Walinomycyna (Polish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Walinomycyna" in Polish language version.

refsWebsite

Global rank Polish rank

26doi.org

2^nd place

6^th place

2worldcat.org

5^th place

2^nd place

2nih.gov

4^th place

7^th place

2pnas.org

1,293^rd place

849^th place

1rupress.org

low place

1springer.com

274^th place

376^th place

1wbc.poznan.pl

5,747^th place

117^th place

1archive.is

87^th place

5^th place

1wiley.com

222^nd place

228^th place

1sciencedirect.com

149^th place

235^th place

1koreascience.kr

low place

archive.is

E. Makrlík, P. Vaňura, J. Hálová. Stability of Ca2+, Zn2+ and Pb2+ complexes with valinomycin in nitrobenzene saturated with water. „Pol. J. Chem.”. 81, s. 1531-1534, 2007. (ang.).

doi.org

H. Brockmann, G. Schmidt-Kastner. Valinomycin I, XXVII. Mitteil. über antibiotica aus actinomyceten. „Chem. Ber.”. 88, s. 57-61, 1955. DOI: 10.1002/cber.19550880111. (niem.).
H. Ristow, J. Salnikow, H. Kleinkauf. Biosynthesis of valinomycin. „FEBS Lett.”. 2, s. 127-130, 1974. DOI: 10.1016/0014-5793(74)80768-4. (ang.).
T. Anke, F. Lipmann. Studies on the biosynthesis of valinomycin. „FEBS Lett.”. 82, s. 337-340, 1977. DOI: 10.1016/0014-5793(77)80615-7. (ang.).
B.C. Pressman, E.J. Harris W.S. Jagger, J.H. Johnson. Antibiotic-mediated transport of alkali ions across lipid barriers. „PNAS”. 58, s. 1949-1956, 1967. DOI: 10.1073/pnas.58.5.1949. (ang.).
B.C. Pressman. Biological applications of ionophores. „Annu. Rev. Biochem.”. 45, s. 501-530, 1976. DOI: 10.1146/annurev.bi.45.070176.002441. (ang.).
C. Moore, B.C. Pressman. Mechanism of action of valinomycin on mitochondria. „Biochem. Biophys. Res. Commun.”. 15, s. 562-567, 1964. DOI: 10.1016/0006-291X(64)90505-4. (ang.).
M. Hofert, B.C. Pressman. Stimulation of oxidative phosphorylation in mitochondria by potassium in the presence of valinomycin. „Biochemistry”. 5, s. 3919-3925, 1965. DOI: 10.1021/bi00876a025. (ang.).
E. Ogata, H. Rasmussen. Valinomycin and mitochondrial ion transport. „Biochemistry”. 5, s. 57-66, 1966. DOI: 10.1021/bi00865a009. (ang.).
M.M. Shemyakin i inni. The structure-antimicrobial relation for valinomycin depsipeptides. „Experientia”. 21, s. 548-552, 1965. DOI: 10.1007/BF02138991. (ang.).
G.D. Smith, W.L. Duax, i inni. Crystal and molecular structure of the triclinic and monoclinic forms of valinomycin, C54H90N6O18. „J. Am. Chem. Soc.”. 97, s. 7242–7247, 1975. DOI: 10.1021/ja00858a008. (ang.).
I.L. Karle. Conformation of valinomycin in a triclinic crystal form. „J. Am. Chem. Soc.”. 97, s. 4379–4386, 1975. DOI: 10.1021/ja00848a041. (ang.).
K. Neupert-Laves, M. Dobler. The Crystal Structure of a K+ Complex of Valinomycin. „Helv. Chim. Acta”. 58, s. 432-442, 1975. DOI: 10.1002/hlca.19750580212. (ang.).
L.K. Steinrauf, J.A. Hamilton, M.N. Sabesan. Crystal structure of valinomycin sodium picrate: Anion effects on valinomycin – cation complexes. „J. Am. Chem. Soc.”. 104, s. 4085-4091, 1982. DOI: 10.1021/ja00379a008. (ang.).
T.R. Forester, W. Smith, J.H.R. Clarke. Antibiotic activity of valinomycin. Molecular dynamics simulations involving the water/membrane interface. „J. Chem. Soc., Faraday Trans.”. 93, s. 613-619, 1997. DOI: 10.1039/A606452C. (ang.).
M.C. Rose, R.W. Henkens. Stability of sodium and potassium complexes of valinomycin. „BBA”. 372, s. 426-435, 1974. DOI: 10.1016/0304-4165(74)90204-9. (ang.).
E. Makrlík, P. Vaňura, P. Selucký. Experimental evidences for some unusual divalent cation complexes of valinomycin. „Monat. fur Chem. – Chemical Monthly”. 139, s. 597-600, 2008. DOI: 10.1007/s00706-007-0816-x. (ang.).
E. Makrlík, P. Vaňura. Stability of the valinomycin – lithium complex in nitrobenzene saturated with water. „J. Radioanal. Nucl. Chem.”. 267, s. 247-249, 2006. DOI: 10.1007/s10967-006-0036-6. (ang.).
M. Daňková, E. Makrlík, P. Vaňura. Stability of the valinomycin-rubidium complex in water saturated nitrobenzene. „J. Radioanal. Nucl. Chem.”. 221, s. 251-253, 1997. DOI: 10.1007/BF02035281. (ang.).
E. Makrlík, P. Vaňura. Stability of complex of Cs+ with valinomycin in nitrobenzene saturated with water. „J. Radioanal. Nucl. Chem.”. 214, s. 339-346, 1996. DOI: 10.1007/BF02164376. (ang.).
J. Kříž, J. Dybal, E. Makrlík. Valinomycin–proton interaction in low-polarity media. „Biopolymers”. 82, s. 536–548, 2006. DOI: 10.1002/bip.20506. (ang.).
J. Kříž, E. Makrlík, P. Vaňura. NMR evidence of a valinomycin–proton complex. „Biopolymers”. 81, s. 104–109, 2006. DOI: 10.1002/bip.20384.
O. Shirai, H. Yamana, T. Ohnuki, Y. Yoshida, S. Kihara. Ion transport across a bilayer lipid membrane facilitated by valinomycin. „J. Electroanal. Chem.”. 570, s. 219–226, 2004. DOI: 10.1016/j.jelechem.2004.03.033. (ang.).
M.C. Pansa, G. Migliori Natalizi, S. Bettini. Toxicity of valinomycin on insects. „J. Invertebr. Pathol.”. 22, s. 148-152, 1973. DOI: 10.1016/0022-2011(73)90126-2. (ang.).
V.V. Teplova, i inni. The higher toxicity of cereulide relative to valinomycin is due to its higher affinity for potassium at physiological plasma concentration. „Toxicol. Appl. Pharmacol”. 210, s. 39-46, 2006. DOI: 10.1016/j.taap.2005.06.012. (ang.).
Y.-Q. Cheng. Deciphering the biosynthetic codes for the potent anti-SARS-CoV cyclodepsipeptide valinomycin in Streptomyces tsusimaensis ATCC 15141. „ChemBioChem”. 7, s. 471-477, 2006. DOI: 10.1002/cbic.200500425. (ang.).
C. Gabrielli, i inni. Investigation of ion-selective electrodes with neutral ionophores and ionic sites by EIS. II. Application to K+ detection. „J. Electroanal. Chem.”. 570, s. 291-304, 2004. DOI: 10.1016/j.jelechem.2004.04.007. (ang.).

koreascience.kr

H.L. Tae, i inni. Antifungal activity of valinomycin, a cyclodepsipeptide from Streptomyces padanus TH-04. „Nat. Prod. Sci.”. 13, s. 144-147, 2007. (ang.).

nih.gov

ncbi.nlm.nih.gov

R. Kanne. Isolation and characterization of a potassium specific ionophore from Streptococcus faecalis. „Z. Naturforschung C”. 32, s. 926-928, 1977. ISSN 0341-0382. (ang.). PubMed
S. Kuroda. Studies on antitumor activity of valinomycin. „Jpn. J. Cancer Chemother.”. 11, s. 2625-2632, 1984. (jap.). PubMed

pnas.org

B.C. Pressman, E.J. Harris W.S. Jagger, J.H. Johnson. Antibiotic-mediated transport of alkali ions across lipid barriers. „PNAS”. 58, s. 1949-1956, 1967. DOI: 10.1073/pnas.58.5.1949. (ang.).
B.C. Pressman. Inducted active transport of ions in mitochondria. „PNAS”. 3, s. 1076-1083, 1965. (ang.).

rupress.org

L. Ernstern, G. Schatz. Mitochondria: A Historical Review. „J. Cell Biol.”. 91, s. 227-255, 1981. (ang.).

sciencedirect.com

O. Shirai, H. Yamana, T. Ohnuki, Y. Yoshida, S. Kihara. Ion transport across a bilayer lipid membrane facilitated by valinomycin. „J. Electroanal. Chem.”. 570, s. 219–226, 2004. DOI: 10.1016/j.jelechem.2004.03.033. (ang.).

springer.com

link.springer.com

L.K. Steinrauf. Crystal structures of valinomycin with potassium tetrachloroaurate and rubidium tetrachloroaurate with comparisons to other monovalent cation complexes. „J. Biosci.”. 8, s. 293-306, 1985. (ang.).

wbc.poznan.pl

G. Schroeder, B. Gierczyk: Syntetyczne receptory jonowe – jonofory. Poznań: Wydawnictwo BETAGRAF P.U.H., 2005, s. 4-33, seria: Chemia Supramolekularna. ISBN 83-89936-05-4. [dostęp 2011-09-08].

wiley.com

onlinelibrary.wiley.com

J. Kříž, E. Makrlík, P. Vaňura. NMR evidence of a valinomycin–proton complex. „Biopolymers”. 81, s. 104–109, 2006. DOI: 10.1002/bip.20384.

worldcat.org

R. Kanne. Isolation and characterization of a potassium specific ionophore from Streptococcus faecalis. „Z. Naturforschung C”. 32, s. 926-928, 1977. ISSN 0341-0382. (ang.). PubMed
M.A. Kroteń, M. Bartoszewicz, I. Święcicka. Cereulide and valinomycin, two important natural dodecadepsipeptides with ionophoretic atcivities. „Pol. J. Microbiol.”. 59, s. 3-10, 2010. ISSN 1733-1331. (ang.).