 |
InterPro: IPR015896 Tetrapyrrole biosynthesis, glutamyl-tRNA reductase, C-terminal
Protein matches
|
UniProtKB Matches: 1167 proteins |
|
Accession
|
IPR015896 4pyrrol_synth_GluRdtase_C |
Secondary
|
IPR000343
|
Type
|
Domain |
Signatures
|
|
InterPro Relationships
|
|
Found in
|
IPR000343 Tetrapyrrole biosynthesis, glutamyl-tRNA reductase
|
GO Term annotation
|
|
Process
|
GO:0033014 tetrapyrrole biosynthetic process
GO:0055114 oxidation reduction
|
|
Function
|
GO:0008883 glutamyl-tRNA reductase activity
GO:0050661 NADP or NADPH binding
|
|
InterPro annotation
|
|
Entry Details in BioMart
|
Abstract
|
Tetrapyrroles are large macrocyclic compounds derived from a common biosynthetic pathway [1]. The end-product, uroporphyrinogen III, is used to synthesise a number of important molecules, including vitamin B12, haem, sirohaem, chlorophyll, coenzyme F430 and phytochromobilin [2].
The first stage in tetrapyrrole synthesis is the synthesis of 5-aminoaevulinic acid ALA via two possible routes: (1) condensation of succinyl CoA and glycine (C4 pathway) using ALA synthase (EC:2.3.1.37), or (2) decarboxylation of glutamate (C5 pathway) via three different enzymes, glutamyl-tRNA synthetase (EC:6.1.1.17) to charge a tRNA with glutamate, glutamyl-tRNA reductase (EC:1.2.1.70) to reduce glutamyl-tRNA to glutamate-1-semialdehyde (GSA), and GSA aminotransferase (EC:5.4.3.8) to catalyse a transamination reaction to produce ALA.
The second stage is to convert ALA to uroporphyrinogen III, the first macrocyclic tetrapyrrolic structure in the pathway. This is achieved by the action of three enzymes in one common pathway: porphobilinogen (PBG) synthase (or ALA dehydratase, EC:4.2.1.24) to condense two ALA molecules to generate porphobilinogen; hydroxymethylbilane synthase (or PBG deaminase, EC:2.5.1.61) to polymerise four PBG molecules into preuroporphyrinogen (tetrapyrrole structure); and uroporphyrinogen III synthase (EC:4.2.1.75) to link two pyrrole units together (rings A and D) to yield uroporphyrinogen III.
Uroporphyrinogen III is the first branch point of the pathway. To synthesise cobalamin (vitamin B12), sirohaem, and coenzyme F430, uroporphyrinogen III needs to be converted into precorrin-2 by the action of uroporphyrinogen III methyltransferase (EC:2.1.1.107). To synthesise haem and chlorophyll, uroporphyrinogen III needs to be decarboxylated into coproporphyrinogen III by the action of uroporphyrinogen III decarboxylase (EC:4.1.1.37) [3].
This entry represents the C-terminal domain of glutamyl-tRNA reductase (EC:1.2.1.70), which reduces glutamyl-tRNA to glutamate-1-semialdehyde during the first stage of tetrapyrrole biosynthesis by the C5 pathway [3, 4]. The enzyme requires NADPH as a cofactor.
|
Structural links
|
|
Database links
|
|
Additional Reading
|
|
Kannangara CG, Gough SP, Bruyant P, Hoober JK, Kahn A, von Wettstein D.
tRNA(Glu) as a cofactor in delta-aminolevulinate biosynthesis: steps that regulate chlorophyll synthesis.
Trends Biochem. Sci. 13 1988 139-43
[PubMed: 3075378]
http://dx.doi.org/10.1016/0968-0004(88)90071-0
|
|
Moser J, Schubert WD, Beier V, Bringemeier I, Jahn D, Heinz DW.
V-shaped structure of glutamyl-tRNA reductase, the first enzyme of tRNA-dependent tetrapyrrole biosynthesis.
EMBO J. 20 2001 6583-90
[PubMed: 11726494]
http://dx.doi.org/10.1093/emboj/20.23.6583
|
|
|
InterPro 23.1
|