InnateDB Protein
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IDBP-476523.3
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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GCH1
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Protein Name
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GTP cyclohydrolase 1
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Synonyms
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DYT14; DYT5; DYT5a; GCH; GTP-CH-1; GTPCH1; HPABH4B;
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000419045
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InnateDB Gene
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IDBG-7150 (GCH1)
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Protein Structure
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Function |
Positively regulates nitric oxide synthesis in umbilical vein endothelial cells (HUVECs). May be involved in dopamine synthesis. May modify pain sensitivity and persistence. Isoform GCH-1 is the functional enzyme, the potential function of the enzymatically inactive isoforms remains unknown. {ECO:0000269PubMed:12176133, ECO:0000269PubMed:16338639, ECO:0000269PubMed:17057711, ECO:0000269PubMed:8068008, ECO:0000269PubMed:9445252}.
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Subcellular Localization |
Cytoplasm. Nucleus.
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Disease Associations |
GTP cyclohydrolase 1 deficiency (GCH1D) [MIM:233910]: A cause of malignant hyperphenylalaninemia due to tetrahydrobiopterin deficiency. It is also responsible for defective neurotransmission due to depletion of the neurotransmitters dopamine and serotonin. The principal symptoms include: psychomotor retardation, tonicity disorders, convulsions, drowsiness, irritability, abnormal movements, hyperthermia, hypersalivation, and difficulty swallowing. Some patients may present a phenotype of intermediate severity between severe hyperphenylalaninemia and mild dystonia type 5 (dystonia- parkinsonism with diurnal fluctuation). In this intermediate phenotype, there is marked motor delay, but no mental retardation and only minimal, if any, hyperphenylalaninemia. {ECO:0000269PubMed:7501255, ECO:0000269PubMed:9667588}. Note=The disease is caused by mutations affecting the gene represented in this entry.Dystonia 5 (DYT5) [MIM:128230]: A DOPA-responsive dystonia. Dystonia is defined by the presence of sustained involuntary muscle contractions, often leading to abnormal postures. DYT5 typically presents in childhood with walking problems due to dystonia of the lower limbs and worsening of the dystonia towards the evening. It is characterized by postural and motor disturbances showing marked diurnal fluctuation. Torsion of the trunk is unusual. Symptoms are alleviated after sleep and aggravated by fatigue and exercise. There is a favorable response to L-DOPA without side effects. {ECO:0000269PubMed:10076897, ECO:0000269PubMed:10208576, ECO:0000269PubMed:10582612, ECO:0000269PubMed:10825351, ECO:0000269PubMed:10987649, ECO:0000269PubMed:11113234, ECO:0000269PubMed:12391354, ECO:0000269PubMed:17101830, ECO:0000269PubMed:7501255, ECO:0000269PubMed:7874165, ECO:0000269PubMed:8852666, ECO:0000269PubMed:8957022, ECO:0000269PubMed:9120469, ECO:0000269PubMed:9328244, ECO:0000269PubMed:9778264}. Note=The disease is caused by mutations affecting the gene represented in this entry.
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Tissue Specificity |
In epidermis, expressed predominantly in basal undifferentiated keratinocytes and in some but not all melanocytes (at protein level). {ECO:0000269PubMed:16778797}.
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 35 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated |
Total |
35
[view]
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Protein-Protein |
34
[view]
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Protein-DNA |
1
[view]
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Protein-RNA |
0
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DNA-DNA |
0
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RNA-RNA |
0
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DNA-RNA |
0
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Predicted by orthology |
Total |
1 [view]
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Molecular Function |
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
IPR001474
GTP cyclohydrolase I
IPR020602
GTP cyclohydrolase I domain
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PFAM |
PF01227
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PRINTS |
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PIRSF |
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SMART |
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TIGRFAMs |
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Modification |
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SwissProt |
P30793
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PhosphoSite |
PhosphoSite-P30793
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TrEMBL |
Q96T74
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UniProt Splice Variant |
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Entrez Gene |
2643
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UniGene |
Hs.86724
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RefSeq |
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HUGO |
HGNC:4193
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OMIM |
600225
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CCDS |
CCDS9720
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HPRD |
02573
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IMGT |
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EMBL |
AF321276
AY137463
BC025415
CH471061
CR536551
L29478
S43856
S44049
S44053
U19256
U19257
U19258
U19259
U19523
U66095
U66097
Z16418
Z29433
Z29434
Z30952
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GenPept |
AAB16861
AAB23164
AAB23165
AAB23166
AAB42186
AAB60633
AAD38866
AAD38868
AAH25415
AAK51704
AAN17459
CAA78908
CAA83213
CAB77391
CAB77392
CAG38788
EAW80647
EAW80648
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