Primary information |
---|
ID | antitb_1137, |
Name | 23689720 |
N-Terminal modification | NK-2 |
C-Terminal Modification | KILRGVCKKIMRTFLRRISKDILTGKK |
Chemical Modification | Free |
Linear/Cyclic | Amidation |
Length | None |
Chirality | Linear |
Nature | 27 |
Source | L |
Origin | Cationic |
Species | Protein Derived |
Strain | Core region of the lymphocytic effector protein NK-lysin, found in NK cells and cytotoxic T cells |
Inhibition Concentration | Mycobacterium smegmatis |
In Vitro/ In vivo | Mycobacterium smegmatis mc2155 (ATCC 700084) |
Cell Line | 7 μg of NK- 2/ml combined with 0.5 ppm of NP-1 kills 90% of M. smegmatis |
Inhibition Concentration | In vitro |
Sequence | 2013 |
Cytotoxicity | RAW264.7 |
In vivo Model | Combination of NP-1 and NK-2 showed 35% reduction in intracellular survival of M. smegmatis |
Lethal Dose | No significant reduction in cell viability either treating alone or combination |
Immune Responce | None |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Permeabilization of the bacterial cell membrane |
Other activities | Cell envelope |
PMID | AgNPs synthesiszed only in the presence of a plant Alstonia macrophylla (NP-1). |
Year of Publication | Antibacterial, Antiprotozoan (Trypanosoma cruzi and Plasmodium falciparum) and antifungal (Candida albicans) |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1138, |
Name | 23689720 |
N-Terminal modification | NK-2 |
C-Terminal Modification | KILRGVCKKIMRTFLRRISKDILTGKK |
Chemical Modification | Free |
Linear/Cyclic | Amidation |
Length | None |
Chirality | Linear |
Nature | 27 |
Source | L |
Origin | Cationic |
Species | Protein Derived |
Strain | Core region of the lymphocytic effector protein NK-lysin, found in NK cells and cytotoxic T cells |
Inhibition Concentration | Mycobacterium smegmatis |
In Vitro/ In vivo | Mycobacterium smegmatis mc2155 (ATCC 700084) |
Cell Line | 7 μg of NK- 2/ml combined with 0.5 ppm of NP-2 kills 90% of M. smegmatis |
Inhibition Concentration | In vitro |
Sequence | 2013 |
Cytotoxicity | RAW264.7 |
In vivo Model | NP-2 in combination with NK-2 killed >52% intra- cellular M. smegmatis. |
Lethal Dose | No significant reduction in cell viability either treating alone or combination |
Immune Responce | None |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Permeabilization of the bacterial cell membrane |
Other activities | Cell envelope |
PMID | AgNPs synthesiszed only in the presence of a fungal Trichoderma sp. (NP-2). |
Year of Publication | Antibacterial, Antiprotozoan (Trypanosoma cruzi and Plasmodium falciparum) and antifungal (Candida albicans) |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1139, |
Name | 23689720 |
N-Terminal modification | NK-2 |
C-Terminal Modification | KILRGVCKKIMRTFLRRISKDILTGKK |
Chemical Modification | Free |
Linear/Cyclic | Amidation |
Length | None |
Chirality | Linear |
Nature | 27 |
Source | L |
Origin | Cationic |
Species | Protein Derived |
Strain | Core region of the lymphocytic effector protein NK-lysin, found in NK cells and cytotoxic T cells |
Inhibition Concentration | Mycobacterium marinum |
In Vitro/ In vivo | Mycobacterium marinum (ATCC 927) |
Cell Line | IC90 = 3.5 μg/ml |
Inhibition Concentration | In vitro |
Sequence | 2013 |
Cytotoxicity | RAW264.7 |
In vivo Model | Moderate killing was observed |
Lethal Dose | No significant reduction in cell viability either treating alone or combination |
Immune Responce | None |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Permeabilization of the bacterial cell membrane |
Other activities | Cell envelope |
PMID | None |
Year of Publication | Antibacterial, Antiprotozoan (Trypanosoma cruzi and Plasmodium falciparum) and antifungal (Candida albicans) |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1806, |
Name | 21396418 |
N-Terminal modification | NK-2 |
C-Terminal Modification | KILRGVCKKIMRTFLRRISKDILTGKK |
Chemical Modification | Free |
Linear/Cyclic | Amidation |
Length | None |
Chirality | Linear |
Nature | 27 |
Source | L |
Origin | Cationic |
Species | Protein Derived |
Strain | Core region of the lymphocytic effector protein NK-lysin |
Inhibition Concentration | Mycobacterium smegmatis |
In Vitro/ In vivo | Mycobacterium smegmatis mc2155 |
Cell Line | After 24 h more than 70% killing of M. smegmatis was found at 30 μM |
Inhibition Concentration | In vitro |
Sequence | 2011 |
Cytotoxicity | mouse macrophage RAW 264.7 |
In vivo Model | 10 μM NK-2 diminished the intracellular bacterial loadwhen compared to the untreated macrophages |
Lethal Dose | Non-toxic |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | NA |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1807, |
Name | 21396418 |
N-Terminal modification | NK-3 |
C-Terminal Modification | KILRGVCKKIMRTFLRRISKDILTGKK |
Chemical Modification | Free |
Linear/Cyclic | Amidation |
Length | None |
Chirality | Linear |
Nature | 27 |
Source | L |
Origin | Cationic |
Species | Protein Derived |
Strain | Core region of the lymphocytic effector protein NK-lysin |
Inhibition Concentration | Mycobacterium bovis |
In Vitro/ In vivo | Mycobacterium bovis BCG Pasteur (ATCC35734) |
Cell Line | After 24 h, more than 78% killing was observed at 30 μM |
Inhibition Concentration | In vitro |
Sequence | 2011 |
Cytotoxicity | mouse macrophage RAW 264.8 |
In vivo Model | 11 μM NK-2 diminished the intracellular bacterial loadwhen compared to the untreated macrophages |
Lethal Dose | Non-toxic |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | NA |
Other activities | NA |
PMID | NA |
Year of Publication | NA |
Tertiary Structure (Technique) | Not Predicted), |