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InterPro: IPR006130 Aspartate/ornithine carbamoyltransferase

Protein matchesHelp
UniProtKB
Matches:
4221 proteins
AccessionHelp IPR006130 Asp/Orn_carbamoylTrfase
SecondaryHelp IPR002029
TypeHelp Family
SignaturesHelp
InterPro RelationshipsHelp
Children IPR002082 Aspartate carbamoyltransferase, eukaryotic
IPR002292 Ornithine carbamoyltransferase
IPR017702 Probable carbamoyltransferase YgeW
Contains IPR006131 Aspartate/ornithine carbamoyltransferase, Asp/Orn-binding domain
IPR006132 Aspartate/ornithine carbamoyltransferase, carbamoyl-P binding
GO Term annotationHelp
Process GO:0006520 cellular amino acid metabolic process
Function GO:0016597 amino acid binding
GO:0016743 carboxyl- or carbamoyltransferase activity
InterPro annotation
BioMart Logo Entry Details in BioMart
AbstractHelp

This family contains two related enzymes:

  1. Aspartate carbamoyltransferase (EC:2.1.3.2) (ATCase) catalyses the conversion of aspartate and carbamoyl phosphate to carbamoylaspartate, the second step in the de novo biosynthesis of pyrimidine nucleotides [1]. In prokaryotes ATCase consists of two subunits: a catalytic chain (gene pyrB) and a regulatory chain (gene pyrI), while in eukaryotes it is a domain in a multi-functional enzyme (called URA2 in yeast, rudimentary in Drosophila, and CAD in mammals [2]) that also catalyses other steps of the biosynthesis of pyrimidines.
  2. Ornithine carbamoyltransferase (EC:2.1.3.3) (OTCase) catalyses the conversion of ornithine and carbamoyl phosphate to citrulline. In mammals this enzyme participates in the urea cycle [3] and is located in the mitochondrial matrix. In prokaryotes and eukaryotic microorganisms it is involved in the biosynthesis of arginine. In some bacterial species it is also involved in the degradation of arginine [4] (the arginine deaminase pathway).

It has been shown [5] that these two enzymes are evolutionary related. The predicted secondary structure of both enzymes are similar and there are some regions of sequence similarities. One of these regions includes three residues which have been shown, by crystallographic studies [6], to be implicated in binding the phosphoryl group of carbamoyl phosphate.

Structural linksHelp
PDB - click here
SCOP: c.78.1.1
CATH: 3.40.50.1370
Database linksHelp
PDBe-motif: PS00097
Enzyme: EC:2.1.3
PROSITE doc: PDOC00091
Blocks: IPB006130

Taxonomic coverageHelp

Overlapping InterPro entriesHelp
IPR006130 Numbers of overlapping proteins Average numbers of overlapping amino acids

Example proteinsHelp
O50039 Ornithine carbamoyltransferase, chloroplastic

P00480 Ornithine carbamoyltransferase, mitochondrial

P05150 Ornithine carbamoyltransferase

P05990 CAD protein

P11725 Ornithine carbamoyltransferase, mitochondrial

More proteins


Example Proteins Key


InterPro entry accession number/name and structure databases Colour code
IPR011702 Glutamine amidotransferase superfamily
IPR002195 Dihydroorotase, conserved site
IPR005479 Carbamoyl phosphate synthetase, large subunit, ATP-binding
IPR011761 ATP-grasp fold
IPR011059 Metal-dependent hydrolase, composite domain
IPR006680 Amidohydrolase 1
IPR000991 Glutamine amidotransferase class-I, C-terminal
IPR002292 Ornithine carbamoyltransferase
IPR005481 Carbamoyl phosphate synthase, large subunit, N-terminal
IPR005480 Carbamoyl phosphate synthetase, large subunit, oligomerisation
IPR013816 ATP-grasp fold, subdomain 2
IPR002082 Aspartate carbamoyltransferase, eukaryotic
IPR013817 Pre-ATP-grasp fold
IPR005483 Carbamoyl phosphate synthase, large subunit
IPR017926 Glutamine amidotransferase type 1
IPR016185 PreATP-grasp-like fold
IPR006130 Aspartate/ornithine carbamoyltransferase
IPR004722 Dihydroorotase multifunctional complex type
IPR002474 Carbamoyl phosphate synthase, small subunit, N-terminal
IPR006132 Aspartate/ornithine carbamoyltransferase, carbamoyl-P binding
IPR006131 Aspartate/ornithine carbamoyltransferase, Asp/Orn-binding domain
IPR011607 MGS-like
IPR006275 Carbamoyl phosphate synthase, large subunit, glutamine-dependent
IPR006274 Carbamoyl phosphate synthase, small subunit
IPR001317 Carbamoyl phosphate synthase, GATase domain
ModBase
SWISS-MODEL
PDB Chain
CATH Domain
SCOP Domain

PublicationsHelp
1. Lerner CG, Switzer RL.
Cloning and structure of the Bacillus subtilis aspartate transcarbamylase gene (pyrB).
J. Biol. Chem. 261 11156-65 1986 [PubMed: 3015959]
http://intl.jbc.org/cgi/reprint/261/24/11156.pdf
2. Davidson JN, Chen KC, Jamison RS, Musmanno LA, Kern CB.
The evolutionary history of the first three enzymes in pyrimidine biosynthesis.
Bioessays 15 157-64 1993 [PubMed: 8098212]
http://dx.doi.org/10.1002/bies.950150303
3. Takiguchi M, Matsubasa T, Amaya Y, Mori M.
Evolutionary aspects of urea cycle enzyme genes.
Bioessays 10 163-6 1989 [PubMed: 2662961]
http://dx.doi.org/10.1002/bies.950100506
4. Baur H, Stalon V, Falmagne P, Luethi E, Haas D.
Primary and quaternary structure of the catabolic ornithine carbamoyltransferase from Pseudomonas aeruginosa. Extensive sequence homology with the anabolic ornithine carbamoyltransferases of Escherichia coli.
Eur. J. Biochem. 166 111-7 1987 [PubMed: 3109911]
http://dx.doi.org/10.1111/j.1432-1033.1987.tb13489.x
5. Houghton JE, Bencini DA, O'Donovan GA, Wild JR.
Protein differentiation: a comparison of aspartate transcarbamoylase and ornithine transcarbamoylase from Escherichia coli K-12.
Proc. Natl. Acad. Sci. U.S.A. 81 4864-8 1984 [PubMed: 6379651]
http://ukpmc.ac.uk/picrender.cgi?tool=EBI&pubmedid=6379651&action=stream&blobtype=pdf
6. Ke HM, Honzatko RB, Lipscomb WN.
Structure of unligated aspartate carbamoyltransferase of Escherichia coli at 2.6-A resolution.
Proc. Natl. Acad. Sci. U.S.A. 81 4037-40 1984 [PubMed: 6377306]
http://ukpmc.ac.uk/articlerender.cgi?tool=EBI&pubmedid=6377306

Additional ReadingHelp
Faure M, Camonis JH, Jacquet M.
Molecular characterization of a Dictyostelium discoideum gene encoding a multifunctional enzyme of the pyrimidine pathway.
Eur. J. Biochem. 179 1989 345-58 [PubMed: 2917570]
http://dx.doi.org/10.1111/j.1432-1033.1989.tb14560.x
De Vos D, Xu Y, Hulpiau P, Vergauwen B, Van Beeumen JJ.
Structural investigation of cold activity and regulation of aspartate carbamoyltransferase from the extreme psychrophilic bacterium Moritella profunda.
J. Mol. Biol. 365 2007 379-95 [PubMed: 17070547]
http://dx.doi.org/10.1016/j.jmb.2006.09.064
Martin PR, Cooperider JW, Mulks MH.
Sequence of the argF gene encoding ornithine transcarbamoylase from Neisseria gonorrhoeae.
Gene 94 1990 139-40 [PubMed: 2121620]
http://dx.doi.org/10.1016/0378-1119(90)90482-7
De Vos D, Xu Y, Aerts T, Van Petegem F, Van Beeumen JJ.
Crystal structure of Sulfolobus acidocaldarius aspartate carbamoyltransferase in complex with its allosteric activator CTP.
Biochem. Biophys. Res. Commun. 372 2008 40-4 [PubMed: 18477471]
http://dx.doi.org/10.1016/j.bbrc.2008.04.173
Stieglitz KA, Xia J, Kantrowitz ER.
The first high pH structure of Escherichia coli aspartate transcarbamoylase.
Proteins 74 2009 318-27 [PubMed: 18618694]
http://dx.doi.org/10.1002/prot.22162
Sankaranarayanan R, Cherney MM, Cherney LT, Garen CR, Moradian F, James MN.
The crystal structures of ornithine carbamoyltransferase from Mycobacterium tuberculosis and its ternary complex with carbamoyl phosphate and L-norvaline reveal the enzyme's catalytic mechanism.
J. Mol. Biol. 375 2008 1052-63 [PubMed: 18062991]
http://dx.doi.org/10.1016/j.jmb.2007.11.025
Cardia JP, Eldo J, Xia J, O'Day EM, Tsuruta H, Gryncel KR, Kantrowitz ER.
Use of L-asparagine and N-phosphonacetyl-L-asparagine to investigate the linkage of catalysis and homotropic cooperativity in E. coli aspartate transcarbomoylase.
Proteins 71 2008 1088-96 [PubMed: 18004787]
http://dx.doi.org/10.1002/prot.21760
Huygen R, Crabeel M, Glansdorff N.
Nucleotide sequence of the ARG3 gene of the yeast Saccharomyces cerevisiae encoding ornithine carbamoyltransferase. Comparison with other carbamoyltransferases.
Eur. J. Biochem. 166 1987 371-7 [PubMed: 3038540]
http://dx.doi.org/10.1111/j.1432-1033.1987.tb13525.x
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InterPro 23.1