Nomenclature
Short Name:
PCTAIRE1
Full Name:
Serine-threonine-protein kinase PCTAIRE-1
Alias:
- CDK16
- PCTAIRE-motif protein kinase 1
- PCTGAIRE
- PCTK1
- Serine/threonine-protein kinase PCTAIRE1
- EC 2.7.11.22
- FLJ16665
- KPT1
- PCTAIRE
- PCTAIRE protein kinase 1
Classification
Type:
Protein-serine/threonine kinase
Group:
CMGC
Family:
CDK
SubFamily:
TAIRE
Specific Links
Structure
Mol. Mass (Da):
55,716
# Amino Acids:
496
# mRNA Isoforms:
3
mRNA Isoforms:
63,458 Da (570 AA; Q00536-2); 56,375 Da (502 AA; Q00536-3); 55,716 Da (496 AA; Q00536)
4D Structure:
Found in a complex containing CABLES1, CDK17 and TDRD7. Interacts with YWHAH, YWHAQ and YWHAZ
1D Structure:
3D Image (rendered using PV Viewer):
PDB ID
Subfamily Alignment
Domain Distribution:
Start | End | Domain |
---|---|---|
165 | 446 | Pkinase |
Kinexus Products
Click on entries below for direct links to relevant products from Kinexus for this protein kinase.
hiddentext
Post-translation Modifications
For detailed information on phosphorylation of this kinase go to PhosphoNET
Acetylated:
K108, K116.
Serine phosphorylated:
S12, S36, S42, S64, S65, S78, S82, S86, S89, S95, S110, S119-, S138, S153-, S155+, S319+, S479, S480.
Threonine phosphorylated:
T14, T88, T111, T135, T175, T178.
Tyrosine phosphorylated:
Y176, Y180.
Ubiquitinated:
K133, K143, K167, K194, K301, K455, K466.
Distribution
Based on gene microarray analysis from the NCBI
Human Tissue Distribution
% Max Expression:
Mean Expression:
Number of Samples:
Standard Deviation:
% Max Expression:
Mean Expression:
Number of Samples:
Standard Deviation:
- 65
1010
39
975
- 12
187
24
79
- 17
272
33
161
- 34
523
162
491
- 55
853
36
666
- 8
117
119
131
- 25
384
51
565
- 59
920
83
1033
- 33
514
24
332
- 17
265
159
205
- 9
139
64
123
- 42
661
286
647
- 13
198
66
184
- 7
113
20
56
- 18
275
57
303
- 10
160
24
91
- 15
239
326
1805
- 22
340
48
369
- 31
485
167
383
- 33
516
162
511
- 20
309
54
265
- 13
200
60
183
- 16
253
44
180
- 22
336
48
220
- 14
217
53
195
- 54
840
102
1057
- 14
218
69
171
- 17
261
48
202
- 16
250
47
202
- 19
289
42
117
- 24
380
42
296
- 100
1557
51
2841
- 33
514
89
942
- 50
786
83
686
- 16
251
48
256
Evolution
Species Conservation
PhosphoNET % Identity:
PhosphoNET % Similarity:
Homologene %
Identity:
PhosphoNET % Identity:
PhosphoNET % Similarity:
Homologene %
Identity:
- 100
100
100 - 58
60.8
100 - 89.3
90.3
99.5 - -
-
98 - -
-
91 - 97.5
98
92 - -
-
- - 97.5
98.9
98 - 95.5
97.3
98 - -
-
- - 76.1
81
- - 69.1
82.9
- - 45.1
59.6
- - 41.9
55.8
80.5 - -
-
- - 35.4
43.9
- - -
-
- - -
-
- - -
-
- - -
-
- - 33
45.3
- - -
-
- - 33.4
46.3
- - -
-
- - -
-
-
For a wider analysis go to PhosphoNET Evolution in PhosphoNET
Binding Proteins
Examples of known interacting proteins
hiddentext
No. | Name – UniProt ID |
---|---|
1 | YWHAG - P61981 |
2 | CDK5 - Q00535 |
3 | YWHAZ - P63104 |
4 | YWHAH - Q04917 |
5 | CDK5R1 - Q15078 |
6 | SEC23A - Q15436 |
7 | PRKACA - P17612 |
8 | YWHAE - P62258 |
9 | CCNB2 - O95067 |
10 | CNNY-Q8ND76 |
Regulation
Activation:
Phosphorylation at Ser-119 induces interaction with 14-3-3 gamma and 14-3-3 zeta.
Inhibition:
Phosphorylation at Ser-153 inhibits phosphotransferase activity.
Synthesis:
NA
Degradation:
NA
Known Upstream Kinases
For further details on these substrates click on the Substrate Short Name or UniProt ID. Phosphosite Location is hyperlinked to PhosphoNET
predictions.
Based on in vitro and/or in vivo phosphorylation data
Kinase Short Name | UniProt ID (Human) | Phosphosite Location | Phosphosite Sequence | Effect of Phosphorylation |
---|
Known Downstream Substrates
For further details on these substrates click on the Substrate Short Name or UniProt ID. Phosphosite Location is hyperlinked to PhosphoNET
predictions.
Based on in vitro and/or in vivo phosphorylation data
Substrate Short Name | UniProt ID (Human) | Phosphosite Location | Phosphosite Sequence | Effect of Phosphorylation |
---|
Protein Kinase Specificity
Matrix of observed frequency (%) of amino acids in aligned protein substrate phosphosites
Matrix Type:
Predicted from the application of the Kinexus Kinase Substrate Predictor Version 2.0 algorithm, which was trained with over 10,000 kinase-protein substrate pairs and 8,000 kinase-peptide substrate pairs.
Domain #:
1
Inhibitors
For further details on these inhibitors click on the Compound Name and enter it into DrugKiNET or click on the ID's
Based on in vitro and/or in vivo phosphorylation data
Compound Name | KD, Ki or IC50 (nM) | PubChem ID | ChEMBL ID | PubMed ID |
---|
Disease Linkage
Gene Expression in Cancers:
TranscriptoNET (www.transcriptonet.ca) analysis with mRNA expression data retrieved from the National Center for Biotechnology Information's Gene Expression Omnibus (GEO) database, which was normalized against 60 abundantly and commonly found proteins, indicated altered expression for this protein kinase as shown here as the percent change from normal tissue controls (%CFC) as supported with the Student T-test in the following types of human cancers: Brain glioblastomas (%CFC= +231, p<0.005); Brain oligodendrogliomas (%CFC= +382, p<0.013); Cervical cancer stage 2A (%CFC= +131, p<0.029); Cervical cancer stage 2B (%CFC= +146, p<0.097); Lung adenocarcinomas (%CFC= +109, p<0.0001); Ovary adenocarcinomas (%CFC= +97, p<0.0008); Prostate cancer - metastatic (%CFC= +77, p<0.0001); Skin fibrosarcomas (%CFC= +182, p<0.002); Skin melanomas - malignant (%CFC= +167, p<0.0001). The COSMIC website notes an up-regulated expression score for PCTAIRE1 in diverse human cancers of 573, which is 1.2-fold of the average score of 462 for the human protein kinases. The down-regulated expression score of 71 for this protein kinase in human cancers was 1.2-fold of the average score of 60 for the human protein kinases.
Mutagenesis Experiments:
Insertional mutagenesis studies in mice support a role for this protein kinase in mouse cancer oncogenesis. BRSK2 mediated phosphorylation of PCTAIRE1 can be inhibited with S12A mutation, which leads to inhibition of insulin secretion. The interaction of PCTAIRE1 and the cyclin CCNY can be inhibited with a S119A mutation. PCTAIRE1 phosphotransferase activity can be constitutively activated through the mutation S153A, leading to increased interaction of PCTAIRE1 and CCNY. Interaction with CCNY can be inhibited with a S153D mutation. The phosphotransferase activity of the PCTAIRE 1 can be inhibited with a K194A mutation, leading to inhibited effect of PCTAIRE1 on insulin secretion. PCTAIRE1 phosphotransferase activity is lost with the K194R mutation.
Mutation Rate in All Cancers:
Percent mutation rates per 100 amino acids length in human cancers: 0.04 % in 24939 diverse cancer specimens. This rate is -41 % lower than the average rate of 0.075 % calculated for human protein kinases in general.
Frequency of Mutated Sites:
None > 4 in 20,222 cancer specimens
Comments:
Only 1 insertion, and no deletions or complex mutations are noted on the COSMIC website.