Gene/Proteome Database (LMPD)

LMPD ID
LMP001188
Gene ID
Species
Homo sapiens (Human)
Gene Name
prostaglandin D2 synthase 21kDa (brain)
Gene Symbol
Synonyms
L-PGDS; LPGDS; PDS; PGD2; PGDS; PGDS2
Alternate Names
prostaglandin-H2 D-isomerase; cerebrin-28; PGD2 synthase; beta-trace protein; prostaglandin D synthase; prostaglandin-D2 synthase; glutathione-independent PGD synthase; glutathione-independent PGD synthetase; lipocalin-type prostaglandin D synthase; lipocalin-type prostaglandin-D synthase
Chromosome
9
Map Location
9q34.2-q34.3
EC Number
5.3.99.2
Summary
The protein encoded by this gene is a glutathione-independent prostaglandin D synthase that catalyzes the conversion of prostaglandin H2 (PGH2) to postaglandin D2 (PGD2). PGD2 functions as a neuromodulator as well as a trophic factor in the central nervous system. PGD2 is also involved in smooth muscle contraction/relaxation and is a potent inhibitor of platelet aggregation. This gene is preferentially expressed in brain. Studies with transgenic mice overexpressing this gene suggest that this gene may be also involved in the regulation of non-rapid eye movement sleep. [provided by RefSeq, Jul 2008]
Orthologs

Proteins

prostaglandin-H2 D-isomerase precursor
Refseq ID NP_000945
Protein GI 32171249
UniProt ID P41222
mRNA ID NM_000954
Length 190
RefSeq Status REVIEWED
MATHHTLWMGLALLGVLGDLQAAPEAQVSVQPNFQQDKFLGRWFSAGLASNSSWLREKKAALSMCKSVVAPATDGGLNLTSTFLRKNQCETRTMLLQPAGSLGSYSYRSPHWGSTYSVSVVETDYDQYALLYSQGSKGPGEDFRMATLYSRTQTPRAELKEKFTAFCKAQGFTEDTIVFLPQTDKCMTEQ
sig_peptide: 1..22 inference: COORDINATES: ab initio prediction:SignalP:4.0 calculated_mol_wt: 2349 peptide sequence: MATHHTLWMGLALLGVLGDLQA

Gene Information

Entrez Gene ID
Gene Name
prostaglandin D2 synthase 21kDa (brain)
Gene Symbol
Species
Homo sapiens

Gene Ontology (GO Annotations)

GO ID Source Type Description
GO:0005794 ISS:UniProtKB C Golgi apparatus
GO:0005789 TAS:Reactome C endoplasmic reticulum membrane
GO:0005576 IDA:UniProtKB C extracellular region
GO:0005615 IDA:UniProtKB C extracellular space
GO:0070062 IDA:UniProtKB C extracellular vesicular exosome
GO:0005634 IEA:UniProtKB-KW C nucleus
GO:0005791 IDA:UniProtKB C rough endoplasmic reticulum
GO:0005504 IDA:UniProtKB F fatty acid binding
GO:0004667 IDA:UniProtKB F prostaglandin-D synthase activity
GO:0005501 ISS:UniProtKB F retinoid binding
GO:0005215 ISS:UniProtKB F transporter activity
GO:0019369 TAS:Reactome P arachidonic acid metabolic process
GO:0019371 TAS:Reactome P cyclooxygenase pathway
GO:0001516 IDA:UniProtKB P prostaglandin biosynthetic process
GO:0045187 ISS:UniProtKB P regulation of circadian sleep/wake cycle, sleep
GO:0051384 IEA:Ensembl P response to glucocorticoid
GO:0044281 TAS:Reactome P small molecule metabolic process
GO:0006810 ISS:UniProtKB P transport

KEGG Pathway Links

KEGG Pathway ID Description
hsa00590 Arachidonic acid metabolism

REACTOME Pathway Links

REACTOME Pathway ID Description
REACT_150149 Synthesis of Prostaglandins (PG) and Thromboxanes (TX)

Domain Information

InterPro Annotations

Accession Description
IPR012674 Calycin
IPR011038 Calycin-like
IPR002345 Lipocalin
IPR022272 Lipocalin family conserved site
IPR000566 Lipocalin/cytosolic fatty-acid binding domain
IPR002972 Prostaglandin D synthase

UniProt Annotations

Entry Information

Gene Name
prostaglandin D2 synthase 21kDa (brain)
Protein Entry
PTGDS_HUMAN
UniProt ID
Species
Human

Comments

Comment Type Description
Catalytic Activity (5Z,13E,15S)-9-alpha,11-alpha-epidioxy-15- hydroxyprosta-5,13-dienoate = (5Z,13E,15S)-9-alpha,15-dihydroxy- 11-oxoprosta-5,13-dienoate.
Developmental Stage Expression in the amniotic fluid increases dramatically during weeks 12 to 25 of pregnancy. Levels decrease slowly after 25 weeks.
Domain Forms a beta-barrel structure that accommodates hydrophobic ligands in its interior.
Function Catalyzes the conversion of PGH2 to PGD2, a prostaglandin involved in smooth muscle contraction/relaxation and a potent inhibitor of platelet aggregation. Involved in a variety of CNS functions, such as sedation, NREM sleep and PGE2-induced allodynia, and may have an anti-apoptotic role in oligodendrocytes. Binds small non-substrate lipophilic molecules, including biliverdin, bilirubin, retinal, retinoic acid and thyroid hormone, and may act as a scavenger for harmful hydrophopic molecules and as a secretory retinoid and thyroid hormone transporter. Possibly involved in development and maintenance of the blood-brain, blood-retina, blood-aqueous humor and blood-testis barrier. It is likely to play important roles in both maturation and maintenance of the central nervous system and male reproductive system. {ECO
Induction By IL1B/interleukin-1 beta and thyroid hormone. Probably induced by dexamethasone, dihydrotestosterone (DHT), progesterone, retinoic acid and retinal. Repressed by the Notch- Hes signaling pathway.
Miscellaneous It has been proposed that the urinary and serum levels may provide a sensitive indicator of renal damage in diabetes mellitus and hypertension. Elevated levels in the coronary circulation may also be associated with angina. Changes in charge and molecular weight microheterogeneity, due to modification of the N-linked oligosaccharides, may be associated with neurodegenerative disease and multiple sclerosis. Detected in meningioma but not in other brain tumors and may be considered a specific cell marker for meningioma. Expression levels in amniotic fluid are altered in abnormal pregnancies. Levels are lower in pregnancies with trisomic fetuses and fetuses with renal abnormalities.
Ptm N- and O-glycosylated. Both N-glycosylation recognition sites are almost quantitatively occupied by N-glycans of the biantennary complex type, with a considerable proportion of structures bearing a bisecting GlcNAc. N-glycan at Asn-78: dHex1Hex5HexNAc4. Agalacto structure as well as sialylated and nonsialylated oligosaccharides bearing alpha2-3- and/or alpha2-6-linked NeuNAc are present. {ECO
Similarity Belongs to the calycin superfamily. Lipocalin family.
Subcellular Location Rough endoplasmic reticulum . Nucleus membrane . Golgi apparatus . Cytoplasm, perinuclear region . Secreted . Note=Detected on rough endoplasmic reticulum of arachnoid and menigioma cells. Localized to the nuclear envelope, Golgi apparatus, secretory vesicles and spherical cytoplasmic structures in arachnoid trabecular cells, and to circular cytoplasmic structures in meningeal macrophages and perivascular microglial cells. In oligodendrocytes, localized to the rough endoplasmic reticulum and nuclear envelope. In retinal pigment epithelial cells, localized to distinct cytoplasmic domains including the perinuclear region. Also secreted.
Subunit Monomer. {ECO
Tissue Specificity Abundant in the brain and CNS, where it is expressed in tissues of the blood-brain barrier and secreted into the cerebro-spinal fluid. Abundantly expressed in the heart. In the male reproductive system, it is expressed in the testis, epididymis and prostate, and is secreted into the seminal fluid. Expressed in the eye and secreted into the aqueous humor. Lower levels detected in various tissue fluids such as serum, normal urine, ascitic fluid and tear fluid. Also found in a number of other organs including ovary, fimbriae of the fallopian tubes, kidney, leukocytes. {ECO
Web Resource Name=SeattleSNPs; URL="http://pga.gs.washington.edu/data/ptgds/";

Identical and Related Proteins

Unique RefSeq proteins for LMP001188 (as displayed in Record Overview)

Protein GI Database Accession Length Protein Name
32171249 RefSeq NP_000945 190 prostaglandin-H2 D-isomerase precursor

Identical Sequences to LMP001188 proteins

Reference Database Accession Length Protein Name
GI:32171249 GenBank ADR97051.1 190 Sequence 561 from patent US 7749695
GI:32171249 GenBank AED45344.1 190 Sequence 852 from patent US 7892730
GI:32171249 GenBank AEJ66628.1 190 Sequence 36 from patent US 7968293
GI:32171249 GenBank AEN52375.1 190 Sequence 2 from patent US 8003765
GI:32171249 GenBank AFK97728.1 190 Sequence 79 from patent US 8158600
GI:32171249 GenBank AIC54985.1 190 PTGDS, partial [synthetic construct]

Related Sequences to LMP001188 proteins

Reference Database Accession Length Protein Name
GI:32171249 GenBank AAV38723.1 191 prostaglandin D2 synthase 21kDa (brain), partial [synthetic construct]
GI:32171249 GenBank AAX29535.1 191 prostaglandin D2 synthase 21kDa, partial [synthetic construct]
GI:32171249 GenBank AAX43094.1 191 prostaglandin D2 synthase, partial [synthetic construct]
GI:32171249 GenBank AAX43095.1 191 prostaglandin D2 synthase, partial [synthetic construct]
GI:32171249 GenBank ACM83526.1 215 Sequence 9024 from patent US 6812339
GI:32171249 PDB 4ORS 190 Chain A, Threedimensional Structure Of The C65a Mutant Of Human Lipocalin-type Prostaglandin D Synthase Apo-form