CMK

General Information


DRACP ID  DRACP04100

Peptide Name   CMK

Sequence  RVKR

Sequence Length  4

UniProt ID  Not available

PubChem CID  Not available

Origin  Synthetic

Type  Synthetic peptide

Classification

  

Active ACP



Activity Information


Hemolytic Activity  Not available

Normal (non-cancerous) Cytotoxicity  Not available

Target  Not available

Affinity  Not available

Mechanism  Not available

Nature  Anticancer; Antiviral



Structure Information


PDB ID  Not available

Predicted Structure  Not available

Helicity  Not available

Linear/Cyclic  Linear

Disulfide/Other Bond  Not available

N-terminal Modification  C10

C-terminal Modification  CMK

Other Modification  None

Chiral  L



Physicochemical Information


Formula  C23H47N11O5

Absent amino acids  ACDEFGHILMNPQSTWY

Common amino acids  R

Mass  61138

Pl  12.52

Basic residues  3

Acidic residues  0

Hydrophobic residues  1

Net charge  3

Boman Index  -3135

Hydrophobicity  -217.5

Aliphatic Index  72.5

Half Life 
  Mammalian: 20 hour
  Yeast: 30 min
  E.coli: >10 hour

Extinction Coefficient cystines  0

Absorbance 280nm  0

Polar residues  0

Amino acid distribution



Literature Information


Literature 1

Pubmed ID 33007239

Title  Furin Inhibitors Block SARS-CoV-2 Spike Protein Cleavage to Suppress Virus Production and Cytopathic Effects

Doi Not available

Year  2020

Literature 2

Pubmed ID 31683742

Title  Decanoyl-Arg-Val-Lys-Arg-Chloromethylketone: An Antiviral Compound That Acts against Flaviviruses through the Inhibition of Furin-Mediated prM Cleavage

Doi Not available

Year  2019

Literature 3

Pubmed ID 23617302

Title  Therapeutic potential of furin inhibitors for the chronic infection of hepatitis B virus

Doi Not available

Year  2013

Patent

Patent ID Not available

Patent Title  Not available

Other Iinformation  Not available

Other Published ID  Not available




DBAASP ID  17117

DRACP is developed by Dr.Zheng's team.