PPIRE19030

Target Protein Information
Protein_Name Lysozyme C
Protein_Sequence MRSLLILVLCFLPLAALGKVFGRCELAAAMKRHGLDNYRGYSLGNWVCAAKFESNFNTQATNRNTDGSTDYGILQINSRWWCNDGRTPGSRNLCNIPCSALLSSDITASVNCAKKIVSDGNGMNAWVAWRNRCKGTDVQAWIRGCRL
Organism_Source Gallus gallus
Functional_Classification glycosidases
Cellular_Localization Extracellular
Gene_Names LYZ
UniProt_ID P00698
Protein-Protein Interaction Networks
Peptide Basic Information
Peptide_Name Cys5-1
Peptide_Sequence NQPSCQDITACLTPQXXK
Peptide_Length 18
Peptide_SMILES CC[C@H](C)[C@H](NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CS)NC(=O)[C@H](CO)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](N)CC(N)=O)C(=O)N[C@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CS)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(N)=O)C(=O)NCC(=O)NCC(=O)N[C@@H](CCCCN)C(=O)O)[C@@H](C)O)[C@@H](C)O
Chemical_Modification X16=biotinylated lysine; X17=norleucine
Cyclization_Method None
Linear/Cyclic Linear
N-terminal_Modification Free
C-terminal_Modification Amide
Amino_Acid_Distribution
Peptide Physicochemical
Molecular_Weight 1861.07
Aliphatic_Index 48.88889
Aromaticity 0.00000
Average_Rotatable_Bonds 3.27778
Charge_at_pH_7 -0.12581
Isoelectric_Point 6.06420
Hydrogen_Bond_Acceptors 30
Hydrogen_Bond_Donors 28
Topological_Polar_Surface_Area 836.81000
X_logP_energy -13.08370
Interaction Information
Affinity KD=38.1 nM
Affinity_Assay Enzyme Inhibition Kinetics
PDB_ID None
Type Affinity ligand
Structure
Reference Information
Document_Type Research Articles
Title The Role of Structure in Antibody Cross-reactivity Between Peptides and Folded Proteins
Release_Year 1998
PMID 9680484
DOI 10.1006/jmbi.1998.1907