HYKK
Hydroxylysine kinase
Also known as: AGPHD1, HYKK_HUMAN, LOC123688
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A2RU49
- Gene
- HYKK
- Ensembl
- ENSG00000188266
- Chromosome
- 15
- Canonical length
- 373 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles,Aggresome,Cytosol
OverviewNCBI Gene
Enables hydroxylysine kinase activity. Predicted to be involved in lysine catabolic process. Predicted to be located in mitochondrial matrix. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
373 residues, UniProt reviewed canonical sequence.
>A2RU49|HYKK
1 MSSGNYQQSE ALSKPTFSEE QASALVESVF GLKVSKVRPL PSYDDQNFHV YVSKTKDGPT
61 EYVLKISNTK ASKNPDLIEV QNHIIMFLKA AGFPTASVCH TKGDNTASLV SVDSGSEIKS
121 YLVRLLTYLP GRPIAELPVS PQLLYEIGKL AAKLDKTLQR FHHPKLSSLH RENFIWNLKN
181 VPLLEKYLYA LGQNRNREIV EHVIHLFKEE VMTKLSHFRE CINHGDLNDH NILIESSKSA
241 SGNAEYQVSG ILDFGDMSYG YYVFEVAITI MYMMIESKSP IQVGGHVLAG FESITPLTAV
301 EKGALFLLVC SRFCQSLVMA AYSCQLYPEN KDYLMVTAKT GWKHLQQMFD MGQKAVEEIW
361 FETAKSYESG ISMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HYKK 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)
- 0.24
- Highest tissue expression
- 12 nTPM
Expression across tissuesHPA
Tissue
- kidney: 12 nTPM
- choroid plexus: 8.2 nTPM
- duodenum: 6.8 nTPM
- small intestine: 6.8 nTPM
- pancreas: 6.5 nTPM
- skeletal muscle: 5.9 nTPM
Single-cell type
- myosatellite cells: 69 nCPM
- late spermatids: 52 nCPM
- enterocytes: 45 nCPM
- respiratory basal cells: 33 nCPM
- proximal tubule cells: 20 nCPM
- distal convoluted tubule cells: 17 nCPM
Immune cell
- naive CD4 T-cell: 3 nTPM
- memory CD4 T-cell: 1.1 nTPM
- naive CD8 T-cell: 0.6 nTPM
- T-reg: 0.5 nTPM
- basophil: 0.4 nTPM
- total PBMC: 0.4 nTPM
Brain region
- basal ganglia: 12 nTPM
- cerebellum: 12 nTPM
- cerebral cortex: 12 nTPM
- white matter: 11 nTPM
- amygdala: 11 nTPM
- hippocampal formation: 11 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about HYKK.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 52 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
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)
- 1.15
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.67
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- amino acid kinase activity
- hydroxylysine kinase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Aminoglycoside phosphotransferase
- Protein kinase-like domain superfamily
- Phosphotransferase enzyme family
- Pseudomonas-type Homoserine Kinase
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads HYKK as an antibody target. Whether an autoantibody or antibody against HYKK could matter depends on whether native HYKK is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HYKK 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 HYKK as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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