-
1
-
-
84870918230
-
Ribosomally synthesized and post-translationally modified peptide natural products: Overview and recommendations for a universal nomenclature
-
Arnison PG, Bibb MJ, Bierbaum G, Bowers AA, Bugni TS, Bulaj G, Camarero JA, Campopiano DJ, Challis GL, Clardy J, Cotter PD, Craik DJ, Dawson M, Dittmann E, Donadio S, Dorrestein PC, Entian K-D, Fischbach MA, Garavelli JS, Göransson U, Gruber CW, Haft DH, Hemscheidt TK, Hertweck C, Hill C, Horswill AR, Jaspars M, Kelly WL, Klinman JP, Kuipers OP, Link AJ, Liu W, Marahiel MA, Mitchell DA, Moll GN, Moore BS, Müller R, Nair SK, Nes IF, Norris GE, Olivera BM, Onaka H, Patchett ML, Piel J, Reaney MJT, Rebuffat S, Ross RP, Sahl H-G, Schmidt EW, Selsted ME, Severinov K, Shen B, Sivonen K, Smith L, Stein T, Süssmuth RE, Tagg JR, Tang G-L, Truman AW, Vederas JC, Walsh CT, Walton JD, Wenzel SC, Willey JM, van der Donk WA (2013) Ribosomally synthesized and post-translationally modified peptide natural products: overview and recommendations for a universal nomenclature. Nat Prod Rep 30:108-160.
-
(2013)
Nat Prod Rep
, vol.30
, pp. 108-160
-
-
Arnison, P.G.1
Bibb, M.J.2
Bierbaum, G.3
Bowers, A.A.4
Bugni, T.S.5
Bulaj, G.6
Camarero, J.A.7
Campopiano, D.J.8
Challis, G.L.9
Clardy, J.10
Cotter, P.D.11
Craik, D.J.12
Dawson, M.13
Dittmann, E.14
Donadio, S.15
Dorrestein, P.C.16
Entian, K.-D.17
Fischbach, M.A.18
Garavelli, J.S.19
Göransson, U.20
Gruber, C.W.21
Haft, D.H.22
Hemscheidt, T.K.23
Hertweck, C.24
Hill, C.25
Horswill, A.R.26
Jaspars, M.27
Kelly, W.L.28
Klinman, J.P.29
Kuipers, O.P.30
Link, A.J.31
Liu, W.32
Marahiel, M.A.33
Mitchell, D.A.34
Moll, G.N.35
Moore, B.S.36
Müller, R.37
Nair, S.K.38
Nes, I.F.39
Norris, G.E.40
Olivera, B.M.41
Onaka, H.42
Patchett, M.L.43
Piel, J.44
Reaney, M.J.T.45
Rebuffat, S.46
Ross, R.P.47
Sahl, H.-G.48
Schmidt, E.W.49
Selsted, M.E.50
Severinov, K.51
Shen, B.52
Sivonen, K.53
Smith, L.54
Stein, T.55
Süssmuth, R.E.56
Tagg, J.R.57
Tang, G.-L.58
Truman, A.W.59
Vederas, J.C.60
Walsh, C.T.61
Walton, J.D.62
Wenzel, S.C.63
Willey, J.M.64
Van Der Donk, W.A.65
more..
-
2
-
-
74049115080
-
Follow the leader: The use of leader peptides to guide natural product biosynthesis
-
Oman TJ, van der Donk WA (2010) Follow the leader: the use of leader peptides to guide natural product biosynthesis. Nat Chem Biol 6:9-18.
-
(2010)
Nat Chem Biol
, vol.6
, pp. 9-18
-
-
Oman, T.J.1
Van Der Donk, W.A.2
-
3
-
-
84861649020
-
Discovery, biosynthesis, and engineering of lantipeptides
-
Knerr PJ, van der Donk WA (2012) Discovery, biosynthesis, and engineering of lantipeptides. Annu Rev Biochem 81:479-505.
-
(2012)
Annu Rev Biochem
, vol.81
, pp. 479-505
-
-
Knerr, P.J.1
Van Der Donk, W.A.2
-
4
-
-
0023912839
-
Prepeptide sequence of epidermin, a ribosomally synthesized antibiotic with four sulphide-rings
-
Schnell N, Entian K-D, Schneider U, Götz F, Zahner H, Kellner R, Jung G (1988) Prepeptide sequence of epidermin, a ribosomally synthesized antibiotic with four sulphide-rings. Nature 333:276-278.
-
(1988)
Nature
, vol.333
, pp. 276-278
-
-
Schnell, N.1
Entian, K.-D.2
Schneider, U.3
Götz, F.4
Zahner, H.5
Kellner, R.6
Jung, G.7
-
5
-
-
78651404410
-
Morphogenetic signaling molecules of the streptomycetes
-
Willey JM, Gaskell AA (2011) Morphogenetic signaling molecules of the streptomycetes. Chem Rev 111:174-187.
-
(2011)
Chem Rev
, vol.111
, pp. 174-187
-
-
Willey, J.M.1
Gaskell, A.A.2
-
6
-
-
84878408977
-
The lantibiotic peptide labyrinthopeptin A1 demonstrates broad anti-HIV and anti-HSV activity with potential for microbicidal applications
-
Ferir G, Petrova MI, Andrei G, Huskens D, Hoorelbeke B, Snoeck R, Vanderleyden J, Balzarini J, Bartoschek S, Brönstrup M, Süssmuth RD, Schols D (2013) The lantibiotic peptide labyrinthopeptin A1 demonstrates broad anti-HIV and anti-HSV activity with potential for microbicidal applications. PLoS One 8:e64010.
-
(2013)
PLoS One
, vol.8
-
-
Ferir, G.1
Petrova, M.I.2
Andrei, G.3
Huskens, D.4
Hoorelbeke, B.5
Snoeck, R.6
Vanderleyden, J.7
Balzarini, J.8
Bartoschek, S.9
Brönstrup, M.10
Süssmuth, R.D.11
Schols, D.12
-
7
-
-
76249088835
-
Labyrinthopeptins: A new class of carbacyclic lantibiotics
-
Meindl K, Schmiederer T, Schneider K, Reicke A, Butz D, Keller S, Guhring H, Vertesy L, Wink J, Hoffmann H, Bronstrup M, Sheldrick GM, Süssmuth RD (2010) Labyrinthopeptins: a new class of carbacyclic lantibiotics. Angew Chem Int Ed 49:1151-1154.
-
(2010)
Angew Chem Int Ed
, vol.49
, pp. 1151-1154
-
-
Meindl, K.1
Schmiederer, T.2
Schneider, K.3
Reicke, A.4
Butz, D.5
Keller, S.6
Guhring, H.7
Vertesy, L.8
Wink, J.9
Hoffmann, H.10
Bronstrup, M.11
Sheldrick, G.M.12
Süssmuth, R.D.13
-
8
-
-
38949166717
-
Biosynthesis, immunity, regulation, mode of action and engineering of the model lantibiotic nisin
-
Lubelski J, Rink R, Khusainov R, Moll GN, Kuipers OP (2008) Biosynthesis, immunity, regulation, mode of action and engineering of the model lantibiotic nisin. Cell Mol Life Sci 65:455-476.
-
(2008)
Cell Mol Life Sci
, vol.65
, pp. 455-476
-
-
Lubelski, J.1
Rink, R.2
Khusainov, R.3
Moll, G.N.4
Kuipers, O.P.5
-
9
-
-
84872016052
-
Generation of an actagardine A variant library through saturation mutagenesis
-
Boakes S, Ayala T, Herman M, Appleyard AN, Dawson MJ, Cortes J (2012) Generation of an actagardine A variant library through saturation mutagenesis. Appl Microbiol Biotechnol 15:1509-1517.
-
(2012)
Appl Microbiol Biotechnol
, vol.15
, pp. 1509-1517
-
-
Boakes, S.1
Ayala, T.2
Herman, M.3
Appleyard, A.N.4
Dawson, M.J.5
Cortes, J.6
-
10
-
-
38349060901
-
Determining the structure and mode of action of microbisporicin, a potent lantibiotic active against multiresistant pathogens
-
Castiglione F, Lazzarini A, Carrano L, Corti E, Ciciliato I, Gastaldo L, Candiani P, Losi D, Marinelli F, Selva E, Parenti F (2008) Determining the structure and mode of action of microbisporicin, a potent lantibiotic active against multiresistant pathogens. Chem Biol 15:22-31.
-
(2008)
Chem Biol
, vol.15
, pp. 22-31
-
-
Castiglione, F.1
Lazzarini, A.2
Carrano, L.3
Corti, E.4
Ciciliato, I.5
Gastaldo, L.6
Candiani, P.7
Losi, D.8
Marinelli, F.9
Selva, E.10
Parenti, F.11
-
11
-
-
79953242162
-
Efficacy of the new lantibiotic NAI-107 in experimental infections induced by multidrugresistant Gram-positive pathogens
-
Jabes D, Brunati C, Candiani G, Riva S, Romano G, Donadio S (2011) Efficacy of the new lantibiotic NAI-107 in experimental infections induced by multidrugresistant Gram-positive pathogens. Antimicrob Agents Chemother 55:1671-1676.
-
(2011)
Antimicrob Agents Chemother
, vol.55
, pp. 1671-1676
-
-
Jabes, D.1
Brunati, C.2
Candiani, G.3
Riva, S.4
Romano, G.5
Donadio, S.6
-
12
-
-
70349096824
-
Emerging treatments in cystic fibrosis
-
Jones AM, Helm JM (2009) Emerging treatments in cystic fibrosis. Drugs 69:1903-1910.
-
(2009)
Drugs
, vol.69
, pp. 1903-1910
-
-
Jones, A.M.1
Helm, J.M.2
-
14
-
-
0034673170
-
Reactions of Pseudomonas 7A glutaminaseasparaginase with diazo analogues of glutamine and asparagine result in unexpected covalent inhibitions and suggests an unusual catalytic triad Thr-Tyr-Glu
-
Ortlund E, Lacount MW, Lewinski K, Lebioda L (2000) Reactions of Pseudomonas 7A glutaminaseasparaginase with diazo analogues of glutamine and asparagine result in unexpected covalent inhibitions and suggests an unusual catalytic triad Thr-Tyr-Glu. Biochemistry 39:1199-1204.
-
(2000)
Biochemistry
, vol.39
, pp. 1199-1204
-
-
Ortlund, E.1
Lacount, M.W.2
Lewinski, K.3
Lebioda, L.4
-
15
-
-
0034604269
-
Identification of catalytic nucleophile of Escherichia coli gamma-glutamyltranspeptidase by gammamonofluorophosphono derivative of glutamic acid: Nterminal thr-391 in small subunit is the nucleophile
-
Inoue M, Hiratake J, Suzuki H, Kumagai H, Sakata K (2000) Identification of catalytic nucleophile of Escherichia coli gamma-glutamyltranspeptidase by gammamonofluorophosphono derivative of glutamic acid: Nterminal thr-391 in small subunit is the nucleophile. Biochemistry 39:7764-7771.
-
(2000)
Biochemistry
, vol.39
, pp. 7764-7771
-
-
Inoue, M.1
Hiratake, J.2
Suzuki, H.3
Kumagai, H.4
Sakata, K.5
-
16
-
-
0344823660
-
SpaC and NisC, the cyclases involved in subtilin and nisin biosynthesis, are zinc proteins
-
Okeley NM, Paul M, Stasser JP, Blackburn N, van der Donk WA (2003) SpaC and NisC, the cyclases involved in subtilin and nisin biosynthesis, are zinc proteins. Biochemistry 42:13613-13624.
-
(2003)
Biochemistry
, vol.42
, pp. 13613-13624
-
-
Okeley, N.M.1
Paul, M.2
Stasser, J.P.3
Blackburn, N.4
Van Der Donk, W.A.5
-
17
-
-
33644854595
-
Structure and mechanism of the lantibiotic cyclase involved in nisin biosynthesis
-
Li B, Yu JP, Brunzelle JS, Moll GN, van der Donk WA, Nair SK (2006) Structure and mechanism of the lantibiotic cyclase involved in nisin biosynthesis. Science 311:1464-1467.
-
(2006)
Science
, vol.311
, pp. 1464-1467
-
-
Li, B.1
Yu, J.P.2
Brunzelle, J.S.3
Moll, G.N.4
Van Der Donk, W.A.5
Nair, S.K.6
-
18
-
-
0032587329
-
Zinc-catalyzed sulfur alkylation: Insights from protein farnesyltransferase
-
Hightower KE, Fierke CA (1999) Zinc-catalyzed sulfur alkylation: insights from protein farnesyltransferase. Curr Opin Chem Biol 3:176-181.
-
(1999)
Curr Opin Chem Biol
, vol.3
, pp. 176-181
-
-
Hightower, K.E.1
Fierke, C.A.2
-
19
-
-
36049001127
-
Comment on "a G protein coupled receptor is a plasma membrane receptor for the plant hormone abscisic acid"
-
author reply 914
-
Johnston CA, Temple BR, Chen JG, Gao Y, Moriyama EN, Jones AM, Siderovski DP, Willard FS (2007) Comment on "A G protein coupled receptor is a plasma membrane receptor for the plant hormone abscisic acid." Science 318:914; author reply 914.
-
(2007)
Science
, vol.318
, pp. 914
-
-
Johnston, C.A.1
Temple, B.R.2
Chen, J.G.3
Gao, Y.4
Moriyama, E.N.5
Jones, A.M.6
Siderovski, D.P.7
Willard, F.S.8
-
20
-
-
0034682901
-
Characterization of p40/GPR69A as a peripheral membrane protein related to the lantibiotic synthetase component C
-
Bauer H, Mayer H, Marchler-Bauer A, Salzer U, Prohaska R (2000) Characterization of p40/GPR69A as a peripheral membrane protein related to the lantibiotic synthetase component C. Biochem Biophys Res Commun 275:69-74.
-
(2000)
Biochem Biophys Res Commun
, vol.275
, pp. 69-74
-
-
Bauer, H.1
Mayer, H.2
Marchler-Bauer, A.3
Salzer, U.4
Prohaska, R.5
-
21
-
-
0035897569
-
Characterization of rat LANCL1, a novel member of the lanthionine synthetase C-like protein family, highly expressed in testis and brain
-
Mayer H, Bauer H, Breuss J, Ziegler S, Prohaska R (2001) Characterization of rat LANCL1, a novel member of the lanthionine synthetase C-like protein family, highly expressed in testis and brain. Gene 269:73-80.
-
(2001)
Gene
, vol.269
, pp. 73-80
-
-
Mayer, H.1
Bauer, H.2
Breuss, J.3
Ziegler, S.4
Prohaska, R.5
-
22
-
-
27644492521
-
Lacticin 481 synthetase phosphorylates its substrate during lantibiotic production
-
Chatterjee C, Miller LM, Leung YL, Xie L, Yi M, Kelleher NL, van der Donk WA (2005) Lacticin 481 synthetase phosphorylates its substrate during lantibiotic production. J Am Chem Soc 127:15332-15333.
-
(2005)
J Am Chem Soc
, vol.127
, pp. 15332-15333
-
-
Chatterjee, C.1
Miller, L.M.2
Leung, Y.L.3
Xie, L.4
Yi, M.5
Kelleher, N.L.6
Van Der Donk, W.A.7
-
23
-
-
3843091511
-
The SapB morphogen is a lantibiotic-like peptide derived from the product of the developmental gene ramS in Streptomyces coelicolor
-
Kodani S, Hudson ME, Durrant MC, Buttner MJ, Nodwell JR, Willey JM (2004) The SapB morphogen is a lantibiotic-like peptide derived from the product of the developmental gene ramS in Streptomyces coelicolor. Proc Natl Acad Sci USA 101:11448-11453.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 11448-11453
-
-
Kodani, S.1
Hudson, M.E.2
Durrant, M.C.3
Buttner, M.J.4
Nodwell, J.R.5
Willey, J.M.6
-
24
-
-
77950563372
-
Discovery of unique lanthionine synthetases reveals new mechanistic and evolutionary insights
-
Goto Y, Li B, Claesen J, Shi Y, Bibb MJ, van der Donk WA (2010) Discovery of unique lanthionine synthetases reveals new mechanistic and evolutionary insights. PLoS Biol 8:e1000339.
-
(2010)
PLoS Biol
, vol.8
-
-
Goto, Y.1
Li, B.2
Claesen, J.3
Shi, Y.4
Bibb, M.J.5
Van Der Donk, W.A.6
-
25
-
-
77953528770
-
In vitro biosynthesis of the prepeptide of type-III lantibiotic labyrinthopeptin A2 including formation of a C-C bond as a post-translational modification
-
Müller WM, Schmiederer T, Ensle P, Süssmuth RD (2010) In vitro biosynthesis of the prepeptide of type-III lantibiotic labyrinthopeptin A2 including formation of a C-C bond as a post-translational modification. Angew Chem Int Ed 49:2436-2440.
-
(2010)
Angew Chem Int Ed
, vol.49
, pp. 2436-2440
-
-
Müller, W.M.1
Schmiederer, T.2
Ensle, P.3
Süssmuth, R.D.4
-
26
-
-
79952097307
-
Mechanistic studies of Ser/Thr dehydration catalyzed by a member of the LanL lanthionine synthetase family
-
Goto Y, Ökesli A, van der Donk WA (2011) Mechanistic studies of Ser/Thr dehydration catalyzed by a member of the LanL lanthionine synthetase family. Biochemistry 50:891-898.
-
(2011)
Biochemistry
, vol.50
, pp. 891-898
-
-
Goto, Y.1
Ökesli, A.2
Van Der Donk, W.A.3
-
27
-
-
33847154642
-
The phosphothreonine lyase activity of a bacterial type III effector family
-
Li H, Xu H, Zhou Y, Zhang J, Long C, Li S, Chen S, Zhou JM, Shao F (2007) The phosphothreonine lyase activity of a bacterial type III effector family. Science 315:1000-1003.
-
(2007)
Science
, vol.315
, pp. 1000-1003
-
-
Li, H.1
Xu, H.2
Zhou, Y.3
Zhang, J.4
Long, C.5
Li, S.6
Chen, S.7
Zhou, J.M.8
Shao, F.9
-
28
-
-
84868094646
-
Biosynthesis of the class III lantipeptide catenulipeptin
-
Wang H, van der Donk WA (2012) Biosynthesis of the class III lantipeptide catenulipeptin. ACS Chem Biol 7: 1529-1535.
-
(2012)
ACS Chem Biol
, vol.7
, pp. 1529-1535
-
-
Wang, H.1
Van Der Donk, W.A.2
-
29
-
-
84866449155
-
Curvopeptin: A new lanthionine-containing class III lantibiotic and its co-substrate promiscuous synthetase
-
Krawczyk B, Völler GH, Völler J, Ensle P, Süssmuth RD (2012) Curvopeptin: a new lanthionine-containing class III lantibiotic and its co-substrate promiscuous synthetase. ChemBioChem 13:2065-2071.
-
(2012)
ChemBioChem
, vol.13
, pp. 2065-2071
-
-
Krawczyk, B.1
Völler, G.H.2
Völler, J.3
Ensle, P.4
Süssmuth, R.D.5
-
30
-
-
38449108932
-
Evolutionary mechanisms underlying secondary metabolite diversity
-
121-140
-
Jenke-Kodama H, Müller R, Dittmann E (2008) Evolutionary mechanisms underlying secondary metabolite diversity. Prog Drug Res 65:119, 121-140.
-
(2008)
Prog Drug Res
, vol.65
, pp. 119
-
-
Jenke-Kodama, H.1
Müller, R.2
Dittmann, E.3
-
31
-
-
0027385948
-
Model studies of lantibiotic biogenesis
-
Toogood PL (1993) Model studies of lantibiotic biogenesis. Tetrahedron Lett 34:7833-7836.
-
(1993)
Tetrahedron Lett
, vol.34
, pp. 7833-7836
-
-
Toogood, P.L.1
-
32
-
-
0034676587
-
Facile chemoselective synthesis of dehydroalanine-containing peptides
-
Okeley NM, Zhu Y, van der Donk WA (2000) Facile chemoselective synthesis of dehydroalanine-containing peptides. Org Lett 2:3603-3606.
-
(2000)
Org Lett
, vol.2
, pp. 3603-3606
-
-
Okeley, N.M.1
Zhu, Y.2
Van Der Donk, W.A.3
-
33
-
-
0034647069
-
Biomimetic synthesis of lantibiotics
-
Burrage S, Raynham T, Williams G, Essex JW, Allen C, Cardno M, Swali V, Bradley M (2000) Biomimetic synthesis of lantibiotics. Chem-Eur J 6:1455-1466.
-
(2000)
Chem-Eur J
, vol.6
, pp. 1455-1466
-
-
Burrage, S.1
Raynham, T.2
Williams, G.3
Essex, J.W.4
Allen, C.5
Cardno, M.6
Swali, V.7
Bradley, M.8
-
34
-
-
0037129424
-
Biomimetic stereoselective formation of methyllanthionine
-
Zhou H, van der Donk WA (2002) Biomimetic stereoselective formation of methyllanthionine. Org Lett 4: 1335-1338.
-
(2002)
Org Lett
, vol.4
, pp. 1335-1338
-
-
Zhou, H.1
Van Der Donk, W.A.2
-
35
-
-
0142094530
-
Biomimetic studies on the mechanism of stereoselective lanthionine formation
-
Zhu Y, Gieselman M, Zhou H, Averin O, van der Donk WA (2003) Biomimetic studies on the mechanism of stereoselective lanthionine formation. Org Biomol Chem 1:3304-3315.
-
(2003)
Org Biomol Chem
, vol.1
, pp. 3304-3315
-
-
Zhu, Y.1
Gieselman, M.2
Zhou, H.3
Averin, O.4
Van Der Donk, W.A.5
-
37
-
-
84878560267
-
Ribosomally synthesized and post-translationally modified peptide natural products: New insights into the role of leader and core peptides during biosynthesis
-
Yang X, van der Donk WA (2013) Ribosomally synthesized and post-translationally modified peptide natural products: new insights into the role of leader and core peptides during biosynthesis. Chem Eur J 19:7662-7677.
-
(2013)
Chem Eur J
, vol.19
, pp. 7662-7677
-
-
Yang, X.1
Van Der Donk, W.A.2
-
38
-
-
70350031573
-
Directionality and coordination of dehydration and ring formation during biosynthesis of the lantibiotic nisin
-
Lubelski J, Khusainov R, Kuipers OP (2009) Directionality and coordination of dehydration and ring formation during biosynthesis of the lantibiotic nisin. J Biol Chem 284:25962-25972.
-
(2009)
J Biol Chem
, vol.284
, pp. 25962-25972
-
-
Lubelski, J.1
Khusainov, R.2
Kuipers, O.P.3
-
39
-
-
69349105507
-
Distributive and directional behavior of lantibiotic synthetases revealed by high-resolution tandem mass spectrometry
-
Lee MV, Ihnken LA, You YO, McClerren AL, van der Donk WA, Kelleher NL (2009) Distributive and directional behavior of lantibiotic synthetases revealed by high-resolution tandem mass spectrometry. J Am Chem Soc 131:12258-12264.
-
(2009)
J Am Chem Soc
, vol.131
, pp. 12258-12264
-
-
Lee, M.V.1
Ihnken, L.A.2
You, Y.O.3
McClerren, A.L.4
Van Der Donk, W.A.5
Kelleher, N.L.6
-
40
-
-
84862528396
-
Deuterium labeled peptides give insights into the directionality of class III lantibiotic synthetase LabKC
-
Krawczyk B, Ensle P, Müller WM, Süssmuth RD (2012) Deuterium labeled peptides give insights into the directionality of class III lantibiotic synthetase LabKC. J Am Chem Soc 134:9922.
-
(2012)
J Am Chem Soc
, vol.134
, pp. 9922
-
-
Krawczyk, B.1
Ensle, P.2
Müller, W.M.3
Süssmuth, R.D.4
-
41
-
-
77950530516
-
To protect peptide pharmaceuticals against peptidases
-
Rink R, Arkema-Meter A, Baudoin I, Post E, Kuipers A, Nelemans SA, Akanbi MH, Moll GN (2010) To protect peptide pharmaceuticals against peptidases. J Pharmacol Toxicol Meth 61:210-218.
-
(2010)
J Pharmacol Toxicol Meth
, vol.61
, pp. 210-218
-
-
Rink, R.1
Arkema-Meter, A.2
Baudoin, I.3
Post, E.4
Kuipers, A.5
Nelemans, S.A.6
Akanbi, M.H.7
Moll, G.N.8
-
42
-
-
36048994654
-
NisC, the cyclase of the lantibiotic nisin, can catalyze cyclization of designed nonlantibiotic peptides
-
Rink R, Kluskens LD, Kuipers A, Driessen AJ, Kuipers OP, Moll GN (2007) NisC, the cyclase of the lantibiotic nisin, can catalyze cyclization of designed nonlantibiotic peptides. Biochemistry 46:13179-13189.
-
(2007)
Biochemistry
, vol.46
, pp. 13179-13189
-
-
Rink, R.1
Kluskens, L.D.2
Kuipers, A.3
Driessen, A.J.4
Kuipers, O.P.5
Moll, G.N.6
-
43
-
-
25444499680
-
Post-translational modification of therapeutic peptides by NisB, the dehydratase of the lantibiotic nisin
-
Kluskens LD, Kuipers A, Rink R, de Boef E, Fekken S, Driessen AJ, Kuipers OP, Moll GN (2005) Post-translational modification of therapeutic peptides by NisB, the dehydratase of the lantibiotic nisin. Biochemistry 44: 12827-12834.
-
(2005)
Biochemistry
, vol.44
, pp. 12827-12834
-
-
Kluskens, L.D.1
Kuipers, A.2
Rink, R.3
De Boef, E.4
Fekken, S.5
Driessen, A.J.6
Kuipers, O.P.7
Moll, G.N.8
-
44
-
-
43549100204
-
Use of lantibiotic synthetases for the preparation of bioactive constrained peptides
-
Levengood MR, van der Donk WA (2008) Use of lantibiotic synthetases for the preparation of bioactive constrained peptides. Bioorg Med Chem Lett 18:3025-3028.
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 3025-3028
-
-
Levengood, M.R.1
Van Der Donk, W.A.2
-
45
-
-
47249108199
-
The importance of the leader sequence for directing lanthionine formation in lacticin 481
-
Patton GC, Paul M, Cooper LE, Chatterjee C, van der Donk WA (2008) The importance of the leader sequence for directing lanthionine formation in lacticin 481. Biochemistry 47:7342-7351.
-
(2008)
Biochemistry
, vol.47
, pp. 7342-7351
-
-
Patton, G.C.1
Paul, M.2
Cooper, L.E.3
Chatterjee, C.4
Van Der Donk, W.A.5
-
46
-
-
0027327107
-
Structure, organization, and expression of the lct gene for lacticin 481, a novel lantibiotic produced by Lactococcus lactis
-
Piard JC, Kuipers OP, Rollema HS, Desmazeaud MJ, de Vos WM (1993) Structure, organization, and expression of the lct gene for lacticin 481, a novel lantibiotic produced by Lactococcus lactis. J Biol Chem 268: 16361-16368.
-
(1993)
J Biol Chem
, vol.268
, pp. 16361-16368
-
-
Piard, J.C.1
Kuipers, O.P.2
Rollema, H.S.3
Desmazeaud, M.J.4
De Vos, W.M.5
-
47
-
-
0027199706
-
Genetics of bacteriocins produced by lactic acid bacteria
-
Klaenhammer TR (1993) Genetics of bacteriocins produced by lactic acid bacteria. FEMS Microbiol Rev 12: 39-85.
-
(1993)
FEMS Microbiol Rev
, vol.12
, pp. 39-85
-
-
Klaenhammer, T.R.1
-
49
-
-
0036185650
-
Two different lantibiotic-like peptides originate from the ericin gene cluster of Bacillus subtilis A1/3
-
Stein T, Borchert S, Conrad B, Feesche J, Hofemeister B, Hofemeister J, Entian K-D (2002) Two different lantibiotic-like peptides originate from the ericin gene cluster of Bacillus subtilis A1/3. J Bacteriol 184:1703-1711.
-
(2002)
J Bacteriol
, vol.184
, pp. 1703-1711
-
-
Stein, T.1
Borchert, S.2
Conrad, B.3
Feesche, J.4
Hofemeister, B.5
Hofemeister, J.6
Entian, K.-D.7
-
50
-
-
77953742146
-
Catalytic promiscuity in the biosynthesis of cyclic peptide secondary metabolites in planktonic marine cyanobacteria
-
Li B, Sher D, Kelly L, Shi Y, Huang K, Knerr PJ, Joewono I, Rusch D, Chisholm SW, van der Donk WA (2010) Catalytic promiscuity in the biosynthesis of cyclic peptide secondary metabolites in planktonic marine cyanobacteria. Proc Natl Acad Sci USA 107: 10430-10435.
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, pp. 10430-10435
-
-
Li, B.1
Sher, D.2
Kelly, L.3
Shi, Y.4
Huang, K.5
Knerr, P.J.6
Joewono, I.7
Rusch, D.8
Chisholm, S.W.9
Van Der Donk, W.A.10
-
51
-
-
77952511174
-
Expansion of ribosomally produced natural products: A nitrile hydratase-and Nif11-related precursor family
-
Haft DH, Basu MK, Mitchell DA (2010) Expansion of ribosomally produced natural products: a nitrile hydratase-and Nif11-related precursor family. BMC Biol 8: 70
-
(2010)
BMC Biol
, vol.8
, pp. 70
-
-
Haft, D.H.1
Basu, M.K.2
Mitchell, D.A.3
-
52
-
-
84861624891
-
Structural characterization of four prochlorosins: A novel class of lantipeptides produced by planktonic marine cyanobacteria
-
Tang W, van der Donk WA (2012) Structural characterization of four prochlorosins: a novel class of lantipeptides produced by planktonic marine cyanobacteria. Biochemistry 51:4271-4279.
-
(2012)
Biochemistry
, vol.51
, pp. 4271-4279
-
-
Tang, W.1
Van Der Donk, W.A.2
-
54
-
-
0000816291
-
Alkyl transfer to metal thiolates: Kinetics, active species identification, and relevance to the DNA methyl phosphotriester repair center of Escherichia coli Ada
-
Wilker JJ, Lippard SJ (1997) Alkyl transfer to metal thiolates: kinetics, active species identification, and relevance to the DNA methyl phosphotriester repair center of Escherichia coli Ada. Inorg Chem 36:969-978.
-
(1997)
Inorg Chem
, vol.36
, pp. 969-978
-
-
Wilker, J.J.1
Lippard, S.J.2
-
55
-
-
0034839228
-
Methylation of neutral pseudotetrahedral zinc thiolate complexes: Model reactions for alkyl group transfer to sulfur by zinc-containing enzymes
-
Warthen CR, Hammes BS, Carrano CJ, Crans DC (2001) Methylation of neutral pseudotetrahedral zinc thiolate complexes: model reactions for alkyl group transfer to sulfur by zinc-containing enzymes. J Biol Inorg Chem 6:82-90.
-
(2001)
J Biol Inorg Chem
, vol.6
, pp. 82-90
-
-
Warthen, C.R.1
Hammes, B.S.2
Carrano, C.J.3
Crans, D.C.4
-
56
-
-
0035914908
-
Functional modeling of cobalamine-independent methionine synthase with pyrazolylborate-zinc-thiolate complexes
-
Brand U, Rombach M, Seebacher J, Vahrenkamp H (2001) Functional modeling of cobalamine-independent methionine synthase with pyrazolylborate-zinc-thiolate complexes. Inorg Chem 40:6151-6157.
-
(2001)
Inorg Chem
, vol.40
, pp. 6151-6157
-
-
Brand, U.1
Rombach, M.2
Seebacher, J.3
Vahrenkamp, H.4
-
57
-
-
0037389593
-
Synthetic modeling of zinc thiolates: Quantitative assessment of hydrogen bonding in modulating sulfur alkylation rates
-
Chiou SJ, Riordan CG, Rheingold AL (2003) Synthetic modeling of zinc thiolates: quantitative assessment of hydrogen bonding in modulating sulfur alkylation rates. Proc Natl Acad Sci USA 100:3695-3700.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 3695-3700
-
-
Chiou, S.J.1
Riordan, C.G.2
Rheingold, A.L.3
-
58
-
-
13844316746
-
Enterococcal cytolysin: A novel two component peptide system that serves as a bacterial defense against eukaryotic and prokaryotic cells
-
Cox CR, Coburn PS, Gilmore MS (2005) Enterococcal cytolysin: a novel two component peptide system that serves as a bacterial defense against eukaryotic and prokaryotic cells. Curr Protein Pept Sci 6:77-84.
-
(2005)
Curr Protein Pept Sci
, vol.6
, pp. 77-84
-
-
Cox, C.R.1
Coburn, P.S.2
Gilmore, M.S.3
-
59
-
-
84874115767
-
The sequence of the enterococcal cytolysin imparts unusual lanthionine stereochemistry
-
Tang W, van der Donk WA (2013) The sequence of the enterococcal cytolysin imparts unusual lanthionine stereochemistry. Nat Chem Biol 9:157-159.
-
(2013)
Nat Chem Biol
, vol.9
, pp. 157-159
-
-
Tang, W.1
Van Der Donk, W.A.2
-
60
-
-
84861445578
-
Characterization of new class III lantibiotics-erythreapeptin, avermipeptin and griseopeptin from Saccharopolyspora erythraea, Streptomyces avermitilis and Streptomyces griseus demonstrates stepwise N-terminal leader processing
-
Völler GH, Krawczyk JM, Pesic A, Krawczyk B, Nachtigall J, Süssmuth RD (2012) Characterization of new class III lantibiotics- erythreapeptin, avermipeptin and griseopeptin from Saccharopolyspora erythraea, Streptomyces avermitilis and Streptomyces griseus demonstrates stepwise N-terminal leader processing. ChemBioChem 13:1174-1183.
-
(2012)
ChemBioChem
, vol.13
, pp. 1174-1183
-
-
Völler, G.H.1
Krawczyk, J.M.2
Pesic, A.3
Krawczyk, B.4
Nachtigall, J.5
Süssmuth, R.D.6
-
61
-
-
4744345463
-
The nisin-lipid II complex reveals a pyrophosphate cage that provides a blueprint for novel antibiotics
-
Hsu ST, Breukink E, Tischenko E, Lutters MA, De Kruijff B, Kaptein R, Bonvin AM, Van Nuland NA (2004) The nisin-lipid II complex reveals a pyrophosphate cage that provides a blueprint for novel antibiotics. Nat Struct Mol Biol 11:963-967.
-
(2004)
Nat Struct Mol Biol
, vol.11
, pp. 963-967
-
-
Hsu, S.T.1
Breukink, E.2
Tischenko, E.3
Lutters, M.A.4
De Kruijff, B.5
Kaptein, R.6
Bonvin, A.M.7
Van Nuland, N.A.8
-
62
-
-
0030041310
-
Structure determination of an immunopotentiator peptide, cinnamycin, complexed with lysophosphatidylethanolamine by 1H-NMR
-
Hosoda K, Ohya M, Kohno T, Maeda T, Endo S, Wakamatsu K (1996) Structure determination of an immunopotentiator peptide, cinnamycin, complexed with lysophosphatidylethanolamine by 1H-NMR. J Biochem 119:226-230.
-
(1996)
J Biochem
, vol.119
, pp. 226-230
-
-
Hosoda, K.1
Ohya, M.2
Kohno, T.3
Maeda, T.4
Endo, S.5
Wakamatsu, K.6
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