PPIRE16379

Target Protein Information
Protein_Name Alpha-2-HS-glycoprotein
Protein_Sequence MKSFVLLFCLAQLWGCHSIPLDPVAGYKEPACDDPDTEQAALAAVDYINKHLPRGYKHTLNQIDSVKVWPRRPTGEVYDIEIDTLETTCHVLDPTPLANCSVRQQTQHAVEGDCDIHVLKQDGQFSVLFTKCDSSPDSAEDVRKLCPDCPLLAPLNDSRVVHAVEVALATFNAESNGSYLQLVEISRAQFVPLPVSVSVEFAVAATDCIAKEVVDPTKCNLLAEKQYGFCKGSVIQKALGGEDVRVTCTLFQTQPVIPQPQPDGAEAEAPSAVPDAAGPTPSAAGPPVASVVVGPSVVAVPLPLHRAHYDLRHTFSGVASVESSSGEAFHVGKTPIVGQPSIPGGPVRLCPGRIRYFKI
Organism_Source Bos taurus
Functional_Classification Accessory factors acute phase glycoproteins
Cellular_Localization Extracellular
Gene_Names AHSG
UniProt_ID P12763
Protein-Protein Interaction Networks
Peptide Basic Information
Peptide_Name Odorranalectin
Peptide_Sequence YASPKCFRYPNGVLACT
Peptide_Length 17
Peptide_SMILES CC(C)C[C@H](NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CC(N)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CS)NC(=O)[C@H](CCCCN)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CO)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CS)C(=O)N[C@H](C(=O)O)[C@@H](C)O
Chemical_Modification None
Cyclization_Method Side chain-side chain cyclization; C6<-->C16; disulfide bond
Linear/Cyclic Cyclic
N-terminal_Modification Free
C-terminal_Modification Free
Amino_Acid_Distribution
Peptide Physicochemical
Molecular_Weight 1890.21
Aliphatic_Index 51.76471
Aromaticity 0.17647
Average_Rotatable_Bonds 3.17647
Charge_at_pH_7 1.87204
Isoelectric_Point 8.77185
Number_of_Hydrogen_Bond_Acceptors 27
Number_of_Hydrogen_Bond_Donors 27
Topological_Polar_Surface_Area 723.27000
X_logP_energy -6.81953
Interaction Information
Affinity KD=0.21 uM
Affinity_Assay Surface Plasmon Resonance
PDB_ID None
Type Affinity ligand
Structure
Reference Information
Document_Type Research Articles
Title Odorranalectin Is a Small Peptide Lectin with Potential for Drug Delivery and Targeting
Release_Year 2008
PMID 18584053
DOI 10.1371/journal.pone.0002381