Peptide Database

Peptide NameUnnamed

Function Ontology

Antimicrobial

Antiviral

Antiviral ▸ Antiviral mechanism ▸ Viral fusion inhibition ▸ Fusion inhibitor

Standard StatusStandard

Sequence Length37 amino acids

Chemical FormulaC228H333N51O64S

DescriptionStandard

        FWNWLSAWIKKTYEEIKKTYEEIKKTYEEIERDWEMV
    

Molecular Weight4844.45 Da

Isoelectric Point (pI)4.97

Net Charge (pH 7.0)-2.23

Net Charge (pH 7.4) -2.46

Charge Density (pH 7.0) -0.0601

GRAVY Index-1.10

Hydrophobic Moment 0.73

Boman Index-0.14

Instability Index54.52

Aliphatic Index 63.24

Aromaticity 0.2162

Extinction Coeff. Reduced 26470.00

Extinction Coeff. Oxidized 26470.00

The radar chart summarizes major physicochemical dimensions for quick comparison, while exact numerical values remain listed on the left.

Amino Acid Composition

TPSA 1912.50

LogP -7.07

H-bond Donors 68.0

H-bond Acceptors 63.0

Rotatable Bonds 163.0

Heavy Atoms 344.0

Ring Count 12.0

Amide Bonds 37.0

3D PDB MODEL

Drag to rotate. Click a residue or atom to inspect it; the selected residue is highlighted in amber in the current view mode. Use the buttons to zoom.

2D CHEMICAL STRUCTURE

Drag to move

Drag to move. Use the buttons to zoom.

RECORD: Rec_0395178 VERIFIED: YES

Provenance & Taxonomy

Organismnot reported [other]

Structure & Mods

Configlinear peptide; DSSP H 94.6%, E 0.0%, T 0.0%, C 5.4% [Linear]

Chiralitycanonical L-amino-acid peptide [L]

N-TermNone

C-TermNone

Bio-Activity Profile

Function

Antiviral Antimicrobial

RECORD: Rec_0415715 VERIFIED: YES

Provenance & Taxonomy

Organismsynthetic construct [Synthetic]

Tax ID32630

Structure & Mods

Configlinear peptide [Linear]

Chiralitycanonical L-amino-acid peptide [L]

Bio-Activity Profile

Function

Antiviral Fusion inhibitor

TargetH9/HIV-1I

Activity0.58 μM

MethodIC50