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InterPro: IPR006130 Aspartate/ornithine carbamoyltransferase
Example proteins
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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 |
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| IPR002195 |
Dihydroorotase, conserved site |
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| IPR005479 |
Carbamoyl phosphate synthetase, large subunit, ATP-binding |
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| IPR011761 |
ATP-grasp fold |
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| IPR011059 |
Metal-dependent hydrolase, composite domain |
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| IPR006680 |
Amidohydrolase 1 |
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| IPR000991 |
Glutamine amidotransferase class-I, C-terminal |
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| IPR002292 |
Ornithine carbamoyltransferase |
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| IPR005481 |
Carbamoyl phosphate synthase, large subunit, N-terminal |
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| IPR005480 |
Carbamoyl phosphate synthetase, large subunit, oligomerisation |
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| IPR013816 |
ATP-grasp fold, subdomain 2 |
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| IPR002082 |
Aspartate carbamoyltransferase, eukaryotic |
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| IPR013817 |
Pre-ATP-grasp fold |
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| IPR005483 |
Carbamoyl phosphate synthase, large subunit |
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| IPR017926 |
Glutamine amidotransferase type 1 |
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| IPR016185 |
PreATP-grasp-like fold |
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| IPR006130 |
Aspartate/ornithine carbamoyltransferase |
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| IPR004722 |
Dihydroorotase multifunctional complex type |
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| IPR002474 |
Carbamoyl phosphate synthase, small subunit, N-terminal |
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| IPR006132 |
Aspartate/ornithine carbamoyltransferase, carbamoyl-P binding |
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| IPR006131 |
Aspartate/ornithine carbamoyltransferase, Asp/Orn-binding domain |
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| IPR011607 |
MGS-like |
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| IPR006275 |
Carbamoyl phosphate synthase, large subunit, glutamine-dependent |
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| IPR006274 |
Carbamoyl phosphate synthase, small subunit |
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| IPR001317 |
Carbamoyl phosphate synthase, GATase domain |
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ModBase |
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SWISS-MODEL |
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PDB Chain |
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CATH Domain |
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SCOP Domain |
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Publications
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1.
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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
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2.
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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
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3.
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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
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4.
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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
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5.
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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
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6.
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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
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Additional Reading
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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
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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
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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
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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
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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
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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
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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
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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
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