Releasing p8662 to FAH
Posted: Fri Oct 28, 2016 7:08 pm
Project p8662 is now being released to FAH.
It is simulation of the enzyme Phenylalanine Hydroylase (PAH), mutations in which cause phenylketonuria (PKU), an inherited disease that affects about 1 in 12000. We are trying to understand the molecular mechanisms by which PAH senses phenylalanine to activate the enzyme
More info: http://fah-web.stanford.edu/cgi-bin/fah ... ned?p=8662
Projects: 8662
stats credit: 1025
timeout: 15.7
deadline 34.3
k-factor v=0.75
number of atoms: 31247
CPUs >= 1 CPUS <= 27 CPUS!=7 CPUS!=11
It is simulation of the enzyme Phenylalanine Hydroylase (PAH), mutations in which cause phenylketonuria (PKU), an inherited disease that affects about 1 in 12000. We are trying to understand the molecular mechanisms by which PAH senses phenylalanine to activate the enzyme
More info: http://fah-web.stanford.edu/cgi-bin/fah ... ned?p=8662
Projects: 8662
stats credit: 1025
timeout: 15.7
deadline 34.3
k-factor v=0.75
number of atoms: 31247
CPUs >= 1 CPUS <= 27 CPUS!=7 CPUS!=11