Tat-a5

General Information


DRACP ID  DRACP00199

Peptide Name   Tat-a5

Sequence  KAQIRAMECNILGRKKRRQRRR

Sequence Length  22

UniProt ID  Not available

PubChem CID  Not available

Origin  HIV-Tat (49-57)

Type  Synthetic peptide

Classification

  

Active ACP Cancer targeted peptides



Activity Information


Cell Line Disease Cancer Classified Activity Assay Testing Time Literature
HCT 116 Colon carcinoma Carcinoma ~80% Cytotoxicity at 100 µM MTT assay 24 h 1

Hemolytic Activity  Not available

Normal (non-cancerous) Cytotoxicity  Not available

Target  HIV-Tat

Affinity  Not available

Mechanism  Tat-a5 could arrest cancer cells at G2/M phase and make them apoptotic; Tat-a5 would have the potential to inhibit tumor angiogenesis

Nature  Anticancer



Structure Information


PDB ID  Not available

Predicted Structure  DRACP00199

Helicity  Not available

Linear/Cyclic  Linear

Disulfide/Other Bond  Not available

N-terminal Modification  Free

C-terminal Modification  Free

Other Modification  None

Chiral  L



Physicochemical Information


Formula  C113H211N49O28S2

Absent amino acids  DFHPSTVWY

Common amino acids  R

Mass  314310

Pl  12.64

Basic residues  10

Acidic residues  1

Hydrophobic residues  5

Net charge  9

Boman Index  -12267

Hydrophobicity  -167.27

Aliphatic Index  62.27

Half Life 
  Mammalian: 1.3 hour
  Yeast: 3 min
  E.coli: 2 min

Extinction Coefficient cystines  0

Absorbance 280nm  0

Polar residues  3

Amino acid distribution



Literature Information


Literature 1

Pubmed ID 18656352

Title  A novel peptide from alpha5 helix of Asterina pectinifera cyclin B conjugated to HIV-Tat(49-59) with cytotoxic and apoptotic effects against human cancer cells

Doi 10.1016/j.bmcl.2008.07.017

Year  2008

Patent

Patent ID Not available

Patent Title  Not available

Other Iinformation  Not available

Other Published ID  Not available




DRACP is developed by Dr.Zheng's team.