TKTL2
Transketolase-like protein 2
Also known as: DKFZP434L1717, FLJ32975, TKTL2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H0I9
- Gene
- TKTL2
- Ensembl
- ENSG00000151005
- Chromosome
- 4
- Canonical length
- 626 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Predicted to enable thiamine pyrophosphate binding activity and transketolase activity. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
626 residues, UniProt reviewed canonical sequence.
>Q9H0I9|TKTL2
1 MMANDAKPDV KTVQVLRDTA NRLRIHSIRA TCASGSGQLT SCCSAAEVVS VLFFHTMKYK
61 QTDPEHPDND RFILSRGHAA PILYAAWVEV GDISESDLLN LRKLHSDLER HPTPRLPFVD
121 VATGSLGQGL GTACGMAYTG KYLDKASYRV FCLMGDGESS EGSVWEAFAF ASHYNLDNLV
181 AVFDVNRLGQ SGPAPLEHGA DIYQNCCEAF GWNTYLVDGH DVEALCQAFW QASQVKNKPT
241 AIVAKTFKGR GIPNIEDAEN WHGKPVPKER ADAIVKLIES QIQTNENLIP KSPVEDSPQI
301 SITDIKMTSP PAYKVGDKIA TQKTYGLALA KLGRANERVI VLSGDTMNST FSEIFRKEHP
361 ERFIECIIAE QNMVSVALGC ATRGRTIAFA GAFAAFFTRA FDQLRMGAIS QANINLIGSH
421 CGVSTGEDGV SQMALEDLAM FRSIPNCTVF YPSDAISTEH AIYLAANTKG MCFIRTSQPE
481 TAVIYTPQEN FEIGQAKVVR HGVNDKVTVI GAGVTLHEAL EAADHLSQQG ISVRVIDPFT
541 IKPLDAATII SSAKATGGRV ITVEDHYREG GIGEAVCAAV SREPDILVHQ LAVSGVPQRG
601 KTSELLDMFG ISTRHIIAAV TLTLMKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TKTL2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.19
- Highest tissue expression
- 54 nTPM
Expression across tissuesHPA
Tissue
- testis: 54 nTPM
- bone marrow: 0.1 nTPM
- retina: 0.1 nTPM
- spleen: 0.1 nTPM
- adipose tissue: 0 nTPM
- adrenal gland: 0 nTPM
Single-cell type
- late primary spermatocytes: 401 nCPM
- early spermatids: 56 nCPM
- late spermatids: 54 nCPM
- early primary spermatocytes: 37 nCPM
- peritubular myoid cells: 1.9 nCPM
- differentiating spermatogonia: 1.7 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- hypothalamus: 0.3 nTPM
- basal ganglia: 0.2 nTPM
- cerebral cortex: 0.2 nTPM
- medulla oblongata: 0.2 nTPM
- pons: 0.2 nTPM
- white matter: 0.2 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.17
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.05
- DepMap mean gene effect
- 0.08
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Transketolase, N-terminal
- Transketolase-like, pyrimidine-binding domain
- Transketolase C-terminal/Pyruvate-ferredoxin oxidoreductase domain II
- Thiamin diphosphate-binding fold
- Transketolase, C-terminal domain
- Transketolase-like
- Transketolase, thiamine diphosphate binding domain
- Transketolase, pyrimidine binding domain
- Transketolase, C-terminal domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TKTL2 as an antibody target. Whether an autoantibody or antibody against TKTL2 could matter depends on whether native TKTL2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TKTL2 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label TKTL2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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