PPIPT00909

Target Protein Information
Protein_Name Ighg protein
Protein_Sequence MDISLSLVFLVLFIKGVQCEVQLVETGGGLVQPGRSLKLSCVASGFTFSSYWMYWIRQAPGKGLEWVSSINTDGGSTYYPDSVKGRFTISRDNAENTVYLQMNSLRSEDTATYYCAKGGEYYGYNYPFDYWGQGVMVTVSSAETTAPSVYPLAPGTALKSNSMVTLGCLVKGYFPEPVTVTWNSGALSSGVHTFPAVLQSGLYTLTSSVTVPSSTWPSQTVTCNVAHPASSTKVDKKIVPRNCGGDCKPCICTGSEVSSVFIFPPKPKDVLTITLTPKVTCVVVDISQDDPEVHFSWFVDDVEVHTAQTRPPEEQFNSTFRSVSELPILHQDWLNGRTFRCKVTSAAFPSPIEKTISKPEGRTQVPHVYTMSPTKEEMTQNEVSITCMVKGFYPPDIYVEWQMNGQPQENYKNTPPTMDTDGSYFLYSKLNVKKEKWQQGNTFTCSVLHEGLHNHHTEKSLSHSPGK
Organism_Source Rattus norvegicus
Functional_Classification Ighg protein
Cellular_Localization Extracellular
Gene_Names Ighg
UniProt_ID Q4VBH1
Protein-Protein Interaction Networks
Peptide Basic Information
Peptide_Name Peptide hybrid 1a
Peptide_Sequence EDDCAWHLGELVWCT
Peptide_Length 15
Peptide_SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](C)NC(=O)[C@H](CS)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](N)CCC(=O)O)C(=O)NCC(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CS)C(=O)N[C@H](C(=O)O)[C@@H](C)O)C(C)C
Chemical_Modification None
Cyclization_Method Side chain-side chain cyclization; C4<->C14; disulfide bond
Linear/Cyclic Linear
N-terminal_Modification PEGylation
C-terminal_Modification Amide
Amino_Acid_Distribution
Peptide Physicochemical
Molecular_Weight 1776.96
Aliphatic_Index 78.00000
Aromaticity 0.13333
Average_Rotatable_Bonds 3.53333
Charge_at_pH_7 -4.03061
Isoelectric_point 3.73726
Number_of_Hydrogen_Bond_Acceptors 24
Number_of_Hydrogen_Bond_Donors 26
Topological_Polar_Surface_Area 700.41000
X_logP_energy -4.08180
Interaction Information
Affinity KD=305 nM
Affinity_Assay Surface Plasmon Resonance
PDB_ID None
Type Affinity ligand
Structure
Reference Information
Document_Type Patent
Title METHOD FOR PREPARING ANTIBODY MONOLAYERS WHICH HAVE CONTROLLED ORIENTATION USING PEPTIDE HYBRID
Release_Year 2010
Patent_ID US20100209945A1