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InterPro: IPR015896 Tetrapyrrole biosynthesis, glutamyl-tRNA reductase, C-terminal

Protein matchesHelp
UniProtKB
Matches:
1167 proteins
AccessionHelp IPR015896 4pyrrol_synth_GluRdtase_C
SecondaryHelp IPR000343
TypeHelp Domain
SignaturesHelp
InterPro RelationshipsHelp
Found in IPR000343 Tetrapyrrole biosynthesis, glutamyl-tRNA reductase
GO Term annotationHelp
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
BioMart Logo Entry Details in BioMart
AbstractHelp

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 linksHelp
SCOP: a.151.1.1
CATH: 1.10.1200.70
Database linksHelp
Enzyme: EC:1.2.1.70
PANDIT: PF00745

Taxonomic coverageHelp

Overlapping InterPro entriesHelp
IPR015896 Numbers of overlapping proteins Average numbers of overlapping amino acids

Example proteinsHelp
A0AJ06 Glutamyl-tRNA reductase

A2Z928 Glutamyl-tRNA reductase, chloroplastic

P28463 Glutamyl-tRNA reductase

P42804 Glutamyl-tRNA reductase 1, chloroplastic

P48077 Glutamyl-tRNA reductase

More proteins


Example Proteins Key


InterPro entry accession number/name and structure databases Colour code
IPR015896 Tetrapyrrole biosynthesis, glutamyl-tRNA reductase, C-terminal
IPR018214 Tetrapyrrole biosynthesis, glutamyl-tRNA reductase, conserved site
IPR016040 NAD(P)-binding domain
IPR006151 Quinate/shikimate 5-dehydrogenase/glutamyl-tRNA reductase
IPR000343 Tetrapyrrole biosynthesis, glutamyl-tRNA reductase
IPR015895 Tetrapyrrole biosynthesis, glutamyl-tRNA reductase, N-terminal
IPR003462 Ornithine cyclodeaminase/mu-crystallin
SWISS-MODEL
ModBase

PublicationsHelp
1. Schulze JO, Schubert WD, Moser J, Jahn D, Heinz DW.
Evolutionary relationship between initial enzymes of tetrapyrrole biosynthesis.
J. Mol. Biol. 358 1212-20 2006 [PubMed: 16564539]
http://dx.doi.org/10.1016/j.jmb.2006.02.064
2. Tanaka R, Tanaka A.
Tetrapyrrole biosynthesis in higher plants.
58 321-46 2007 [PubMed: 17227226]
http://dx.doi.org/10.1146/annurev.arplant.57.032905.105448
3. Raux E, Schubert HL, Warren MJ.
Biosynthesis of cobalamin (vitamin B12): a bacterial conundrum.
Cell. Mol. Life Sci. 57 1880-93 2000 [PubMed: 11215515]
http://dx.doi.org/10.1007/PL00000670
4. Jahn D, Verkamp E, Soll D.
Glutamyl-transfer RNA: a precursor of heme and chlorophyll biosynthesis.
Trends Biochem. Sci. 17 215-8 1992 [PubMed: 1502723]
http://dx.doi.org/10.1016/0968-0004(92)90380-R

Additional ReadingHelp
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
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InterPro 23.1