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I-(Dhb)-AI-(Dha)-LA-(Abu)-PGAK-(Abu)-GALMGANVK-(Abu)-A-(Abu)-ANASIHV-(Dha)-K details
Primary information
ID antitb_1149,
Name21468208
N-Terminal modificationNisin V
C-Terminal ModificationI-(Dhb)-AI-(Dha)-LA-(Abu)-PGAK-(Abu)-GALMGANVK-(Abu)-A-(Abu)-ANASIHV-(Dha)-K
Chemical ModificationFree
Linear/CyclicFree
LengthDha= Didehydroalanine, Dhb= Didehydroaminobutyric acid, Abu= 2-aminobutyric acid, Lanthionine (Ala-S-Ala) formation from 3-7 Ala, and β-methyllanthionine (Abu-S-Ala) from 8-11, 13-19, 23-26, 25-28 in between Abu and Ala
ChiralityCyclic (5 hinge region dur to presence of lanthion
Nature34
SourceL
SpeciesNatural
StrainProduced by Lactococcus lactis
Inhibition ConcentrationMycobacterium smegmatis
In Vitro/ In vivoMycobacterium smegmatis MC2155
Cell Line2.2 mm zone of activity as compared to Nisin A
Inhibition ConcentrationIn vitro
Sequence2010
CytotoxicityNone
In vivo ModelNA
Lethal DoseNA
Immune ResponceNone
Mechanism of ActionNA
TargetNA
Combination TherapyNA
Other activitiesNA
PMIDNone
Year of PublicationAntibacterial (Shigella, Pseudomonas and Salmonella, S. aureus, S. agalactiae and L. monocytogenes)
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1150,
Name21468208
N-Terminal modificationNisin V
C-Terminal ModificationI-(Dhb)-AI-(Dha)-LA-(Abu)-PGAK-(Abu)-GALMGANVK-(Abu)-A-(Abu)-ANASIHV-(Dha)-K
Chemical ModificationFree
Linear/CyclicFree
LengthDha= Didehydroalanine, Dhb= Didehydroaminobutyric acid, Abu= 2-aminobutyric acid, Lanthionine (Ala-S-Ala) formation from 3-7 Ala, and β-methyllanthionine (Abu-S-Ala) from 8-11, 13-19, 23-26, 25-28 in between Abu and Ala
ChiralityCyclic (5 hinge region dur to presence of lanthion
Nature34
SourceL
SpeciesNatural
StrainProduced by Lactococcus lactis
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis H37Ra
Cell Line10% decrease in relative growth as compared to Nicin A
Inhibition ConcentrationIn vitro
Sequence2010
CytotoxicityNone
In vivo ModelNA
Lethal DoseNA
Immune ResponceNone
Mechanism of ActionNA
TargetNA
Combination TherapyNA
Other activitiesNA
PMIDNone
Year of PublicationAntibacterial (Shigella, Pseudomonas and Salmonella, S. aureus, S. agalactiae and L. monocytogenes)
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1151,
Name21468208
N-Terminal modificationNisin V
C-Terminal ModificationI-(Dhb)-AI-(Dha)-LA-(Abu)-PGAK-(Abu)-GALMGANVK-(Abu)-A-(Abu)-ANASIHV-(Dha)-K
Chemical ModificationFree
Linear/CyclicFree
LengthDha= Didehydroalanine, Dhb= Didehydroaminobutyric acid, Abu= 2-aminobutyric acid, Lanthionine (Ala-S-Ala) formation from 3-7 Ala, and β-methyllanthionine (Abu-S-Ala) from 8-11, 13-19, 23-26, 25-28 in between Abu and Ala
ChiralityCyclic (5 hinge region dur to presence of lanthion
Nature34
SourceL
SpeciesNatural
StrainProduced by Lactococcus lactis
Inhibition ConcentrationMycobacterium kansasii
In Vitro/ In vivoMycobacterium kansasii CIT11/06
Cell Line20% decrease in relative growth as compared to Nicin A
Inhibition ConcentrationIn vitro
Sequence2010
CytotoxicityNone
In vivo ModelNA
Lethal DoseNA
Immune ResponceNone
Mechanism of ActionNA
TargetNA
Combination TherapyNA
Other activitiesNA
PMIDNone
Year of PublicationAntibacterial (Shigella, Pseudomonas and Salmonella, S. aureus, S. agalactiae and L. monocytogenes)
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1152,
Name21468208
N-Terminal modificationNisin V
C-Terminal ModificationI-(Dhb)-AI-(Dha)-LA-(Abu)-PGAK-(Abu)-GALMGANVK-(Abu)-A-(Abu)-ANASIHV-(Dha)-K
Chemical ModificationFree
Linear/CyclicFree
LengthDha= Didehydroalanine, Dhb= Didehydroaminobutyric acid, Abu= 2-aminobutyric acid, Lanthionine (Ala-S-Ala) formation from 3-7 Ala, and β-methyllanthionine (Abu-S-Ala) from 8-11, 13-19, 23-26, 25-28 in between Abu and Ala
ChiralityCyclic (5 hinge region dur to presence of lanthion
Nature34
SourceL
SpeciesNatural
StrainProduced by Lactococcus lactis
Inhibition ConcentrationMycobacterium avium
In Vitro/ In vivoMycobacterium avium subsp. Hominissuis (CIT05/03)
Cell Line16% decrease in relative growth as compared to Nicin A
Inhibition ConcentrationIn vitro
Sequence2010
CytotoxicityNone
In vivo ModelNA
Lethal DoseNA
Immune ResponceNone
Mechanism of ActionNA
TargetNA
Combination TherapyNA
Other activitiesNA
PMIDNone
Year of PublicationAntibacterial (Shigella, Pseudomonas and Salmonella, S. aureus, S. agalactiae and L. monocytogenes)
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1153,
Name21468208
N-Terminal modificationNisin V
C-Terminal ModificationI-(Dhb)-AI-(Dha)-LA-(Abu)-PGAK-(Abu)-GALMGANVK-(Abu)-A-(Abu)-ANASIHV-(Dha)-K
Chemical ModificationFree
Linear/CyclicFree
LengthDha= Didehydroalanine, Dhb= Didehydroaminobutyric acid, Abu= 2-aminobutyric acid, Lanthionine (Ala-S-Ala) formation from 3-7 Ala, and β-methyllanthionine (Abu-S-Ala) from 8-11, 13-19, 23-26, 25-28 in between Abu and Ala
ChiralityCyclic (5 hinge region dur to presence of lanthion
Nature34
SourceL
SpeciesNatural
StrainProduced by Lactococcus lactis
Inhibition ConcentrationMycobacterium avium
In Vitro/ In vivoMycobacterium avium paratuberculosis (ATCC 19698)
Cell Line23% decrease in relative growth as compared to Nicin A
Inhibition ConcentrationIn vitro
Sequence2010
CytotoxicityNone
In vivo ModelNA
Lethal DoseNA
Immune ResponceNone
Mechanism of ActionNA
TargetNA
Combination TherapyNA
Other activitiesNA
PMIDNone
Year of PublicationAntibacterial (Shigella, Pseudomonas and Salmonella, S. aureus, S. agalactiae and L. monocytogenes)
Tertiary Structure
(Technique)
Not Predicted),