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RGGRLCYCRRRFCVCVGR details
Primary information
ID antitb_1134,
Name11328767
N-Terminal modificationProtegrin-1 (PG-1)
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthInternal disulphide bond (between Cys 6-15 and Cys 8-13)
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainIsolated from porcine leukocytes
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis H37Rv (ATCC 25618)
Cell Line50 mg/L causes approx 65 % growth inhibition
Inhibition ConcentrationIn vitro
Sequence2001
CytotoxicityNone
In vivo ModelNA
Lethal DoseNA
Immune ResponceNone
Mechanism of ActionNA
TargetNA
Combination TherapyDisrupt the membrane architecture
Other activitiesCell envelope
PMIDNone
Year of PublicationAntibacterial against salmonella, staphylococcus and neisseria
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1135,
Name11328767
N-Terminal modificationProtegrin-1 (PG-1)
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthInternal disulphide bond (between Cys 6-15 and Cys 8-13)
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainIsolated from porcine leukocytes
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis E1380/94 MDR (Isoniazid, rifampicin, streptomycin, ethambutol) strain
Cell Line50 mg/L causes approx 39 % growth inhibition
Inhibition ConcentrationIn vitro
Sequence2001
CytotoxicityNone
In vivo ModelNA
Lethal DoseNA
Immune ResponceNone
Mechanism of ActionNA
TargetNA
Combination TherapyDisrupt the membrane architecture
Other activitiesCell envelope
PMIDNone
Year of PublicationAntibacterial against salmonella, staphylococcus and neisseria
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1563,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis H37Rv
Cell LineCFU/well 3.20 ± 0.15 at peptide concentration 64μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
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_1564,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis H37Rv
Cell LineCFU/well 2.70 ± 0.15 at peptide concentration 64μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
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_1565,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis H37Rv
Cell LineCFU/well 0.88± 0.30 at peptide concentration 4 μg/ml +INH 0.06 μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
Immune ResponceNA
Mechanism of ActionNA
TargetNA
Combination TherapyBacterial membrane pore formation
Other activitiesNA
PMIDINH +peptide
Year of PublicationNA
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1566,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis H37Rv
Cell LineCFU/well 3.19 ± 0.15 at peptide concentration 64 μg/ml +INH 0.06 μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
Immune ResponceNA
Mechanism of ActionNA
TargetNA
Combination TherapyBacterial membrane pore formation
Other activitiesNA
PMIDINH+Peptide
Year of PublicationNA
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1567,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis H37Rv
Cell LineCFU/well 3.19 ± 0.15 at peptide concentration 4 μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
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_1568,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis H37Rv
Cell LineCFU/well 3.58 ± 0.47 at peptide concentration 8 μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
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_1569,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis H37Rv
Cell LineCFU/well 3.16 ± 0.21 at peptide concentration 16 μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
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_1570,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis H37Rv
Cell LineCFU/well 2.97 ± 0.40 at peptide concentration 32 μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
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_1571,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis H37Rv
Cell LineCFU/well 2.70 ± 0.10 at peptide concentration 64 μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
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_1572,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis H37Rv
Cell LineCFU/well 1.72 ± 0.46 at peptide concentration 128 μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
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_1573,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis RM22
Cell LineCFU/well 3.08 ± 0.09 at peptide concentration 4 μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
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_1574,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature19
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis RM23
Cell LineCFU/well 2.97 ± 0.06 at peptide concentration 4 μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
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_1575,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature20
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis RM24
Cell LineCFU/well 3.11 ± 0.09 at peptide concentration 4 μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
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_1576,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature21
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis RM25
Cell LineCFU/well 3.19 ± 0.05 at peptide concentration 4 μg/ml +INH 4μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
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_1577,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature22
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis RM26
Cell LineCFU/well 3.08 ± 0.09 at peptide concentration 64 μg/ml +INH 4μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
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_1578,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis RM22
Cell LineCFU/well 3.10 ± 0.08 at peptide concentration 8 μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
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_1579,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis RM22
Cell LineCFU/well 3.00 ± 0.10 at peptide concentration 16 μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
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_1580,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis RM22
Cell LineCFU/well 3.05 ± 0.11 at peptide concentration 32 μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
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_1581,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis RM22
Cell LineCFU/well 2.88 ± 0.06at peptide concentration 64 μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
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_1582,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis RM22
Cell LineCFU/well 2.71 ± 0.09 at peptide concentration 128 μg/ml
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
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_1603,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis H37Rv
Cell LineCFU/well 0.68 ± 0.30 at peptide 64ul + 4 ul of INH
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
Immune ResponceNA
Mechanism of ActionNA
TargetNA
Combination TherapyBacterial membrane pore formation
Other activitiesNA
PMIDPeptide(64 ul) + INH(4 ul)
Year of PublicationNA
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1604,
Name15245864
N-Terminal modificationProtegrin -1
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-14
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
StrainDerived from porcine leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis RM22
Cell LineCFU/well 1.99 ± 0.44 at peptide 64ul + 4 ul of INH
Inhibition Concentrationin vitro
Sequence2004
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
Immune ResponceNA
Mechanism of ActionNA
TargetNA
Combination TherapyBacterial membrane pore formation
Other activitiesNA
PMIDPeptide(64 ul) + INH(4 ul)
Year of PublicationNA
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1708,
Name8641802
N-Terminal modificationPorcine leucocyte peptide (PG-1)
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-13
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
Strain porcine neutrophil leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis Ra 7632G
Cell LineReduction in CFU at 50 μg/ml
Inhibition Concentrationin vitro
Sequence1996
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
Immune ResponceNA
Mechanism of ActionNA
TargetNA
Combination TherapyMicrobial membrane disruption
Other activitiesNA
PMIDNA
Year of PublicationNA
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1709,
Name8641802
N-Terminal modificationPorcine leucocyte peptide (PG-1)
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-14
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
Strain porcine neutrophil leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis Ra 9034G
Cell LineReduction in CFU at 50 μg/ml
Inhibition Concentrationin vitro
Sequence1996
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
Immune ResponceNA
Mechanism of ActionNA
TargetNA
Combination TherapyMicrobial membrane disruption
Other activitiesNA
PMIDNA
Year of PublicationNA
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1710,
Name8641802
N-Terminal modificationPorcine leucocyte peptide (PG-1)
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-15
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
Strain porcine neutrophil leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis Ra 11170G
Cell LineReduction in CFU at 50 μg/ml
Inhibition Concentrationin vitro
Sequence1996
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
Immune ResponceNA
Mechanism of ActionNA
TargetNA
Combination TherapyMicrobial membrane disruption
Other activitiesNA
PMIDNA
Year of PublicationNA
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1711,
Name8641802
N-Terminal modificationPorcine leucocyte peptide (PG-1)
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-16
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
Strain porcine neutrophil leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis H37 Ra
Cell LineIC50= 5 μg/ml
Inhibition Concentrationin vitro
Sequence1996
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
Immune ResponceNA
Mechanism of ActionNA
TargetNA
Combination TherapyMicrobial membrane disruption
Other activitiesNA
PMIDNA
Year of PublicationNA
Tertiary Structure
(Technique)
Not Predicted),
Primary information
ID antitb_1712,
Name8641802
N-Terminal modificationPorcine leucocyte peptide (PG-1)
C-Terminal ModificationRGGRLCYCRRRFCVCVGR
Chemical ModificationFree
Linear/CyclicFree
LengthDisulphide linkage 6-15 and 8-17
ChiralityCyclic
Nature18
SourceL
OriginCationic
SpeciesNatural
Strain porcine neutrophil leucocyte
Inhibition ConcentrationMycobacterium tuberculosis
In Vitro/ In vivoMycobacterium tuberculosis H37 Ra
Cell LineMIC = 50 μg/ml
Inhibition Concentrationin vitro
Sequence1996
CytotoxicityNA
In vivo ModelNA
Lethal DoseNA
Immune ResponceNA
Mechanism of ActionNA
TargetNA
Combination TherapyMicrobial membrane disruption
Other activitiesNA
PMIDNA
Year of PublicationNA
Tertiary Structure
(Technique)
Not Predicted),