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Forbavselse gullig Matematisk 3r 3 methyl d ornitine and lys Om tuberkulose Tentacle

3R)-3-methyl-D-ornithine | C6H14N2O2 | CID 51055215 - PubChem
3R)-3-methyl-D-ornithine | C6H14N2O2 | CID 51055215 - PubChem

3R)-3-methyl-D-ornithine | C6H14N2O2 | CID 51055215 - PubChem
3R)-3-methyl-D-ornithine | C6H14N2O2 | CID 51055215 - PubChem

Molecules | Free Full-Text | GC-MS Discrimination of Citrulline from  Ornithine and Homocitrulline from Lysine by Chemical Derivatization:  Evidence of Formation of N5-Carboxy-ornithine and N6-Carboxy-lysine
Molecules | Free Full-Text | GC-MS Discrimination of Citrulline from Ornithine and Homocitrulline from Lysine by Chemical Derivatization: Evidence of Formation of N5-Carboxy-ornithine and N6-Carboxy-lysine

Biosynthesis of the 22nd Genetically Encoded Amino Acid Pyrrolysine:  Structure and Reaction Mechanism of PylC at 1.5 Å Resolution - ScienceDirect
Biosynthesis of the 22nd Genetically Encoded Amino Acid Pyrrolysine: Structure and Reaction Mechanism of PylC at 1.5 Å Resolution - ScienceDirect

PowerPoint プレゼンテーション
PowerPoint プレゼンテーション

Product Index
Product Index

CheckMyBlob | Ligands
CheckMyBlob | Ligands

Evaluation of Metalloendopeptidase Lys-N Protease Performance under  Different Sample Handling Conditions | Journal of Proteome Research
Evaluation of Metalloendopeptidase Lys-N Protease Performance under Different Sample Handling Conditions | Journal of Proteome Research

Amino acid - Wikipedia
Amino acid - Wikipedia

Buy Amino Acids | Research Chemicals - Peptide Synthesis Tools Products |  Biosynth
Buy Amino Acids | Research Chemicals - Peptide Synthesis Tools Products | Biosynth

Molecules | Free Full-Text | GC-MS Discrimination of Citrulline from  Ornithine and Homocitrulline from Lysine by Chemical Derivatization:  Evidence of Formation of N5-Carboxy-ornithine and N6-Carboxy-lysine
Molecules | Free Full-Text | GC-MS Discrimination of Citrulline from Ornithine and Homocitrulline from Lysine by Chemical Derivatization: Evidence of Formation of N5-Carboxy-ornithine and N6-Carboxy-lysine

D-Glutamic Acid - an overview | ScienceDirect Topics
D-Glutamic Acid - an overview | ScienceDirect Topics

RCSB PDB - 4FFL: PylC in complex with L-lysine
RCSB PDB - 4FFL: PylC in complex with L-lysine

Unusual Amino Acids in Medicinal Chemistry | Journal of Medicinal Chemistry
Unusual Amino Acids in Medicinal Chemistry | Journal of Medicinal Chemistry

KR20120093310A - 2-amino-3-methyl-hex-5-enoic acid and its use in the  production of peptides such as bacitracins - Google Patents
KR20120093310A - 2-amino-3-methyl-hex-5-enoic acid and its use in the production of peptides such as bacitracins - Google Patents

Proteinogenic amino acid - Wikipedia
Proteinogenic amino acid - Wikipedia

3-Methylornithine - Wikipedia
3-Methylornithine - Wikipedia

Cell-Penetrating Peptides Using Cyclic α,α-Disubstituted α-Amino Acids with  Basic Functional Groups | ACS Biomaterials Science & Engineering
Cell-Penetrating Peptides Using Cyclic α,α-Disubstituted α-Amino Acids with Basic Functional Groups | ACS Biomaterials Science & Engineering

3R)-3-methyl-D-ornithine | C6H14N2O2 | CID 51055215 - PubChem
3R)-3-methyl-D-ornithine | C6H14N2O2 | CID 51055215 - PubChem

3-Methylornithine - Wikipedia
3-Methylornithine - Wikipedia

Structure and Reaction Mechanism of Pyrrolysine Synthase (PylD) - Quitterer  - 2013 - Angewandte Chemie International Edition - Wiley Online Library
Structure and Reaction Mechanism of Pyrrolysine Synthase (PylD) - Quitterer - 2013 - Angewandte Chemie International Edition - Wiley Online Library

D-Glutamic Acid - an overview | ScienceDirect Topics
D-Glutamic Acid - an overview | ScienceDirect Topics

3R)-3-methyl-D-ornithine(1+) | C6H15N2O2+ | CID 57339220 - PubChem
3R)-3-methyl-D-ornithine(1+) | C6H15N2O2+ | CID 57339220 - PubChem

Antibiotics | Free Full-Text | The Desotamide Family of Antibiotics
Antibiotics | Free Full-Text | The Desotamide Family of Antibiotics

KR20120093310A - 2-amino-3-methyl-hex-5-enoic acid and its use in the  production of peptides such as bacitracins - Google Patents
KR20120093310A - 2-amino-3-methyl-hex-5-enoic acid and its use in the production of peptides such as bacitracins - Google Patents

Antibiotics | Free Full-Text | Structure–Activity Relationship  Studies of Substitutions of Cationic Amino Acid Residues on Antimicrobial  Peptides
Antibiotics | Free Full-Text | Structure–Activity Relationship Studies of Substitutions of Cationic Amino Acid Residues on Antimicrobial Peptides