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MLLKKLLKKM details
Primary information
ID antitb_1247,
Name24314557
N-Terminal modificationM(LLKK)2M
C-Terminal ModificationMLLKKLLKKM
Chemical ModificationFree
Linear/CyclicFree
LengthNone
ChiralityLinear
Nature10
SourceL
OriginCationic
SpeciesSynthetic
Inhibition ConcentrationMycobacterium smegmatis
In Vitro/ In vivoMycobacterium smegmatis (ATCC No. 14468)
Cell LineMIC = 62.5 mg/L
Inhibition ConcentrationIn vitro
Sequence2014
CytotoxicityRat red blood cells (rRBCs)
In vivo ModelNA
Lethal DoseVery low, i.e. 50% hemolysis concentration (HC50) > 1000 mg/L
Immune ResponceNone
Mechanism of ActionNA
TargetNA
Combination TherapyMembrane-lytic mechanism
Other activitiesCell envelope
PMIDNone
Year of PublicationAntibacterial
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1248,
Name24314557
N-Terminal modificationM(LLKK)2M
C-Terminal ModificationMLLKKLLKKM
Chemical ModificationFree
Linear/CyclicFree
LengthNone
ChiralityLinear
Nature10
SourceL
OriginCationic
SpeciesSynthetic
Inhibition ConcentrationMycobacterium smegmatis
In Vitro/ In vivoMycobacterium smegmatis (ATCC No. 14468)
Cell LineMIC = 15.6 mg/L
Inhibition ConcentrationIn vitro
Sequence2014
CytotoxicityRat red blood cells (rRBCs)
In vivo ModelNA
Lethal DoseVery low, i.e. 50% hemolysis concentration (HC50) > 1000 mg/L
Immune ResponceNone
Mechanism of ActionNA
TargetNA
Combination TherapyMembrane-lytic mechanism
Other activitiesCell envelope
PMIDRifampicin, shows synergy
Year of PublicationAntibacterial
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1249,
Name24314557
N-Terminal modificationM(LLKK)2M
C-Terminal ModificationMLLKKLLKKM
Chemical ModificationFree
Linear/CyclicFree
LengthNone
ChiralityLinear
Nature10
SourceL
OriginCationic
SpeciesSynthetic
Inhibition ConcentrationMycobacterium smegmatis
In Vitro/ In vivoMycobacterium smegmatis resistant agianst rifampicin
Cell LineMIC = 62.5 mg/L
Inhibition ConcentrationIn vitro
Sequence2014
CytotoxicityRat red blood cells (rRBCs)
In vivo ModelNA
Lethal DoseVery low, i.e. 50% hemolysis concentration (HC50) > 1000 mg/L
Immune ResponceNone
Mechanism of ActionNA
TargetNA
Combination TherapyMembrane-lytic mechanism
Other activitiesCell envelope
PMIDNone
Year of PublicationAntibacterial
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1250,
Name24314557
N-Terminal modificationM(LLKK)2M
C-Terminal ModificationMLLKKLLKKM
Chemical ModificationFree
Linear/CyclicFree
LengthNone
ChiralityLinear
Nature10
SourceL
OriginCationic
SpeciesSynthetic
Inhibition ConcentrationMycobacterium smegmatis
In Vitro/ In vivoMycobacterium smegmatis resistant agianst rifampicin
Cell LineMIC = 15.6 mg/L
Inhibition ConcentrationIn vitro
Sequence2014
CytotoxicityRat red blood cells (rRBCs)
In vivo ModelNA
Lethal DoseVery low, i.e. 50% hemolysis concentration (HC50) > 1000 mg/L
Immune ResponceNone
Mechanism of ActionNA
TargetNA
Combination TherapyMembrane-lytic mechanism
Other activitiesCell envelope
PMIDRifampicin, shows synergy
Year of PublicationAntibacterial
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1251,
Name24314557
N-Terminal modificationM(LLKK)2M
C-Terminal ModificationMLLKKLLKKM
Chemical ModificationFree
Linear/CyclicFree
LengthNone
ChiralityLinear
Nature10
SourceL
OriginCationic
SpeciesSynthetic
Inhibition ConcentrationMycobacterium bovis
In Vitro/ In vivoMycobacterium bovis BCG lux
Cell LineMIC = 15.6 mg/L
Inhibition ConcentrationIn vitro
Sequence2014
CytotoxicityRat red blood cells (rRBCs)
In vivo ModelNA
Lethal DoseVery low, i.e. 50% hemolysis concentration (HC50) > 1000 mg/L
Immune ResponceNone
Mechanism of ActionNA
TargetNA
Combination TherapyMembrane-lytic mechanism
Other activitiesCell envelope
PMIDNone
Year of PublicationAntibacterial
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1252,
Name24314557
N-Terminal modificationM(LLKK)2M
C-Terminal ModificationMLLKKLLKKM
Chemical ModificationFree
Linear/CyclicFree
LengthNone
ChiralityLinear
Nature10
SourceL
OriginCationic
SpeciesSynthetic
Inhibition ConcentrationMycobacterium bovis
In Vitro/ In vivoMycobacterium bovis BCG lux
Cell LineMIC = 3.91 mg/L
Inhibition ConcentrationIn vitro
Sequence2014
CytotoxicityRat red blood cells (rRBCs)
In vivo ModelNA
Lethal DoseVery low, i.e. 50% hemolysis concentration (HC50) > 1000 mg/L
Immune ResponceNone
Mechanism of ActionNA
TargetNA
Combination TherapyMembrane-lytic mechanism
Other activitiesCell envelope
PMIDRifampicin, shows synergy
Year of PublicationAntibacterial
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1253,
Name24314557
N-Terminal modificationM(LLKK)2M
C-Terminal ModificationMLLKKLLKKM
Chemical ModificationFree
Linear/CyclicFree
LengthNone
ChiralityLinear
Nature10
SourceL
OriginCationic
SpeciesSynthetic
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis H37Rv
Cell LineMIC = 125 mg/L
Inhibition ConcentrationIn vitro
Sequence2014
CytotoxicityRat red blood cells (rRBCs)
In vivo ModelNA
Lethal DoseVery low, i.e. 50% hemolysis concentration (HC50) > 1000 mg/L
Immune ResponceNone
Mechanism of ActionNA
TargetNA
Combination TherapyMembrane-lytic mechanism
Other activitiesCell envelope
PMIDNone
Year of PublicationAntibacterial
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1254,
Name24314557
N-Terminal modificationM(LLKK)2M
C-Terminal ModificationMLLKKLLKKM
Chemical ModificationFree
Linear/CyclicFree
LengthNone
ChiralityLinear
Nature10
SourceL
OriginCationic
SpeciesSynthetic
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis H37Rv
Cell LineMIC = 7.81 mg/L
Inhibition ConcentrationIn vitro
Sequence2014
CytotoxicityRat red blood cells (rRBCs)
In vivo ModelNA
Lethal DoseVery low, i.e. 50% hemolysis concentration (HC50) > 1000 mg/L
Immune ResponceNone
Mechanism of ActionNA
TargetNA
Combination TherapyMembrane-lytic mechanism
Other activitiesCell envelope
PMIDRifampicin, shows synergy
Year of PublicationAntibacterial
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1255,
Name24314557
N-Terminal modificationM(LLKK)2M
C-Terminal ModificationMLLKKLLKKM
Chemical ModificationFree
Linear/CyclicFree
LengthNone
ChiralityLinear
Nature10
SourceL
OriginCationic
SpeciesSynthetic
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis CSU87 reistant to rifampicin, isoniazid, ethambutol, streptomycin and kanamycin
Cell LineMIC = 62.5 mg/L
Inhibition ConcentrationIn vitro
Sequence2014
CytotoxicityRat red blood cells (rRBCs)
In vivo ModelNA
Lethal DoseVery low, i.e. 50% hemolysis concentration (HC50) > 1000 mg/L
Immune ResponceNone
Mechanism of ActionNA
TargetNA
Combination TherapyMembrane-lytic mechanism
Other activitiesCell envelope
PMIDNone
Year of PublicationAntibacterial
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1620,
Name26380930
N-Terminal modificationMM
C-Terminal ModificationMLLKKLLKKM
Chemical ModificationFree
Linear/CyclicAmidation
LengthNone
ChiralityLinear
Nature10
SourceL
OriginCationic
SpeciesSynthetic
Inhibition ConcentrationMycobacterium smegmatis
In Vitro/ In vivoMycobacterium smegmatis ATCC14468
Cell LineMIC = 62.5 μg/ml
Inhibition Concentrationin vitro
Sequence2015
CytotoxicityRAW 264.7 mouse macrophage
In vivo ModelNA
Lethal DoseHC50= >500 μg/ml
Immune ResponceNA
Mechanism of ActionNA
TargetNA
Combination TherapyBacterial membrane pore formation
Other activitiesNA
PMIDNA
Year of PublicationNA
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1626,
Name26380930
N-Terminal modificationMM
C-Terminal ModificationMLLKKLLKKM
Chemical ModificationFree
Linear/CyclicAmidation
LengthNone
ChiralityLinear
Nature10
SourceL
OriginCationic
SpeciesSynthetic
Inhibition ConcentrationMycobacterium smegmatis
In Vitro/ In vivoMycobacterium smegmatis ATCC14468
Cell LineMIC = 15.6 μg/ml
Inhibition Concentrationin vitro
Sequence2015
CytotoxicityRAW 264.7 mouse macrophage
In vivo ModelNA
Lethal DoseHC50= >500 μg/ml
Immune ResponceNA
Mechanism of ActionNA
TargetNA
Combination TherapyBacterial membrane pore formation
Other activitiesNA
PMIDPeptide + Rifampicin (0.98 μg/ml)
Year of PublicationNA
Tertiary Structure
(Technique)
Not Predicted),