Protein detail

GNAS3

Neuroendocrine secretory protein 55 (NESP55) [Cleaved into: LHAL tetrapeptide; GPIPIRRH peptide]

Entry name
GNAS3
UniProt ID
EVMP confidence score
0.38
Supporting publications (n)
1
Transmembrane count
Protein classification
Cancer-related genesDisease related genesHuman disease related genesPotential drug targetsPredicted intracellular proteinsPredicted membrane proteinsTransporters
EVMP confidence score

Annotation confidence score; open for threshold definitions.

Extremely high >= 0.85High >= 0.70Medium >= 0.55Low >= 0.40
Basic Information11
Protein Names
Neuroendocrine secretory protein 55 (NESP55) [Cleaved into: LHAL tetrapeptide; GPIPIRRH peptide]
Protein Class (7)
Cancer-related genesDisease related genesHuman disease related genesPotential drug targetsPredicted intracellular proteinsPredicted membrane proteinsTransporters
Protein Function (11)
  • Cancer-related genes:Mutational cancer driver genes
  • Predicted intracellular proteins
  • Human disease related genes:Congenital malformations:Congenital malformations of the musculoskeletal system
  • Human disease related genes:Endocrine and metabolic diseases:Hypothalamus and pituitary gland diseases
  • Human disease related genes:Musculoskeletal diseases:Skeletal diseases
  • Potential drug targets
  • Human disease related genes:Endocrine and metabolic diseases:Parathyroid diseases
  • Cancer-related genes:Candidate cancer biomarkers
  • Transporters:Accessory Factors Involved in Transport
  • Disease related genes
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Entrez Gene Symbol
Gene Synonym (7)
GNAS1GNASXLGPSANESPNESP55SCG6SgVI
Gene Description
GNAS complex locus
Chromosome
20
Position
58839718-58911192
Supporting publications (n)
1
EVMP confidence score
0.38
Fluorescence & Localization2
Tissue Specificskeletal muscleCell SpecificLate spermatids
Function & Pathway8
Protein Function (11)
  • Cancer-related genes:Mutational cancer driver genes
  • Predicted intracellular proteins
  • Human disease related genes:Congenital malformations:Congenital malformations of the musculoskeletal system
  • Human disease related genes:Endocrine and metabolic diseases:Hypothalamus and pituitary gland diseases
  • Human disease related genes:Musculoskeletal diseases:Skeletal diseases
  • Potential drug targets
  • Human disease related genes:Endocrine and metabolic diseases:Parathyroid diseases
  • Cancer-related genes:Candidate cancer biomarkers
  • Transporters:Accessory Factors Involved in Transport
  • Disease related genes
Page 1 of 2
Canonical Pathways (3)
  • M56 Pid lpa4 pathway
  • M8 Pid endothelin pathway
  • M15 Pid lysophospholipid pathway
Mediation Categories (5)
Clinical-translation mediationFusion and delivery mediationImmune mediationMetabolism mediationReceptor-signaling mediation
Relations & Evidence188

Ligand-Receptor Signaling (88)

88 records.

CategoryParentDatabaseTransmitterReceiverSecretedPlasma Membrane (Transmembrane)Plasma Membrane (Peripheral)
intracellularintracellularComPPINoNoYesNoNo
intracellularintracellularComPPINoNoYesNoNo
intracellularintracellularComPPINoNoYesNoNo
intracellularintracellularGO_IntercellNoNoYesNoNo
intracellularintracellularUniProt_locationNoNoYesNoNo
intracellularintracellularUniProt_locationNoNoYesNoNo
intracellularintracellularUniProt_locationNoNoYesNoNo
intracellularintracellularUniProt_locationNoNoYesNoNo
intracellularintracellularOmniPathNoNoYesNoNo
intracellularintracellularOmniPathNoNoYesNoNo
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Regulatory Interaction Network (93)

93 records.

Source Protein SymbolSource UniProt IDTarget Protein SymbolTarget UniProt IDIs DirectedIs StimulationIs InhibitionDatabaseReferences
HRH1P35367GNAS3O95467YesYesNoSIGNORSIGNOR:31160049
FZD7O75084GNAS3O95467YesYesNoSIGNORSIGNOR:22944199
NMBRP28336GNAS3O95467YesYesNoSIGNORSIGNOR:31160049
FFAR1O14842GNAS3O95467YesYesNoSIGNORSIGNOR:31160049
GNAS3O95467RACK1P63244YesNoYesSIGNORSIGNOR:34657150
GNAS3O95467AXIN1O15169YesYesNoSIGNORSIGNOR:16293724
GP132Q9UNW8GNAS3O95467YesYesNoSIGNORSIGNOR:31160049
ADRB3P13945GNAS3O95467YesYesNoKEGG-MEDICUSHPRDWangSIGNORHPRD:8011597SIGNOR:31160049
MCHR1Q99705GNAS3O95467YesYesNoSIGNORSIGNOR:31160049
GHSRQ92847GNAS3O95467YesYesNoSIGNORSIGNOR:31160049
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Protein Complex Composition (7)

7 records.

Component NameComponent Gene SymbolsComponent UniProt IDStoichiometryDatabaseDatabase IDsReferences
GNAS-L-GNB1-GNG1 complexGNASGNB5GNGT1O14775P63092P632110:0:0CORUMCORUM:714625733868
GNAS-L-GNB5-GNG12 complexGNASGNB5GNG12O14775P63092Q9UBI60:0:0CORUMCORUM:720825733868
GNAS-L-GNB5-GNG13 complexGNASGNB5GNG13O14775P63092Q9P2W30:0:0CORUMCORUM:721325733868
GNAS-L-GNB5-GNG4 complexGNASGNB5GNG4O14775P50150P630920:0:0CORUMCORUM:716425733868
GNAS-L-GNB5-GNG8 complexGNASGNB5GNG8O14775P63092Q9UK080:0:0CORUMCORUM:717925733868
DPCDGNASMTORRPAP3RPL26RUVBL1RUVBL2TTI1O43156O95467P42345P61254Q9BVM2Q9H6T3Q9Y230Q9Y2651:1:1:1:1:1:1:1NetworkBlastCompleatCompleat:HC7677
GNASP630924PDBPDB:7e5e
Sequence, Structure & Domains8

Sequences

Length
245
Mass
28,029
Sequence
MDRRSRAQQWRRARHNYNDLCPPIGRRAATALLWLSCSIALLRALATSNARAQQRAAAQQRRSFLNAHHRSGAQVFPESPESESDHEHEEADLELSLPECLEYEEEFDYETESETESEIESETDFETEPETAPTTEPETEPEDDRGPVVPKHSTFGQSLTQRLHALKLRSPDASPSRAPPSTQEPQSPREGEELKPEDKDPRDPEESKEPKEEKQRRRCKPKKPTRRDASPESPSKKGPIPIRRH
Alternative Products
Event=Alternative splicing; Named isoforms=8; Name=Nesp55; IsoId=O95467-1; Sequence=Displayed; Name=XLas-1; IsoId=Q5JWF2-1; Sequence=External; Name=XLas-2; IsoId=Q5JWF2-2; Sequence=External; Name=XLas-3; IsoId=Q5JWF2-3; Sequence=External; Name=Gnas-1; Synonyms=Alpha-S2, GNASl, Alpha-S-long; IsoId=P63092-1, P04895-1; Sequence=External; Name=Gnas-2; Synonyms=Alpha-S1, GNASs, Alpha-S-short; IsoId=P63092-2, P04895-2; Sequence=External; Name=3; IsoId=P63092-3; Sequence=External; Name=4; IsoId=P63092-4; Sequence=External

Domain & Motif Annotations

Compositional Bias
101..129; Acidic residues; 171..181; Low complexity; 187..215; Basic and acidic residues; 216..225; Basic residues
Region
70..245; Disordered
Protein Families
NESP55 family
Sequence Similarities
Belongs to the NESP55 family.
Clinical Relevance6
Supporting Publications1
PMIDTitleAbstract
32384937Alzheimer's disease progression characterized by alterations in the molecular profiles and biogenesis of brain extracellular vesicles.No abstract available