PDK3

Pyruvate dehydrogenase kinase 3 Q15120 PDK3_HUMAN
Protein Coding Chr X Xp22.11 Swiss-Prot reviewed Entrez 5165
Mutations
165
CL 19 · Tissue 142
Samples
159
CL 18 · Tissue 137
Peptides
132
unique mutant peptides
Transcripts
3
isoforms mutated

Stats by Source

Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Total = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Total can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

TotalCell lineTissue
Mutations16519142
Samples15918137
Peptides13214116

Function

PDK3 · Pyruvate dehydrogenase kinase 3

The pyruvate dehydrogenase (PDH) complex is a nuclear-encoded mitochondrial multienzyme complex that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2). It provides the primary link between glycolysis and the tricarboxylic acid (TCA) cycle, and thus is one of the major enzymes responsible for the regulation of glucose metabolism. The enzymatic activity of PDH is regulated by a phosphorylation/dephosphorylation cycle, and phosphorylation results in inactivation of PDH. The protein encoded by this gene is one of the three pyruvate dehydrogenase kinases that inhibits the PDH complex by phosphorylation of the E1 alpha subunit. This gene is predominantly expressed in the heart and skeletal muscles. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010].

Isoforms & Proteins

3 transcripts · UniProt mapping is sequence-verified (AA-safe)

About the isoform mapping
Isoforms & Proteins

Each Ensembl transcript (ENST) this gene is mutated on, with its matched UniProt accession.

The mapping is sequence-verified: the UniProt sequence is identical to the transcript translation, so amino-acid positions line up exactly. A * marks an unreviewed (TrEMBL) entry.

Counts are mutations and unique mutant peptides on each transcript.

TranscriptUniProtMutationsPeptides
ENST00000379162 Q15120 159 128
ENST00000568479 Q15120-2 5 3
ENST00000648777 Q15120 1 1

Gene Properties

Type
Protein Coding
Chromosome
X
Cytoband
Xp22.11
Entrez ID
Aliases
CMTX6GS1-358P8.4

Recurrent Mutations

All 128 amino-acid changes on canonical ENST00000379162 · needle height = samples · drag the mini-map to zoom

What this lollipop shows
Recurrent Mutations

A lollipop / needle plot – the standard way to show recurrent mutations along a protein (as used by cBioPortal and MutationMapper).

X-axis = amino-acid position in the protein.

Needle height & head size = how often that exact amino-acid change was observed (its recurrence). Tall/large heads are mutational hotspots.

The most recurrent changes are labelled; hover any needle for the change, position and counts.

Mutation frequency across cancer types

% of samples with a missense/complex mutation in PDK3 · cell line vs tissue

How this frequency is counted
Cancer-type mutation frequency

For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in PDK3 – counted as distinct samples (a sample counts once no matter how many mutations it has).

Split into cell line and tissue; each cell shows mutated / total and the percentage. Cohorts with <20 samples are omitted. Ordered by combined frequency.

Cancer typeCell linesTissue samples
Endometrial Carcinoma
3/42 7%
18/612 3%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Melanoma
2/210 1%
25/1899 1%
Small Cell Lung Carcinoma
0/9 0%
7/752 1%
Colorectal Carcinoma
6/143 4%
16/3239 0%
Squamous Cell Lung Carcinoma
0/57 0%
5/810 1%
Head and Neck Carcinoma
2/85 2%
7/1574 0%
Other Sarcomas
0/69 0%
4/699 1%
Ovarian Carcinoma
1/109 1%
4/998 0%
Non-Small Cell Lung Carcinoma
0/304 0%
6/1390 0%
Gastric Carcinoma
0/74 0%
6/1809 0%
Other Solid Cancers
0/94 0%
5/1515 0%
Hepatocellular Carcinoma
0/46 0%
7/2210 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Neuroendocrine Tumour
1/154 1%
1/577 0%
Thyroid Gland Carcinoma
0/45 0%
4/1592 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Non-Cancerous
0/104 0%
2/830 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Prostate Carcinoma
0/13 0%
4/2105 0%
Glioma
0/52 0%
4/2127 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Pancreatic Carcinoma
0/89 0%
2/1611 0%
Kidney Carcinoma
0/85 0%
2/1862 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
2/2550 0%
Breast Carcinoma
2/144 1%
0/3264 0%
B-Lymphoblastic Leukemia
0/55 0%
1/2640 0%

Mutation Distribution

Where PDK3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in PDK3 were found in each tissue, across the whole database.

Each bar is a tissue (cell-line and tissue names are merged to the standard tissue), split into cell line and tissue (patient tumour) contributions.

This shows the cancer-context where this gene is recurrently altered.

GTEx Expression

Median TPM across 54 healthy tissues

GTEx Portal ↗
About the expression data
GTEx Expression

Median gene expression (TPM) in normal, non-cancer human tissues from the GTEx project.

Useful for judging tumour specificity – a strong neoantigen target ideally comes from a gene with low expression in healthy tissues.

Scroll or drag the mini-axis below the chart to browse all tissues.

Mutations

All 165 mutations in PDK3

About the mutation list
Mutations

Every mutation record for this gene, across all samples and sources.

The Sample column links to the cell line (cell-line samples) or the tissue type (tissue samples).

Use the Type / Source filters, the search box, and column sorting to explore; each CAN-IMMUNE ID opens the full mutation & peptide view.

IDSampleTranscriptAA Change CDSTypeSourceMutant PeptideWild-type Peptide