Entity Details

Primary name GCYA1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ02108
EntryNameGCYA1_HUMAN
FullNameGuanylate cyclase soluble subunit alpha-1
TaxID9606
Evidenceevidence at protein level
Length690
SequenceStatuscomplete
DateCreated1993-07-01
DateModified2021-06-02

Ontological Relatives

GenesGUCY1A1

GO terms

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GOName
GO:0004383 guanylate cyclase activity
GO:0005525 GTP binding
GO:0006182 cGMP biosynthetic process
GO:0007263 nitric oxide mediated signal transduction
GO:0008015 blood circulation
GO:0008074 guanylate cyclase complex, soluble
GO:0008217 regulation of blood pressure
GO:0010750 positive regulation of nitric oxide mediated signal transduction
GO:0020037 heme binding
GO:0038023 signaling receptor activity
GO:0060087 relaxation of vascular associated smooth muscle
GO:0098925 retrograde trans-synaptic signaling by nitric oxide, modulating synaptic transmission
GO:0098978 glutamatergic synapse
GO:0098982 GABA-ergic synapse

Subcellular Location

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Subcellular Location
Cytoplasm

Domains

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DomainNameCategoryType
IPR001054 Adenylyl cyclase class-3/4/guanylyl cyclaseDomainDomain
IPR011644 Heme NO-bindingDomainDomain
IPR011645 Haem NO binding associatedDomainDomain
IPR018297 Adenylyl cyclase class-4/guanylyl cyclase, conserved siteSiteConserved site
IPR024096 NO signalling/Golgi transport ligand-binding domain superfamilyFamilyHomologous superfamily
IPR029787 Nucleotide cyclaseFamilyHomologous superfamily
IPR038158 H-NOX domain superfamilyFamilyHomologous superfamily
IPR042463 Haem NO binding associated domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
615750 OMIMMoyamoya disease 6 with or without achalasia (MYMY6)A form of Moyamoya disease, a progressive cerebral angiopathy characterized by bilateral intracranial carotid artery stenosis and telangiectatic vessels in the region of the basal ganglia. The abnormal vessels resemble a 'puff of smoke' (moyamoya) on cerebral angiogram. Affected individuals can develop transient ischemic attacks and/or cerebral infarction, and rupture of the collateral vessels can cause intracranial hemorrhage. Hemiplegia of sudden onset and epileptic seizures constitute the prevailing presentation in childhood, while subarachnoid bleeding occurs more frequently in adults. MYMY6 is characterized by severe cerebral angiopathy and onset of severe achalasia in infancy or early childhood. The disease is caused by variants affecting the gene represented in this entry.