PSPH
Sign in to saveAlso known as PSP, PSPHD, phosphoserine phosphatase
Phosphoserine phosphatase is an enzyme that in humans is encoded by the PSPH gene.
Gene data
PSPH- Name
- phosphoserine phosphatase
- Type
- protein-coding
- Aliases
- PSP, PSPHD
The protein encoded by this gene belongs to a subfamily of the phosphotransferases. This encoded enzyme is responsible for the third and last step in L-serine formation. It catalyzes magnesium-dependent hydrolysis of L-phosphoserine and is also involved in an exchange reaction between L-serine and L-phosphoserine. Deficiency of this protein is thought to be linked to Williams syndrome. [provided by RefSeq, Jul 2008].
via MyGene.info
Gene · Ensembl
phosphoserine phosphatase
- Symbol
- PSPH
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 7:56,010,119-56,051,609
- Strand
- Reverse (−)
- Assembly
- GRCh38
View on Ensembl →
via Ensembl · EMBL-EBI
Wikidata facts
- Image
- Protein PSPH PDB 1l8l.png
Show 5 more facts
- HomoloGene ID
- 31245
- exact match
- identifiers.org/ncbigene/5723
- genomic end
- 56119297
- genomic start
- 56078744
- cytogenetic location
- 7p11.2
via Wikidata · CC0
~1 min read
Article
5 sectionsContents
- Function
- Clinical significance
- References
- Further reading
- External links
Phosphoserine phosphatase is an enzyme that in humans is encoded by the PSPH gene.
== Function ==
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Q180686
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Ensembl genome database project
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enzyme
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human genome
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Q229883
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