المؤلفون: Gochin, Miriam, Khorosheva, Valentina, Case, Martin A

المصدر: Journal of the American Chemical Society. 124(37)

مصطلحات موضوعية: 2, 2'-Dipyridyl: chemistry, Amino Acid Sequence, Cobalt: chemistry, Computer Simulation, Kinetics, Leucine: chemistry, Metalloproteins: chemical synthesis, chemistry, Models, Chemical, Models, Molecular, Molecular Sequence Data, Nickel: chemistry, Nuclear Magnetic Resonance, Biomolecular: methods, Oligopeptides: chemical synthesis, chemistry, Protein Isoforms, Protein Structure, Secondary, Protein Structure, Tertiary, Spectrophotometry, Ultraviolet

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/3n29686q

المؤلفون: Andersen, Ole A, Nathubhai, Amit, Dixon, Mark J, Eggleston, Ian M, van Aalten, Daan M F

المصدر: Andersen , O A , Nathubhai , A , Dixon , M J , Eggleston , I M & van Aalten , D M F 2008 , ' Structure-based dissection of the natural product cyclopentapeptide chitinase inhibitor argifin ' , Cell Chemical Biology , vol. 15 , no. 3 , pp. 295-301 . https://doi.org/10.1016/j.chembiol.2008.02.015

مصطلحات موضوعية: Arginine/analogs & derivatives, Aspergillus fumigatus/enzymology, Biological Products/chemical synthesis, Chitinases/antagonists & inhibitors, Crystallography, X-Ray, Drug Design, Oligopeptides/chemical synthesis, Peptide Fragments/metabolism, Peptides, Cyclic/chemical synthesis, Structure-Activity Relationship, Urea/analogs & derivatives

وصف الملف: application/pdf

Relation: https://pure.northampton.ac.uk/en/publications/0ae8d91c-756d-4df8-a00b-ed151214d1f2

الاتاحة: https://pure.northampton.ac.uk/en/publications/0ae8d91c-756d-4df8-a00b-ed151214d1f2
https://doi.org/10.1016/j.chembiol.2008.02.015
https://pure.northampton.ac.uk/ws/files/55121633/Cell_Cem_Biol_2008.pdf

المساهمون: Byeong Woo Park, Ki Suk Kim, Kyung Sup Kim, Eun Kyung Kim, Kyong Sik Lee, Min Kyu Heo, Park, Byeong Woo, Kim, Eun Kyung, Kim, Eun-Kyung

المصدر: T200303043.pdf

مصطلحات موضوعية: Amino Acid Sequence, Animals, Cell Division/drug effects, Cell Line, Mice, Oligopeptides/chemical synthesis, Oligopeptides/pharmacology, Peptide Fragments/chemical synthesis, Peptide Fragments/pharmacology, Receptor, ErbB-2/chemistry, Recombinant Proteins/chemical synthesis, Recombinant Proteins/pharmacology, Technology, Pharmaceutical, Transfection, HER2/neu, mimetic peptide, biologic therapy

وصف الملف: 58~64

Relation: YONSEI MEDICAL JOURNAL; J02813; OAK-2003-00289; https://ir.ymlib.yonsei.ac.kr/handle/22282913/113449; T200303043; YONSEI MEDICAL JOURNAL, Vol.44(1) : 58-64, 2003

الاتاحة: https://ir.ymlib.yonsei.ac.kr/handle/22282913/113449
https://doi.org/10.3349/ymj.2003.44.1.58

المؤلفون: Bodor, N, Tóth-Sarudy, E, Holm, T, Pallagi, I, Vass, E, Buchwald, P, Langel, U

المصدر: J Pharm Pharmacol. 59(8):1065-76

مصطلحات موضوعية: Amino Acids/chemistry, Aminocaproic Acids/chemistry, Arginine/analogs & derivatives/chemical synthesis/*chemistry, Biological Transport, Circular Dichroism, Drug Carriers/chemical synthesis/*chemistry, Fluorescein, Hela Cells, Humans, Models, Molecular, Oligopeptides/chemical synthesis/*chemistry, Protein Conformation, Spectroscopy, Fourier Transform Infrared, Structure-Activity Relationship

وصف الملف: print

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-20671
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_uids=17725848&dopt=Citation

المؤلفون: Jaremko, Mariusz, Jaremko, Lukasz, Mazur, Adam, Makowski, Maciej, Lisowski, Marek

المصدر: Amino acids 45(4), 865-875 (2013). doi:10.1007/s00726-013-1534-9

مصطلحات موضوعية: info:eu-repo/classification/ddc/540, Circular Dichroism, Magnetic Resonance Spectroscopy, Oligopeptides: chemical synthesis, Oligopeptides: chemistry, Phenylalanine: chemistry, Protein Conformation, Protein Stability, Stereoisomerism, Oligopeptides, Phenylalanine

جغرافية الموضوع: DE

Relation: info:eu-repo/semantics/altIdentifier/issn/0939-4451; info:eu-repo/semantics/altIdentifier/issn/1438-2199; info:eu-repo/semantics/altIdentifier/pmid/pmid:23812673; https://pub.dzne.de/record/137044; https://pub.dzne.de/search?p=id:%22DZNE-2020-03366%22

الاتاحة: https://pub.dzne.de/record/137044
https://pub.dzne.de/search?p=id:%22DZNE-2020-03366%22

المؤلفون: Huhn, C., Ruhaak, L.R., Wuhrer, M., Deelder, A.D.

المصدر: Journal of proteomics 75, 1515 - 1528 (2012). doi:10.1016/j.jprot.2011.11.028

مصطلحات موضوعية: info:eu-repo/classification/ddc/570, Blood Proteins: analysis, Glycosylation, Humans, Oligopeptides: chemical synthesis, Oligopeptides: chemistry, Peptide Library, Polysaccharides: analysis, Polysaccharides: chemistry, Proteomics: methods, Blood Proteins, Oligopeptides, Polysaccharides, On-bead glycan release, Glycan analysis, Protein enrichment and depletion, Protein capturing, ProteoMiner beads, DNA sequencer

جغرافية الموضوع: DE

Relation: info:eu-repo/semantics/altIdentifier/issn/1874-3919; info:eu-repo/semantics/altIdentifier/pmid/pmid:22154983; info:eu-repo/semantics/altIdentifier/wos/WOS:000300924700006; https://juser.fz-juelich.de/record/19782; https://juser.fz-juelich.de/search?p=id:%22PreJuSER-19782%22

الاتاحة: https://juser.fz-juelich.de/record/19782
https://juser.fz-juelich.de/search?p=id:%22PreJuSER-19782%22

المؤلفون: Clifton, I. J., Ge, W., Adlington, R. M., Baldwin, J. E., Rutledge, P. J.

المصدر: Archives of biochemistry and biophysics 516, 103-107 (2011). doi:10.1016/j.abb.2011.09.014

مصطلحات موضوعية: info:eu-repo/classification/ddc/500, Catalytic Domain, Crystallography, X-Ray, Iron: chemistry, Methionine: analogs & derivatives, Methionine: chemistry, Models, Molecular, Oligopeptides: chemical synthesis, Oligopeptides: chemistry, Oxidoreductases: chemistry, Oxidoreductases: metabolism, Static Electricity, Substrate Specificity, Sulfides: chemistry, Oligopeptides, Sulfides, 5-(2-aminoadipyl)cysteinylvaline, Methionine, Iron, Oxidoreductases, isopenicillin N synthetase

جغرافية الموضوع: DE

Relation: info:eu-repo/semantics/altIdentifier/pmid/pmid:22001738; info:eu-repo/semantics/altIdentifier/issn/0003-9861; info:eu-repo/semantics/altIdentifier/issn/1096-0384; info:eu-repo/semantics/altIdentifier/wos/WOS:000297716700003; https://bib-pubdb1.desy.de/record/139099; https://bib-pubdb1.desy.de/search?p=id:%22PHPPUBDB-22954%22

الاتاحة: https://bib-pubdb1.desy.de/record/139099
https://bib-pubdb1.desy.de/search?p=id:%22PHPPUBDB-22954%22

المؤلفون: Znabet, Anass, Polak, Marloes M, Janssen, Elwin, de Kanter, Frans J J, Turner, Nicholas J, Orru, Romano V A, Ruijter, Eelco

المصدر: Znabet , A , Polak , M M , Janssen , E , de Kanter , F J J , Turner , N J , Orru , R V A & Ruijter , E 2010 , ' A highly efficient synthesis of telaprevir by strategic use of biocatalysis and multicomponent reactions ' , Chemical Commununications , vol. 46 , no. 42 , pp. 7918-7920 . https://doi.org/10.1039/c0cc02823a

مصطلحات موضوعية: Antiviral Agents/chemical synthesis, Biocatalysis, Dimerization, Oligopeptides/chemical synthesis, Oxidation-Reduction, Serine Proteinase Inhibitors/chemical synthesis

الاتاحة: https://research.vu.nl/en/publications/8727d01f-d6b0-48f3-9b80-44ff64af9880
https://doi.org/10.1039/c0cc02823a
https://hdl.handle.net/1871.1/8727d01f-d6b0-48f3-9b80-44ff64af9880

المؤلفون: Chen, MQ, Weng, LH, Chang, XW, Zhang, DW, Jiang, ZF, Song, KS, Zhang, YH, Zhu, NY, Yang, D

مصطلحات موضوعية: Amino Acids - Chemistry, Circular Dichroism, Crystallography, X-Ray, Cyclopropanes - Chemical Synthesis - Chemistry, Dipeptides - Chemistry, Models, Molecular, Molecular Conformation, Molecular Sequence Data, Molecular Structure, Nitrogen - Chemistry, Nuclear Magnetic Resonance, Biomolecular, Oligopeptides - Chemical Synthesis - Chemistry, Oxygen - Chemistry

Relation: Journal of Organic Chemistry; http://www.scopus.com/mlt/select.url?eid=2-s2.0-77954561183&selection=ref&src=s&origin=recordpage; Journal Of Organic Chemistry, 2010, v. 75 n. 14, p. 4796-4805; 4805; 181176; WOS:000279569500015; 14; eid_2-s2.0-77954561183; 4796; http://hdl.handle.net/10722/168469; 75

الاتاحة: https://doi.org/10.1021/jo100810m
http://hdl.handle.net/10722/168469

المؤلفون: Molesworth, Samuel P., Osburn, Sandra M., Van Stipdonk, Michael J.

المساهمون: Wichita State University. Department of Chemistry

المصدر: NLM

مصطلحات موضوعية: Research Support, Non-U.S. Gov't, U.S. Gov't, Non-P.H.S, Amino Acid Sequence, Base Sequence, Ions/classification, Isomerism, Molecular Sequence Data, Molecular Structure, Oligopeptides/chemical synthesis, Spectrometry, Mass, Electrospray Ionization/classification

جغرافية الموضوع: United States

وصف الملف: 2174-81

Relation: Journal of the American Society for Mass Spectrometry; J. Am. Soc. Mass Spectrom.; 9010412; S1044-0305(09)00589-3; Journal of the American Society for Mass Spectrometry. 2009 Nov; 20(11): 2174-81.; http://dx.doi.org/10.1016/j.jasms.2009.07.023; http://hdl.handle.net/10057/4266

الاتاحة: http://hdl.handle.net/10057/4266
https://doi.org/10.1016/j.jasms.2009.07.023

المؤلفون: Wu, YD, Chen, F, Song, KS, Yang, D

مصطلحات موضوعية: Hydrogen Bonding, Amino Acids - Chemistry, Spectrophotometry, Infrared, Protein Structure, Secondary, Oligopeptides - Chemical Synthesis - Chemistry, Circular Dichroism

Relation: Journal of the American Chemical Society; http://www.scopus.com/mlt/select.url?eid=2-s2.0-40149088073&selection=ref&src=s&origin=recordpage; Journal Of The American Chemical Society, 2008, v. 130 n. 2, p. 743-755; 755; 151121; WOS:000252292500070; eid_2-s2.0-40149088073; 743; http://hdl.handle.net/10722/168278; 130

الاتاحة: https://doi.org/10.1021/ja0772750
http://hdl.handle.net/10722/168278

المؤلفون: Wu, Lisa Y, Anderson, Marc O, Toriyabe, Yoko, Maung, Jack, Campbell, Tammy Y, Tajon, Cheryl, Kazak, Marat, Moser, Jamie, Berkman, Clifford E

مصطلحات موضوعية: Glutamate Carboxypeptidase II - antagonists & inhibitors, Amides - chemical synthesis, Stereoisomerism, Humans, Crystallography, X-Ray, Male, Structure-Activity Relationship, Zinc - chemistry, Computer Simulation, Drug Design, Molecular Structure, Binding Sites, Glutamate Carboxypeptidase II - chemistry, Oligopeptides - chemistry, Amides - pharmacology, Oligopeptides - chemical synthesis, Phosphoric Acids - chemical synthesis, Recombinant Proteins - antagonists & inhibitors, Phosphoric Acids - chemistry, Models, Molecular, Recombinant Proteins - chemistry, Antigens, Surface - chemistry, Phosphoric Acids - pharmacology, Small Molecule Libraries, Amides - chemistry, Organometallic Compounds - chemistry, Oligopeptides - pharmacology

Relation: ispartof: Bioorganic & medicinal chemistry spage 7434 epage 7443 issue 23 vol 15; PMC2065856; WOS:000253489100022; 2376/115075; https://doi.org/10.1016/j.bmc.2007.07.028; 99900548121101842; alma:01ALLIANCE_WSU/bibs/99900548121101842

الاتاحة: https://doi.org/10.1016/j.bmc.2007.07.028
https://rex.libraries.wsu.edu/esploro/outputs/journalArticle/The-molecular-pruning-of-a-phosphoramidate/99900548121101842

المؤلفون: Villard, V., Kalyuzhniy, O., Riccio, O., Potekhin, S., Melnik, T.N., Kajava, A.V., Rüegg, C., Corradin, G.

المصدر: Journal of Peptide Science, vol. 12, no. 3, pp. 206-212

مصطلحات موضوعية: Cell Adhesion/drug effects, Cell Adhesion/physiology, Cell Line, Tumor, Humans, Integrin alphaVbeta3/chemistry, Integrin alphaVbeta3/drug effects, Ligands, Oligopeptides/chemical synthesis, Oligopeptides/chemistry, Protein Structure, Secondary/physiology, Tertiary/physiology, Structure-Activity Relationship

Relation: info:eu-repo/semantics/altIdentifier/pmid/16103993; info:eu-repo/semantics/altIdentifier/pissn/1075-2617; https://serval.unil.ch/notice/serval:BIB_6D785D120087

الاتاحة: https://serval.unil.ch/notice/serval:BIB_6D785D120087
https://doi.org/10.1002/psc.707

المؤلفون: Checinska, L., Mebs, S., Hübschle, C. B., Förster, D., Morgenroth, W., Luger, P.

المصدر: Organic & biomolecular chemistry 4, 3242-3251 (2006). doi:10.1039/b607744g

مصطلحات موضوعية: info:eu-repo/classification/ddc/540, Alanine, Crystallography, X-Ray, Hydrogen Bonding, Models, Molecular, Molecular Conformation, Oligopeptides: chemical synthesis, Oligopeptides: chemistry, Static Electricity, Tyrosine, Oligopeptides

جغرافية الموضوع: DE

Relation: info:eu-repo/semantics/altIdentifier/pmid/pmid:17036112; info:eu-repo/semantics/altIdentifier/issn/1477-0520; info:eu-repo/semantics/altIdentifier/wos/WOS:000239915500013; info:eu-repo/semantics/altIdentifier/issn/1477-0539; https://bib-pubdb1.desy.de/record/78777; https://bib-pubdb1.desy.de/search?p=id:%22PHPPUBDB-365%22

الاتاحة: https://bib-pubdb1.desy.de/record/78777
https://bib-pubdb1.desy.de/search?p=id:%22PHPPUBDB-365%22

المؤلفون: Ma, J, Liang, W, Zhao, Q, Zhou, Z, Pei, D, Ziebuhr, J, Hilgenfeld, R, Yuen, KY, Wong, L, Gao, G, Chen, S, Chen, Z, Ma, D, Rao, Z, Bartlam, M, Yang, H, Xie, W, Xue, X, Yang, K

مصطلحات موضوعية: Oxazoles - Chemical Synthesis - Pharmacology, Protein Conformation, Viral Proteins - Antagonists & Inhibitors, Tumor Cells, Cultured, Transmissible Gastroenteritis Virus - Enzymology, Sars Virus - Enzymology, Pyrrolidinones - Chemical Synthesis - Pharmacology, Animals, Antiviral Agents - Chemical Synthesis - Pharmacology, Binding Sites, Coronavirus - Enzymology, Crystallography, X-Ray, Cysteine Endopeptidases - Chemistry - Metabolism, Cysteine Proteinase Inhibitors - Chemical Synthesis - Pharmacology, Drug Design, Humans, Kinetics, Mice, Molecular Sequence Data, Oligopeptides - Chemical Synthesis - Pharmacology

Relation: PLoS biology.; Plos Biology., 2005, v. 3 n. 10, p. e324; WOS:000232404600009; 10; eid_2-s2.0-26444498493; e324; http://hdl.handle.net/10722/157435

الاتاحة: https://doi.org/10.1371/journal.pbio.0030324
http://hdl.handle.net/10722/157435

المؤلفون: Donella-Deana, Arianna, Marin, Oriano, Cesaro, Luca, Gunby, Rosalind H., Ferrarese, Anna, Coluccia, Addolorata M. L., Tartari, Carmen J., Mologni, Luca, Scapozza, Leonardo, Gambacorti-Passerini, Carlo, Pinna, Lorenzo A.

المصدر: ISSN: 0006-2960 ; Biochemistry, vol. 44, no. 23 (2005) p. 8533-8542.

مصطلحات موضوعية: info:eu-repo/classification/ddc/615, Amino Acid Sequence, Amino Acid Substitution, Cell Line, Tumor, Enzyme Activation, Humans, Lymphoma, Large-Cell, Anaplastic/enzymology, Molecular Sequence Data, Oligopeptides/chemical synthesis, Peptides/chemical synthesis, Phosphorylation, Protein Structure, Tertiary, Protein-Tyrosine Kinases/chemistry/metabolism, Receptor Protein-Tyrosine Kinases/chemistry/metabolism, Substrate Specificity, Tyrosine/metabolism

Relation: info:eu-repo/semantics/altIdentifier/pmid/15938644; https://archive-ouverte.unige.ch/unige:81203; unige:81203

الاتاحة: https://archive-ouverte.unige.ch/unige:81203

المؤلفون: Anbalagan, Victor, Silva, A. T. M., Rajagopalachary, S, Bulleigh, Kellis, Talaty, Erach R., Van Stipdonk, Michael J.

المساهمون: Wichita State University. Department of Chemistry

المصدر: NLM

مصطلحات موضوعية: Research Support, Non-U.S. Gov't, U.S. Gov't, Non-P.H.S, Amino Acids/chemistry, Cations/chemistry, Mass Spectrometry, Metals/chemistry, Molecular Structure, Oligopeptides/chemistry, Oligopeptides/chemical synthesis

جغرافية الموضوع: England

وصف الملف: 495-504

Relation: Journal of mass spectrometry : JMS; J Mass Spectrom; 9504818; Journal of mass spectrometry : JMS. 2004 May; 39(5): 495-504.; http://dx.doi.org/10.1002/jms.610; http://hdl.handle.net/10057/4323

الاتاحة: http://hdl.handle.net/10057/4323
https://doi.org/10.1002/jms.610

المؤلفون: Desjobert, Cécile, Richard de Soultrait, Vaea, Faure, Aurélie, Parissi, Vincent, Litvak, Simon, Tarrago-Litvak, Laura, Fournier, Michel

المساهمون: Laboratoire REGER : réplication et expression des génomes eucaryotes et rétroviraux (LRREGER), Université Bordeaux Segalen - Bordeaux 2-Centre National de la Recherche Scientifique (CNRS), This work was supported by the Agence Nationale de Recherche contre le SIDA (ANRS), the Centre National de la Recherche Scientifique (CNRS), and the Université Victor Segalen Bordeaux 2. C.D. was supported by an MNERT doctoral fellowship, and V.R.S. and V.P. were supported by fellowships from the “Ensemble contre le SIDA” (Sidaction)., We thank J. F. Mouscadet (UMR-CNRS 8532, Villejuif, France) for the generous gift of the histidine-tagged HIV-1 IN plasmid constructions. The manuscript was edited by Ray Cooke (Department of Foreign Languages, University of Bordeaux 2).

المصدر: ISSN: 0006-2960.

مصطلحات موضوعية: MESH: Bacteriophage M13, MESH: Binding, Competitive, MESH: DNA-Binding Proteins/chemical synthesis, MESH: DNA-Binding Proteins/metabolism, MESH: HIV Integrase Inhibitors/chemical synthesis, MESH: Dimerization, MESH: HIV Integrase/chemistry, MESH: HIV Integrase/metabolism, MESH: HIV Integrase Inhibitors/chemistry, MESH: HIV Integrase Inhibitors/metabolism, MESH: Oligopeptides/chemical synthesis, MESH: Oligopeptides/chemistry, MESH: Substrate Specificity, MESH: Oligopeptides/metabolism, MESH: Peptide Library, MESH: Protein Binding, MESH: Transcription, Genetic, MESH: Capsid Proteins, MESH: Viral Fusion Proteins/chemical synthesis, MESH: Viral Fusion Proteins/metabolism, MESH: Virus Integration, MESH: Catalysis, MESH: Catalytic Domain, [SDV]Life Sciences [q-bio], [SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology, [SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology

Relation: hal-02421530; https://hal.science/hal-02421530

الاتاحة: https://hal.science/hal-02421530
https://doi.org/10.1021/bi049385e

المؤلفون: Addolorata Coluccia, Luca Mologni, Rosalind H. Gunby, Luca Cesaro, Arianna Donella-Deana, Lorenzo A. Pinna, C. Gambacorti-Passerini, Carmen J. Tartari, Leonardo Scapozza, Anna Ferrarese, Oriano Marin

المساهمون: Donella deana, A, Marin, O, Cesaro, L, Gunby, R, Ferrarese, A, Tartari, C, Mologni, L, Scapozza, L, GAMBACORTI PASSERINI, C, Pinna, L

المصدر: Biochemistry, Vol. 44, No 23 (2005) pp. 8533-8542

مصطلحات موضوعية: ALK (anaplastic lymphoma kinase), Lymphoma, Peptides/chemical synthesis, Peptide, Biochemistry, Substrate Specificity, alk, anaplastic lymphoma, hemic and lymphatic diseases, Receptor Protein-Tyrosine Kinases/chemistry/metabolism, Anaplastic lymphoma kinase, Protein phosphorylation, Anaplastic Lymphoma Kinase, Tyrosine, Phosphorylation, Peptide sequence, chemistry.chemical_classification, ddc:615, Tumor, Synthetic peptides, Kinase, Protein-Tyrosine Kinases, Large-Cell, Lymphoma, Large-Cell, Anaplastic, Tyrosine/metabolism, Tyrosine kinase, Oligopeptides, Anaplastic/enzymology, Protein Structure, Solid-phase synthesis, Molecular Sequence Data, Biology, Cell Line, Oligopeptides/chemical synthesis, Cell Line, Tumor, Humans, Amino Acid Sequence, Receptor Protein-Tyrosine Kinases, Molecular biology, protein phosphorylation, Protein Structure, Tertiary, Enzyme Activation, chemistry, Amino Acid Substitution, Peptides, Tertiary, Protein-Tyrosine Kinases/chemistry/metabolism

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e1f6e7326e9237e0426d378cfc767dd
https://archive-ouverte.unige.ch/unige:81203

المؤلفون: Xie, Guiyang, Uttamchandani, Mahesh, Chen, Grace Y.J., Bu, Xianzhang, Lin, San San, Wong, Ka Man, Yan, Weili, Yao, Shao Q., Guo, Zhihong

مصطلحات موضوعية: Acetylcysteine: chemistry, Anti-Infective Agents: chemical synthesis, Anti-Infective Agents: pharmacokinetics, Esterases: metabolism, Kinetics, Oligopeptides: chemical synthesis, Oligopeptides: pharmacokinetics, Substrate Specificity, Sulfhydryl Compounds: chemistry, Tyrocidine: metabolism

Relation: https://repository.hkust.edu.hk/ir/Record/1783.1-29726; Bioorganic & medicinal chemistry letters, v. 12, (6), 2002, MAR 25, p. 989-992; https://doi.org/10.1016/S0960-894X(02)00067-7; http://lbdiscover.ust.hk/uresolver?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rfr_id=info:sid/HKUST:SPI&rft.genre=article&rft.issn=0960-894X&rft.volume=12&rft.issue=6&rft.date=2002&rft.spage=989&rft.epage=992&rft.aulast=Xie&rft.aufirst=GY&rft.atitle=Substrate+spectrum+of+tyrocidine+thioesterase+probed+with+randomized+peptide+N-acetylcysteamine+thioesters; http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=LinksAMR&SrcApp=PARTNER_APP&DestLinkType=FullRecord&DestApp=WOS&KeyUT=000175291700037; http://www.scopus.com/record/display.url?eid=2-s2.0-0037170820&origin=inward

الاتاحة: https://repository.hkust.edu.hk/ir/Record/1783.1-29726
https://doi.org/10.1016/S0960-894X(02)00067-7
http://lbdiscover.ust.hk/uresolver?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rfr_id=info:sid/HKUST:SPI&rft.genre=article&rft.issn=0960-894X&rft.volume=12&rft.issue=6&rft.date=2002&rft.spage=989&rft.epage=992&rft.aulast=Xie&rft.aufirst=GY&rft.atitle=Substrate+spectrum+of+tyrocidine+thioesterase+probed+with+randomized+peptide+N-acetylcysteamine+thioesters
http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=LinksAMR&SrcApp=PARTNER_APP&DestLinkType=FullRecord&DestApp=WOS&KeyUT=000175291700037
http://www.scopus.com/record/display.url?eid=2-s2.0-0037170820&origin=inward