General Information of the Molecule (ID: Mol04319)
Name
Guanine nucleotide-binding protein G(i) subunit alpha-2 (GNAI2) ,Homo sapiens
Synonyms
Adenylate cyclase-inhibiting G alpha protein
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Molecule Type
Protein
Gene Name
GNAI2
Gene ID
2771
Sequence
MGCTVSAEDKAAAERSKMIDKNLREDGEKAAREVKLLLLGAGESGKSTIVKQMKIIHEDG
YSEEECRQYRAVVYSNTIQSIMAIVKAMGNLQIDFADPSRADDARQLFALSCTAEEQGV
L PDDLSGVIRRLWADHGVQACFGRSREYQLNDSAAYYLNDLERIAQSDYIPTQQDVLRT
RV KTTGIVETHFTFKDLHFKMFDVGGQRSERKKWIHCFEGVTAIIFCVALSAYDLVLAE
DEE MNRMHESMKLFDSICNNKWFTDTSIILFLNKKDLFEEKITHSPLTICFPEYTGANK
YDEA ASYIQSKFEDLNKRKDTKEIYTHFTCATDTKNVQFVFDAVTDVIIKNNLKDCGLF
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Function
Guanine nucleotide-binding proteins are involvedas modulators or transducers in various transmembrane signalingsystems. The G proteins are involved in hormonal regulation ofadenylate cyclase: they inhibit the cyclase in response to beta-adrenergic stimuli. May play a role in cell division.{ECO:0000269|PubMed:17635935}.; [Isoform sGi2]: Regulates the cell surface density ofdopamine receptors DRD2 by sequestrating them as an intracellular pool.{ECO:0000269|PubMed:17550964}.
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Uniprot ID
GNAI2_HUMAN
Ensembl ID
ENSG0000011435317
HGNC ID
HGNC:4385
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Kingdom: Metazoa
Phylum: Chordata
Class: Mammalia
Order: Primates
Family: Hominidae
Genus: Homo
Species: Homo sapiens
Type(s) of Resistant Mechanism of This Molecule
  UAPP: Unusual Activation of Pro-survival Pathway
Drug Resistance Data Categorized by Drug
Approved Drug(s)
1 drug(s) in total
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Cabazitaxel
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Drug Resistance Data Categorized by Their Corresponding Mechanisms
  Unusual Activation of Pro-survival Pathway (UAPP) Click to Show/Hide
Disease Class: Prostate cancer [ICD-11: 2C82.0] [1]
Resistant Disease Prostate cancer [ICD-11: 2C82.0]
Resistant Drug Cabazitaxel
Molecule Alteration Phosphorylation
Up-regulation
Experimental Note Revealed Based on the Cell Line Data
Cell Pathway Regulation Oxytocin signaling pathway Activation hsa04921
In Vitro Model DU145CR cells prostate Homo sapiens (Human) N.A.
Experiment for
Molecule Alteration
MS analysis
Mechanism Description Pathway analysis revealed that clusters in two cases showed up-regulation of the oxytocin (OXT) receptor-signaling pathway. Spatial gene expression analysis of CBZ-resistant prostate cancer tissues confirmed the heterogeneous expression of OXT-signaling molecules. We identified the OXT-signaling pathway as a potential target for CBZ-resistant CRPC using single-cell transcriptomic analysis of CTCs. CLO may potentially overcome CBZ resistance in CRPC by inhibiting the OXT-signaling pathway.
References
Ref 1 G-protein signaling of oxytocin receptor as a potential target for cabazitaxel-resistant prostate cancer. PNAS Nexus. 2024 Jan 4;3(1):pgae002.

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