, and contains two catalytic alpha subunits and two regulatory beta subunits. Protein kinase CK2 complexes are found in nearly every subcellular compartment, and can phosphorylate many protein substrates in addition to casein.

4 GO annotations of molecular function

Name Definition
ATP binding Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator.
protein N-terminus binding Binding to a protein N-terminus, the end of any peptide chain at which the 2-amino (or 2-imino) function of a constituent amino acid is not attached in peptide linkage to another amino-acid residue.
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.

14 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 cycle The progression of biochemical and morphological phases and events that occur in a cell during successive cell replication or nuclear replication events. Canonically, the cell cycle comprises the replication and segregation of genetic material followed by the division of the cell, but in endocycles or syncytial cells nuclear replication or nuclear division may not be followed by cell division.
cerebral cortex development The progression of the cerebral cortex over time from its initial formation until its mature state. The cerebral cortex is the outer layered region of the telencephalon.
liver regeneration The regrowth of lost or destroyed liver.
negative regulation of apoptotic signaling pathway Any process that stops, prevents or reduces the frequency, rate or extent of apoptotic signaling pathway.
negative regulation of ubiquitin-dependent protein catabolic process Any process that stops, prevents, or reduces the frequency, rate or extent of ubiquitin-dependent protein catabolic process.
peptidyl-serine phosphorylation The phosphorylation of peptidyl-serine to form peptidyl-O-phospho-L-serine.
peptidyl-threonine phosphorylation The phosphorylation of peptidyl-threonine to form peptidyl-O-phospho-L-threonine.
positive regulation of protein targeting to mitochondrion Any process that activates or increases the frequency, rate or extent of protein targeting to mitochondrion.
regulation of autophagy of mitochondrion Any process that modulates the frequency, rate or extent of mitochondrion degradation by an autophagic process.
regulation of cell cycle Any process that modulates the rate or extent of progression through the cell cycle.
regulation of chromosome separation Any process that modulates the frequency, rate or extent of chromosome separation.
spermatogenesis The developmental process by which male germ line stem cells self renew or give rise to successive cell types resulting in the development of a spermatozoa.
Wnt signaling pathway The series of molecular signals initiated by binding of a Wnt protein to a frizzled family receptor on the surface of the target cell and ending with a change in cell state.

7 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
P19454 CKA2 Casein kinase II subunit alpha' Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) PR
P15790 CKA1 Casein kinase II subunit alpha Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) PR
P20427 CSNK2A2 Casein kinase II subunit alpha' Bos taurus (Bovine) PR
P21869 Casein kinase II subunit alpha' Gallus gallus (Chicken) PR
P68400 CSNK2A1 Casein kinase II subunit alpha Homo sapiens (Human) PR
O64816 CKA4 Casein kinase II subunit alpha-4, chloroplastic Arabidopsis thaliana (Mouse-ear cress) PR
Q08466 CKA2 Casein kinase II subunit alpha-2 Arabidopsis thaliana (Mouse-ear cress) PR
10 20 30 40 50 60
MPGPAAGSRA RVYAEVNSLR SREYWDYEAH VPSWGNQDDY QLVRKLGRGK YSEVFEAINI
70 80 90 100 110 120
TNNERVVVKI LKPVKKKKIK REVKILENLR GGTNIIKLID TVKDPVSKTP ALVFEYINNT
130 140 150 160 170 180
DFKQLYQILT DFDIRFYMYE LLKALDYCHS KGIMHRDVKP HNVMIDHQQK KLRLIDWGLA
190 200 210 220 230 240
EFYHPAQEYN VRVASRYFKG PELLVDYQMY DYSLDMWSLG CMLASMIFRR EPFFHGQDNY
250 260 270 280 290 300
DQLVRIAKVL GTEELYGYLK KYHIDLDPHF NDILGQHSRK RWENFIHSEN RHLVSPEALD
310 320 330 340
LLDKLLRYDH QQRLTAKEAM EHPYFYPVVK EQSQPCADNA VLSSGLTAAR