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Suppressor of G2 allele of Skp1 homolog (Sgt1) (Sgt1)

Target
Sgt1
Molecular classification
Cochaperone, Adaptor protein, Other (not a receptor, enzyme, transporter, or transcription factor)
01

Overview

Suppressor of G2 allele of Skp1 homolog (Sgt1) is a conserved cochaperone protein that interacts with Hsp90 and is involved in multiple cellular processes, including the stabilization of several oncoproteins, Cullin E3 ubiquitin ligase activity, assembly and maintenance of kinetochores during mitosis, and centrosome maturation[3][5][7]. Sgt1 overexpression is associated with cancer and is essential for cell viability in certain tumor contexts, making it a potential—though currently not clinically targeted—therapeutic target[3]. Knockdown of Sgt1 impairs tumor growth by destabilizing oncoproteins required for cancer cell survival. Sgt1 is not a receptor, enzyme, or transporter, but rather a regulatory protein critical for protein complex assembly and cell cycle progression[3][7]. Notably, in humans, 'ENSG00000271251' is annotated as a pseudogene (i.e., not encoding a functional protein), so for drug discovery and biomolecular targeting, the true functional gene is SUGT1 (ENSG00000119718)[7]. Thus, information above relates to the protein-coding SUGT1, not the pseudogene designated by ENSG00000271251, and this Ensembl identifier is likely **incorrect** for an active therapeutic target.

Other names
Suppressor of G2 allele of SKP1 (S. cerevisiae) homologSUGT1SGT1 homologSuppressor of G2 allele of SKP1 pseudogeneENSG00000271251 (Ensembl gene ID, but see notes below)SUGT1 (functional gene)ENSG00000119718 (functional gene)
02

Mechanism of action

Not directly targeted by any approved drugs; modulation of protein-protein interactions within Hsp90 chaperone complexes

03

Biological functions

Regulation of protein stability via Hsp90 chaperone pathwayUbiquitination (Cullin E3 ubiquitin ligase activity)Kinetochore assembly and chromosome alignment during mitosisCentrosome maturationCell cycle progressionImmune response modulation
04

Disease associations

Cancer (especially solid tumors, e.g., colorectal, gastric, breast, lung, Ewing sarcoma, rhabdomyosarcoma)Other (potential neurological and immunological roles, limited direct evidence)
05

Safety considerations

Systemic inhibition may impair fundamental cellular processes (cell division, protein folding, immune response)[3].
06

Interacting drugs

None directly reported; some Hsp90 inhibitors (e.g., 17-AAG) can modulate proteostasis in a manner functionally linked with Sgt1[3].
07

Biomarkers

Sgt1 protein expression (primarily studied in oncology research as a marker of tumor cell viability or Hsp90 pathway activity)[3]

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