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Updated November 2019

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Nomenclature

Short Name:
NuaK1
Full Name:
AMPK-related protein kinase 5
Alias:
  • AMP-activated protein kinase family member 5
  • ARK5
  • NUAK family, SNF1-like kinase, 1
  • NUAK2
  • Probable KIAA0537
  • EC 2.7.11.1
  • KIAA053
  • KIAA0537
  • Kinase NuaK1

Classification

Type:
Protein-serine/threonine kinase
Group:
CAMK
Family:
CAMKL
SubFamily:
NuaK
 
 

Specific Links

Entrez-Gene Entry: 9891
Entrez-Protein Entry: NP_055655
GeneCards Entry: NUAK
KinBASE Entry: NUAK1
OMIM Entry: 608130
Pfam Entry: O60285
PhosphoNET Entry: O60285
Phosphosite Plus Entry: 802
ScanSite Entry: O60285
Source Entry: NUAK1
UniProt Entry: O60285
Kinexus Products: NuaK1
NUAK family SNF1-like kinase 1; AMPK-related protein kinase 5 T211 phosphosite-specific antibody AB-PK737
Cdc25C (205-225), KinSub - Cdc25C phosphatase (V205-R225, human) peptide; Chktide peptide - Powder PE-01ACN95
NUAK family SNF1-like kinase 1 / AMPK-related protein kinase 5 (F208-G214, human) pT211 phosphopeptide - Powder PE-04AKS99

General Links

ClustalW2
GPS-Cuckoo
Human Protein Atlas
Kinase.com
Kinase Research
Kinasource
Kinomer
Netphorest
NetworKIN
Phosida
PhosphoElm
Protein Blast
ScanSite
String

Structure

Mol. Mass (Da):
74,305
# Amino Acids:
661
# mRNA Isoforms:
2
mRNA Isoforms:
74,305 Da (661 AA; O60285); 23,824 Da (208 AA; O60285-2)
4D Structure:
NA
1D Structure:
Retrieve Gene Sequence
Retrieve Full Protein Sequence
Retrieve Catalytic Domain Sequence
 
Subfamily Alignment
subfamily domain
 
Domain Distribution:
Start End Domain
55 306 Pkinase
 

Kinexus Products

Click on entries below for direct links to relevant products from Kinexus for this protein kinase.
hiddentext
○ NUAK family SNF1-like kinase 1; AMPK-related protein kinase 5 T211 phosphosite-specific antibody AB-PK737
○ Cdc25C (205-225), KinSub - Cdc25C phosphatase (V205-R225, human) peptide; Chktide peptide - Powder PE-01ACN95
○ NUAK family SNF1-like kinase 1 / AMPK-related protein kinase 5 (F208-G214, human) pT211 phosphopeptide - Powder PE-04AKS99
 

Post-translation Modifications

For detailed information on phosphorylation of this kinase go to PhosphoNET
Methylated:
R284.
Serine phosphorylated:

S22, S145, S388, S444, S445, S455, S459, S476, S480, S499, S516, S518, S562, S564, S600+.
Threonine phosphorylated:

T211+, T356.
Tyrosine phosphorylated:

Y141, Y143, Y565.
 

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:
  • adipose
    12

    769

    16

    782

  • adrenal
    2

    148

    10

    39

  • bladder
    1

    67

    7

    87

  • brain
    17

    1153

    60

    787

  • breast
    12

    765

    14

    666

  • cervix
    16

    1068

    52

    2237

  • colon
    5

    347

    19

    571

  • heart
    9

    578

    33

    946

  • intestine
    5

    302

    10

    229

  • kidney
    2

    129

    51

    67

  • liver
    2

    107

    20

    77

  • lung
    11

    744

    101

    758

  • lymphnode
    1.1

    74

    18

    63

  • ovary
    3

    184

    9

    98

  • pancreas
    1.2

    77

    16

    59

  • pituitary
    1.3

    84

    8

    37

  • prostate
    2

    138

    105

    59

  • salivarygland
    1

    67

    14

    57

  • skeletalmuscle"
    4

    239

    49

    126

  • skin
    15

    990

    56

    784

  • spinalcord
    4

    232

    16

    144

  • spleen
    0.6

    43

    17

    43

  • stomach
    1

    66

    8

    67

  • testis
    1

    63

    14

    54

  • thymus
    1.4

    95

    16

    73

  • thyroid
    13

    835

    42

    1343

  • tonsil
    0.9

    57

    21

    59

  • trachea
    1.3

    87

    14

    61

  • uterus
    3

    211

    14

    154

  • reticulocytes"
    2

    152

    14

    45

  • t-lymphocytes
    7

    432

    18

    313

  • b-lymphocytes
    100

    6616

    27

    8345

  • neutrophils
    5

    309

    43

    740

  • macrophages
    12

    768

    26

    668

  • sperm
    1

    69

    22

    97

 

Evolution

Species Conservation
PhosphoNET % Identity:
PhosphoNET % Similarity:
Homologene %
Identity:
PhosphoNET % Identity:
PhosphoNET % Similarity:
Homologene %
Identity:
  • tableheader
    100

    100

    100
  • tableheader
    99.7

    99.8

    100
  • tableheader
    97.9

    98

    99
  • tableheader
    -

    -

    95
  • tableheader
    -

    -

    -
  • tableheader
    91.7

    94.4

    92
  • tableheader
    -

    -

    -
  • tableheader
    90.9

    93.8

    91.5
  • tableheader
    55.7

    68.1

    91
  • tableheader
    -

    -

    -
  • tableheader
    84.3

    88

    -
  • tableheader
    26.2

    42.9

    83
  • tableheader
    48.6

    61.4

    -
  • tableheader
    23.6

    36.2

    69
  • tableheader
    -

    -

    -
  • tableheader
    24.4

    33.6

    -
  • tableheader
    -

    -

    -
  • tableheader
    22.5

    35.8

    -
  • tableheader
    -

    -

    -
  • tableheader
    -

    -

    -
  • tableheader
    -

    -

    -
  • tableheader
    -

    -

    -
  • tableheader
    31.2

    49.3

    -
  • tableheader
    26.8

    46.1

    -
  • tableheader
    -

    -

    -
For a wider analysis go to PhosphoNET Evolution in PhosphoNET
 

Binding Proteins

Examples of known interacting proteins
hiddentext
No. Name – UniProt ID
1 CASP6 - P55212
2 SIK1 - P57059
3 MARK3 - P27448
4 BRSK2 - Q8IWQ3
5 MARK1 - Q9P0L2
6 SIK2 - Q9H0K1
7 MARK4 - Q96L34
8 NUAK2 - Q9H093
9 BRSK1 - Q8TDC3
10 MARK2 - Q7KZI7
11 PRKAA1 - Q13131
12 SIK3 - Q9Y2K2
13 PRKAG1 - P54619
14 HSP90AA1 - P07900
15 HSPA1A - P08107
 

Regulation

Activation:
Activated by phosphorylation at Thr-211 and Ser-600.
Inhibition:
NA
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
LKB1 Q15831 T211 QKDKFLQTFCGSPLY +
NDR2 Q9Y2H1 T211 QKDKFLQTFCGSPLY +
Akt1 P31749 S600 PARQRIRSCVSAENF +
AKT3 Q9Y243 S600 PARQRIRSCVSAENF +
 

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
Caspase 6 P55212 S257 TLVNRKVSQRRVDFC
LATS1 O95835 S464 NIPVRSNSFNNPLGN -
p53 P04637 S15 PSVEPPLSQETFSDL +
p53 P04637 S392 FKTEGPDSD______ +
 

Protein Kinase Specificity

Matrix of observed frequency (%) of amino acids in aligned protein substrate phosphosites

Kinections GIF
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
TTT-3002 IC50 < 2 nM
Lestaurtinib Kd = 3.7 nM 126565 22037378
Staurosporine Kd = 4.4 nM 5279 18183025
AZ960 IC50 < 10 nM 25099184 18775810
NVP-TAE684 Kd = 13 nM 16038120 509032 22037378
WZ3146 Kd < 20 nM 44607360 20033049
BCP9000906 IC50 < 25 nM 5494425 21156 22037377
Cdk1/2 Inhibitor III IC50 < 25 nM 5330812 261720 22037377
Gö6976 IC50 < 25 nM 3501 302449 22037377
GSK-3 Inhibitor XIII IC50 < 25 nM 6419766 359482 22037377
IDR E804 IC50 < 25 nM 6419764 1802727 22037377
K-252a; Nocardiopsis sp. IC50 < 25 nM 3813 281948 22037377
NU6140 IC50 < 25 nM 10202471 1802728 22037377
PKR Inhibitor IC50 < 25 nM 6490494 235641 22037377
SB218078 IC50 < 25 nM 447446 289422 22037377
SU11652 IC50 < 25 nM 24906267 13485 22037377
TG101348 Kd = 34 nM 16722836 1287853 22037378
Amgen TBK 1 inhibitor (Compound II) IC50 < 40 nM
BX795 IC50 < 40 nM 10077147 577784
N-Benzoylstaurosporine Kd = 41 nM 56603681 608533 18183025
Sunitinib Kd = 48 nM 5329102 535 18183025
AG-E-60384 IC50 > 50 nM 6419741 413188 22037377
Alsterpaullone IC50 > 50 nM 5005498 50894 22037377
Alsterpaullone; 2-Cyanoethyl IC50 > 50 nM 16760286 260138 22037377
ALX-270-403-M001 IC50 > 50 nM 22037377
Bosutinib IC50 > 50 nM 5328940 288441 22037377
Indirubin-3′-monoxime IC50 > 50 nM 5326739 22037377
JAK3 Inhibitor VI IC50 > 50 nM 16760524 22037377
PF-03814735 IC50 < 50 nM 49830590 20354118
SU6656 IC50 > 50 nM 5353978 605003 22037377
SU9516 IC50 > 50 nM 5289419 258805 22037377
Syk Inhibitor IC50 > 50 nM 6419747 104279 22037377
Aurora A Inhibitor 1 (DF) IC50 = 52.2 nM 21992004
Wyeth PDK1 Inhibitor Compound 1 IC50 < 60 nM
JNKIN7 IC50 < 80 nM 57340685
Princeton's TrkA inhibitor compound 20h IC50 < 80 nM
R406 IC50 < 80 nM 11984591
WZ4002 Kd = 91 nM 44607530 20033049
AT9283 IC50 > 100 nM 24905142 19143567
BML-275 IC50 = 100 nM 11524144 478629
GSK-3 Inhibitor IX IC50 = 100 nM 5287844 409450
GSK650394A IC50 = 100 nM 25022668 558642
GW 843682X IC50 = 100 nM 9826308 514499
LDN193189 IC50 = 100 nM 25195294 513147
MRT67307 IC50 = 100 nM 44464263
Novartis 12a (PKD1) IC50 = 100 nM
Staurosporine aglycone IC50 < 100 nM 3035817 281948
CHEMBL1240703 Kd = 110 nM 52945601 1240703 19654408
1;9-Pyrazoloanthrone IC50 > 150 nM 8515 7064 22037377
Aloisine A IC50 > 150 nM 5326843 75680 22037377
Aloisine; RP106 IC50 > 150 nM 44350092 126343 22037377
Bisindolylmaleimide I IC50 > 150 nM 2396 7463 22037377
IKK-2 Inhibitor IV IC50 > 150 nM 9903786 257167 22037377
Kenpaullone IC50 > 150 nM 3820 296586 22037377
Semaxinib IC50 > 150 nM 5329098 276711 22037377
SU11274 IC50 > 150 nM 9549297 261641 22037377
Syk Inhibitor II IC50 > 150 nM 16760670 22037377
VEGFR2 Kinase Inhibitor II IC50 > 150 nM 5329155 88606 22037377
Nintedanib Kd = 160 nM 9809715 502835 22037378
JNJ-7706621 Kd = 180 nM 5330790 191003 18183025
Aurora A Inhibitor 23 (DF) Kd < 200 nM 21992004
Tozasertib Kd = 200 nM 5494449 572878 18183025
Dovitinib Kd = 240 nM 57336746 18183025
Gö6983 IC50 > 250 nM 3499 261491 22037377
H-89 IC50 > 250 nM 449241 104264 22037377
STO609 IC50 > 250 nM 51371511 22037377
TWS119 IC50 > 250 nM 9549289 405759 22037377
Aurora A Inhibitor 29 (DF) Kd < 400 nM 21992004
IPA-3 IC50 < 400 nM 521106 472940
Ro-31-8220 IC50 < 400 nM 5083 6291
GSK690693 Kd = 420 nM 16725726 494089 22037378
SU14813 Kd = 460 nM 10138259 1721885 18183025
CGP74514A IC50 = 500 nM 2794188 367625 22037377
GSK-3 Inhibitor X IC50 = 500 nM 6538818 430226 22037377
JNK Inhibitor; Negative Control IC50 = 500 nM 11665831 22037377
Pazopanib IC50 = 500 nM 10113978 477772 22037377
GW441756 hydrochloride IC50 < 600 nM 16219400
K00596a IC50 < 600 nM 9549298 200027
Ruxolitinib IC50 < 600 nM 25126798 1789941
Tofacitinib IC50 < 600 nM 9926791 221959
PHA-665752 Kd = 620 nM 10461815 450786 22037378
BMS-690514 Kd < 800 nM 11349170 21531814
ETP 46464 IC50 < 800 nM
GSK461364A IC50 < 800 nM 15983966 1908394
IKK-3 inhibitor IX IC50 < 800 nM 11626927 373751
PP242 IC50 < 800 nM 25243800
Quercetagetin IC50 < 800 nM 5281680 413552
BI-D1870 IC50 = 1 µM 25023738 573107
CHEMBL383899 IC50 > 1 µM 9549303 383899 22037377
Compound 52 IC50 > 1 µM 2856 22037377
CZC-25146 IC50 = 1 µM
Flt-3 Inhibitor II IC50 > 1 µM 11601743 377193 22037377
Flt-3 Inhibitor III IC50 > 1 µM 11772958 22037377
GSK-3b Inhibitor XI IC50 > 1 µM 10020713 272629 22037377
GSK2334470 IC50 = 1 µM 46215815 1765740
GSK269962A IC50 = 1 µM 16095342 220241
GSK429286 IC50 = 1 µM 11373846 375312
H-1152; Glycyl IC50 = 1 µM 16760635
HG-10-102-01 IC50 = 1 µM
Icotinib IC50 > 1 µM 22024915 22112293
IKK-2 Inhibitor VIII IC50 = 1 µM 66576999 368427
JNKIN8 IC50 = 1 µM 57340686
KIN 112 IC50 = 1 µM
MK5108 IC50 > 1 µM 24748204 20053775
Purvalanol A IC50 = 1 µM 456214 23327
Purvalanol B IC50 = 1 µM 448991 23254
Silmitasertib IC50 > 1 µM 24748573 21174434
SNS314 IC50 > 1 µM 16047143 514582 18678489
Syk Inhibitor IV IC50 = 1 µM 10200390
VEGFR2 Kinase Inhibitor I IC50 > 1 µM 6419834 86943 22037377
WHI-P154 IC50 > 1 µM 3795 473773 22037377
Neratinib Kd = 1.5 µM 9915743 180022 22037378
CHEMBL248757 Ki > 1.503 µM 44444843 248757 17935989
Ruboxistaurin Kd = 1.8 µM 153999 91829 18183025
HG-9-91-01 IC50 > 3 µM
IRAK-1-4 Inhibitor I IC50 < 3 µM 11983295 379787
SureCN4875304 IC50 > 3.5 µM 46871765 20472445
BAY11-7082 IC50 < 4 µM 5353431 403183
JNJ-28871063 IC50 > 4 µM 17747413 17975007
(5Z)-7-Oxozeaenol IC50 > 4.5 µM 1077979
Akt Inhibitor VIII IC50 > 4.5 µM 10196499 258844
GDC-0941 IC50 > 4.5 µM 17755052 521851
IRAK-4 kinase inhibitor b IC50 > 4.5 µM
 

Disease Linkage

General Disease Association:

Developmental disorders
Specific Diseases (Non-cancerous):

Omphalocele
Comments:
Omphalocele is a rare syndrome typically characterized by the liver, intestines, and sometimes other organs being located outside of the abdomen. These organs are surrounded in a sack, but can still lead to high rates of mortality. The tissues affected by Omphalocele can include the liver, skin, and heart. A K84A mutation in NuaK1 can lead to inhibited kinase phosphotransferase activity and can lead to senescence of the cell (consisting of biologically old cell characteristics).
 
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: Barrett's esophagus epithelial metaplasia (%CFC= +84, p<0.034); Brain glioblastomas (%CFC= +863, p<0.004); Brain oligodendrogliomas (%CFC= +825, p<0.084); Breast epithelial hyperplastic enlarged lobular units (HELU) (%CFC= -72, p<0.016); Colorectal adenocarcinomas (early onset) (%CFC= +116, p<0.002); Oral squamous cell carcinomas (OSCC) (%CFC= +742, p<0.001); Ovary adenocarcinomas (%CFC= +190, p<0.002); Pituitary adenomas (ACTH-secreting) (%CFC= +68); Skin fibrosarcomas (%CFC= -45); Skin melanomas - malignant (%CFC= -82, p<0.002); and Vulvar intraepithelial neoplasia (%CFC= -67, p<0.0002).
Mutagenesis Experiments:

Insertional mutagenesis studies in mice have not yet revealed a role for this protein kinase in mouse cancer oncogenesis. A T211A NuaK1 mutation can inhibit LKB1-mediated activation and phosphorylation of NuaK1, while ablating induction of senescence. The I400K and L401K mutations can lead to interrupted NuaK1 complex with PPP1CB, and inhibiting regulation of PP1 activity. Phosphorylation via AKT1 can be prevented through an S600A mutation.
Mutation Rate in All Cancers:

Percent mutation rates per 100 amino acids length in human cancers: 0.1 % in 24434 diverse cancer specimens. This rate is only 37 % higher than the average rate of 0.075 % calculated for human protein kinases in general.
Frequency of Mutated Sites:

None > 3 in 20,034 cancer specimens
Comments:
Only 1 deletion, and no insertions or complex mutations are noted on the COSMIC website.
 
COSMIC Entry:
NUAK1_ENST00000261402
OMIM Entry:
608130
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