Target intelligence / Profile preview

Iron-sulfur cluster assembly protein (ISCU (major scaffold protein); other gene/protein names include ISCU, ISCA, NFS1, SufA, etc.)

Target
ISCU (major scaffold protein); other gene/protein names include ISCU, ISCA, NFS1, SufA, etc.
Molecular classification
Scaffold protein, Enzyme, Chaperone, Accessory protein, Assembly factor, Other (given the broad family)
01

Overview

Iron-sulfur cluster assembly proteins are a diverse group of proteins essential for the maturation of iron-sulfur (Fe-S) clusters, ubiquitous prosthetic groups required for fundamental cell processes including electron transport, gene regulation, catalysis, iron metabolism, and DNA repair[6][1][7]. The assembly pathway involves cysteine desulfurases that liberate sulfur from cysteine, scaffold proteins (such as ISCU) that serve as platforms for cluster assembly, and carrier proteins/chaperones that facilitate transfer to target apoproteins[2][3][9]. Dysfunction in any part of the assembly process can result in diseases such as Friedreich’s ataxia or severe metabolic disorders[4][1]. These proteins are critical for cell viability and not considered direct therapeutic or drug targets, but serve crucial roles in cell biology and pathology[10][6].

Other names
Iron-sulfur cluster scaffold proteinFe-S cluster assembly proteinISCU (for the canonical scaffold protein in the ISC pathway)Iron-sulfur cluster biosynthesis protein
02

Biological functions

Iron-sulfur cluster biosynthesisElectron transport (indirectly, by enabling Fe-S protein function)DNA repairEnergy production (oxidative phosphorylation)Regulation of iron metabolismGene regulationEnzyme catalysis (through Fe-S cluster provision)
03

Disease associations

Neurodegenerative disease (e.g., Friedreich's ataxia due to frataxin deficiency impacting Fe-S assembly)Mitochondrial diseaseMetabolic disorderOther (defective Fe-S cluster assembly leads to global cell dysfunction)
04

Safety considerations

Potential toxicity or widespread cell dysfunction if Fe-S cluster assembly is inhibitedLethality or severe metabolic impairment due to global effects
05

Biomarkers

Frataxin deficiencyDefective ISCU gene or protein levelsDeficiency in Fe-S protein activity (secondary effect)

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