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Peptide record

TPDB92486

[WR]5 Antibacterial Anticancer Cell-penetrating Peptides Toxicity standard
10 amino acids
Basic Information
3D PDB MODEL
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TPDB92486
[WR]5
Antibacterial Anticancer Cell-penetrating Peptides Toxicity
Anti-infective peptides Cancer-related peptides Toxicity and safety peptides Delivery and barrier-penetrating peptides
Peptipedia CPPsite3.0
standard
No
A 10-aa standard natural multi-activity (Antibacterial, Anticancer, Cell-penetrating Peptides, and other sources) peptide sequence curated from Peptipedia and CPPsite3.0, with an available 3D structural model.
N-terminal: Conjugated with FITC
Sequence
WRWRWRWRWR
Physicochemical Analysis
C85H112N30O11
ANDCEQGHILKMFPSTYV
RW
1730.02
13.00
5
0
5
+5
-5.20
-2.700
0.00
Mammalian: 2.8 hour Yeast: 3 min E.coli: 2 min
27500
1589.58
0
Residue Composition
number
0
A
5
R
0
N
0
D
0
C
0
E
0
Q
0
G
0
H
0
I
0
L
0
K
0
M
0
F
0
P
0
S
0
T
5
W
0
Y
0
V
Amino Acid Distribution
A: 0 R: 5 N: 0 D: 0 C: 0 E: 0 Q: 0 G: 0 H: 0 I: 0 L: 0 K: 0 M: 0 F: 0 P: 0 S: 0 T: 0 W: 5 Y: 0 V: 0
Chemical Descriptors
10
C85H112N30O11
1730.02
13.00
+5
-5.20
-2.700
Free
L
Cyclic
Conjugated with FITC
N[C@@H](CCCN=C)C(=O)N[C@@H](CC1=CN=C(C)/C/1=C\C)C(=O)N[C@@H](CCCN=C)C(=O)N[C@@H](CC1=CN=C(C)/C/1=C\C)C(=O)N[C@@H](CCCN=C)C(=O)N[C@@H](CC1=CN=C(C)/C/1=C\C)C(=O)N[C@@H](CCCN=C)C(=O)N[C@@H](CC1=C(C(=NC1)C)CC)C(=O)N[C@@H](CCCN=C)C(=O)N[C@@H](CC1=CN=C(C)/C/1=C\C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCN=C)C(=O)N[C@@H](CC1=CN=C(C)/C/1=C\C)C(=O)N[C@@H](CCCN=C)C(=O)N[C@@H](CC1=CN=C(C)/C/1=C\C)C(=O)N[C@@H](CCCN=C)C(=O)N[C@@H](CC1=CN=C(C)/C/1=C\C)C(=O)N[C@@H](CCCN=C)C(=O)N[C@@H](CC1=CN=C(C)/C/1=C\C)C(=O)N[C@@H](CCCN=C)C(=O)N[C@@H](CC1=CN=C(C)/C/1=C\C)C(=O)O
Evidence Records 2 records
Evidence 1 Activity

Activity

Cell-penetrating Peptides

Target

CCRF-CEM, Sk-Ov-3, Hek-293 And MDA-MB-231 Cells

Source & Reference

CPPsite3.0
CPPsite3

Other

Source Activity Label Source Definition
Cell-penetrating Peptides
CPPsite3.0 experimentally validated cell-penetrating peptide annotation.
Natural residues Cyclic L
Synthetic
Carboxyfluorescein-labeled phosphopeptide (F′-GpYEEI)
F′-GpYEEI (2 μM) with [WR]5 enhanced the uptake by 3.6- and 2-fold in CCRF-CEM and SK-OV-3 cells, respectively.
In vitro
CCSSSSCCCCSSSCCCCCCCC
Evidence 2 Activity

Activity

Cell-penetrating Peptides

Target

CCRF-CEM, Sk-Ov-3, Hek-293 And MDA-MB-231 Cells

Source & Reference

CPPsite3.0
CPPsite3

Other

Natural residues Cyclic L
Synthetic
Carboxyfluorescein-labeled anti-HIV drugs (lamivudine (F′-3TC), emtricitabine (F′-FTC), Stavudine (F′-d4T))
In vitro
CCSSSSCCCCSSSCCCCCCCC
Additional Detail Fields 1 fields
CCSSSSCCCCSSSCCCCCCCC