309 related articles for article (PubMed ID: 14570477)
1. Design of amino acid sulfonamides as transition-state analogue inhibitors of arginase.
Cama E; Shin H; Christianson DW
J Am Chem Soc; 2003 Oct; 125(43):13052-7. PubMed ID: 14570477
[TBL] [Abstract][Full Text] [Related]
2. Design of amino acid aldehydes as transition-state analogue inhibitors of arginase.
Shin H; Cama E; Christianson DW
J Am Chem Soc; 2004 Aug; 126(33):10278-84. PubMed ID: 15315440
[TBL] [Abstract][Full Text] [Related]
3. Arginase-boronic acid complex highlights a physiological role in erectile function.
Cox JD; Kim NN; Traish AM; Christianson DW
Nat Struct Biol; 1999 Nov; 6(11):1043-7. PubMed ID: 10542097
[TBL] [Abstract][Full Text] [Related]
4. Inhibitor coordination interactions in the binuclear manganese cluster of arginase.
Cama E; Pethe S; Boucher JL; Han S; Emig FA; Ash DE; Viola RE; Mansuy D; Christianson DW
Biochemistry; 2004 Jul; 43(28):8987-99. PubMed ID: 15248756
[TBL] [Abstract][Full Text] [Related]
5. Arginase: structure, mechanism, and physiological role in male and female sexual arousal.
Christianson DW
Acc Chem Res; 2005 Mar; 38(3):191-201. PubMed ID: 15766238
[TBL] [Abstract][Full Text] [Related]
6. Synthesis and evaluation of new omega-borono-alpha-amino acids as rat liver arginase inhibitors.
Busnel O; Carreaux F; Carboni B; Pethe S; Goff SV; Mansuy D; Boucher JL
Bioorg Med Chem; 2005 Apr; 13(7):2373-9. PubMed ID: 15755639
[TBL] [Abstract][Full Text] [Related]
7. Probing erectile function: S-(2-boronoethyl)-L-cysteine binds to arginase as a transition state analogue and enhances smooth muscle relaxation in human penile corpus cavernosum.
Kim NN; Cox JD; Baggio RF; Emig FA; Mistry SK; Harper SL; Speicher DW; Morris SM; Ash DE; Traish A; Christianson DW
Biochemistry; 2001 Mar; 40(9):2678-88. PubMed ID: 11258879
[TBL] [Abstract][Full Text] [Related]
8. Molecular modeling of Helicobacter pylori arginase and the inhibitor coordination interactions.
Azizian H; Bahrami H; Pasalar P; Amanlou M
J Mol Graph Model; 2010 Apr; 28(7):626-35. PubMed ID: 20080052
[TBL] [Abstract][Full Text] [Related]
9. Synthesis of quaternary α-amino acid-based arginase inhibitors via the Ugi reaction.
Golebiowski A; Whitehouse D; Beckett RP; Van Zandt M; Ji MK; Ryder TR; Jagdmann E; Andreoli M; Lee Y; Sheeler R; Conway B; Olczak J; Mazur M; Czestkowski W; Piotrowska W; Cousido-Siah A; Ruiz FX; Mitschler A; Podjarny A; Schroeter H
Bioorg Med Chem Lett; 2013 Sep; 23(17):4837-41. PubMed ID: 23886684
[TBL] [Abstract][Full Text] [Related]
10. L-arginine binding to liver arginase requires proton transfer to gateway residue His141 and coordination of the guanidinium group to the dimanganese(II,II) center.
Khangulov SV; Sossong TM; Ash DE; Dismukes GC
Biochemistry; 1998 Jun; 37(23):8539-50. PubMed ID: 9622506
[TBL] [Abstract][Full Text] [Related]
11. Carbonic anhydrase inhibitors: the X-ray crystal structure of the adduct of N-hydroxysulfamide with isozyme II explains why this new zinc binding function is effective in the design of potent inhibitors.
Temperini C; Winum JY; Montero JL; Scozzafava A; Supuran CT
Bioorg Med Chem Lett; 2007 May; 17(10):2795-801. PubMed ID: 17346964
[TBL] [Abstract][Full Text] [Related]
12. T-state inhibitors of E. coli aspartate transcarbamoylase that prevent the allosteric transition.
Heng S; Stieglitz KA; Eldo J; Xia J; Cardia JP; Kantrowitz ER
Biochemistry; 2006 Aug; 45(33):10062-71. PubMed ID: 16906764
[TBL] [Abstract][Full Text] [Related]
13. Binding of α,α-disubstituted amino acids to arginase suggests new avenues for inhibitor design.
Ilies M; Di Costanzo L; Dowling DP; Thorn KJ; Christianson DW
J Med Chem; 2011 Aug; 54(15):5432-43. PubMed ID: 21728378
[TBL] [Abstract][Full Text] [Related]
14. Carbonic anhydrase inhibitors: X-ray crystallographic studies for the binding of 5-amino-1,3,4-thiadiazole-2-sulfonamide and 5-(4-amino-3-chloro-5-fluorophenylsulfonamido)-1,3,4-thiadiazole-2-sulfonamide to human isoform II.
Menchise V; De Simone G; Di Fiore A; Scozzafava A; Supuran CT
Bioorg Med Chem Lett; 2006 Dec; 16(24):6204-8. PubMed ID: 17000110
[TBL] [Abstract][Full Text] [Related]
15. Mechanistic and metabolic inferences from the binding of substrate analogues and products to arginase.
Cox JD; Cama E; Colleluori DM; Pethe S; Boucher JL; Mansuy D; Ash DE; Christianson DW
Biochemistry; 2001 Mar; 40(9):2689-701. PubMed ID: 11258880
[TBL] [Abstract][Full Text] [Related]
16. Carbonic anhydrase inhibitors: Valdecoxib binds to a different active site region of the human isoform II as compared to the structurally related cyclooxygenase II "selective" inhibitor celecoxib.
Di Fiore A; Pedone C; D'Ambrosio K; Scozzafava A; De Simone G; Supuran CT
Bioorg Med Chem Lett; 2006 Jan; 16(2):437-42. PubMed ID: 16290146
[TBL] [Abstract][Full Text] [Related]
17. 2-aminoimidazole amino acids as inhibitors of the binuclear manganese metalloenzyme human arginase I.
Ilies M; Di Costanzo L; North ML; Scott JA; Christianson DW
J Med Chem; 2010 May; 53(10):4266-76. PubMed ID: 20441173
[TBL] [Abstract][Full Text] [Related]
18. Synthesis of a new trifluoromethylketone analogue of l-arginine and contrasting inhibitory activity against human arginase I and histone deacetylase 8.
Ilies M; Dowling DP; Lombardi PM; Christianson DW
Bioorg Med Chem Lett; 2011 Oct; 21(19):5854-8. PubMed ID: 21875805
[TBL] [Abstract][Full Text] [Related]
19. Crystal structures of Leishmania mexicana arginase complexed with α,α-disubstituted boronic amino-acid inhibitors.
Hai Y; Christianson DW
Acta Crystallogr F Struct Biol Commun; 2016 Apr; 72(Pt 4):300-6. PubMed ID: 27050264
[TBL] [Abstract][Full Text] [Related]
20. Human arginase II: crystal structure and physiological role in male and female sexual arousal.
Cama E; Colleluori DM; Emig FA; Shin H; Kim SW; Kim NN; Traish AM; Ash DE; Christianson DW
Biochemistry; 2003 Jul; 42(28):8445-51. PubMed ID: 12859189
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
