Structure
No three-dimensional record for this entry.
- Class
- Organic compound
- Formula
- C14H21N6O8PS
- Mass
- 464.397 g/mol
- Charge
- 0
- InChIKey
- GTCBZVYHMVYZBU-WFMPWKQPSA-N
- SMILES
- Nc1ncnc2c1ncn2[C@@H]1O[C@H](COP(=O)([O-])OC(=O)[C@@H]([NH3+])CCS)[C@@H](O)[C@H]1O
- Look it up
- ChEBIBy InChIKey
Identity from ChEBI. Not evidence.
What it touches on the way
Mechanistic reach
1 entity
1 entities reached.
0 reported hops1 assembled from the scaffold
What the reference databases state
Statements
3 statements
3 statements · 1 reference database · Subject: L-homocysteinyl-AMP · Sources: Rhea
- L-homocysteine is converted to L-homocysteinyl-AMPCompoundRhea RHEA:83879Inferred only
- L-homocysteinyl-AMP is converted to L-homocysteine thiolactoneCompoundRhea RHEA:83883Inferred only
- L-homocysteinyl-AMP is a substrate of MARS1ProteinRhea RHEA:83883Inferred only
Reactions
2 reactions
L-homocysteine+ATP(4-)+hydronL-homocysteinyl-AMP+diphosphate(3-)
Catalysed by MARS1
Reaction pageLeft to rightBalanced
Rhea RHEA:83879CC BY 4.0Reference data
L-homocysteinyl-AMPL-homocysteine thiolactone+AMP+hydron
Catalysed by MARS1
Reaction pageLeft to rightBalanced
Rhea RHEA:83883CC BY 4.0Reference data
Other names
2 names
Resolves to: L-homocysteinyl-AMP
- Also called
- (L-homocysteinyl)adenylateL-homocysteinyl-adenylate