Target intelligence / Profile preview

iron-containing enzyme

Molecular classification
Enzyme, Metalloprotein, Oxidoreductase (main subclass), Oxygenase (heme/non-heme subclasses), Transferase, Lyase, Isomerase, etc. (dependent on specific enzyme), Iron–sulfur protein (subset), Heme protein (subset)
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Overview

Iron-containing enzymes are a heterogeneous group of metalloenzymes characterized by the presence of iron in their active sites, typically as mononuclear or dinuclear iron ions, within heme groups or iron–sulfur clusters. They play crucial roles in biologically essential processes including oxygen binding and activation, electron transport, cellular respiration, detoxification, biosynthesis, DNA replication, and immune defense. The most prominent families include heme enzymes (such as cytochrome P450, catalases, peroxidases), iron–sulfur cluster proteins (involved in electron transport and metabolic regulation), and non-heme iron enzymes (such as monooxygenases, dioxygenases). Iron-containing enzymes are prevalent therapeutic targets, especially in drug metabolism (via cytochrome P450), anti-infective development, cancer therapy, and management of iron-related disorders. Due to their central metabolic and regulatory roles, safety concerns arise with iron homeostasis disruption, potential generation of toxic ROS, and wide impact across cell physiology. Because "various iron-containing enzymes" is not a specific target but a structural class, more precise identification is required for clinical or research applications.

Other names
iron enzymemetalloenzyme (with iron)iron–sulfur protein (subset)heme enzyme (subset)non-heme iron enzyme (subset)
02

Mechanism of action

Generalized mechanisms include enzyme inhibition (competitive and non-competitive), disruption of iron binding or removal of iron cofactor (chelation), alteration of redox state (blocking oxidation or reduction), and antagonism of downstream metabolic effects.

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Biological functions

Oxygen transport (e.g. hemoglobin, myoglobin)Electron transfer (e.g. cytochromes, iron–sulfur cluster proteins)Oxidative metabolism and biosynthesis (cytochrome P450, catalase, peroxidases)DNA synthesis and repair (ribonucleotide reductase)Detoxification (catalase, peroxidase)Cellular metabolism (e.g. amino acid oxidases, fatty acid desaturases)Immune response and inflammation (myeloperoxidase, nitric oxide synthase, indoleamine 2,3-dioxygenase)Cell growth and proliferation (via metabolic control)
04

Disease associations

Cancer (altered iron enzyme activity or ROS generation)Infection (immune defense, microbial iron metabolism)Neurodegenerative diseases (oxidative stress, iron dysregulation)Cardiovascular disease (oxidative metabolism, ROS, iron overload)Inflammation (immune cell iron handling, ROS balance)Other (anemia, iron overload disorders, rare enzyme deficiencies)
05

Safety considerations

Off-target oxidative stress due to ROS (reactive oxygen species) generation or disruptionTissue iron overload (toxicity, organ damage)Drug–drug interactions (especially with cytochrome P450 enzyme system)Narrow therapeutic index for iron chelator or enzyme inhibitorsAnemia or deficiency if enzymes required for iron homeostasis are disrupted
06

Interacting drugs

Azole antifungals (inhibit cytochrome P450 enzymes)

5 more in the full profile.

07

Biomarkers

Serum ferritinTransferrin saturationTotal iron binding capacityHeme enzyme activity (e.g. cytochrome P450 activity in drug metabolism)Iron–sulfur protein levels (in rare metabolic panels)

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