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(METH-Ala)-(D-Pip)-L-( D-Allo-ILE)-Pip-(D-Pip) details |
Primary information | |
---|---|
ID | antitb_1846, |
Name | 24224794 |
N-Terminal modification | Hytramycin I |
C-Terminal Modification | (METH-Ala)-(D-Pip)-L-( D-Allo-ILE)-Pip-(D-Pip) |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | METH-ALA= Methylated alanine, D-Pip = piperazic acid moieties, D-Allo-ILE= D form of Allo-isoleucine |
Chirality | Cyclic (Intrachain bond between 1-6) |
Nature | 6 |
Source | Mix |
Species | Natural |
Strain | From Streptomyces hygroscopicus strain ECUM 14046 |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis H37Rv |
Cell Line | MIC = 6.0 μg/mL |
Inhibition Concentration | In vitro |
Sequence | 2013 |
Cytotoxicity | None |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | NA |
Other activities | NA |
PMID | NA |
Year of Publication | Antibacterial (Escherichia coli (ATCC 25922), Staphylococcus aureus (ATCC 29213), Acinetobacter baumannii (ATCC BAA-747), Enterococcus faecalis (ATCC 29212), and Pseudomonas aeruginosa (ATCC 27853) |
Tertiary Structure (Technique) | Not Predicted), |
Primary information | |
---|---|
ID | antitb_1847, |
Name | 24224794 |
N-Terminal modification | Hytramycin I |
C-Terminal Modification | (METH-Ala)-(D-Pip)-L-( D-Allo-ILE)-Pip-(D-Pip) |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | METH-ALA= Methylated alanine, D-Pip = piperazic acid moieties, D-Allo-ILE= D form of Allo-isoleucine |
Chirality | Cyclic (Intrachain bond between 1-6) |
Nature | 6 |
Source | Mix |
Species | Natural |
Strain | From Streptomyces hygroscopicus strain ECUM 14046 |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Clinical isolate, X004439 |
Cell Line | MIC = 4.4 μg/mL |
Inhibition Concentration | In vitro |
Sequence | 2013 |
Cytotoxicity | None |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | NA |
Other activities | NA |
PMID | NA |
Year of Publication | Antibacterial (Escherichia coli (ATCC 25922), Staphylococcus aureus (ATCC 29213), Acinetobacter baumannii (ATCC BAA-747), Enterococcus faecalis (ATCC 29212), and Pseudomonas aeruginosa (ATCC 27853) |
Tertiary Structure (Technique) | Not Predicted), |
Primary information | |
---|---|
ID | antitb_1848, |
Name | 24224794 |
N-Terminal modification | Hytramycin I |
C-Terminal Modification | (METH-Ala)-(D-Pip)-L-( D-Allo-ILE)-Pip-(D-Pip) |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | METH-ALA= Methylated alanine, D-Pip = piperazic acid moieties, D-Allo-ILE= D form of Allo-isoleucine |
Chirality | Cyclic (Intrachain bond between 1-6) |
Nature | 6 |
Source | Mix |
Species | Natural |
Strain | From Streptomyces hygroscopicus strain ECUM 14046 |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Clinical isolate, X004244 |
Cell Line | MIC = 4.7 μg/mL |
Inhibition Concentration | In vitro |
Sequence | 2013 |
Cytotoxicity | None |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | NA |
Other activities | NA |
PMID | NA |
Year of Publication | Antibacterial (Escherichia coli (ATCC 25922), Staphylococcus aureus (ATCC 29213), Acinetobacter baumannii (ATCC BAA-747), Enterococcus faecalis (ATCC 29212), and Pseudomonas aeruginosa (ATCC 27853) |
Tertiary Structure (Technique) | Not Predicted), |
Primary information | |
---|---|
ID | antitb_1849, |
Name | 24224794 |
N-Terminal modification | Hytramycin I |
C-Terminal Modification | (METH-Ala)-(D-Pip)-L-( D-Allo-ILE)-Pip-(D-Pip) |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | METH-ALA= Methylated alanine, D-Pip = piperazic acid moieties, D-Allo-ILE= D form of Allo-isoleucine |
Chirality | Cyclic (Intrachain bond between 1-6) |
Nature | 6 |
Source | Mix |
Species | Natural |
Strain | From Streptomyces hygroscopicus strain ECUM 14046 |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Clinical isolate, X005282 |
Cell Line | MIC = 4.7 μg/mL |
Inhibition Concentration | In vitro |
Sequence | 2013 |
Cytotoxicity | None |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | NA |
Other activities | NA |
PMID | NA |
Year of Publication | Antibacterial (Escherichia coli (ATCC 25922), Staphylococcus aureus (ATCC 29213), Acinetobacter baumannii (ATCC BAA-747), Enterococcus faecalis (ATCC 29212), and Pseudomonas aeruginosa (ATCC 27853) |
Tertiary Structure (Technique) | Not Predicted), |
Primary information | |
---|---|
ID | antitb_1850, |
Name | 24224794 |
N-Terminal modification | Hytramycin I |
C-Terminal Modification | (METH-Ala)-(D-Pip)-L-( D-Allo-ILE)-Pip-(D-Pip) |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | METH-ALA= Methylated alanine, D-Pip = piperazic acid moieties, D-Allo-ILE= D form of Allo-isoleucine |
Chirality | Cyclic (Intrachain bond between 1-6) |
Nature | 6 |
Source | Mix |
Species | Natural |
Strain | From Streptomyces hygroscopicus strain ECUM 14046 |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Clinical isolate, X005319 |
Cell Line | MIC = 4.8 μg/mL |
Inhibition Concentration | In vitro |
Sequence | 2013 |
Cytotoxicity | None |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | NA |
Other activities | NA |
PMID | NA |
Year of Publication | Antibacterial (Escherichia coli (ATCC 25922), Staphylococcus aureus (ATCC 29213), Acinetobacter baumannii (ATCC BAA-747), Enterococcus faecalis (ATCC 29212), and Pseudomonas aeruginosa (ATCC 27853) |
Tertiary Structure (Technique) | Not Predicted), |
Primary information | |
---|---|
ID | antitb_1851, |
Name | 24224794 |
N-Terminal modification | Hytramycin I |
C-Terminal Modification | (METH-Ala)-(D-Pip)-L-( D-Allo-ILE)-Pip-(D-Pip) |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | METH-ALA= Methylated alanine, D-Pip = piperazic acid moieties, D-Allo-ILE= D form of Allo-isoleucine |
Chirality | Cyclic (Intrachain bond between 1-6) |
Nature | 6 |
Source | Mix |
Species | Natural |
Strain | From Streptomyces hygroscopicus strain ECUM 14046 |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Clinical isolate, X001354 |
Cell Line | MIC = 4.7 μg/mL |
Inhibition Concentration | In vitro |
Sequence | 2013 |
Cytotoxicity | None |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | NA |
Other activities | NA |
PMID | NA |
Year of Publication | Antibacterial (Escherichia coli (ATCC 25922), Staphylococcus aureus (ATCC 29213), Acinetobacter baumannii (ATCC BAA-747), Enterococcus faecalis (ATCC 29212), and Pseudomonas aeruginosa (ATCC 27853) |
Tertiary Structure (Technique) | Not Predicted), |
Primary information | |
---|---|
ID | antitb_1852, |
Name | 24224794 |
N-Terminal modification | Hytramycin I |
C-Terminal Modification | (METH-Ala)-(D-Pip)-L-( D-Allo-ILE)-Pip-(D-Pip) |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | METH-ALA= Methylated alanine, D-Pip = piperazic acid moieties, D-Allo-ILE= D form of Allo-isoleucine |
Chirality | Cyclic (Intrachain bond between 1-6) |
Nature | 6 |
Source | Mix |
Species | Natural |
Strain | From Streptomyces hygroscopicus strain ECUM 14046 |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Clinical isolate, X003899 |
Cell Line | MIC = 4.8 μg/mL |
Inhibition Concentration | In vitro |
Sequence | 2013 |
Cytotoxicity | None |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | NA |
Other activities | NA |
PMID | NA |
Year of Publication | Antibacterial (Escherichia coli (ATCC 25922), Staphylococcus aureus (ATCC 29213), Acinetobacter baumannii (ATCC BAA-747), Enterococcus faecalis (ATCC 29212), and Pseudomonas aeruginosa (ATCC 27853) |
Tertiary Structure (Technique) | Not Predicted), |
Primary information | |
---|---|
ID | antitb_1853, |
Name | 24224794 |
N-Terminal modification | Hytramycin I |
C-Terminal Modification | (METH-Ala)-(D-Pip)-L-( D-Allo-ILE)-Pip-(D-Pip) |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | METH-ALA= Methylated alanine, D-Pip = piperazic acid moieties, D-Allo-ILE= D form of Allo-isoleucine |
Chirality | Cyclic (Intrachain bond between 1-6) |
Nature | 6 |
Source | Mix |
Species | Natural |
Strain | From Streptomyces hygroscopicus strain ECUM 14046 |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis resistant to streptomycin (rSM, ATCC 35820) |
Cell Line | MIC = 4.7 μg/mL |
Inhibition Concentration | In vitro |
Sequence | 2013 |
Cytotoxicity | None |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | NA |
Other activities | NA |
PMID | NA |
Year of Publication | Antibacterial (Escherichia coli (ATCC 25922), Staphylococcus aureus (ATCC 29213), Acinetobacter baumannii (ATCC BAA-747), Enterococcus faecalis (ATCC 29212), and Pseudomonas aeruginosa (ATCC 27853) |
Tertiary Structure (Technique) | Not Predicted), |
Primary information | |
---|---|
ID | antitb_1854, |
Name | 24224794 |
N-Terminal modification | Hytramycin I |
C-Terminal Modification | (METH-Ala)-(D-Pip)-L-( D-Allo-ILE)-Pip-(D-Pip) |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | METH-ALA= Methylated alanine, D-Pip = piperazic acid moieties, D-Allo-ILE= D form of Allo-isoleucine |
Chirality | Cyclic (Intrachain bond between 1-6) |
Nature | 6 |
Source | Mix |
Species | Natural |
Strain | From Streptomyces hygroscopicus strain ECUM 14046 |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis resistant to rifampin (rRMP, ATCC 35838) |
Cell Line | MIC = 4.7 μg/mL |
Inhibition Concentration | In vitro |
Sequence | 2013 |
Cytotoxicity | None |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | NA |
Other activities | NA |
PMID | NA |
Year of Publication | Antibacterial (Escherichia coli (ATCC 25922), Staphylococcus aureus (ATCC 29213), Acinetobacter baumannii (ATCC BAA-747), Enterococcus faecalis (ATCC 29212), and Pseudomonas aeruginosa (ATCC 27853) |
Tertiary Structure (Technique) | Not Predicted), |
Primary information | |
---|---|
ID | antitb_1855, |
Name | 24224794 |
N-Terminal modification | Hytramycin I |
C-Terminal Modification | (METH-Ala)-(D-Pip)-L-( D-Allo-ILE)-Pip-(D-Pip) |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | METH-ALA= Methylated alanine, D-Pip = piperazic acid moieties, D-Allo-ILE= D form of Allo-isoleucine |
Chirality | Cyclic (Intrachain bond between 1-6) |
Nature | 6 |
Source | Mix |
Species | Natural |
Strain | From Streptomyces hygroscopicus strain ECUM 14046 |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis resistant to kanamycin (rKM, ATCC 35827) |
Cell Line | MIC = 4.9 μg/mL |
Inhibition Concentration | In vitro |
Sequence | 2013 |
Cytotoxicity | None |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | NA |
Other activities | NA |
PMID | NA |
Year of Publication | Antibacterial (Escherichia coli (ATCC 25922), Staphylococcus aureus (ATCC 29213), Acinetobacter baumannii (ATCC BAA-747), Enterococcus faecalis (ATCC 29212), and Pseudomonas aeruginosa (ATCC 27853) |
Tertiary Structure (Technique) | Not Predicted), |
Primary information | |
---|---|
ID | antitb_1856, |
Name | 24224794 |
N-Terminal modification | Hytramycin I |
C-Terminal Modification | (METH-Ala)-(D-Pip)-L-( D-Allo-ILE)-Pip-(D-Pip) |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | METH-ALA= Methylated alanine, D-Pip = piperazic acid moieties, D-Allo-ILE= D form of Allo-isoleucine |
Chirality | Cyclic (Intrachain bond between 1-6) |
Nature | 6 |
Source | Mix |
Species | Natural |
Strain | From Streptomyces hygroscopicus strain ECUM 14046 |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis resistant to isoniazid (rINH, ATCC 35822) |
Cell Line | MIC = 4.7 μg/mL |
Inhibition Concentration | In vitro |
Sequence | 2013 |
Cytotoxicity | None |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | NA |
Other activities | NA |
PMID | NA |
Year of Publication | Antibacterial (Escherichia coli (ATCC 25922), Staphylococcus aureus (ATCC 29213), Acinetobacter baumannii (ATCC BAA-747), Enterococcus faecalis (ATCC 29212), and Pseudomonas aeruginosa (ATCC 27853) |
Tertiary Structure (Technique) | Not Predicted), |
Primary information | |
---|---|
ID | antitb_1857, |
Name | 24224794 |
N-Terminal modification | Hytramycin I |
C-Terminal Modification | (METH-Ala)-(D-Pip)-L-( D-Allo-ILE)-Pip-(D-Pip) |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | METH-ALA= Methylated alanine, D-Pip = piperazic acid moieties, D-Allo-ILE= D form of Allo-isoleucine |
Chirality | Cyclic (Intrachain bond between 1-6) |
Nature | 6 |
Source | Mix |
Species | Natural |
Strain | From Streptomyces hygroscopicus strain ECUM 14046 |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis resistant to cycloserine (rCS, ATCC 35826) |
Cell Line | MIC = 7.4 μg/mL |
Inhibition Concentration | In vitro |
Sequence | 2013 |
Cytotoxicity | None |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | NA |
Other activities | NA |
PMID | NA |
Year of Publication | Antibacterial (Escherichia coli (ATCC 25922), Staphylococcus aureus (ATCC 29213), Acinetobacter baumannii (ATCC BAA-747), Enterococcus faecalis (ATCC 29212), and Pseudomonas aeruginosa (ATCC 27853) |
Tertiary Structure (Technique) | Not Predicted), |
Primary information | |
---|---|
ID | antitb_1858, |
Name | 24224794 |
N-Terminal modification | Hytramycin I |
C-Terminal Modification | (METH-Ala)-(D-Pip)-L-( D-Allo-ILE)-Pip-(D-Pip) |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | METH-ALA= Methylated alanine, D-Pip = piperazic acid moieties, D-Allo-ILE= D form of Allo-isoleucine |
Chirality | Cyclic (Intrachain bond between 1-6) |
Nature | 6 |
Source | Mix |
Species | Natural |
Strain | From Streptomyces hygroscopicus strain ECUM 14046 |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis resistant to moxifloxacin (rMOX) |
Cell Line | MIC = 4.0 μg/mL |
Inhibition Concentration | In vitro |
Sequence | 2013 |
Cytotoxicity | None |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | NA |
Other activities | NA |
PMID | NA |
Year of Publication | Antibacterial (Escherichia coli (ATCC 25922), Staphylococcus aureus (ATCC 29213), Acinetobacter baumannii (ATCC BAA-747), Enterococcus faecalis (ATCC 29212), and Pseudomonas aeruginosa (ATCC 27853) |
Tertiary Structure (Technique) | Not Predicted), |
Primary information | |
---|---|
ID | antitb_1859, |
Name | 24224794 |
N-Terminal modification | Hytramycin I |
C-Terminal Modification | (METH-Ala)-(D-Pip)-L-( D-Allo-ILE)-Pip-(D-Pip) |
Chemical Modification | Free |
Linear/Cyclic | Free |
Length | METH-ALA= Methylated alanine, D-Pip = piperazic acid moieties, D-Allo-ILE= D form of Allo-isoleucine |
Chirality | Cyclic (Intrachain bond between 1-6) |
Nature | 6 |
Source | Mix |
Species | Natural |
Strain | From Streptomyces hygroscopicus strain ECUM 14046 |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis resistant to capreomycin (rCAP) |
Cell Line | MIC = 4.8 μg/mL |
Inhibition Concentration | In vitro |
Sequence | 2013 |
Cytotoxicity | None |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | NA |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | NA |
Other activities | NA |
PMID | NA |
Year of Publication | Antibacterial (Escherichia coli (ATCC 25922), Staphylococcus aureus (ATCC 29213), Acinetobacter baumannii (ATCC BAA-747), Enterococcus faecalis (ATCC 29212), and Pseudomonas aeruginosa (ATCC 27853) |
Tertiary Structure (Technique) | Not Predicted), |