Entity Details

Primary name SYN1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP17600
EntryNameSYN1_HUMAN
FullNameSynapsin-1
TaxID9606
Evidenceevidence at protein level
Length705
SequenceStatuscomplete
DateCreated1990-08-01
DateModified2021-06-02

Ontological Relatives

GenesSYN1

GO terms

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GOName
GO:0000795 synaptonemal complex
GO:0003779 actin binding
GO:0005215 transporter activity
GO:0005524 ATP binding
GO:0005794 Golgi apparatus
GO:0005829 cytosol
GO:0005856 cytoskeleton
GO:0007268 chemical synaptic transmission
GO:0007269 neurotransmitter secretion
GO:0008021 synaptic vesicle
GO:0014069 postsynaptic density
GO:0019901 protein kinase binding
GO:0030424 axon
GO:0030425 dendrite
GO:0030672 synaptic vesicle membrane
GO:0042802 identical protein binding
GO:0046928 regulation of neurotransmitter secretion
GO:0048306 calcium-dependent protein binding
GO:0048666 neuron development
GO:0048786 presynaptic active zone
GO:0050808 synapse organization
GO:0097091 synaptic vesicle clustering
GO:0098685 Schaffer collateral - CA1 synapse
GO:0098693 regulation of synaptic vesicle cycle
GO:0098850 extrinsic component of synaptic vesicle membrane
GO:0098993 anchored component of synaptic vesicle membrane
GO:2000300 regulation of synaptic vesicle exocytosis

Subcellular Location

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Subcellular Location
Cell junction
Golgi apparatus

Domains

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DomainNameCategoryType
IPR001359 SynapsinFamilyFamily
IPR013815 ATP-grasp fold, subdomain 1FamilyHomologous superfamily
IPR016185 Pre-ATP-grasp domain superfamilyFamilyHomologous superfamily
IPR019735 Synapsin, conserved siteSiteConserved site
IPR019736 Synapsin, phosphorylation sitePTMPTM
IPR020897 Synapsin, pre-ATP-grasp domainDomainDomain
IPR020898 Synapsin, ATP-binding domainDomainDomain
IPR028713 Synapsin-1FamilyFamily

Diseases

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Disease IDSourceNameDescription
300491 OMIMEpilepsy X-linked, with variable learning disabilities and behavior disorders (XELBD)A neurologic disorder characterized by variable combinations of epilepsy, learning difficulties, macrocephaly, and aggressive behavior. The disease is caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB02930 Adenosine 5'-[gamma-thio]triphosphateDrugbanksmall molecule

Interactions

33 interactions

InteractorPartnerSourcesPublicationsLink
SYN1_HUMANKAT5_HUMANBioGRID, HPRD, IntAct16169070 details
SYN1_HUMANSYN1_HUMANBioGRID, HPRD, IntAct16169070 28533388 9463375 details
SYN1_HUMANVIME_HUMANBioGRID, HPRD, IntAct16169070 details
SYN1_HUMANEGFR_HUMANIntAct20029029 31980649 details
SYN1_HUMANSYUA_HUMANBioGRID, IntAct17893145 22163275 details
SYN1_HUMANRBCC1_HUMANBioGRID, MINT25640309 details
SYN1_HUMANGRB2_HUMANBioGRID, HPRD10899172 8022809 8552632 details
SYN1_HUMANSYN2_HUMANBioGRID, HPRD10358015 details
SYN1_HUMANCAPON_HUMANBioGRID, HPRD11867766 details
SYN1_HUMANNOS1_HUMANBioGRID11867766 details
SYN1_HUMANBLM_HUMANBioGRID15829507 details
SYN1_HUMANITSN2_HUMANBioGRID22558309 details
SYN1_HUMANERG_HUMANBioGRID24591637 details
SYN1_HUMANSYN3_HUMANHPRD10358015 details
SYN1_HUMANNCF1_HUMANBioGRID, HPRD10899172 details
SYN1_HUMANBIN1_HUMANBioGRID, HPRD10899172 details
SYN1_HUMANAMPH_HUMANBioGRID, HPRD10899172 details
SYN1_HUMANSRC_HUMANBioGRID, HPRD10899172 details
SYN1_HUMANP85A_HUMANBioGRID, HPRD10899172 details
SYN1_HUMANCRK_HUMANBioGRID, HPRD10899172 details
SYN1_HUMANPRKN_HUMANBioGRID11431533 details
SYN1_HUMANPLCG1_HUMANHPRD10899172 details
SYN1_HUMANPROF2_HUMANHPRD9463375 details
SYN1_HUMANSPTN1_HUMANHPRD1905928 details
SYN1_HUMANKAPCA_HUMANHPRD10571231 12237306 details
SYN1_HUMANKCC1A_HUMANHPRD10571231 12237306 9395448 details
SYN1_HUMANPAK2_HUMANHPRD10571231 12237306 details
SYN1_HUMANS10A1_HUMANHPRD15147519 details
SYN1_HUMANPAK1_HUMANHPRD12237306 details
SYN1_HUMANPAK3_HUMANHPRD12237306 details
SYN1_HUMANMK03_HUMANHPRD10725920 details
SYN1_HUMANCDK5_HUMANHPRD8702879 details
SYN1_HUMANRASA1_HUMANHPRD10899172 details