PSPH

PSPH
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	1L8L, 1L8O, 1NNL
Identifiers
Aliases	PSPH, PSP, PSPHD, phosphoserine phosphatase
External IDs	OMIM: 172480; MGI: 97788; HomoloGene: 31245; GeneCards: PSPH; OMA:PSPH - orthologs
Gene location (Human)
Chr.	Chromosome 7 (human)
End	56,051,604 bp
Gene location (Mouse)
Chr.	Chromosome 5 (mouse)
End	129,864,513 bp
RNA expression pattern
	Top expressed in
	right uterine tube; ; stromal cell of endometrium; ; C1 segment; ; ventricular zone; ; right adrenal cortex; ; gonad; ; muscle of thigh; ; nucleus accumbens; ; prefrontal cortex; ; caudate nucleus;
	Top expressed in
	seminal vesicula; ; yolk sac; ; lip; ; skin of external ear; ; calvaria; ; ventricular zone; ; endothelial cell of lymphatic vessel; ; medial ganglionic eminence; ; vestibular sensory epithelium; ; epidermis;
	More reference expression data
	; ; ; ;
	More reference expression data
Gene ontology
Molecular function	calcium ion binding; protein homodimerization activity; metal ion binding; hydrolase activity; magnesium ion binding; phosphatase activity;
Cellular component	cytosol; neuron projection; cytoplasm;
Biological process	response to testosterone; response to mechanical stimulus; response to nutrient levels; L-serine metabolic process; cellular amino acid biosynthetic process; dephosphorylation; L-serine biosynthetic process;
	Sources:Amigo / QuickGO
Orthologs
	5723
	100678
	ENSG00000146733
	ENSMUSG00000029446
	P78330
	Q99LS3
	NM_004577
	NM_133900
NP_004568; NP_001357432; NP_001357433; NP_001357434; NP_001357435;
	NP_001357436; NP_001357437; NP_001357438; NP_001357439; NP_001357440; NP_001357441; NP_001357442; NP_001357443; NP_001357444; NP_001357445; NP_001357446; NP_001357447; NP_001357448; NP_001357449; NP_001357450; NP_001357451
	NP_598661
	Wikidata
View/Edit Human	View/Edit Mouse

Phosphoserine phosphatase is an enzyme that in humans is encoded by the PSPH gene.^[5]^[6]^[7]

Function

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.^[7]

Clinical significance

Homozygous or compound heterozygous mutations in PSPH cause Neu–Laxova syndrome^[8] and Phosphoserine phosphatase deficiency.^[9]^[10]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000146733 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000029446 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Koch GA, Eddy RL, Haley LL, Byers MG, McAvoy M, Shows TB (Apr 1983). "Assignment of the human phosphoserine phosphatase gene (PSP) to the pter leads to q22 region of chromosome 7". Cytogenetics and Cell Genetics. 35 (1): 67–9. doi:10.1159/000131839. PMID 6297854.
^ Collet JF, Gerin I, Rider MH, Veiga-da-Cunha M, Van Schaftingen E (May 1997). "Human L-3-phosphoserine phosphatase: sequence, expression and evidence for a phosphoenzyme intermediate". FEBS Letters. 408 (3): 281–4. doi:10.1016/S0014-5793(97)00438-9. PMID 9188776. S2CID 6952728.
^ ^a ^b "Entrez Gene: PSPH phosphoserine phosphatase".
^ Acuna-Hidalgo R, Schanze D, Kariminejad A, Nordgren A, Kariminejad MH, Conner P, Grigelioniene G, Nilsson D, Nordenskjöld M, Wedell A, Freyer C, Wredenberg A, Wieczorek D, Gillessen-Kaesbach G, Kayserili H, Elcioglu N, Ghaderi-Sohi S, Goodarzi P, Setayesh H, van de Vorst M, Steehouwer M, Pfundt R, Krabichler B, Curry C, MacKenzie MG, Boycott KM, Gilissen C, Janecke AR, Hoischen A, Zenker M (Sep 2014). "Neu-Laxova syndrome is a heterogeneous metabolic disorder caused by defects in enzymes of the L-serine biosynthesis pathway". American Journal of Human Genetics. 95 (3): 285–93. doi:10.1016/j.ajhg.2014.07.012. PMC 4157144. PMID 25152457.
^ Veiga-da-Cunha M, Collet JF, Prieur B, Jaeken J, Peeraer Y, Rabbijns A, Van Schaftingen E (Feb 2004). "Mutations responsible for 3-phosphoserine phosphatase deficiency". European Journal of Human Genetics. 12 (2): 163–6. doi:10.1038/sj.ejhg.5201083. PMID 14673469.
^ Jaeken J, Detheux M, Fryns JP, Collet JF, Alliet P, Van Schaftingen E (Jul 1997). "Phosphoserine phosphatase deficiency in a patient with Williams syndrome". Journal of Medical Genetics. 34 (7): 594–6. doi:10.1136/jmg.34.7.594. PMC 1051004. PMID 9222972.

External links

Overview of all the structural information available in the PDB for UniProt: P78330 (Phosphoserine phosphatase) at the PDBe-KB.

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000146733 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000029446 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid6297854-5] Koch GA, Eddy RL, Haley LL, Byers MG, McAvoy M, Shows TB (Apr 1983). "Assignment of the human phosphoserine phosphatase gene (PSP) to the pter leads to q22 region of chromosome 7". Cytogenetics and Cell Genetics. 35 (1): 67–9. doi:10.1159/000131839. PMID 6297854.

[pmid9188776-6] Collet JF, Gerin I, Rider MH, Veiga-da-Cunha M, Van Schaftingen E (May 1997). "Human L-3-phosphoserine phosphatase: sequence, expression and evidence for a phosphoenzyme intermediate". FEBS Letters. 408 (3): 281–4. doi:10.1016/S0014-5793(97)00438-9. PMID 9188776. S2CID 6952728.

[entrez-7] "Entrez Gene: PSPH phosphoserine phosphatase".

[8] Acuna-Hidalgo R, Schanze D, Kariminejad A, Nordgren A, Kariminejad MH, Conner P, Grigelioniene G, Nilsson D, Nordenskjöld M, Wedell A, Freyer C, Wredenberg A, Wieczorek D, Gillessen-Kaesbach G, Kayserili H, Elcioglu N, Ghaderi-Sohi S, Goodarzi P, Setayesh H, van de Vorst M, Steehouwer M, Pfundt R, Krabichler B, Curry C, MacKenzie MG, Boycott KM, Gilissen C, Janecke AR, Hoischen A, Zenker M (Sep 2014). "Neu-Laxova syndrome is a heterogeneous metabolic disorder caused by defects in enzymes of the L-serine biosynthesis pathway". American Journal of Human Genetics. 95 (3): 285–93. doi:10.1016/j.ajhg.2014.07.012. PMC 4157144. PMID 25152457.

[9] Veiga-da-Cunha M, Collet JF, Prieur B, Jaeken J, Peeraer Y, Rabbijns A, Van Schaftingen E (Feb 2004). "Mutations responsible for 3-phosphoserine phosphatase deficiency". European Journal of Human Genetics. 12 (2): 163–6. doi:10.1038/sj.ejhg.5201083. PMID 14673469.

[10] Jaeken J, Detheux M, Fryns JP, Collet JF, Alliet P, Van Schaftingen E (Jul 1997). "Phosphoserine phosphatase deficiency in a patient with Williams syndrome". Journal of Medical Genetics. 34 (7): 594–6. doi:10.1136/jmg.34.7.594. PMC 1051004. PMID 9222972.

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PSPH

Function

Clinical significance

References

Further reading

External links

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