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Peptide record

TPDB05196

Antibacterial Anticancer Antifungal Antiparasitic Antiviral Toxicity standard
28 amino acids
Basic Information
3D PDB MODEL
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TPDB05196
Antibacterial Anticancer Antifungal Antiparasitic Antiviral Toxicity
Anti-infective peptides Cancer-related peptides Toxicity and safety peptides
AntiBP3 Peptipedia AntiCP 2.0 iACP-DRLF Antifungipept i2APP AI4AVP dbAMP 3.0 DRAMP DRAVP 2.0 ToxinPred 3.0
standard
No
A 28-aa standard natural multi-activity (Antibacterial, Anticancer, Antifungal, and other sources) peptide sequence curated from AntiBP3, Peptipedia, AntiCP 2.0, and other sources, with an available 3D structural model.
Sequence
GTACGESCYVLPCFTVGCTCTSSQCFKN
Physicochemical Analysis
C120H185N31O41S6
RDHIMW
C
2910.33
5.90
1
1
7
-0
0.21
0.389
38.21
Mammalian: 30 hour Yeast: >20 hour E.coli: >10 hour
1865
64.08
16
Residue Composition
number
1
A
0
R
1
N
0
D
6
C
1
E
1
Q
3
G
0
H
0
I
1
L
1
K
0
M
2
F
1
P
3
S
4
T
0
W
1
Y
2
V
Amino Acid Distribution
A: 1 R: 0 N: 1 D: 0 C: 6 E: 1 Q: 1 G: 3 H: 0 I: 0 L: 1 K: 1 M: 0 F: 2 P: 1 S: 3 T: 4 W: 0 Y: 1 V: 2
Chemical Descriptors
28
C120H185N31O41S6
2910.33
5.90
-0
0.21
0.389
Evidence Records 6 records
Evidence 1 Activity

Activity

Antibacterial

Source & Reference

DRAMP

Other

It inhibited HIV-1 infection in cultured human T-lymphoblast (CEM-SS) cells (EC50 130 nM).
Evidence 2 Activity

Activity

Antifungal

Source & Reference

DRAMP Antifungipept

Other

It inhibited HIV-1 infection in cultured human T-lymphoblast (CEM-SS) cells (EC50 130 nM).
Evidence 3 Activity

Activity

Antiparasitic

Source & Reference

dbAMP 3.0 DRAMP

Other

Source Activity Label Source Definition
Antiparasitic
dbAMP 3.0 classified under the Anti-parasitic function class.
It inhibited HIV-1 infection in cultured human T-lymphoblast (CEM-SS) cells (EC50 130 nM).
Evidence 4 Activity

Activity

Antiviral

Source & Reference

dbAMP 3.0 DRAMP DRAVP 2.0

Other

Source Activity Label Source Definition
Antiviral
dbAMP 3.0 classified under the Anti-viral function class.
It inhibited HIV-1 infection in cultured human T-lymphoblast (CEM-SS) cells (EC50 130 nM).
Evidence 5 Activity

Activity

IC50
Toxicity
0.56 µM
Cytotoxic
IC50 | 0.56 | µM | target cell: CEM-SS cells

Target

CEM-SS cells

Source & Reference

NA
DBAASP
Cyclotides as natural anti-HIV agents | Biopolymers | 2008
Evidence 6 Activity

Activity

IC50
Toxicity
560 nM
Cytotoxic
Cytotoxicity: [Ref.18008336]CEM-SS cells:IC50=560 nM.

Source & Reference

NA
DRAMP
J Org Chem. 2000 Jan 14 65(1):124-128.##Biopolymers. 2008 90(1):51-60.