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Amino Acid Metabolism [[electronic resource]]
Amino Acid Metabolism [[electronic resource]]
Autore Bender David A
Edizione [3rd ed.]
Pubbl/distr/stampa Hoboken, : Wiley, 2012
Descrizione fisica 1 online resource (480 p.)
Disciplina 572.65
572/.65
Soggetto topico Amino acids - Metabolism
Amino Acids, Peptides, and Proteins
Metabolic Phenomena
Drugs
Metabolism
Amino Acids
ISBN 1-118-35818-X
1-283-54246-3
9786613854919
1-118-35817-1
1-118-35751-5
1-118-35819-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto 1.4.1 Purine synthesis 1.4.1.1 Phosphoribosyl pyrophosphate (PRPP) synthetase; 1.4.1.2 PRPP amidotransferase; 1.4.2 Purine catabolism and salvage; 1.4.2.1 Adenosine deaminase deficiency - severe combined immune deficiency; 1.4.2.2 Gout and hyperuricaemia; 1.4.2.3 HGPRT deficiency - the Lesch-Nyhan syndrome; 1.4.3 Pyrimidine synthesis; 1.4.3.1 Orotic aciduria; 1.4.4 Pyrimidine catabolism and salvage; 1.5 Deamination of amino acids; 1.5.1 Amino acid oxidases; 1.5.2 Amine oxidases; 1.5.3 Glutamate and alanine dehydrogenases; 1.5.4 Non-oxidative deamination of amino acids
1.5.5 Glutaminase and asparaginase 1.6 Excretion of nitrogenous waste; 1.6.1 Uricotelic and purinotelic species; 1.6.2 Ureotelic species; 1.6.2.1 Urea synthesis; 1.6.2.2 Inborn errors of metabolism affecting the urea synthesis cycle; 1.6.2.3 Entero-hepatic circulation of urea; 1.6.2.4 Canavanine; 1.7 Other nitrogenous compounds in human urine; 1.7.1 Aminoacidurias; Further reading; 2: Nitrogen Balance and Protein Turnover - Protein and Amino Acids in Human Nutrition; 2.1 Nitrogen balance and protein requirements; 2.1.1 Protein digestion and absorption
2.1.2 Protein digestibility and unavailable amino acids in dietary proteins 2.1.3 Obligatory nitrogen losses; 2.1.4 Dynamic equilibrium and tissue protein turnover; 2.1.5 Tissue protein catabolism; 2.1.5.1 Lysosomal autophagy; 2.1.5.2 Ubiquitin and the proteasome; 2.1.5.3 Active site proteolysis of apo-enzymes; 2.1.6 Whole body protein turnover; 2.1.6.1 The constant infusion, labelled precursor method; 2.1.6.2 The constant infusion, labelled end product method; 2.1.6.3 Rates of whole-body protein turnover; 2.1.6.4 The catabolic drive and amino acid oxidation
2.1.6.5 The energy cost of protein turnover
Record Nr. UNINA-9910139693803321
Bender David A  
Hoboken, : Wiley, 2012
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Amino Acid Metabolism
Amino Acid Metabolism
Autore Bender David A
Edizione [3rd ed.]
Pubbl/distr/stampa Hoboken, : Wiley, 2012
Descrizione fisica 1 online resource (480 p.)
Disciplina 572.65
572/.65
Soggetto topico Amino acids - Metabolism
Amino Acids, Peptides, and Proteins
Metabolism
Pharmaceutical Preparations
Amino Acids
ISBN 9786613854919
9781118358184
111835818X
9781283542463
1283542463
9781118358177
1118358171
9781118357514
1118357515
9781118358191
1118358198
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto 1.4.1 Purine synthesis 1.4.1.1 Phosphoribosyl pyrophosphate (PRPP) synthetase; 1.4.1.2 PRPP amidotransferase; 1.4.2 Purine catabolism and salvage; 1.4.2.1 Adenosine deaminase deficiency - severe combined immune deficiency; 1.4.2.2 Gout and hyperuricaemia; 1.4.2.3 HGPRT deficiency - the Lesch-Nyhan syndrome; 1.4.3 Pyrimidine synthesis; 1.4.3.1 Orotic aciduria; 1.4.4 Pyrimidine catabolism and salvage; 1.5 Deamination of amino acids; 1.5.1 Amino acid oxidases; 1.5.2 Amine oxidases; 1.5.3 Glutamate and alanine dehydrogenases; 1.5.4 Non-oxidative deamination of amino acids
1.5.5 Glutaminase and asparaginase 1.6 Excretion of nitrogenous waste; 1.6.1 Uricotelic and purinotelic species; 1.6.2 Ureotelic species; 1.6.2.1 Urea synthesis; 1.6.2.2 Inborn errors of metabolism affecting the urea synthesis cycle; 1.6.2.3 Entero-hepatic circulation of urea; 1.6.2.4 Canavanine; 1.7 Other nitrogenous compounds in human urine; 1.7.1 Aminoacidurias; Further reading; 2: Nitrogen Balance and Protein Turnover - Protein and Amino Acids in Human Nutrition; 2.1 Nitrogen balance and protein requirements; 2.1.1 Protein digestion and absorption
2.1.2 Protein digestibility and unavailable amino acids in dietary proteins 2.1.3 Obligatory nitrogen losses; 2.1.4 Dynamic equilibrium and tissue protein turnover; 2.1.5 Tissue protein catabolism; 2.1.5.1 Lysosomal autophagy; 2.1.5.2 Ubiquitin and the proteasome; 2.1.5.3 Active site proteolysis of apo-enzymes; 2.1.6 Whole body protein turnover; 2.1.6.1 The constant infusion, labelled precursor method; 2.1.6.2 The constant infusion, labelled end product method; 2.1.6.3 Rates of whole-body protein turnover; 2.1.6.4 The catabolic drive and amino acid oxidation
2.1.6.5 The energy cost of protein turnover
Record Nr. UNINA-9910820769603321
Bender David A  
Hoboken, : Wiley, 2012
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Amino acids and peptides / / G.C. Barrett and D.T. Elmore [[electronic resource]]
Amino acids and peptides / / G.C. Barrett and D.T. Elmore [[electronic resource]]
Autore Barrett G. C. <1935->
Pubbl/distr/stampa Cambridge : , : Cambridge University Press, , 1998
Descrizione fisica 1 online resource (xv, 224 pages) : digital, PDF file(s)
Disciplina 572/.65
Soggetto topico Amino acids
Peptides
ISBN 1-107-11238-9
0-511-03952-2
9786612388941
1-282-38894-0
0-511-64273-3
1-139-16382-5
0-511-15126-8
0-511-55552-0
0-511-05294-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; Half-title; Title; Copyright; Contents; Foreword; 1 Introduction; 2 Conformations of amino acids and peptides; 3 Physicochemical properties of amino acids and peptides; 4 Reactions and analytical methods for amino acids and peptides; 5 Determination of the primary structures of peptides and proteins; 6 Synthesis of amino acids; 7 Methods for the synthesis of peptides; 8 Biological roles of amino acids and peptides; 9 Some aspects of amino-acid and peptide drug design; Subject index
Altri titoli varianti Amino Acids & Peptides
Record Nr. UNINA-9910449849503321
Barrett G. C. <1935->  
Cambridge : , : Cambridge University Press, , 1998
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Amino acids and peptides / / G.C. Barrett and D.T. Elmore [[electronic resource]]
Amino acids and peptides / / G.C. Barrett and D.T. Elmore [[electronic resource]]
Autore Barrett G. C. <1935->
Pubbl/distr/stampa Cambridge : , : Cambridge University Press, , 1998
Descrizione fisica 1 online resource (xv, 224 pages) : digital, PDF file(s)
Disciplina 572/.65
Soggetto topico Amino acids
Peptides
ISBN 1-107-11238-9
0-511-03952-2
9786612388941
1-282-38894-0
0-511-64273-3
1-139-16382-5
0-511-15126-8
0-511-55552-0
0-511-05294-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; Half-title; Title; Copyright; Contents; Foreword; 1 Introduction; 2 Conformations of amino acids and peptides; 3 Physicochemical properties of amino acids and peptides; 4 Reactions and analytical methods for amino acids and peptides; 5 Determination of the primary structures of peptides and proteins; 6 Synthesis of amino acids; 7 Methods for the synthesis of peptides; 8 Biological roles of amino acids and peptides; 9 Some aspects of amino-acid and peptide drug design; Subject index
Altri titoli varianti Amino Acids & Peptides
Record Nr. UNINA-9910777355103321
Barrett G. C. <1935->  
Cambridge : , : Cambridge University Press, , 1998
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Amino group chemistry : from synthesis to the life sciences / / edited by Alfredo Ricci
Amino group chemistry : from synthesis to the life sciences / / edited by Alfredo Ricci
Pubbl/distr/stampa Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2008
Descrizione fisica 1 online resource (410 p.)
Disciplina 547.042
572/.65
Soggetto topico Amino acids
Soggetto genere / forma Electronic books.
ISBN 1-282-78423-4
9786612784231
3-527-62126-1
3-527-62127-X
Classificazione 35.62
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione ger
Nota di contenuto Amino Group Chemistry; Contents; Preface; List of Contributors; 1 Simple Molecules, Highly Efficient Amination; 1.1 Introduction; 1.2 Hydroxylamine Derivatives; 1.2.1 O-Sulfonylhydroxylamine; 1.2.2 O-Phosphinylhydroxylamine; 1.2.3 O-Acylhydroxylamine; 1.2.4 O-Trimethylsilylhydroxylamine; 1.2.5 Experimental Procedures; 1.3 Oxime Derivatives; 1.3.1 Synthesis of Primary Amines by Electrophilic Amination of Carbanions; 1.3.2 Experimental Procedures; 1.4 Azo Compounds; 1.4.1 Azodicarboxylates; 1.4.1.1 Allylic Amination through Ene-Type Reactions; 1.4.1.2 Hydrohydrazination of Alkenes
1.4.2 Arylazo Sulfones1.4.3 Experimental Procedures; 1.5 Oxaziridine Derivatives; 1.5.1 Electrophilic Amination of Carbon Nucleophiles; 1.5.2 Amination of Allylic and Propargylic Sulfides by Use of a Ketomalonate-Derived Oxaziridine; 1.5.3 Experimental Procedures; 1.6 Chloramine-T; 1.6.1 Aminochalcogenation of Alkenes; 1.6.2 Aminohydroxylation of Alkenes; 1.6.3 Aziridination of Alkenes; 1.6.4 Other Applications; 1.6.5 Experimental Procedures; 1.7 N-Sulfonyliminophenyliodinane; 1.7.1 Transition Metal-Catalyzed Amination of Alkenes; 1.7.2 Experimental Procedures
1.8 Transition Metal-Nitride Complexes1.8.1 Nitrogen Atom Transfer Mediated by Transition Metal/Nitride Complexes; 1.8.2 Experimental Procedures; 1.9 Azido Derivatives; 1.9.1 Electrophilic Amination of Organometallic Reagents with Organic Azides; 1.9.2 Radical-Mediated Amination with Sulfonyl Azides; 1.9.3 Hydroazidation of Alkenes with Sulfonyl Azides; 1.9.4 Experimental Procedures; 1.10 Gabriel-Type Reagents; 1.10.1 Nucleophilic Amination Reactions; 1.10.2 Experimental Procedure; 1.11 Conclusion; 2 Catalytic C-H Amination with Nitrenes; 2.1 Introduction; 2.2 Historical Overview
2.3 Hypervalent Iodine-Mediated C-H Amination2.3.1 Intramolecular C-H Amination; 2.3.1.1 From NH(2) Carbamates; 2.3.1.2 From NH(2) Sulfamates; 2.3.1.3 From Other Nitrogen Functionalities; 2.3.2 Intermolecular C-H Amination; 2.3.2.1 General Scope and Limitations; 2.3.2.2 Recent Major Improvements; 2.4 Other Nitrene Precursors for C-H Amination; 2.4.1 Azides; 2.4.2 Haloamines; 2.4.3 Carbamate Derivatives; 2.5 Amination of Aromatic C-H Bonds; 2.6 Applications in Total Synthesis; 2.6.1 Application of Intramolecular C-H Amination with Carbamates
2.6.2 Application of Intramolecular C-H Amination with Sulfamates2.6.3 Application of Intermolecular C-H Amination; 2.7 Conclusions; 3 Nitroalkenes as Amination Tools; 3.1 Introduction; 3.2 General Strategies for the Synthesis of Nitroalkenes; 3.3 Synthesis of Alkylamines; 3.3.1 Monoamines; 3.3.2 Amino Acid Derivatives; 3.3.3 Amino Alcohols; 3.3.4 Diamino Derivatives; 3.4 Pyrrolidine Derivatives; 3.4.1 Pyrrolidinones; 3.4.2 Pyrrolidines; 3.5 Piperidines and Piperazines; 3.6 Pyrrolizidines and Related Derivatives; 3.7 Arene-Fused Nitrogen Heterocycles; 3.7.1 Pyrroloindole Derivatives
3.7.2 Carbolines and their Tryptamine Precursors
Record Nr. UNINA-9910144276703321
Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Amino group chemistry : from synthesis to the life sciences / / edited by Alfredo Ricci
Amino group chemistry : from synthesis to the life sciences / / edited by Alfredo Ricci
Pubbl/distr/stampa Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2008
Descrizione fisica 1 online resource (410 p.)
Disciplina 547.042
572/.65
Soggetto topico Amino acids
ISBN 1-282-78423-4
9786612784231
3-527-62126-1
3-527-62127-X
Classificazione 35.62
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione ger
Nota di contenuto Amino Group Chemistry; Contents; Preface; List of Contributors; 1 Simple Molecules, Highly Efficient Amination; 1.1 Introduction; 1.2 Hydroxylamine Derivatives; 1.2.1 O-Sulfonylhydroxylamine; 1.2.2 O-Phosphinylhydroxylamine; 1.2.3 O-Acylhydroxylamine; 1.2.4 O-Trimethylsilylhydroxylamine; 1.2.5 Experimental Procedures; 1.3 Oxime Derivatives; 1.3.1 Synthesis of Primary Amines by Electrophilic Amination of Carbanions; 1.3.2 Experimental Procedures; 1.4 Azo Compounds; 1.4.1 Azodicarboxylates; 1.4.1.1 Allylic Amination through Ene-Type Reactions; 1.4.1.2 Hydrohydrazination of Alkenes
1.4.2 Arylazo Sulfones1.4.3 Experimental Procedures; 1.5 Oxaziridine Derivatives; 1.5.1 Electrophilic Amination of Carbon Nucleophiles; 1.5.2 Amination of Allylic and Propargylic Sulfides by Use of a Ketomalonate-Derived Oxaziridine; 1.5.3 Experimental Procedures; 1.6 Chloramine-T; 1.6.1 Aminochalcogenation of Alkenes; 1.6.2 Aminohydroxylation of Alkenes; 1.6.3 Aziridination of Alkenes; 1.6.4 Other Applications; 1.6.5 Experimental Procedures; 1.7 N-Sulfonyliminophenyliodinane; 1.7.1 Transition Metal-Catalyzed Amination of Alkenes; 1.7.2 Experimental Procedures
1.8 Transition Metal-Nitride Complexes1.8.1 Nitrogen Atom Transfer Mediated by Transition Metal/Nitride Complexes; 1.8.2 Experimental Procedures; 1.9 Azido Derivatives; 1.9.1 Electrophilic Amination of Organometallic Reagents with Organic Azides; 1.9.2 Radical-Mediated Amination with Sulfonyl Azides; 1.9.3 Hydroazidation of Alkenes with Sulfonyl Azides; 1.9.4 Experimental Procedures; 1.10 Gabriel-Type Reagents; 1.10.1 Nucleophilic Amination Reactions; 1.10.2 Experimental Procedure; 1.11 Conclusion; 2 Catalytic C-H Amination with Nitrenes; 2.1 Introduction; 2.2 Historical Overview
2.3 Hypervalent Iodine-Mediated C-H Amination2.3.1 Intramolecular C-H Amination; 2.3.1.1 From NH(2) Carbamates; 2.3.1.2 From NH(2) Sulfamates; 2.3.1.3 From Other Nitrogen Functionalities; 2.3.2 Intermolecular C-H Amination; 2.3.2.1 General Scope and Limitations; 2.3.2.2 Recent Major Improvements; 2.4 Other Nitrene Precursors for C-H Amination; 2.4.1 Azides; 2.4.2 Haloamines; 2.4.3 Carbamate Derivatives; 2.5 Amination of Aromatic C-H Bonds; 2.6 Applications in Total Synthesis; 2.6.1 Application of Intramolecular C-H Amination with Carbamates
2.6.2 Application of Intramolecular C-H Amination with Sulfamates2.6.3 Application of Intermolecular C-H Amination; 2.7 Conclusions; 3 Nitroalkenes as Amination Tools; 3.1 Introduction; 3.2 General Strategies for the Synthesis of Nitroalkenes; 3.3 Synthesis of Alkylamines; 3.3.1 Monoamines; 3.3.2 Amino Acid Derivatives; 3.3.3 Amino Alcohols; 3.3.4 Diamino Derivatives; 3.4 Pyrrolidine Derivatives; 3.4.1 Pyrrolidinones; 3.4.2 Pyrrolidines; 3.5 Piperidines and Piperazines; 3.6 Pyrrolizidines and Related Derivatives; 3.7 Arene-Fused Nitrogen Heterocycles; 3.7.1 Pyrroloindole Derivatives
3.7.2 Carbolines and their Tryptamine Precursors
Record Nr. UNINA-9910830098903321
Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Bioactive peptides : applications for improving nutrition and health / / Richard Owusu-Apenten
Bioactive peptides : applications for improving nutrition and health / / Richard Owusu-Apenten
Autore Owusu-Apenten R. K.
Pubbl/distr/stampa Boca Raton : , : CRC Press, , 2010
Descrizione fisica 1 online resource (416 p.)
Disciplina 572/.65
Soggetto topico Peptide drugs
Dietary supplements
Proteins - Metabolism
Proteins in human nutrition
Appetite stimulants
Soggetto genere / forma Electronic books.
ISBN 0-429-13297-2
1-4398-1363-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front cover; Contents; Preface; Acknowledgments; Author; Chapter 1: Nutrition and the HostResponse to Infectionand Injury; Chapter 2: Bioactive Peptidesfor Nutrition and Health; Chapter 3: Dietary ProteinRequirements for Health; Chapter 4: Protein Turnoverand Economics within the Body; Chapter 5: Major Processes forMuscle Gain and Loss; Chapter 6: Inflammation and InnateImmune Response; Chapter 7: Infection and Sepsis; Chapter 8: Anabolic Dysfunction; Chapter 9: Bioactive Peptidesfor Alleviating Illness Anorexia; Index; Back cover
Record Nr. UNINA-9910459266003321
Owusu-Apenten R. K.  
Boca Raton : , : CRC Press, , 2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Bioactive peptides : applications for improving nutrition and health / / Richard Owusu-Apenten
Bioactive peptides : applications for improving nutrition and health / / Richard Owusu-Apenten
Autore Owusu-Apenten R. K.
Pubbl/distr/stampa Boca Raton : , : CRC Press, , 2010
Descrizione fisica 1 online resource (416 p.)
Disciplina 572/.65
Soggetto topico Peptide drugs
Dietary supplements
Proteins - Metabolism
Proteins in human nutrition
Appetite stimulants
ISBN 0-429-13297-2
1-4398-1363-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front cover; Contents; Preface; Acknowledgments; Author; Chapter 1: Nutrition and the HostResponse to Infectionand Injury; Chapter 2: Bioactive Peptidesfor Nutrition and Health; Chapter 3: Dietary ProteinRequirements for Health; Chapter 4: Protein Turnoverand Economics within the Body; Chapter 5: Major Processes forMuscle Gain and Loss; Chapter 6: Inflammation and InnateImmune Response; Chapter 7: Infection and Sepsis; Chapter 8: Anabolic Dysfunction; Chapter 9: Bioactive Peptidesfor Alleviating Illness Anorexia; Index; Back cover
Record Nr. UNINA-9910784904303321
Owusu-Apenten R. K.  
Boca Raton : , : CRC Press, , 2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Bioactive peptides : applications for improving nutrition and health / / Richard Owusu-Apenten
Bioactive peptides : applications for improving nutrition and health / / Richard Owusu-Apenten
Autore Owusu-Apenten R. K.
Pubbl/distr/stampa Boca Raton : , : CRC Press, , 2010
Descrizione fisica 1 online resource (416 p.)
Disciplina 572/.65
Soggetto topico Peptide drugs
Dietary supplements
Proteins - Metabolism
Proteins in human nutrition
Appetite stimulants
ISBN 0-429-13297-2
1-4398-1363-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front cover; Contents; Preface; Acknowledgments; Author; Chapter 1: Nutrition and the HostResponse to Infectionand Injury; Chapter 2: Bioactive Peptidesfor Nutrition and Health; Chapter 3: Dietary ProteinRequirements for Health; Chapter 4: Protein Turnoverand Economics within the Body; Chapter 5: Major Processes forMuscle Gain and Loss; Chapter 6: Inflammation and InnateImmune Response; Chapter 7: Infection and Sepsis; Chapter 8: Anabolic Dysfunction; Chapter 9: Bioactive Peptidesfor Alleviating Illness Anorexia; Index; Back cover
Record Nr. UNINA-9910799963903321
Owusu-Apenten R. K.  
Boca Raton : , : CRC Press, , 2010
Materiale a stampa
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Gramicidin and related ion channel-forming peptides [[electronic resource] /] / [editors, Derek J. Chadwick and Gail Cardew]
Gramicidin and related ion channel-forming peptides [[electronic resource] /] / [editors, Derek J. Chadwick and Gail Cardew]
Pubbl/distr/stampa Chichester ; ; New York, : Wiley, 1999
Descrizione fisica 1 online resource (286 p.)
Disciplina 572.65
572/.65
Altri autori (Persone) ChadwickDerek
CardewGail
Collana Novartis Foundation symposium
Soggetto topico Gramicidins
Ionophores
Ion channels
Soggetto genere / forma Electronic books.
ISBN 1-282-45526-5
9786612455261
0-470-51571-6
0-470-51572-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto GRAMICIDIN AND RELATED ION PEPTIDES CHANNEL-FORMING; Contents; Participants; Introduction: gramicidin, a model ion channel; Correlations of structure, dynamics and function in the gramicidin channel by solid-state NMR spectroscopy; X-ray crystallographic structures of gramicidin and their relation to the Streptomyces Zividuns potassium channel structure; General discussion I; Design and characterization of gramicidin channels with side chain or backbone mutations; Engineering charge selectivity in alamethicin channels; Lorentzian noise in single gramicidin A channel forrnarnidiniurn currents
Can we use rate constants and state models to describe ion transport through gramicidin channels?The binding site of sodium in the gramicidin A channel; The mechanism of channel formation by alarnethicin as viewed by molecular dynamics simulations; General discussion I1; Ionic interactions in multiply occupied channels; Peptide influences on lipids; Peptide-lipid interactions and mechanisms of antimicrobial peptides; Folding patterns of membrane proteins: diversity and the limitations of their prediction
Molecular basis of the charge selectivity of nicotinic acetylcholine receptor and related ligand-gated ion channelsThe gramicidin-based biosensor: a functioning nano-machine; Final general discussion; Summary: what we have learned about gramicidin and other ion channels; Index of contributors; Subject Index
Record Nr. UNINA-9910144736703321
Chichester ; ; New York, : Wiley, 1999
Materiale a stampa
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