Record in detail
General Info
- lamp_id:L01A000223
- Name:KAB1_OLDAF
- FullName:Kalata-B1
- Source:Oldenlandia affinis
- Mass:2916.3 Da
- Sequence Length:29 aa
- Isoelectric Point:5.93
- Activity:Antibacterial, Antifungal
- Sequence
VCGETCVGGTCNTPGCTCSWPVCTRNGLP - Function:Probably participates in a plant defense mechanism. Has antibiotic activity. Has a diuretic effect. Has a uterotonic effect in humans. Active against the Gram-positive S. aureus with a minimum inhibition concentration of approximately 0.2 microM. Relatively ineffective against Gram-negative bacteria such as E.coli and P.aeruginosa. Inhibitory effect on the growth and development of larvae from H.punctigera. The unmodified form has hemolytic activity, the oxidized form lacks hemolytic activity. If the protein is linearized, hemolytic activity is lost.
Cross-Linking
- Cross-linking
- 1 Database:CAMP CAMPSQ202
- 2 Database:dbAMP dbAMP_11671
- 3 Database:SATPdb satpdb16048
- 4 Database:Uniprot P56254
Top similar AMPs
- Top similar AMPs on LAMP
- 1. L01A000223 From 1 To 29 E-value: 0.00000000004 Score: 58.5
VCGETCVGGTCNTPGCTCSWPVCTRNGLP - 2. L02A001048 From 1 To 29 E-value: 0.00000000009 Score: 57.4
ICGETCVGGTCNTPGCSCSWPVCTRNGLP - 3. L13A024911 From 1 To 29 E-value: 0.00000000009 Score: 57.4
VCGETCVGGTCNTPGCTCSWPVCTRDGLP - 4. L02A000729 From 1 To 28 E-value: 0.0000000001 Score: 57
CGETCVGGTCNTPGCTCSWPVCTRNGLP - 5. L02A001806 From 1 To 28 E-value: 0.0000000003 Score: 55.8
CGETCVGGTCNTPGCACSWPVCTRNGLP
Structure
- Domains
- 1 Name:Cyclotide Interpro Link:IPR005535
- 2 Name:Cyclotide_moebius_CS Interpro Link:IPR012324
- Structures
- 1
PDB:1JJZ
Method:NMR
Chains:A=89-116 - 2
PDB:1K48
Method:NMR
Chains:A=89-116 - 3
PDB:1KAL
Method:NMR
Chains:A=89-109 - 4
PDB:1N1U
Method:NMR
Chains:A=94-120 - 5
PDB:1NB1
Method:NMR
Chains:A=93-120 - 6
PDB:1ORX
Method:NMR
Chains:A=92-115 - 7
PDB:2F2I
Method:NMR
Chains:A=93-120 - 8
PDB:2F2J
Method:NMR
Chains:A=93-120 - 9
PDB:2JUE
Method:NMR
Chains:A=93-120 - 10
PDB:2KHB
Method:NMR
Chains:A=89-117
Activity
- Antibacterial Activities
- 1 Target: K. oxytoca MIC: 159.81 μg/ml (54.7989 μM)
- 2 Target: S. aureus MIC: 0.76 μg/ml (0.260604 μM)
- 3 Target: M. luteus MIC: 117.82 μg/ml (40.4005 μM)
- 4 Target: C. kefyr MIC: 62.41 μg/ml (21.4004 μM)
Toxicity
- Toxicity
No toxicity records found on LAMP database
Reference
- Reference
- [1] Juul J.,Sletten K.,Campbell I.D.,Craik D.J.,Saether O.,
- Title:Elucidation of the primary and three-dimensional structure of the uterotonic polypeptide kalata B1.
- Journal:Biochemistry, 1995, 34, 4147-4158 [MEDLINE:95217878]
- [2] Chiu K.-W.,Yang J.-L.,Lu Y.-A.,Tam J.P.,
- Title:An unusual structural motif of antimicrobial peptides containing end-to-end macrocycle and cystine-knot disulfides.
- Journal:Proc. Natl. Acad. Sci. U.S.A., 1999, 96, 8913-8918 [MEDLINE:99362685]
- [3] Anderson M.A.,Craik D.J.,Waine C.,West J.,Jennings C.V.,
- Title:Biosynthesis and insecticidal properties of plant cyclotides: the cyclic knotted proteins from Oldenlandia affinis.
- Journal:Proc. Natl. Acad. Sci. U.S.A., 2001, 98, 10614-10619 [MEDLINE:21438013]
- [4] Volkman B.F.,Sletten K.,Gran L.,Skjeldal L.,
- Title:Refined structure and metal binding site of the kalata B1 peptide.
- Journal:Arch. Biochem. Biophys., 2002, 399, 142-148 [PubMed:11888199]
- [5] Craik D.J.,Clark R.J.,Daly N.L.,
- Title:Disulfide folding pathways of cystine knot proteins. Tying the knot within the circular backbone of the cyclotides.
- Journal:J. Biol. Chem., 2003, 278, 6314-6322 [PubMed:12482862]
- [6] Craik D.J.,Sando L.,Clark R.J.,Daly N.L.,Barry D.G.,
- Title:Linearization of a naturally occurring circular protein maintains structure but eliminates hemolytic activity.
- Journal:Biochemistry, 2003, 42, 6688-6695 [PubMed:12779323]
- [7] Craik D.J.,Waine C.,Plan M.R.R.,Daly N.L.,Rosengren K.J.,
- Title:Twists, knots, and rings in proteins. Structural definition of the cyclotide framework.
- Journal:J. Biol. Chem., 2003, 278, 8606-8616 [PubMed:12482868]
- [8] Colgrave M.L.,Daly N.L.,Clark R.J.,Goeransson U.,Plan M.R.R.,
- Title:The cyclotide fingerprint in Oldenlandia affinis: elucidation of chemically modified, linear and novel macrocyclic peptides.
- Journal:ChemBioChem, 2007, 8, 1001-1011 [PubMed:17534989]
Comments
- Comments
No comments found on LAMP database