-
2
-
-
0033036795
-
Structure-activity relationships of naturally occurring and synthetic opioid tetrapeptides acting on locus coeruleus neurons
-
Yang YR, Chiu TH & Chen CL (1999) Structure-activity relationships of naturally occurring and synthetic opioid tetrapeptides acting on locus coeruleus neurons. Eur J Pharmacol 372, 229-236.
-
(1999)
Eur J Pharmacol
, vol.372
, pp. 229-236
-
-
Yang, Y.R.1
Chiu, T.H.2
Chen, C.L.3
-
3
-
-
2142823653
-
Recent advances in the investigation of the bioactive conformation of peptides active at the μ-opioid receptor. Conformational analysis of endomorphins
-
Gentilucci L & Tolomelli A (2004) Recent advances in the investigation of the bioactive conformation of peptides active at the μ-opioid receptor. Conformational analysis of endomorphins. Curr Topics Med Chem 4, 105-121.
-
(2004)
Curr Topics Med Chem
, vol.4
, pp. 105-121
-
-
Gentilucci, L.1
Tolomelli, A.2
-
5
-
-
0035258571
-
Structural studies on C-amidated amino acids and peptides: Crystal structures of hydrochloride salts of C-amidated Ile, Val, Thr, Ser, Met, Trp, Gln and Arg, and comparison with their C-unamidated ones
-
In Y, Fujii M, Sasada Y & Ishida T (2001) Structural studies on C-amidated amino acids and peptides: Crystal structures of hydrochloride salts of C-amidated Ile, Val, Thr, Ser, Met, Trp, Gln and Arg, and comparison with their C-unamidated ones. Acta Cryst B57, 72-81.
-
(2001)
Acta Cryst
, vol.B57
, pp. 72-81
-
-
In, Y.1
Fujii, M.2
Sasada, Y.3
Ishida, T.4
-
6
-
-
0035181504
-
1H NMR spectroscopy and molecular modeling calculation
-
1H NMR spectroscopy and molecular modeling calculation. J Peptide Res 58, 399-412.
-
(2001)
J Peptide Res
, vol.58
, pp. 399-412
-
-
In, Y.1
Minoura, K.2
Ohishi, H.3
Minakata, H.4
Kamigauchi, M.5
Sugiura, M.6
Ishida, T.7
-
7
-
-
0030933655
-
A potent and selective endogenous agonist for the μ-opioid receptor
-
Zadina JE, Hackler L, Ge LJ & Kastin AJ (1997) A potent and selective endogenous agonist for the μ-opioid receptor. Nature 386, 499-502.
-
(1997)
Nature
, vol.386
, pp. 499-502
-
-
Zadina, J.E.1
Hackler, L.2
Ge, L.J.3
Kastin, A.J.4
-
9
-
-
0027049066
-
Differential stereochemical requirements of μ vs. δ opioid receptors for ligand binding and signal transduction: Development of a class of potent and highly δ-selective peptide antagonists
-
Schiller PW, Nguyen TMD, Weltrowska G, Wilkes BC, Marsden. J, Lemieux C & Chung NN (1992) Differential stereochemical requirements of μ vs. δ opioid receptors for ligand binding and signal transduction: Development of a class of potent and highly δ-selective peptide antagonists. Proc Natl Acad Sci USA 89, 11871-11875.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 11871-11875
-
-
Schiller, P.W.1
Nguyen, T.M.D.2
Weltrowska, G.3
Wilkes, B.C.4
Marsden, J.5
Lemieux, C.6
Chung, N.N.7
-
10
-
-
0017620408
-
ACTH: A short introductory review
-
Schwyzer R (1977) ACTH: a short introductory review. Ann N Y Acad Sci 297, 3-26.
-
(1977)
Ann N Y Acad Sci
, vol.297
, pp. 3-26
-
-
Schwyzer, R.1
-
11
-
-
26244434030
-
1H-NMR spectroscopy and X-ray structure analysis
-
1H-NMR spectroscopy and X-ray structure analysis. Peptide Sci 200, 427-430.
-
(2005)
Peptide Sci
, vol.200
, pp. 427-430
-
-
In, Y.1
Minoura, K.2
Ishida, T.3
-
12
-
-
0035368628
-
Receptor constants for endomorphin-1 and endomorphin-1-ol indicate differences in efficacy and receptor occupancy
-
Al-Khrasani M, Orosz G, Kocsis L, Farkas V, Magyar A, Lengyel I, Benyhe S, Borsodi A & Ronai AZ (2001) Receptor constants for endomorphin-1 and endomorphin-1-ol indicate differences in efficacy and receptor occupancy. Eur J Pharmacol 421, 61-67.
-
(2001)
Eur J Pharmacol
, vol.421
, pp. 61-67
-
-
Al-Khrasani, M.1
Orosz, G.2
Kocsis, L.3
Farkas, V.4
Magyar, A.5
Lengyel, I.6
Benyhe, S.7
Borsodi, A.8
Ronai, A.Z.9
-
13
-
-
0017687154
-
Conformational states of enkephalins in solution
-
Khaled MA, Long MM, Thompson WD, Bradley RJ, Brown GB & Urry DW (1977) Conformational states of enkephalins in solution. Biochem Biophys Res Commun 76, 224-231.
-
(1977)
Biochem Biophys Res Commun
, vol.76
, pp. 224-231
-
-
Khaled, M.A.1
Long, M.M.2
Thompson, W.D.3
Bradley, R.J.4
Brown, G.B.5
Urry, D.W.6
-
14
-
-
0020003386
-
1H nuclear-magnetic-resonance study of met-enkephalin in solvent mixtures. Conformational transition from dimethylsulphoxide to water
-
1H nuclear-magnetic- resonance study of met-enkephalin in solvent mixtures. Conformational transition from dimethylsulphoxide to water. Eur J Biochem 122, 215-222.
-
(1982)
Eur J Biochem
, vol.122
, pp. 215-222
-
-
Zetta, L.1
Cabassi, F.2
-
15
-
-
0344500751
-
Preferred conformation of endomorphin-1 in aqueous and membrane-mimetic environments
-
Fiori S, Renner C, Cramer J, Pegoraro S & Moroder L (1999) Preferred conformation of endomorphin-1 in aqueous and membrane-mimetic environments. J Mol Biol 291, 163-175.
-
(1999)
J Mol Biol
, vol.291
, pp. 163-175
-
-
Fiori, S.1
Renner, C.2
Cramer, J.3
Pegoraro, S.4
Moroder, L.5
-
16
-
-
17144452429
-
Conformational analysis of the endogenous μ-opioid agonist endomorphin-1 using NMR spectroscopy and molecular modeling
-
Podlogar BL, Paterlini G, Ferguson DM, Leo GC, Demeter DA, Brown FK & Reitz AB (1998) Conformational analysis of the endogenous μ-opioid agonist endomorphin-1 using NMR spectroscopy and molecular modeling. FEBS Lett 439, 13-20.
-
(1998)
FEBS Lett
, vol.439
, pp. 13-20
-
-
Podlogar, B.L.1
Paterlini, G.2
Ferguson, D.M.3
Leo, G.C.4
Demeter, D.A.5
Brown, F.K.6
Reitz, A.B.7
-
17
-
-
0030919988
-
2), a highly potent μ-receptor selective opioid agonist: Comparison with proposed model structures
-
2), a highly potent μ-receptor selective opioid agonist: comparison with proposed model structures. J Peptide Res 49, 384-393.
-
(1997)
J Peptide Res
, vol.49
, pp. 384-393
-
-
Flippen-Anderson, J.L.1
Deschamps, J.R.2
George, C.3
Reddy, P.A.4
Lewin, A.H.5
Brine, G.A.6
Sheldrick, G.7
Nikiforovich, G.8
-
18
-
-
0036382880
-
The structure of an endomorphin analogue incorporating 1-aminocyclohexane-1-carboxylic acid for proline is similar to the β-turn of Leu-enkephalin
-
Doi M, Asano A, Komura E & Ueda Y (2002) The structure of an endomorphin analogue incorporating 1-aminocyclohexane-1-carboxylic acid for proline is similar to the β-turn of Leu-enkephalin. Biochem Biophys Res Commun 297, 138-142.
-
(2002)
Biochem Biophys Res Commun
, vol.297
, pp. 138-142
-
-
Doi, M.1
Asano, A.2
Komura, E.3
Ueda, Y.4
-
19
-
-
18444361816
-
Side chain modifications change the binding and agonist properties of endomorphin 2
-
Lengyel I, Orosz G, Biyashev D, Kocsis L, Al-Khrasani M, Ronai A, Tomboly Cs, FurstZs Toth G & Borsodi A (2002) Side chain modifications change the binding and agonist properties of endomorphin 2. Biochem Biophys Res Commun 290, 153-161.
-
(2002)
Biochem Biophys Res Commun
, vol.290
, pp. 153-161
-
-
Lengyel, I.1
Orosz, G.2
Biyashev, D.3
Kocsis, L.4
Al-Khrasani, M.5
Ronai, A.6
Tomboly, Cs.7
FurstZs Toth, G.8
Borsodi, A.9
-
20
-
-
0036945574
-
Development and validation of opioid ligand-receptor interaction models: The structural basis of mu vs. delta selectivity
-
Mosberg HI & Fowler CB (2002) Development and validation of opioid ligand-receptor interaction models: The structural basis of mu vs. delta selectivity. J Peptide Res 60, 329-335.
-
(2002)
J Peptide Res
, vol.60
, pp. 329-335
-
-
Mosberg, H.I.1
Fowler, C.B.2
-
21
-
-
0031018775
-
Key residues defining the μ-opioid receptor binding pocket: A site-directed mutagenesis study
-
Mansour A, Taylor LP, Fine JL, Thompson RC, Hoversten MT, Mosberg HI, Watson SJ & Akil H (1997) Key residues defining the μ-opioid receptor binding pocket: a site-directed mutagenesis study. J Neurochem 86, 344-353.
-
(1997)
J Neurochem
, vol.86
, pp. 344-353
-
-
Mansour, A.1
Taylor, L.P.2
Fine, J.L.3
Thompson, R.C.4
Hoversten, M.T.5
Mosberg, H.I.6
Watson, S.J.7
Akil, H.8
-
22
-
-
3042599035
-
Development of potent bifunctional endomorphin-2 analogues with mixed μ-/δ-opioid agonist and δ-opioid antagonist properties
-
Fujita Y, Tsuda Y, Li T, Motoyama T, Takahashi M, Shimizu Y, Yokoi T, Sasaki Y, Ambo A, Kita A, Jinsmaa Y, Bryant SD, Lazarus LH & Okada Y (2004) Development of potent bifunctional endomorphin-2 analogues with mixed μ-/δ-opioid agonist and δ-opioid antagonist properties. J Med Chem 47, 3591-3599.
-
(2004)
J Med Chem
, vol.47
, pp. 3591-3599
-
-
Fujita, Y.1
Tsuda, Y.2
Li, T.3
Motoyama, T.4
Takahashi, M.5
Shimizu, Y.6
Yokoi, T.7
Sasaki, Y.8
Ambo, A.9
Kita, A.10
Jinsmaa, Y.11
Bryant, S.D.12
Lazarus, L.H.13
Okada, Y.14
-
23
-
-
49349130990
-
Spin-spin coupling and the conformational states of peptide systems
-
Bystrov VF (1976) Spin-spin coupling and the conformational states of peptide systems. Prog Nucl Magn Reson Spectrosc 10, 41-81.
-
(1976)
Prog Nucl Magn Reson Spectrosc
, vol.10
, pp. 41-81
-
-
Bystrov, V.F.1
-
24
-
-
0015830934
-
Dihedral angle-vicinal proton coupling constant correlation for the α-β bond of amino acid residues
-
Kopple KD, Wiley GR & Tauke R (1973) Dihedral angle-vicinal proton coupling constant correlation for the α-β bond of amino acid residues. Biopolymers 12, 627-636.
-
(1973)
Biopolymers
, vol.12
, pp. 627-636
-
-
Kopple, K.D.1
Wiley, G.R.2
Tauke, R.3
-
25
-
-
0000939457
-
The three-dimensional structure of α1-purothionin in solution: Combined use of nuclear magnetic resonance, distance geometry and restrained molecular dynamics
-
Clore GM, Nigles M, Sukumaran DK, Bruenger AT, Karplus M & Gronenborn AM (1986) The three-dimensional structure of α1-purothionin in solution: combined use of nuclear magnetic resonance, distance geometry and restrained molecular dynamics. EMBO J 5, 2729-2735.
-
(1986)
EMBO J
, vol.5
, pp. 2729-2735
-
-
Clore, G.M.1
Nigles, M.2
Sukumaran, D.K.3
Bruenger, A.T.4
Karplus, M.5
Gronenborn, A.M.6
-
26
-
-
0024285896
-
Determination of three-dimensional structures of proteins from interproton distance data by hybrid distance geometry-dynamical simulated annealing calculations
-
Nilges M, Clore GM & Gronenborn AM (1988) Determination of three-dimensional structures of proteins from interproton distance data by hybrid distance geometry-dynamical simulated annealing calculations. FEBS Lett 229, 317-324.
-
(1988)
FEBS Lett
, vol.229
, pp. 317-324
-
-
Nilges, M.1
Clore, G.M.2
Gronenborn, A.M.3
-
27
-
-
26244458227
-
-
INSIGHT/DISCOVER. Accelrys Software Inc, San Diego, CA
-
INSIGHT/DISCOVER. Accelrys Software Inc, San Diego, CA.
-
-
-
-
31
-
-
0347383758
-
Modeller: Generation and refinement of homology-based protein structure models
-
Fiser A & Sali A (2003) Modeller: generation and refinement of homology-based protein structure models. Methods Enzymol 374, 461-491.
-
(2003)
Methods Enzymol
, vol.374
, pp. 461-491
-
-
Fiser, A.1
Sali, A.2
|