Nomenclature
Short Name:
GAK
Full Name:
Cyclin G-associated kinase
Alias:
- Cyclin G associated kinase
- EC 2.7.11.1
- Kinase GAK
Classification
Type:
Protein-serine/threonine kinase
Group:
Other
Family:
NAK
SubFamily:
NA
Structure
Mol. Mass (Da):
143,191
# Amino Acids:
1311
# mRNA Isoforms:
2
mRNA Isoforms:
143,191 Da (1311 AA; O14976); 134,464 Da (1232 AA; O14976-2)
4D Structure:
NA
1D Structure:
3D Image (rendered using PV Viewer):
PDB ID
Subfamily Alignment
Domain Distribution:
Start | End | Domain |
---|---|---|
40 | 314 | Pkinase |
1247 | 1311 | DnaJ |
399 | 566 | Phosphatase tensin-type |
572 | 710 | C2 tensin-type |
1247 | 1311 | J |
Post-translation Modifications
For detailed information on phosphorylation of this kinase go to PhosphoNET
Acetylated:
K395.
Serine phosphorylated:
S16, S73, S277, S290, S340, S421, S456, S540, S770, S778, S780, S783, S785, S811, S812, S815, S817, S826, S829, S834, S837, S838, S939, S1096, S1118, S1130, S1154, S1176, S1185.
Threonine phosphorylated:
T776, T794, T805, T908, T1213.
Tyrosine phosphorylated:
Y153, Y201, Y204, Y235, Y276, Y285, Y338, Y367, Y371, Y403, Y615, Y764, Y1149.
Ubiquitinated:
K90, K175, K325, K390, K405, K432.
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:
- 48
755
42
837
- 16
248
21
239
- 16
245
29
243
- 32
506
148
581
- 61
952
33
671
- 7
114
117
123
- 34
523
47
539
- 59
927
73
2023
- 58
903
24
605
- 16
255
138
227
- 13
209
57
224
- 49
762
259
679
- 14
213
62
183
- 14
218
16
217
- 21
335
48
423
- 12
195
23
189
- 28
444
231
2971
- 31
485
40
363
- 6
100
157
112
- 41
635
162
648
- 15
236
46
252
- 18
282
52
312
- 20
308
32
288
- 26
403
42
424
- 23
360
45
369
- 67
1046
96
1561
- 15
235
65
199
- 21
335
41
311
- 15
240
42
197
- 12
189
42
164
- 60
943
30
961
- 100
1561
51
2272
- 11
169
51
156
- 72
1119
78
854
- 97
1513
48
1686
Evolution
Species Conservation
PhosphoNET % Identity:
PhosphoNET % Similarity:
Homologene %
Identity:
PhosphoNET % Identity:
PhosphoNET % Similarity:
Homologene %
Identity:
- 100
100
100 - 99.6
99.8
100 - 88.6
89.2
97 - -
-
82.5 - -
-
87 - 47.8
52.2
85 - -
-
- - 82.6
88.5
83 - 82.4
88.3
83 - -
-
- - 74.2
83.3
- - 70.2
80.3
72 - -
-
69 - 66.7
78
74 - -
-
- - -
-
42 - -
-
- - -
-
- - -
-
- - -
-
- - -
-
- - -
-
- - -
-
- - -
-
- - -
-
-
For a wider analysis go to PhosphoNET Evolution in PhosphoNET
Binding Proteins
Examples of known interacting proteins
hiddentext
No. | Name – UniProt ID |
---|---|
1 | AR - P10275 |
2 | CREBBP - Q92793 |
3 | HSPA8 - P11142 |
4 | CCNG1 - P51959 |
5 | CLTC - Q00610 |
6 | CDK5 - Q00535 |
7 | AP2M1 - Q96CW1 |
8 | AP1M1 - Q9BXS5 |
9 | AP1M2 - Q9Y6Q5 |
10 | ARHGAP4 - P98171 |
11 | USO1 - O60763 |
12 | IL12RB2 - Q99665 |
13 | DNM2 - P50570 |
14 | DNM1 - Q05193 |
15 | DNM3 - Q9UQ16 |
Regulation
Activation:
NA
Inhibition:
NA
Synthesis:
NA
Degradation:
NA
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
General Disease Association:
Neurological disorders
Specific Diseases (Non-cancerous):
Parkinson's disease (PD)
Comments:
Parkinson's disease (PD) is a neurodegenerative movement disorder, characterized by the degeneration of the dopaminergic neurons in the substantia nigra of the midbrain. Symptoms of PD include trembling of hands, arms, legs, and face, stiffness in the arms and legs, bradykinesia, and poor coordination and balance. Based mainly on genome-wide association studies, GAK has been implicated as a suceptibility gene for the development of PD. In addition, a significant correlation was demonstrated between the rs1564282 allele of GAK and the risk for PD in a Taiwanese population, supporting a role for GAK in the pathogenesis of PD.
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: Classical Hodgkin lymphomas (%CFC= +87, p<0.092); and Ovary adenocarcinomas (%CFC= +137, p<0.027). The COSMIC website notes an up-regulated expression score for GAK in diverse human cancers of 383, which is 0.8-fold of the average score of 462 for the human protein kinases. The down-regulated expression score of 259 for this protein kinase in human cancers was 4.3-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.
Mutation Rate in All Cancers:
Percent mutation rates per 100 amino acids length in human cancers: 0.06 % in 24977 diverse cancer specimens. This rate is only -14 % lower than the average rate of 0.075 % calculated for human protein kinases in general.
Mutation Rate in Specific Cancers:
Highest percent mutation rates per 100 amino acids length in human cancers: 0.29 % in 1093 large intestine cancers tested; 0.28 % in 805 skin cancers tested; 0.23 % in 589 stomach cancers tested; 0.18 % in 602 endometrium cancers tested; 0.17 % in 500 urinary tract cancers tested; 0.13 % in 1807 lung cancers tested.
Frequency of Mutated Sites:
None > 2 in 20,244 cancer specimens
Comments:
Only 6 deletions, 1 insertion and no complex mutations are noted on the COSMIC website.