-
2
-
-
17144404555
-
Dipeptidyl peptidase IV and related enzymes in cell biology and liver disorders
-
Gorrell MD. Dipeptidyl peptidase IV and related enzymes in cell biology and liver disorders. Clin Sci 2005;108:277-292.
-
(2005)
Clin Sci
, vol.108
, pp. 277-292
-
-
Gorrell, M.D.1
-
3
-
-
17144374877
-
Glucagon-like peptide 1 receptor agonists and dipeptidyl peptidase IV inhibitors: New therapeutic agents for the treatment of type 2 diabetes
-
Sinclair EM, Drucker DJ. Glucagon-like peptide 1 receptor agonists and dipeptidyl peptidase IV inhibitors: new therapeutic agents for the treatment of type 2 diabetes. Curr Opin Endocrinol Diabetes 2005;12:146-151.
-
(2005)
Curr Opin Endocrinol Diabetes
, vol.12
, pp. 146-151
-
-
Sinclair, E.M.1
Drucker, D.J.2
-
4
-
-
0347367026
-
Structural requirements for catalysis, expression, and dimerization in the CD26/DPIV gene family
-
Ajami K, Abbott CA, Obradovic M, Gysbers V, Kahne T, McCaughan GW, Gorrell MD. Structural requirements for catalysis, expression, and dimerization in the CD26/DPIV gene family. Biochemistry 2003;42:694-701.
-
(2003)
Biochemistry
, vol.42
, pp. 694-701
-
-
Ajami, K.1
Abbott, C.A.2
Obradovic, M.3
Gysbers, V.4
Kahne, T.5
McCaughan, G.W.6
Gorrell, M.D.7
-
5
-
-
0000038304
-
Binding to human dipeptidyl peptidase IV by adenosine deaminase and antibodies that inhibit ligand binding involves overlapping, discontinuous sites on a predicted beta propeller domain
-
Abbott CA, McCaughan GW, Levy MT, Church WB, Gorrell MD. Binding to human dipeptidyl peptidase IV by adenosine deaminase and antibodies that inhibit ligand binding involves overlapping, discontinuous sites on a predicted beta propeller domain. Eur J Biochem 1999;266:798-810.
-
(1999)
Eur J Biochem
, vol.266
, pp. 798-810
-
-
Abbott, C.A.1
McCaughan, G.W.2
Levy, M.T.3
Church, W.B.4
Gorrell, M.D.5
-
6
-
-
0043073112
-
Prolyl peptidases: A serine protease subfamily with high potential for drug discovery
-
Rosenblum JS, Kozarich JW. Prolyl peptidases: a serine protease subfamily with high potential for drug discovery. Curr Opin Chem Biol 2003;7:496-504.
-
(2003)
Curr Opin Chem Biol
, vol.7
, pp. 496-504
-
-
Rosenblum, J.S.1
Kozarich, J.W.2
-
7
-
-
0037219684
-
Crystal structure of human dipeptidyl peptidase IV/CD26 in complex with a substrate analog
-
Rasmussen HB, Branner S, Wiberg FC, Wagtmann N. Crystal structure of human dipeptidyl peptidase IV/CD26 in complex with a substrate analog. Nat Struct Biol 2003;10:19-25.
-
(2003)
Nat Struct Biol
, vol.10
, pp. 19-25
-
-
Rasmussen, H.B.1
Branner, S.2
Wiberg, F.C.3
Wagtmann, N.4
-
8
-
-
21244503095
-
Structural and kinetic analysis of the substrate specificity of human fibroblast activation protein alpha
-
Aertgeerts K, Levin I, Shi L, Snell GP, Jennings A, Prasad GS, Zhang Y, Kraus ML, Salakian S, Sridhar V, Wijnands R, Tennant MG. Structural and kinetic analysis of the substrate specificity of human fibroblast activation protein alpha. J Biol Chem 2005; 280:19441-19444.
-
(2005)
J Biol Chem
, vol.280
, pp. 19441-19444
-
-
Aertgeerts, K.1
Levin, I.2
Shi, L.3
Snell, G.P.4
Jennings, A.5
Prasad, G.S.6
Zhang, Y.7
Kraus, M.L.8
Salakian, S.9
Sridhar, V.10
Wijnands, R.11
Tennant, M.G.12
-
9
-
-
5144227957
-
Structure of a human A-type potassium channel interacting protein DPPX, a member of the dipeptidyl aminopeptidase family
-
Strop P, Bankovich AJ, Hansen KC, Garcia KC, Brunger AT. Structure of a human A-type potassium channel interacting protein DPPX, a member of the dipeptidyl aminopeptidase family. J Mol Biol 2004;343:1055-1065.
-
(2004)
J Mol Biol
, vol.343
, pp. 1055-1065
-
-
Strop, P.1
Bankovich, A.J.2
Hansen, K.C.3
Garcia, K.C.4
Brunger, A.T.5
-
10
-
-
0032563162
-
Prolyl oligopeptidase: An unusual beta-propeller domain regulates proteolysis
-
Fulop V, Bocskei Z, Polgar L. Prolyl oligopeptidase: an unusual beta-propeller domain regulates proteolysis. Cell 1998;94:161-170.
-
(1998)
Cell
, vol.94
, pp. 161-170
-
-
Fulop, V.1
Bocskei, Z.2
Polgar, L.3
-
11
-
-
27744590673
-
Inhibitors of proline-specific dipeptidyl peptidases: DPP-IV inhibitors as a novel approach for the treatment of Type 2 diabetes
-
Augustyns K, Van der Veken P, Haemers A. Inhibitors of proline-specific dipeptidyl peptidases: DPP-IV inhibitors as a novel approach for the treatment of Type 2 diabetes. Expert Opin Ther Patents 2005;15:1387-1407.
-
(2005)
Expert Opin Ther Patents
, vol.15
, pp. 1387-1407
-
-
Augustyns, K.1
Van Der Veken, P.2
Haemers, A.3
-
12
-
-
2642519637
-
Treatment of type 2 diabetes mellitus with agonists of the GLP-1 receptor or DPP-IV inhibitors
-
Holst JJ. Treatment of type 2 diabetes mellitus with agonists of the GLP-1 receptor or DPP-IV inhibitors. Expert Opin Emerg Drugs 2004;9:155-166.
-
(2004)
Expert Opin Emerg Drugs
, vol.9
, pp. 155-166
-
-
Holst, J.J.1
-
13
-
-
3843072211
-
Dipeptidyl peptidase IV inhibitors for the treatment of diabetes
-
Weber AE. Dipeptidyl peptidase IV inhibitors for the treatment of diabetes. J Med Chem 2004;47:4135-4141.
-
(2004)
J Med Chem
, vol.47
, pp. 4135-4141
-
-
Weber, A.E.1
-
14
-
-
27744540889
-
Improved glycaemic control with dipeptidyl peptidase-4 inhibition in patients with type 2 diabetes: Vildagliptin (LAF237) dose response
-
Ristic S, Byiers S, Foley J, Holmes D. Improved glycaemic control with dipeptidyl peptidase-4 inhibition in patients with type 2 diabetes: vildagliptin (LAF237) dose response. Diabetes Obes Metab 2005;7:692-698.
-
(2005)
Diabetes Obes Metab
, vol.7
, pp. 692-698
-
-
Ristic, S.1
Byiers, S.2
Foley, J.3
Holmes, D.4
-
15
-
-
0037777695
-
1-[[(3-hydroxy-1-adamantyl)amino]acetyl]-2-cyano-(S)-pyrrolidine: A potent, selective, and orally bioavailable dipeptidyl peptidase IV inhibitor with antihyperglycemic properties
-
Villhauer EB, Brinkman JA, Naderi GB, Burkey BF, Dunning BE, Prasad K, Mangold BL, Russell ME, Hughes TE. 1-[[(3-hydroxy-1-adamantyl)amino]acetyl]-2- cyano-(S)-pyrrolidine: a potent, selective, and orally bioavailable dipeptidyl peptidase IV inhibitor with antihyperglycemic properties. J Med Chem 2003;46:2774-2789.
-
(2003)
J Med Chem
, vol.46
, pp. 2774-2789
-
-
Villhauer, E.B.1
Brinkman, J.A.2
Naderi, G.B.3
Burkey, B.F.4
Dunning, B.E.5
Prasad, K.6
Mangold, B.L.7
Russell, M.E.8
Hughes, T.E.9
-
16
-
-
0037030602
-
1-[2-[(5-Cyanopyridin-2-yl)amino]ethylamino]acetyl-2-(S) -pyrrolidinecarbon itrile: A potent, selective, and orally bioavailable dipeptidyl peptidase IV inhibitor with antihyperglycemic properties
-
Villhauer EB, Brinkman JA, Naderi GB, Dunning BE, Mangold BL, Mone MD, Russell ME, Weldon SC, Hughes TE. 1-[2-[(5-Cyanopyridin-2-yl)amino]ethylamino] acetyl-2-(S)-pyrrolidinecarbon itrile: a potent, selective, and orally bioavailable dipeptidyl peptidase IV inhibitor with antihyperglycemic properties. J Med Chem 2002;45:2362-2365.
-
(2002)
J Med Chem
, vol.45
, pp. 2362-2365
-
-
Villhauer, E.B.1
Brinkman, J.A.2
Naderi, G.B.3
Dunning, B.E.4
Mangold, B.L.5
Mone, M.D.6
Russell, M.E.7
Weldon, S.C.8
Hughes, T.E.9
-
17
-
-
0038793576
-
High-resolution structure of human apo dipeptidyl peptidase IV/ CD26 and its complex with 1-[([2-[(5-iodopyridin-2-yl)amino]-ethyl]amino)-acetyl]-2- cyano-(S)-pyrrol idine
-
Oefner C, D'Arcy A, Mac SA, Pierau S, Gardiner R, Dale GE. High-resolution structure of human apo dipeptidyl peptidase IV/ CD26 and its complex with 1-[([2-[(5-iodopyridin-2-yl)amino]-ethyl]amino)-acetyl]-2-cyano-(S) -pyrrol idine. Acta Crystallogr D Biol Crystallogr 2003;59:1206-1212.
-
(2003)
Acta Crystallogr D Biol Crystallogr
, vol.59
, pp. 1206-1212
-
-
Oefner, C.1
D'Arcy, A.2
Mac, S.A.3
Pierau, S.4
Gardiner, R.5
Dale, G.E.6
-
18
-
-
19944427998
-
(2R)-4-oxo-4-[3-(trifluoromethyl)-5,6-dihydro[1,2,4]triazolo[4,3-a] pyrazin-7(8H)-yl]-1-(2,4,5-trifluoropnenyl)butan-2-amine: A potent, orally active dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes
-
Kim D, Wang L, Beconi M, Eiermann GJ, Fisher MH, He H, Hickey GJ, Kowalchick JE, Leiting B, Lyons K, Marsilio F, McCann ME, Patel RA, Petrov A, Scapin G, Patel SB, Roy RS, Wu JK, Wyvratt MJ, Zhang BB, Zhu L, Thornberry NA, Weber AE. (2R)-4-oxo-4-[3-(trifluoromethyl)-5,6-dihydro[1,2,4]triazolo[4,3-a] pyrazin-7(8H)-yl]-1-(2,4,5-trifluoropnenyl)butan-2-amine: a potent, orally active dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes. J Med Chem 2005;48:141-151.
-
(2005)
J Med Chem
, vol.48
, pp. 141-151
-
-
Kim, D.1
Wang, L.2
Beconi, M.3
Eiermann, G.J.4
Fisher, M.H.5
He, H.6
Hickey, G.J.7
Kowalchick, J.E.8
Leiting, B.9
Lyons, K.10
Marsilio, F.11
McCann, M.E.12
Patel, R.A.13
Petrov, A.14
Scapin, G.15
Patel, S.B.16
Roy, R.S.17
Wu, J.K.18
Wyvratt, M.J.19
Zhang, B.B.20
Zhu, L.21
Thornberry, N.A.22
Weber, A.E.23
more..
-
19
-
-
25844459084
-
Dipeptidyl peptidase IV inhibition for the treatment of type 2 diabetes: Potential importance of selectivity over dipeptidyl peptidases 8 and 9
-
Lankas GR, Leiting B, Roy RS, Eiermann GJ, Beconi MG, Biftu T, Chan CC, Edmondson S, Feeney WP, He H, Ippolito DE, Kim D, Lyons KA, Ok HO, Patel RA, Petrov AN, Pryor KA, Qian X, Reigle L, Woods A, Wu JK, Zaller D, Zhang X, Zhu L, Weber AE, Thornberry NA. Dipeptidyl peptidase IV inhibition for the treatment of type 2 diabetes: potential importance of selectivity over dipeptidyl peptidases 8 and 9. Diabetes 2005;54:2988-2994.
-
(2005)
Diabetes
, vol.54
, pp. 2988-2994
-
-
Lankas, G.R.1
Leiting, B.2
Roy, R.S.3
Eiermann, G.J.4
Beconi, M.G.5
Biftu, T.6
Chan, C.C.7
Edmondson, S.8
Feeney, W.P.9
He, H.10
Ippolito, D.E.11
Kim, D.12
Lyons, K.A.13
Ok, H.O.14
Patel, R.A.15
Petrov, A.N.16
Pryor, K.A.17
Qian, X.18
Reigle, L.19
Woods, A.20
Wu, J.K.21
Zaller, D.22
Zhang, X.23
Zhu, L.24
Weber, A.E.25
Thornberry, N.A.26
more..
-
20
-
-
4544227213
-
Inhibition of DPP8/9; Results in toxicity in preclinical species: Potential importance of selective dipeptidyl peptidase IV inhibition for treatment of type 2 DM
-
Orlando, FL, June 4-8, (Abstract 7-OR)
-
Lankas GR, Leiting B, Sinha RS, Eiermann GJ, Biftu T, Kim D, Ok H, Weber AE, Thornberry NA. Inhibition of DPP8/9; Results in toxicity in preclinical species: potential importance of selective dipeptidyl peptidase IV inhibition for treatment of type 2 DM, Presented at the American Diabetes Association 64th Scientific Session, Orlando, FL, June 4-8, 2004 (Abstract 7-OR).
-
(2004)
American Diabetes Association 64th Scientific Session
-
-
Lankas, G.R.1
Leiting, B.2
Sinha, R.S.3
Eiermann, G.J.4
Biftu, T.5
Kim, D.6
Ok, H.7
Weber, A.E.8
Thornberry, N.A.9
-
21
-
-
12844260161
-
Comparative protein structure modeling and its applications to drug discovery
-
Jacobson MP, Sali A. Comparative protein structure modeling and its applications to drug discovery. Ann Rep Med Chem 2004;39:259-276.
-
(2004)
Ann Rep Med Chem
, vol.39
, pp. 259-276
-
-
Jacobson, M.P.1
Sali, A.2
-
22
-
-
33645734536
-
Protein structure modeling in the proteomics era
-
Fiser A. Protein structure modeling in the proteomics era. Expert Rev Proteomics 2004;1:97-110.
-
(2004)
Expert Rev Proteomics
, vol.1
, pp. 97-110
-
-
Fiser, A.1
-
23
-
-
3142758686
-
Automated protein structure homology modeling: A progress report
-
Kopp J, Schwede T. Automated protein structure homology modeling: a progress report. Pharmacogenomics 2004;5:405-416.
-
(2004)
Pharmacogenomics
, vol.5
, pp. 405-416
-
-
Kopp, J.1
Schwede, T.2
-
25
-
-
0027968068
-
CLUSTAL W: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
-
Thompson JD, Higgins DG, Gibson TJ. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res 1994;22:4673-4680.
-
(1994)
Nucleic Acids Res
, vol.22
, pp. 4673-4680
-
-
Thompson, J.D.1
Higgins, D.G.2
Gibson, T.J.3
-
26
-
-
0002051540
-
BioEdit: A user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT
-
Hall TA. BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucl Acids Symp Ser 1999;41:95-98.
-
(1999)
Nucl Acids Symp Ser
, vol.41
, pp. 95-98
-
-
Hall, T.A.1
-
27
-
-
33845668798
-
-
Schrödinger, LLC, Portland, OR
-
Prime 1.2, Schrödinger, LLC, Portland, OR.
-
Prime 1.2
-
-
-
28
-
-
1842532008
-
A hierarchical approach to all-atom protein loop prediction
-
Jacobson MP, Pincus DL, Rapp CS, Day TJ, Honig B, Shaw DE, Friesner RA. A hierarchical approach to all-atom protein loop prediction. Proteins 2004;55:351-367.
-
(2004)
Proteins
, vol.55
, pp. 351-367
-
-
Jacobson, M.P.1
Pincus, D.L.2
Rapp, C.S.3
Day, T.J.4
Honig, B.5
Shaw, D.E.6
Friesner, R.A.7
-
29
-
-
0033135619
-
Prediction of loop geometries using a generalized born model of solvation effects
-
Rapp CS, Friesner RA. Prediction of loop geometries using a generalized born model of solvation effects. Proteins 1999;35:173-183.
-
(1999)
Proteins
, vol.35
, pp. 173-183
-
-
Rapp, C.S.1
Friesner, R.A.2
-
31
-
-
0037459171
-
The structure and function of human dipeptidyl peptidase IV, possessing a unique eight-bladed β-propeller fold
-
Hiramatsu H, Kyono K, Higashiyama Y, Fukushima C, Shima H, Sugiyama S, Inaka K, Yamamoto A, Shimizu R. The structure and function of human dipeptidyl peptidase IV, possessing a unique eight-bladed β-propeller fold. Biochem Biophys Res Commun 2003;302:849-854.
-
(2003)
Biochem Biophys Res Commun
, vol.302
, pp. 849-854
-
-
Hiramatsu, H.1
Kyono, K.2
Higashiyama, Y.3
Fukushima, C.4
Shima, H.5
Sugiyama, S.6
Inaka, K.7
Yamamoto, A.8
Shimizu, R.9
-
32
-
-
1642534610
-
Crystal structure of human dipeptidyl peptidase IV in complex with a decapeptide reveals details on substrate specificity and tetrahedral intermediate formation
-
Aertgeerts K, Ye S, Tennant MG, Kraus ML, Rogers J, Sang BC, Skene RJ, Webb DR, Prasad GS. Crystal structure of human dipeptidyl peptidase IV in complex with a decapeptide reveals details on substrate specificity and tetrahedral intermediate formation. Protein Sci 2004;13:412-421.
-
(2004)
Protein Sci
, vol.13
, pp. 412-421
-
-
Aertgeerts, K.1
Ye, S.2
Tennant, M.G.3
Kraus, M.L.4
Rogers, J.5
Sang, B.C.6
Skene, R.J.7
Webb, D.R.8
Prasad, G.S.9
-
33
-
-
32044465048
-
The reversed binding of b-phenethylamine inhibitors of DPP-IV. X-ray structures and properties of novel fragment and elaborated inhibitors
-
Nordhoff S, Cerezo-Gálvez S, Feurer A, Hill O, Matassa VG, Metz G, Rummey C, Thiemann M, Edwards PJ. The reversed binding of b-phenethylamine inhibitors of DPP-IV. X-ray structures and properties of novel fragment and elaborated inhibitors. Bioorg Med Chem Lett 2006;16:1744-1748.
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 1744-1748
-
-
Nordhoff, S.1
Cerezo-Gálvez, S.2
Feurer, A.3
Hill, O.4
Matassa, V.G.5
Metz, G.6
Rummey, C.7
Thiemann, M.8
Edwards, P.J.9
-
34
-
-
4544237622
-
Tyrosine 547 constitutes an essential part of the catalytic mechanism of dipeptidyl peptidase TV
-
Bjelke JR, Christensen J, Branner S, Wagtmann N, Olsen C, Kanstrup AB, Rasmussen HB. Tyrosine 547 constitutes an essential part of the catalytic mechanism of dipeptidyl peptidase TV. J Biol Chem 2004;279:34691-34697.
-
(2004)
J Biol Chem
, vol.279
, pp. 34691-34697
-
-
Bjelke, J.R.1
Christensen, J.2
Branner, S.3
Wagtmann, N.4
Olsen, C.5
Kanstrup, A.B.6
Rasmussen, H.B.7
-
35
-
-
1542314925
-
Aminomethylpyrimidines as novel DPP-IV inhibitors: A 10(5)-fold activity increase by optimization of aromatic substituents
-
Peters JU, Weber S, Kritter S, Weiss P, Wallier A, Boehringer M, Hennig M, Kuhn B, Loeffler BM. Aminomethylpyrimidines as novel DPP-IV inhibitors: a 10(5)-fold activity increase by optimization of aromatic substituents. Bioorg Med Chem Lett 2004;14:1491-1493.
-
(2004)
Bioorg Med Chem Lett
, vol.14
, pp. 1491-1493
-
-
Peters, J.U.1
Weber, S.2
Kritter, S.3
Weiss, P.4
Wallier, A.5
Boehringer, M.6
Hennig, M.7
Kuhn, B.8
Loeffler, B.M.9
-
36
-
-
0042131827
-
Structural basis of proline-specific exopeptidase activity as observed in human dipeptidyl peptidase-IV
-
Thoma R, Loffler B, Stihle M, Huber W, Ruf A, Hennig M. Structural basis of proline-specific exopeptidase activity as observed in human dipeptidyl peptidase-IV. Structure 2003;11: 947-959.
-
(2003)
Structure
, vol.11
, pp. 947-959
-
-
Thoma, R.1
Loffler, B.2
Stihle, M.3
Huber, W.4
Ruf, A.5
Hennig, M.6
-
37
-
-
0037966007
-
The crystal structure of dipeptidyl peptidase IV (CD26) reveals its functional regulation and enzymatic mechanism
-
Engel M, Hoffmann T, Wagner L, Wermann M, Heiser U, Kiefersauer R, Huber R, Bode W, Demuth HU, Brandstetter H. The crystal structure of dipeptidyl peptidase IV (CD26) reveals its functional regulation and enzymatic mechanism. Proc Natl Acad Sci USA 2003;100:5063-5068.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 5063-5068
-
-
Engel, M.1
Hoffmann, T.2
Wagner, L.3
Wermann, M.4
Heiser, U.5
Kiefersauer, R.6
Huber, R.7
Bode, W.8
Demuth, H.U.9
Brandstetter, H.10
-
38
-
-
5644261220
-
Crystal structure of CD26/dipeptidyl-peptidase IV in complex with adenosine deaminase reveals a highly amphiphilic interface
-
Weihofen WA, Liu J, Reutter W, Saenger W, Fan H. Crystal structure of CD26/dipeptidyl-peptidase IV in complex with adenosine deaminase reveals a highly amphiphilic interface. J Biol Chem 2004;279:43330-43335.
-
(2004)
J Biol Chem
, vol.279
, pp. 43330-43335
-
-
Weihofen, W.A.1
Liu, J.2
Reutter, W.3
Saenger, W.4
Fan, H.5
-
39
-
-
0033780088
-
Cloning, expression and chromosomal localization of a novel human dipeptidyl peptidase (DPP) IV homolog, DPP8
-
Abbott CA, Yu DM, Woollatt E, Sutherland GR, McCaughan GW, Gorrell MD. Cloning, expression and chromosomal localization of a novel human dipeptidyl peptidase (DPP) IV homolog, DPP8. Eur J Biochem 2000;267:6140-6150.
-
(2000)
Eur J Biochem
, vol.267
, pp. 6140-6150
-
-
Abbott, C.A.1
Yu, D.M.2
Woollatt, E.3
Sutherland, G.R.4
McCaughan, G.W.5
Gorrell, M.D.6
-
40
-
-
0034471660
-
Development of a tertiary-structure model of the C-terminal domain of DPP IV
-
Brandt W. Development of a tertiary-structure model of the C-terminal domain of DPP IV. Adv Exp Med Biol 2000;477:97-101.
-
(2000)
Adv Exp Med Biol
, vol.477
, pp. 97-101
-
-
Brandt, W.1
-
41
-
-
33845676398
-
-
http://www.ncbi.nlm.nih.gov/BLAST/
-
-
-
-
42
-
-
3042734543
-
Dipeptidyl peptidase 9 has two forms, a broad tissue distribution, cytoplasmic localization and DPIV-like peptidase activity
-
Ajami K, Abbott CA, McCaughan GW, Gorrell MD. Dipeptidyl peptidase 9 has two forms, a broad tissue distribution, cytoplasmic localization and DPIV-like peptidase activity. Biochim Biophys Acta 2004;1679:18-28.
-
(2004)
Biochim Biophys Acta
, vol.1679
, pp. 18-28
-
-
Ajami, K.1
Abbott, C.A.2
McCaughan, G.W.3
Gorrell, M.D.4
-
43
-
-
3242809886
-
The crystal structure of human dipeptidyl peptidase IV (DPPIV) complex with diprotin A
-
Hiramatsu H, Yamamoto A, Kyono K, Higashiyama Y, Fukushima C, Shima H, Sugiyama S, Inaka K, Shimizu R. The crystal structure of human dipeptidyl peptidase IV (DPPIV) complex with diprotin A. Biol Chem 2004;385:561-564.
-
(2004)
Biol Chem
, vol.385
, pp. 561-564
-
-
Hiramatsu, H.1
Yamamoto, A.2
Kyono, K.3
Higashiyama, Y.4
Fukushima, C.5
Shima, H.6
Sugiyama, S.7
Inaka, K.8
Shimizu, R.9
-
44
-
-
31544450787
-
Novel procedure for modeling ligand/receptor induced fit effects
-
Sherman W, Day T, Jacobson MP, Friesner RA, Farid R. Novel procedure for modeling ligand/receptor induced fit effects. J Med Chem 2006;49:534-553.
-
(2006)
J Med Chem
, vol.49
, pp. 534-553
-
-
Sherman, W.1
Day, T.2
Jacobson, M.P.3
Friesner, R.A.4
Farid, R.5
-
45
-
-
0242301182
-
Ligand-supported homology modelling of protein binding-sites using knowledge-based potentials
-
Evers A, Gohlke H, Klebe G. Ligand-supported homology modelling of protein binding-sites using knowledge-based potentials. J Mol Biol 2003;334:327-345.
-
(2003)
J Mol Biol
, vol.334
, pp. 327-345
-
-
Evers, A.1
Gohlke, H.2
Klebe, G.3
-
46
-
-
20444390974
-
Glutamic acid analogues as potent dipeptidyl peptidase IV and 8 inhibitors
-
Lu IL, Lee SJ, Tsu H, Wu SY, Kao KH, Chien CH, Chang YY, Chen YS, Cheng JH, Chang CN, Chen TW, Chang SP, Chen X, Jiaang WT. Glutamic acid analogues as potent dipeptidyl peptidase IV and 8 inhibitors. Bioorg Med Chem Lett 2005;15:3271-3275.
-
(2005)
Bioorg Med Chem Lett
, vol.15
, pp. 3271-3275
-
-
Lu, I.L.1
Lee, S.J.2
Tsu, H.3
Wu, S.Y.4
Kao, K.H.5
Chien, C.H.6
Chang, Y.Y.7
Chen, Y.S.8
Cheng, J.H.9
Chang, C.N.10
Chen, T.W.11
Chang, S.P.12
Chen, X.13
Jiaang, W.T.14
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