Compound

N-(4-oxoglutaryl)-L-cysteinylglycine

A peptide anion obtained by deprotonation of the carboxy groups of N-(4-oxoglutaryl)-L-cysteinylglycine; major species at pH 7.3.

Definition from ChEBI (CHEBI:138256), read 2026-09-23. CC BY 4.0.

CHEBI:138256ChEBI

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Structure

2D depiction · 3D model shown

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A generated conformer of N-(4-oxoglutaryl)-L-cysteinylglycine — one low-energy arrangement PubChem computed, not a measured structure. Hydrogens are not drawn; the formula counts them.

Class: Organic compound, anion
Formula: C10H12N2O7S
Mass: 304.28 g/mol
Charge: -2
InChIKey: PMIVQUCENWNWHX-YFKPBYRVSA-L
SMILES: O=C([O-])CNC(=O)[C@H](CS)NC(=O)CCC(=O)C(=O)[O-]
Look it up: ChEBI PubChem By InChIKey

Identity from ChEBI, geometry from PubChem. Not evidence.

What it touches on the way

Mechanistic reach

1 entity

1 entities reached.

0 reported hops1 assembled from the scaffold

NIT1ProteinUNIPROT:Q86X76substrate ofInferred only3 paths3 endpoints

What the reference databases state

Statements

3 statements

3 statements · 1 reference database · Subject: N-(4-oxoglutaryl)-L-cysteinylglycine · Sources: Rhea

Order

N-(4-oxoglutaryl)-L-cysteinylglycine is converted to L-cysteinylglycineCompoundRhea RHEA:54532Inferred only
L-cysteinylglycine is converted to N-(4-oxoglutaryl)-L-cysteinylglycineCompoundRhea RHEA:54532Inferred only
N-(4-oxoglutaryl)-L-cysteinylglycine is a substrate of NIT1ProteinRhea RHEA:54532Inferred only

Reactions

1 reaction

N-(4-oxoglutaryl)-L-cysteinylglycine+waterL-cysteinylglycine+2-oxoglutarate(2-)
Catalysed by NIT1
Reaction pageDirection not assertedBalanced
Rhea RHEA:54532CC BY 4.0Reference data

Other names

1 name

Resolves to: N-(4-oxoglutaryl)-L-cysteinylglycine

Systematic name: 5-({(2R)-1-[(carboxylatomethyl)amino]-1-oxo-3-sulfanylpropan-2-yl}amino)-2,5-dioxopentanoate