SEPHS2
Selenide, water dikinase 2
Also known as: SPS2, SPS2_HUMAN, SPS2b
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q99611
- Gene
- SEPHS2
- Ensembl
- ENSG00000179918
- Chromosome
- 16
- Canonical length
- 448 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes an enzyme that catalyzes the production of monoselenophosphate (MSP) from selenide and ATP. MSP is the selenium donor required for synthesis of selenocysteine (Sec), which is co-translationally incorporated into selenoproteins at in-frame UGA codons that normally signal translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, the Sec insertion sequence (SECIS) element, which is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. This protein is itself a selenoprotein containing a Sec residue at its active site, suggesting the existence of an autoregulatory mechanism. It is preferentially expressed in tissues implicated in the synthesis of selenoproteins and in sites of blood cell development. A pseudogene for this locus has been identified on chromosome 5. [provided by RefSeq, May 2017]
Canonical amino-acid sequenceUniProt
448 residues, UniProt reviewed canonical sequence.
>Q99611|SEPHS2
1 MAEASATGAC GEAMAAAEGS SGPAGLTLGR SFSNYRPFEP QALGLSPSWR LTGFSGMKGU
61 GCKVPQEALL KLLAGLTRPD VRPPLGRGLV GGQEEASQEA GLPAGAGPSP TFPALGIGMD
121 SCVIPLRHGG LSLVQTTDFF YPLVEDPYMM GRIACANVLS DLYAMGITEC DNMLMLLSVS
181 QSMSEEEREK VTPLMVKGFR DAAEEGGTAV TGGQTVVNPW IIIGGVATVV CQPNEFIMPD
241 SAVVGDVLVL TKPLGTQVAV NAHQWLDNPE RWNKVKMVVS REEVELAYQE AMFNMATLNR
301 TAAGLMHTFN AHAATDITGF GILGHSQNLA KQQRNEVSFV IHNLPIIAKM AAVSKASGRF
361 GLLQGTSAET SGGLLICLPR EQAARFCSEI KSSKYGEGHQ AWIVGIVEKG NRTARIIDKP
421 RVIEVLPRGA TAAVLAPDSS NASSEPSSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SEPHS2 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
- Highest tissue expression
- 377 nTPM
Expression across tissuesHPA
Tissue
- liver: 377 nTPM
- kidney: 148 nTPM
- duodenum: 128 nTPM
- small intestine: 100 nTPM
- colon: 71 nTPM
- rectum: 62 nTPM
Single-cell type
- hepatocytes: 414 nCPM
- enterocytes: 373 nCPM
- colonocytes: 213 nCPM
- megakaryocytes: 142 nCPM
- parietal cells: 140 nCPM
- hofbauer cells: 133 nCPM
Immune cell
- NK-cell: 32 nTPM
- eosinophil: 30 nTPM
- naive CD4 T-cell: 25 nTPM
- T-reg: 23 nTPM
- MAIT T-cell: 22 nTPM
- myeloid DC: 22 nTPM
Brain region
- choroid plexus: 30 nTPM
- hypothalamus: 29 nTPM
- thalamus: 29 nTPM
- white matter: 27 nTPM
- pons: 27 nTPM
- midbrain: 26 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
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.76
- DepMap mean gene effect
- -0.7
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- selenium compound metabolic process
- selenocysteine biosynthetic process
- selenocysteine metabolic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SEPHS2 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SEPHS2 as an antibody target. Whether an autoantibody or antibody against SEPHS2 could matter depends on whether native SEPHS2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SEPHS2 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 SEPHS2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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