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"In silico"


From Wikipedia
If the target host* of a phage therapy treatment is not an animal the term "biocontrol" (as in phage-mediated biocontrol of bacteria) is usually employed, rather than "phage therapy".

In silico
From:"Genomics,Proteomics and Clinical Bacteriology",N.Woodford and Alan P.Johnson

Phrase that emphasizes the fact that many molecular biologists spend increasing amounts of their time in front of a computer screen, generating hypotheses that can subsequently be tested and (hopefully) confirmed in the laboratory.


Phage Therapy is influenced by:

Phage therapy is influenced by:

Country : the epidemiological situation is different from country to country in terms of circulating bacteria and bacteriophages. Example: lytic phages from Italy may be no active on the same bacteria (genus and species) isolated from another country and vice versa.
Temporariness
Mutation rate
Phenotypical delay
Phage cocktail

My point of view

Sunday 27 February 2011

Receptor?

All these proteins are Transmembrane Helices.


D29p08
hypothetical protein

minor tail subunit

D29p28
hypothetical protein

D29p33
hypothetical protein

D29p36
hypothetical protein

D29p59
hypothetical protein




gp26

Bxz2p28
gp30

Bxz2p29
gp31

Bxz2p31
gp33

Bxz2p33
gp35

Bxz2p58
gp60

Bxz2p63
gp65






638291237
TM4_17 putative tape-measure protein
TM4_27

TM4_30

TM4_32

TM4_33

TM4_44

TM4_54

TM4_75

TM4_79

TM4_86


The question is if among these proteins there is a common phage receptor.