Primary information |
---|
ID | antitb_1135, |
Name | 11328767 |
N-Terminal modification | Protegrin-1 (PG-1) |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Internal disulphide bond (between Cys 6-15 and Cys 8-13) |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Isolated from porcine leukocytes |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis E1380/94 MDR (Isoniazid, rifampicin, streptomycin, ethambutol) strain |
Cell Line | 50 mg/L causes approx 39 % growth inhibition |
Inhibition Concentration | In vitro |
Sequence | 2001 |
Cytotoxicity | None |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | None |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Disrupt the membrane architecture |
Other activities | Cell envelope |
PMID | None |
Year of Publication | Antibacterial against salmonella, staphylococcus and neisseria |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1563, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis H37Rv |
Cell Line | CFU/well 3.20 ± 0.15 at peptide concentration 64μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1564, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis H37Rv |
Cell Line | CFU/well 2.70 ± 0.15 at peptide concentration 64μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1565, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis H37Rv |
Cell Line | CFU/well 0.88± 0.30 at peptide concentration 4 μg/ml +INH 0.06 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | INH +peptide |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1566, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis H37Rv |
Cell Line | CFU/well 3.19 ± 0.15 at peptide concentration 64 μg/ml +INH 0.06 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | INH+Peptide |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1567, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis H37Rv |
Cell Line | CFU/well 3.19 ± 0.15 at peptide concentration 4 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1568, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis H37Rv |
Cell Line | CFU/well 3.58 ± 0.47 at peptide concentration 8 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1569, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis H37Rv |
Cell Line | CFU/well 3.16 ± 0.21 at peptide concentration 16 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1570, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis H37Rv |
Cell Line | CFU/well 2.97 ± 0.40 at peptide concentration 32 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1571, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis H37Rv |
Cell Line | CFU/well 2.70 ± 0.10 at peptide concentration 64 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1572, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis H37Rv |
Cell Line | CFU/well 1.72 ± 0.46 at peptide concentration 128 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1573, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis RM22 |
Cell Line | CFU/well 3.08 ± 0.09 at peptide concentration 4 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1574, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 19 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis RM23 |
Cell Line | CFU/well 2.97 ± 0.06 at peptide concentration 4 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1575, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 20 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis RM24 |
Cell Line | CFU/well 3.11 ± 0.09 at peptide concentration 4 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1576, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 21 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis RM25 |
Cell Line | CFU/well 3.19 ± 0.05 at peptide concentration 4 μg/ml +INH 4μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1577, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 22 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis RM26 |
Cell Line | CFU/well 3.08 ± 0.09 at peptide concentration 64 μg/ml +INH 4μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1578, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis RM22 |
Cell Line | CFU/well 3.10 ± 0.08 at peptide concentration 8 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1579, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis RM22 |
Cell Line | CFU/well 3.00 ± 0.10 at peptide concentration 16 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1580, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis RM22 |
Cell Line | CFU/well 3.05 ± 0.11 at peptide concentration 32 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1581, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis RM22 |
Cell Line | CFU/well 2.88 ± 0.06at peptide concentration 64 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1582, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis RM22 |
Cell Line | CFU/well 2.71 ± 0.09 at peptide concentration 128 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1603, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis H37Rv |
Cell Line | CFU/well 0.68 ± 0.30 at peptide 64ul + 4 ul of INH |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | Peptide(64 ul) + INH(4 ul) |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1604, |
Name | 15245864 |
N-Terminal modification | Protegrin -1 |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-14 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | Derived from porcine leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis RM22 |
Cell Line | CFU/well 1.99 ± 0.44 at peptide 64ul + 4 ul of INH |
Inhibition Concentration | in vitro |
Sequence | 2004 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Bacterial membrane pore formation |
Other activities | NA |
PMID | Peptide(64 ul) + INH(4 ul) |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1708, |
Name | 8641802 |
N-Terminal modification | Porcine leucocyte peptide (PG-1) |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-13 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | porcine neutrophil leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis Ra 7632G |
Cell Line | Reduction in CFU at 50 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 1996 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Microbial membrane disruption |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1709, |
Name | 8641802 |
N-Terminal modification | Porcine leucocyte peptide (PG-1) |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-14 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | porcine neutrophil leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis Ra 9034G |
Cell Line | Reduction in CFU at 50 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 1996 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Microbial membrane disruption |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1710, |
Name | 8641802 |
N-Terminal modification | Porcine leucocyte peptide (PG-1) |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-15 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | porcine neutrophil leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis Ra 11170G |
Cell Line | Reduction in CFU at 50 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 1996 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Microbial membrane disruption |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1711, |
Name | 8641802 |
N-Terminal modification | Porcine leucocyte peptide (PG-1) |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-16 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | porcine neutrophil leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis H37 Ra |
Cell Line | IC50= 5 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 1996 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Microbial membrane disruption |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1712, |
Name | 8641802 |
N-Terminal modification | Porcine leucocyte peptide (PG-1) |
C-Terminal Modification | RGGRLCYCRRRFCVCVGR |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | Disulphide linkage 6-15 and 8-17 |
Chirality | Cyclic |
Nature | 18 |
Source | L |
Origin | Cationic |
Species | Natural |
Strain | porcine neutrophil leucocyte |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis H37 Ra |
Cell Line | MIC = 50 μg/ml |
Inhibition Concentration | in vitro |
Sequence | 1996 |
Cytotoxicity | NA |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Microbial membrane disruption |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |