Target intelligence / Profile preview

Small ubiquitin-like modifier 3 (SUMO3)

Target
SUMO3
Molecular classification
Ubiquitin-like modifier, Posttranslational modification enzyme, Other (modifier protein)
01

Overview

Small ubiquitin-like modifier 3 (SUMO3) is a member of the SUMO family of proteins that function as posttranslational modifiers in eukaryotic cells. SUMO3 is covalently conjugated to lysine residues on target proteins through an enzymatic cascade (involving E1, E2, and E3 enzymes), in a process called sumoylation. Unlike ubiquitin, which often tags proteins for degradation, SUMO3 modification typically alters protein localization, activity, stability, and interactions without triggering degradation. Biological roles of SUMO3 include regulating nuclear transport, DNA replication and repair, mitosis, transcriptional regulation, and stress responses. SUMO3 is highly similar to SUMO2 (sharing ~97% sequence identity) and these two are frequently studied together as “SUMO2/3.” Aberrant sumoylation involving SUMO3 is implicated in cancer, immune reactions, and cellular stress, but no currently approved drugs directly target SUMO3. SUMO pathway modulation is a subject of basic research and potential therapeutic investigation

Other names
Small ubiquitin-related modifier 3SMT3ASMT3H1SUMO-3Smt3ASmt3BSMT3 suppressor of mif two 3 homolog 1SMT3 suppressor of mif two 3 homolog 3Ubiquitin-like protein SMT3AUbiquitin-like protein SMT3Bsmall ubiquitin-like modifier 3SUMO2 (historical confusion/overlap in nomenclature, but SUMO2 and SUMO3 are encoded by distinct genes in humans)
02

Mechanism of action

Not applicable (SUMO3 modifies target proteins via *sumoylation*, a covalent and reversible posttranslational modification of lysine residues, but it is not directly drug-targeted)

03

Biological functions

Protein sumoylation/posttranslational modificationNuclear transportDNA replication and repairMitosisTranscriptional regulationSignal transductionApoptosisProtein stability
04

Disease associations

Cancer (implicated in cancer-related pathways)Immune responseInfectionOther (specific roles under investigation; not a primary disease gene itself)
05

Safety considerations

None directly related to SUMO3 modulation in therapies, as it is not a direct drug target; however, dysregulation of the sumoylation pathway is associated with disrupted cellular function, cell cycle, and possibly tumorigenesis, raising concerns for indirect targeting
06

Interacting drugs

None known (no direct small-molecule SUMO3-targeting drugs approved or in clinical use)
07

Biomarkers

None established (SUMO3 and sumoylation alterations are being studied as *potential* cancer and cellular stress biomarkers, but are not standard in clinical practice)

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