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Updated November 2019

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Nomenclature

Short Name:
MYO3A
Full Name:
Myosin IIIA
Alias:
  • Class III myosin
  • EC 2.7.11.1
  • MY3A
  • Myosin IIIA

Classification

Type:
Protein-serine/threonine kinase
Group:
STE
Family:
STE20
SubFamily:
NinaC
 
 

Specific Links

Entrez-Gene Entry: 53904
Entrez-Protein Entry: NP_059129
GeneCards Entry: DFNB30
KinBASE Entry: MYO3A
OMIM Entry: 606808
Pfam Entry: Q8NEV4
PhosphoNET Entry: Q8NEV4
Phosphosite Plus Entry: 822
ScanSite Entry: Q8NEV4
Source Entry: MYO3A
UCSD-Nature Entry: A003760
UniProt Entry: Q8NEV4

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):
186208
# Amino Acids:
1616
# mRNA Isoforms:
2
mRNA Isoforms:
186,208 Da (1616 AA; Q8NEV4); 27,678 Da (247 AA; Q8NEV4-2)
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
21 287 Pkinase
340 1041 MYSc
1055 1084 IQ
1082 1111 IQ
1346 1375 IQ
 

Post-translation Modifications

For detailed information on phosphorylation of this kinase go to PhosphoNET
Acetylated:
K1306.
Serine phosphorylated:

S73, S177, S688, S1167, S1280, S1355.
Threonine phosphorylated:

T178, T184, T188, T302, T853, T908, T919, T1279.
Tyrosine phosphorylated:

Y82, Y85, Y509, Y1125, Y1394, Y1396, Y1459, .
 

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
    56

    666

    25

    819

  • adrenal
    0.5

    6

    10

    7

  • bladder
    4

    48

    22

    78

  • brain
    22

    259

    122

    2022

  • breast
    30

    359

    31

    246

  • cervix
    0.5

    6

    55

    7

  • colon
    0.4

    5

    35

    6

  • heart
    19

    222

    36

    425

  • intestine
    17

    204

    10

    212

  • kidney
    3

    37

    72

    63

  • liver
    4

    43

    36

    78

  • lung
    41

    484

    109

    511

  • lymphnode
    3

    34

    36

    90

  • ovary
    0.7

    8

    6

    10

  • pancreas
    4

    43

    9

    72

  • pituitary
    0.3

    4

    17

    4

  • prostate
    5

    55

    132

    50

  • salivarygland
    3

    38

    30

    64

  • skeletalmuscle"
    1.1

    13

    88

    21

  • skin
    27

    318

    107

    257

  • spinalcord
    3

    34

    39

    69

  • spleen
    3

    37

    31

    77

  • stomach
    4

    42

    33

    82

  • testis
    4

    50

    39

    51

  • thymus
    5

    55

    32

    94

  • thyroid
    30

    359

    78

    449

  • tonsil
    2

    28

    33

    62

  • trachea
    3

    36

    37

    88

  • uterus
    3

    31

    37

    77

  • reticulocytes"
    11

    127

    28

    118

  • t-lymphocytes
    31

    373

    18

    275

  • b-lymphocytes
    100

    1194

    31

    2447

  • neutrophils
    14

    172

    67

    550

  • macrophages
    56

    663

    78

    588

  • sperm
    18

    209

    48

    298

 

Evolution

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

    100

    100
  • tableheader
    98

    98.5

    99
  • tableheader
    95.4

    97.1

    96
  • tableheader
    -

    -

    86.5
  • tableheader
    -

    -

    -
  • tableheader
    75.5

    80.4

    87
  • tableheader
    -

    -

    -
  • tableheader
    81.7

    88.9

    82
  • tableheader
    71.8

    78.5

    83
  • tableheader
    -

    -

    -
  • tableheader
    60.1

    72.6

    -
  • tableheader
    67.5

    79.1

    71
  • tableheader
    -

    -

    65
  • tableheader
    56.3

    70.3

    62
  • tableheader
    -

    -

    -
  • tableheader
    28.2

    46.5

    38
  • tableheader
    41

    58

    -
  • tableheader
    -

    -

    -
  • tableheader
    -

    -

    -
  • tableheader
    -

    -

    -
  • tableheader
    -

    -

    -
  • tableheader
    -

    -

    -
  • tableheader
    -

    -

    -
  • tableheader
    -

    -

    -
  • tableheader
    -

    -

    -
For a wider analysis go to PhosphoNET Evolution in PhosphoNET
 

Binding Proteins

Examples of known interacting proteins
hiddentext
No. Name – UniProt ID
1 TGFBR1 - P36897
 

Regulation

Activation:
NA
Inhibition:
NA
Synthesis:
NA
Degradation:
NA
 

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
AST-487 Kd = 41 nM 11409972 574738 18183025
NVP-TAE684 Kd = 67 nM 16038120 509032 22037378
Lestaurtinib Kd = 260 nM 126565 22037378
Staurosporine Kd = 500 nM 5279 18183025
KW2449 Kd = 740 nM 11427553 1908397 22037378
PP242 Kd = 830 nM 25243800 22037378
WZ3146 Kd > 1 µM 44607360 20033049
WZ4002 Kd > 1 µM 44607530 20033049
SU14813 Kd = 1.4 µM 10138259 1721885 22037378
Axitinib Kd = 1.9 µM 6450551 1289926 22037378
Foretinib Kd = 2.8 µM 42642645 1230609 22037378
Sunitinib Kd = 3.1 µM 5329102 535 22037378
BMS-690514 Kd < 4 µM 11349170 21531814
 

Disease Linkage

General Disease Association:

Ear disorders
Specific Diseases (Non-cancerous):

Deafness, autosomal recessive 30; Deafness, autosomal recessive 76; Dfnb30 nonsyndromic hearing loss and deafness
Comments:
Three different recessive mutations leading to loss of function have been shown to cause deafness, autosomal recessive, 30, or other nonsyndromic progressive hearing loss diseases.
 
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 human Bladder carcinomas (%CFC= -50, p<0.0004). The COSMIC website notes an up-regulated expression score for MYO3A in diverse human cancers of 364, which is 0.8-fold of the average score of 462 for the human protein kinases. The down-regulated expression score of 0 for this protein kinase in human cancers was 100% lower than the average score of 60 for the human protein kinases.
Mutagenesis Experiments:

Insertional mutagenesis studies in mice have not yet revealed 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: 0.13 % in 25086 diverse cancer specimens. This rate is 1.7-fold higher 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: 0.62 % in 10 peritoneum cancers tested; 0.5 % in 1270 large intestine cancers tested; 0.38 % in 589 stomach cancers tested; 0.33 % in 603 endometrium cancers tested; 0.23 % in 1824 lung cancers tested; 0.15 % in 834 ovary cancers tested; 0.15 % in 710 oesophagus cancers tested; 0.14 % in 548 urinary tract cancers tested; 0.14 % in 1512 liver cancers tested; 0.11 % in 1372 breast cancers tested; 0.1 % in 881 prostate cancers tested; 0.09 % in 1364 kidney cancers tested; 0.08 % in 2082 central nervous system cancers tested; 0.05 % in 273 cervix cancers tested; 0.04 % in 152 biliary tract cancers tested.
Frequency of Mutated Sites:

Most frequent mutations with the number of reports indicated in brackets: N525S (4); N525K (2); N525H (2).
Comments:
Eighteen deletions (12 at M1192fs*1), 3 insertions and no complex mutations are noted on the COSMIC website.
 
COSMIC Entry:
MYO3A
OMIM Entry:
606808
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