165 related articles for article (PubMed ID: 1359877)
41. Nucleotide ligands protect the inter-domain regions of the multifunctional polypeptide CAD against limited proteolysis, and also stabilize the thermolabile part-reactions of the carbamoyl-phosphate synthase II domains within the CAD polypeptide.
Carrey EA
Biochem J; 1986 Jun; 236(2):327-35. PubMed ID: 3638965
[TBL] [Abstract][Full Text] [Related]
42. In vitro phosphorylation of a synthetic collagen peptide by cyclic AMP-dependent protein kinase.
Glass DB; May JM
Coll Relat Res; 1984 Jan; 4(1):63-74. PubMed ID: 6327183
[TBL] [Abstract][Full Text] [Related]
43. Multi-enzyme complex of glutamine-dependent carbamoyl-phosphate synthetase with aspartate carbamoyltransferase and dihydroorotase from rat ascites-hepatoma cells. Purification, molecular properties and limited proteolysis.
Mori M; Tatibana M
Eur J Biochem; 1978 May; 86(2):381-8. PubMed ID: 26565
[No Abstract] [Full Text] [Related]
44. Dihydroorotase from the hyperthermophile Aquifex aeolicus is activated by stoichiometric association with aspartate transcarbamoylase and forms a one-pot reactor for pyrimidine biosynthesis.
Zhang P; Martin PD; Purcarea C; Vaishnav A; Brunzelle JS; Fernando R; Guy-Evans HI; Evans DR; Edwards BF
Biochemistry; 2009 Feb; 48(4):766-78. PubMed ID: 19128030
[TBL] [Abstract][Full Text] [Related]
45. Getting CAD in shape: the atomic structure of human dihydroorotase domain.
Hermoso JA
Structure; 2014 Feb; 22(2):179-81. PubMed ID: 24507779
[TBL] [Abstract][Full Text] [Related]
46. Protein kinase substrate recognition studied using the recombinant catalytic domain of AMP-activated protein kinase and a model substrate.
Scott JW; Norman DG; Hawley SA; Kontogiannis L; Hardie DG
J Mol Biol; 2002 Mar; 317(2):309-23. PubMed ID: 11902845
[TBL] [Abstract][Full Text] [Related]
47. Creation of a putative third metal binding site in type II dihydroorotases significantly enhances enzyme activity.
Huang YH; Huang CY
Protein Pept Lett; 2015; 22(12):1117-22. PubMed ID: 26446564
[TBL] [Abstract][Full Text] [Related]
48. Localization of the multifunctional protein CAD in astrocytes of rodent brain.
Cammer W; Downing M
J Histochem Cytochem; 1991 May; 39(5):695-700. PubMed ID: 1673139
[TBL] [Abstract][Full Text] [Related]
49. The use of synthetic peptides for defining the specificity of tyrosine protein kinases.
Casnellie JE; Krebs EG
Adv Enzyme Regul; 1984; 22():501-15. PubMed ID: 6540972
[TBL] [Abstract][Full Text] [Related]
50. 3-Hydroxy-3-methylglutaryl-coenzyme A reductase kinase and sucrose-phosphate synthase kinase activities in cauliflower florets: Ca2+ dependence and substrate specificities.
Toroser D; Huber SC
Arch Biochem Biophys; 1998 Jul; 355(2):291-300. PubMed ID: 9675040
[TBL] [Abstract][Full Text] [Related]
51. Estrogen receptor/Sp1 complexes are required for induction of cad gene expression by 17beta-estradiol in breast cancer cells.
Khan S; Abdelrahim M; Samudio I; Safe S
Endocrinology; 2003 Jun; 144(6):2325-35. PubMed ID: 12746293
[TBL] [Abstract][Full Text] [Related]
52. Quantitative phosphoproteomics reveal mTORC1 activates de novo pyrimidine synthesis.
Robitaille AM; Christen S; Shimobayashi M; Cornu M; Fava LL; Moes S; Prescianotto-Baschong C; Sauer U; Jenoe P; Hall MN
Science; 2013 Mar; 339(6125):1320-3. PubMed ID: 23429704
[TBL] [Abstract][Full Text] [Related]
53. Comparison of substrate specificity of myosin kinase and cyclic AMP-dependent protein kinase.
Pearson RB; Forrest S; Davis M; Martin TJ; Kemp BE
Biochim Biophys Acta; 1984 May; 786(3):261-6. PubMed ID: 6547060
[TBL] [Abstract][Full Text] [Related]
54. Appearance of CAD activity, the rate-limiting enzyme for pyrimidine biosynthesis, as B cells progress into and through the G1 stage of the cell cycle.
Morford G; Davidson JN; Snow EC
Cell Immunol; 1994 Oct; 158(1):96-104. PubMed ID: 7916269
[TBL] [Abstract][Full Text] [Related]
55. A novel splicing regulator shares a nuclear import pathway with SR proteins.
Lai MC; Kuo HW; Chang WC; Tarn WY
EMBO J; 2003 Mar; 22(6):1359-69. PubMed ID: 12628928
[TBL] [Abstract][Full Text] [Related]
56. Identification of elements critical for phosphorylation of 3-hydroxy-3-methylglutaryl coenzyme A reductase by adenosine monophosphate-activated protein kinase: protein engineering of the naturally nonphosphorylatable 3-hydroxy-3-methylglutaryl coenzyme A reductase from Pseudomonas mevalonii.
Friesen JA; Rodwell VW
Biochemistry; 1997 Feb; 36(5):1157-62. PubMed ID: 9033407
[TBL] [Abstract][Full Text] [Related]
57. Deciphering CAD: Structure and function of a mega-enzymatic pyrimidine factory in health and disease.
Del Caño-Ochoa F; Ramón-Maiques S
Protein Sci; 2021 Oct; 30(10):1995-2008. PubMed ID: 34288185
[TBL] [Abstract][Full Text] [Related]
58. The aspartate transcarbamoylase-dihydroorotase complex in Deinococcus radiophilus has an active dihydroorotase.
McPhail D; Shepherdson M
Arch Microbiol; 2006 Mar; 185(1):78-81. PubMed ID: 16395552
[TBL] [Abstract][Full Text] [Related]
59. N- and C-termini modulate the effects of pH and phosphorylation on hepatic 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase.
Kurland IJ; Chapman B; El-Maghrabi MR
Biochem J; 2000 Apr; 347(Pt 2):459-67. PubMed ID: 10749675
[TBL] [Abstract][Full Text] [Related]
60. cAMP-dependent protein kinase, but not the cGMP-dependent enzyme, rapidly phosphorylates delta-CREB, and a synthetic delta-CREB peptide.
Colbran JL; Roach PJ; Fiol CJ; Dixon JE; Andrisani OM; Corbin JD
Biochem Cell Biol; 1992; 70(10-11):1277-82. PubMed ID: 1338414
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
