This work is licensed under a Creative Commons Attribution 4.0 International License.
PMAP-23 [R10W][Q13W]
General Information
DRACP ID DRACP02179
Peptide Name PMAP-23 [R10W][Q13W]
Sequence RIIDLLWRVWRPWKPKFVTVWVR
Sequence Length 23
UniProt ID P49930
PubChem CID 16129746
Origin Synthetic (Derived from PMAP-23)
Type Synthetic peptide
Classification
Active ACP
Activity Information
| Cell Line | Disease | Cancer Classified | Activity | Assay | Testing Time | Literature |
|---|---|---|---|---|---|---|
| Jurkat | Childhood T acute lymphoblastic leukemia; Precursor T-cell acute lymphoblastic leukemia | Leukemia | IC50=16 µM | MTT assay | 3 days | 1 |
| SNU-601 | Gastric signet ring cell adenocarcinoma | Carcinoma | IC50=21 µM | MTT assay | 3 days | 1 |
Hemolytic Activity Not available
Normal (non-cancerous) Cytotoxicity Not available
Target Not available
Affinity Not available
Mechanism Not available
Nature Anticancer; Antimicrobial; Antifungal
Structure Information
Helicity Not available
Linear/Cyclic Linear
Disulfide/Other Bond Not available
N-terminal Modification Free
C-terminal Modification Amidation
Other Modification None
Chiral L
Physicochemical Information
Formula C151H229N41O27
Absent amino acids ACEGHMNQSY
Common amino acids RVW
Mass 344332
Pl 12.52
Basic residues 6
Acidic residues 1
Hydrophobic residues 13
Net charge 5
Boman Index -3393
Hydrophobicity -2.61
Aliphatic Index 118.26
Half Life
Mammalian: 1 hour
Yeast: 2 min
E.coli: 2 min
Extinction Coefficient cystines 22000
Absorbance 280nm 1000
Polar residues 1
Amino acid distribution
Literature Information
Literature 1
Pubmed ID 12054589
Title Design of novel peptide analogs with potent fungicidal activity, based on PMAP-23 antimicrobial peptide isolated from porcine myeloid
Doi 10.1016/S0006-291X(02)00222-X
Year 2002
Patent
Patent ID Not available
Patent Title Not available
Other Iinformation Not available
Other Published ID Not available
External Code
DBAASP ID DBAASPS_3055
This work is licensed under a Creative Commons Attribution 4.0 International License.