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proteins
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Quantitative metabolomics services for biomarker discovery and validation.
Specializing in ready to use metabolomics kits.
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Proteins
Displaying proteins
1026 - 1050
of
2133
in total
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Uniprot ID
Gene Name
Name
Type
Metabolites
P64608
Details
mlaE
Probable phospholipid ABC transporter permease protein mlaE
Enzyme
P64606
Details
mlaE
Probable phospholipid ABC transporter permease protein mlaE
Enzyme
PS(16:0/16:0)
PA(16:0/16:0)
CDP-DG(16:0/16:0)
CDP-DG(16:0/18:0)
CDP-DG(16:0/18:1(11Z))
CDP-DG(16:0/18:1(9Z))
CDP-DG(18:0/16:0)
CDP-DG(18:0/18:0)
CDP-DG(18:0/18:1(11Z))
CDP-DG(18:0/18:1(9Z))
CDP-DG(18:1(11Z)/16:0)
CDP-DG(18:1(11Z)/18:0)
CDP-DG(18:1(11Z)/18:1(11Z))
CDP-DG(18:1(11Z)/18:1(9Z))
CDP-DG(18:1(11Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))
CDP-DG(18:1(9Z)/16:0)
CDP-DG(18:1(9Z)/18:0)
CDP-DG(18:1(9Z)/18:1(11Z))
PA(16:0/18:1(11Z))
PA(16:0/18:1(9Z))
PA(16:0/18:2(9Z,12Z))
PA(18:0/18:2(9Z,12Z))
PA(18:1(11Z)/18:1(11Z))
PA(18:1(11Z)/18:1(9Z))
PA(18:1(9Z)/18:1(11Z))
PA(18:1(9Z)/18:1(9Z))
PE(14:0/14:0)
PE(14:0/16:0)
PE(14:0/16:1(9Z))
PE(14:0/18:1(11Z))
PE(16:0/14:0)
PE(16:0/16:0)
PE(16:0/16:1(9Z))
PE(16:0/18:1(11Z))
PE(16:1(9Z)/14:0)
PE(16:1(9Z)/16:0)
PE(16:1(9Z)/16:1(9Z))
PE(16:1(9Z)/18:1(11Z))
PE(18:1(11Z)/14:0)
PE(18:1(11Z)/16:0)
PE(18:1(11Z)/16:1(9Z))
PE(18:1(11Z)/18:1(11Z))
PG(16:0/16:0)
PG(16:0/16:1(9Z))
PG(16:0/18:1(11Z))
PG(16:1(9Z)/16:0)
PG(16:1(9Z)/16:1(9Z))
PG(16:1(9Z)/18:1(11Z))
PG(18:1(11Z)/16:0)
PG(18:1(11Z)/16:1(9Z))
PG(18:1(11Z)/18:1(11Z))
CL(18:1(9Z)/18:1(9Z)/18:1(9Z)/18:1(9Z))
PA(16:0e/18:0)
PA(P-16:0e/18:2(9Z,12Z))
PA(20:4(5Z,8Z,11Z,14Z)e/2:0)
PS(14:0/14:0)
PS(14:0/16:0)
PS(14:0/16:1(9Z))
PS(16:0/14:0)
PS(16:0/16:1(9Z))
PS(16:1(9Z)/14:0)
PS(16:1(9Z)/16:0)
PS(16:1(9Z)/16:1(9Z))
PG(14:0/14:0)
PE(17:0/16:0)
PE(17:0/17:0)
PE(17:0/19:0)
PE(19:0/14:0)
PE(19:0/16:0)
PE(19:0/17:0)
PE(19:0/19:0)
PG(14:0/16:0)
PG(17:0/17:0)
PS(16:0/18:1(11Z))
PE(14:0/17:0)
PE(14:0/19:0)
PE(16:0/17:0)
PE(16:0/19:0)
PE(17:0/14:0)
PG(14:0/17:0)
PG(19:0/14:0)
PG(19:0/16:0)
PG(19:0/17:0)
PG(19:0/19:0)
PG(16:1(9Z)/14:0)
PS(14:0/17:0)
PS(14:0/19:0)
PS(16:0/17:0)
PS(16:0/19:0)
PS(18:1(11Z)/14:0)
PG(14:0/19:0)
PS(17:0/14:0)
PS(17:0/19:0)
PS(19:0/14:0)
PS(19:0/16:0)
PS(19:0/17:0)
PS(19:0/19:0)
PG(14:0/18:1(11Z))
PG(17:0/16:0)
PS(14:0/18:1(11Z))
PS(18:1(11Z)/16:0)
PG(14:0/16:1(9Z))
PS(18:1(11Z)/18:1(11Z))
PS(18:1(11Z)/16:1(9Z))
PS(17:0/16:0)
PS(17:0/17:0)
PS(16:1(9Z)/18:1(11Z))
PE(18:1(11Z)/17:0)
PE(18:1(11Z)/19:0)
PE(17:0/16:1(9Z))
PE(19:0/18:1(11Z))
PE(17:0/18:1(11Z))
PG(16:0/14:0)
PE(19:0/16:1(9Z))
PE(16:1(9Z)/17:0)
PE(16:1(9Z)/19:0)
PG(18:1(11Z)/17:0)
PG(18:1(11Z)/19:0)
PG(17:0/18:1(11Z))
PG(17:0/16:1(9Z))
PG(19:0/18:1(11Z))
PG(19:0/16:1(9Z))
PG(16:1(9Z)/17:0)
PG(16:0/17:0)
PG(16:1(9Z)/19:0)
PS(18:1(11Z)/17:0)
PS(18:1(11Z)/19:0)
PS(17:0/18:1(11Z))
PS(17:0/16:1(9Z))
PS(19:0/18:1(11Z))
PS(19:0/16:1(9Z))
PS(16:1(9Z)/17:0)
PS(16:1(9Z)/19:0)
PG(16:0/19:0)
PG(18:1(11Z)/14:0)
PG(17:0/14:0)
PG(17:0/19:0)
PG(14:0/17:0cycw7c)
PG(15:0/17:0cycw7c)
PG(16:0/17:0cycw7c)
PG(16:0/18:0)
PG(16:0/19:0cycw8c)
PE(10:0/10:0)
PE(10:0/12:0)
PE(10:0/14:0)
PE(10:0/15:0)
PE(10:0/16:0)
PE(10:0/16:1(9Z))
PE(10:0/17:0cycw7c)
PE(10:0/18:0)
PE(10:0/18:1(11Z))
PE(10:0/19:1(12Z))
PE(10:0/19:0cycw8c)
PE(12:0/10:0)
PE(12:0/12:0)
PE(12:0/14:0)
PE(12:0/15:0)
PE(12:0/16:0)
PE(12:0/16:1(9Z))
PE(12:0/17:0cycw7c)
PE(12:0/18:0)
PE(12:0/18:1(11Z))
PE(12:0/19:1(12Z))
PE(12:0/19:0cycw8c)
PE(14:0/10:0)
PE(14:0/12:0)
PE(14:0/17:0cycw7c)
PE(15:0/10:0)
PE(15:0/12:0)
PE(15:0/17:0cycw7c)
PE(16:0/10:0)
PE(16:0/12:0)
PE(16:0/17:0cycw7c)
PE(16:0/19:0cycw8c)
PE(16:1(9Z)/10:0)
PE(16:1(9Z)/12:0)
PE(17:0cycw7c/10:0)
PE(17:0cycw7c/12:0)
PE(17:0cycw7c/17:0cycw7c)
PE(18:0/10:0)
PE(18:0/12:0)
PE(18:0/17:0cycw7c)
PE(18:1(11Z)/10:0)
PE(18:1(11Z)/12:0)
PE(19:1(12Z)/10:0)
PE(19:1(12Z)/12:0)
PE(19:0cycw8c/10:0)
PE(19:0cycw8c/12:0)
PE(19:0cycw8c/17:0cycw7c)
CDP-DG(10:0/10:0)
CDP-DG(10:0/12:0)
CDP-DG(10:0/14:0)
CDP-DG(10:0/15:0)
CDP-DG(10:0/16:0)
CDP-DG(10:0/16:1(9Z))
CDP-DG(10:0/18:0)
CDP-DG(10:0/18:1(9Z))
CDP-DG(10:0/19:1(9Z))
CDP-DG(12:0/10:0)
CDP-DG(12:0/14:0)
CDP-DG(12:0/15:0)
CDP-DG(12:0/16:0)
CDP-DG(12:0/16:1(9Z))
CDP-DG(12:0/18:0)
CDP-DG(12:0/18:1(9Z))
CDP-DG(12:0/19:1(9Z))
CDP-DG(14:0/10:0)
CDP-DG(14:0/12:0)
CDP-DG(14:0/15:0)
CDP-DG(14:0/16:0)
CDP-DG(14:0/16:1(9Z))
CDP-DG(14:0/18:0)
CDP-DG(14:0/18:1(9Z))
CDP-DG(14:0/19:1(9Z))
CDP-DG(15:0/10:0)
CDP-DG(15:0/12:0)
CDP-DG(15:0/14:0)
CDP-DG(15:0/15:0)
CDP-DG(15:0/16:0)
CDP-DG(15:0/16:1(9Z))
CDP-DG(15:0/18:0)
CDP-DG(15:0/18:1(9Z))
CDP-DG(15:0/19:1(9Z))
CDP-DG(16:0/10:0)
CDP-DG(16:0/12:0)
CDP-DG(16:0/14:0)
CDP-DG(16:0/15:0)
CDP-DG(16:0/16:1(9Z))
CDP-DG(16:0/19:1(9Z))
CDP-DG(16:1(9Z)/10:0)
CDP-DG(16:1(9Z)/12:0)
CDP-DG(16:1(9Z)/14:0)
CDP-DG(16:1(9Z)/15:0)
CDP-DG(16:1(9Z)/16:0)
CDP-DG(16:1(9Z)/18:0)
CDP-DG(16:1(9Z)/18:1(9Z))
CDP-DG(16:1(9Z)/19:1(9Z))
CDP-DG(18:0/10:0)
CDP-DG(18:0/12:0)
CDP-DG(18:0/14:0)
CDP-DG(18:0/15:0)
CDP-DG(18:0/16:1(9Z))
CDP-DG(18:0/19:1(9Z))
CDP-DG(18:1(9Z)/10:0)
CDP-DG(18:1(9Z)/12:0)
CDP-DG(18:1(9Z)/14:0)
CDP-DG(18:1(9Z)/15:0)
CDP-DG(18:1(9Z)/16:1(9Z))
CDP-DG(18:1(9Z)/18:1(9Z))
CDP-DG(18:1(9Z)/19:1(9Z))
CDP-DG(19:1(9Z)/10:0)
CDP-DG(19:1(9Z)/12:0)
CDP-DG(19:1(9Z)/14:0)
CDP-DG(19:1(9Z)/15:0)
CDP-DG(19:1(9Z)/16:0)
CDP-DG(19:1(9Z)/16:1(9Z))
CDP-DG(19:1(9Z)/18:0)
CDP-DG(19:1(9Z)/18:1(9Z))
CDP-DG(19:1(9Z)/19:1(9Z))
PE(10:0(3-OH)/10:0)
PE(10:0(3-OH)/10:0(3-OH))
PE(10:0(3-OH)/12:0)
PE(10:0(3-OH)/12:0(3-OH))
PE(10:0(3-OH)/14:0)
PE(10:0(3-OH)/14:0(3-OH))
PE(10:0(3-OH)/15:0)
PE(10:0(3-OH)/15:0cyclo)
PE(10:0(3-OH)/16:0)
PE(10:0(3-OH)/16:1(9Z))
PE(10:0(3-OH)/17:0cycw7c)
PE(10:0(3-OH)/18:1(9Z))
PE(10:0(3-OH)/19:0cycv8c)
PE(10:0(3-OH)/19:iso)
PE(10:0/10:0(3-OH))
PE(10:0/12:0(3-OH))
PE(10:0/14:0(3-OH))
PE(10:0/19:iso)
PE(12:0(3-OH)/10:0)
PE(12:0(3-OH)/10:0(3-OH))
PE(12:0(3-OH)/12:0)
PE(12:0(3-OH)/12:0(3-OH))
PE(12:0(3-OH)/14:0)
PE(12:0(3-OH)/14:0(3-OH))
PE(12:0(3-OH)/15:0)
PE(12:0(3-OH)/15:0cyclo)
PE(12:0(3-OH)/16:0)
PE(12:0(3-OH)/16:1(9Z))
PE(12:0(3-OH)/17:0cycw7c)
PE(12:0(3-OH)/18:1(9Z))
PE(12:0(3-OH)/19:0cycv8c)
PE(12:0(3-OH)/19:iso)
PE(12:0/10:0(3-OH))
PE(12:0/12:0(3-OH))
PE(12:0/14:0(3-OH))
PE(12:0/19:iso)
PE(14:0(3-OH)/10:0)
PE(14:0(3-OH)/10:0(3-OH))
PE(14:0(3-OH)/12:0)
PE(14:0(3-OH)/12:0(3-OH))
PE(14:0(3-OH)/14:0)
PE(14:0(3-OH)/14:0(3-OH))
PE(14:0(3-OH)/15:0)
PE(14:0(3-OH)/15:0cyclo)
PE(14:0(3-OH)/16:0)
PE(14:0(3-OH)/16:1(9Z))
PE(14:0(3-OH)/17:0cycw7c)
PE(14:0(3-OH)/18:1(9Z))
PE(14:0(3-OH)/19:0cycv8c)
PE(14:0(3-OH)/19:iso)
PE(14:0/10:0(3-OH))
PE(14:0/12:0(3-OH))
PE(14:0/14:0(3-OH))
PE(14:0/19:iso)
PE(15:0/10:0(3-OH))
PE(15:0/12:0(3-OH))
PE(15:0/14:0(3-OH))
PE(15:0/19:iso)
PE(15:0cyclo/10:0(3-OH))
PE(15:0cyclo/12:0(3-OH))
PE(15:0cyclo/14:0(3-OH))
PE(15:0cyclo/19:iso)
PE(16:0/10:0(3-OH))
PE(16:0/12:0(3-OH))
PE(16:0/14:0(3-OH))
PE(16:0/19:iso)
PE(16:1(9Z)/10:0(3-OH))
PE(16:1(9Z)/12:0(3-OH))
PE(16:1(9Z)/14:0(3-OH))
PE(16:1(9Z)/19:iso)
PE(17:0cycw7c/10:0(3-OH))
PE(17:0cycw7c/12:0(3-OH))
PE(17:0cycw7c/14:0(3-OH))
PE(17:0cycw7c/19:iso)
PE(18:1(9Z)/10:0(3-OH))
PE(18:1(9Z)/12:0(3-OH))
PE(18:1(9Z)/14:0(3-OH))
PE(18:1(9Z)/19:iso)
PE(19:0cycv8c/10:0(3-OH))
PE(19:0cycv8c/12:0(3-OH))
PE(19:0cycv8c/14:0(3-OH))
PE(19:0cycv8c/19:iso)
PE(19:iso/10:0)
PE(19:iso/10:0(3-OH))
PE(19:iso/12:0)
PE(19:iso/12:0(3-OH))
PE(19:iso/14:0)
PE(19:iso/14:0(3-OH))
PE(19:iso/15:0)
PE(19:iso/15:0cyclo)
PE(19:iso/16:0)
PE(19:iso/16:1(9Z))
PE(19:iso/17:0cycw7c)
PE(19:iso/18:1(9Z))
PE(19:iso/19:0cycv8c)
PE(19:iso/19:iso)
PS(10:0(3-OH)/10:0)
PS(10:0(3-OH)/10:0(3-OH))
PS(10:0(3-OH)/12:0)
PS(10:0(3-OH)/12:0(3-OH))
PS(10:0(3-OH)/14:0)
PS(10:0(3-OH)/14:0(3-OH))
PS(10:0(3-OH)/15:0)
PS(10:0(3-OH)/15:0cyclo)
PS(10:0(3-OH)/16:0)
PS(10:0(3-OH)/16:1(9Z))
PS(10:0(3-OH)/17:0cycw7c)
PS(10:0(3-OH)/18:1(9Z))
PS(10:0(3-OH)/19:0cycv8c)
PS(10:0(3-OH)/19:iso)
PS(10:0/10:0(3-OH))
PS(10:0/12:0(3-OH))
PS(10:0/14:0(3-OH))
PS(10:0/19:iso)
PS(12:0(3-OH)/10:0)
PS(12:0(3-OH)/10:0(3-OH))
PS(12:0(3-OH)/12:0)
PS(12:0(3-OH)/12:0(3-OH))
PS(12:0(3-OH)/14:0)
PS(12:0(3-OH)/14:0(3-OH))
PS(12:0(3-OH)/15:0)
PS(12:0(3-OH)/15:0cyclo)
PS(12:0(3-OH)/16:0)
PS(12:0(3-OH)/16:1(9Z))
PS(12:0(3-OH)/17:0cycw7c)
PS(12:0(3-OH)/18:1(9Z))
PS(12:0(3-OH)/19:0cycv8c)
PS(12:0(3-OH)/19:iso)
PS(12:0/10:0(3-OH))
PS(12:0/12:0(3-OH))
PS(12:0/14:0(3-OH))
PS(12:0/19:iso)
PS(14:0(3-OH)/10:0)
PS(14:0(3-OH)/10:0(3-OH))
PS(14:0(3-OH)/12:0)
PS(14:0(3-OH)/12:0(3-OH))
PS(14:0(3-OH)/14:0)
PS(14:0(3-OH)/14:0(3-OH))
PS(14:0(3-OH)/15:0)
PS(14:0(3-OH)/15:0cyclo)
PS(14:0(3-OH)/16:0)
PS(14:0(3-OH)/16:1(9Z))
PS(14:0(3-OH)/17:0cycw7c)
PS(14:0(3-OH)/18:1(9Z))
PS(14:0(3-OH)/19:0cycv8c)
PS(14:0(3-OH)/19:iso)
PS(14:0/10:0(3-OH))
PS(14:0/12:0(3-OH))
PS(14:0/14:0(3-OH))
PS(14:0/19:iso)
PS(15:0/10:0(3-OH))
PS(15:0/12:0(3-OH))
PS(15:0/14:0(3-OH))
PS(15:0/19:iso)
PS(15:0cyclo/10:0(3-OH))
PS(15:0cyclo/12:0(3-OH))
PS(15:0cyclo/14:0(3-OH))
PS(15:0cyclo/19:iso)
PS(16:0/10:0(3-OH))
PS(16:0/12:0(3-OH))
PS(16:0/14:0(3-OH))
PS(16:0/19:iso)
PS(16:1(9Z)/10:0(3-OH))
PS(16:1(9Z)/12:0(3-OH))
PS(16:1(9Z)/14:0(3-OH))
PS(16:1(9Z)/19:iso)
PS(17:0cycw7c/10:0(3-OH))
PS(17:0cycw7c/12:0(3-OH))
PS(17:0cycw7c/14:0(3-OH))
PS(17:0cycw7c/19:iso)
PS(18:1(9Z)/10:0(3-OH))
PS(18:1(9Z)/12:0(3-OH))
PS(18:1(9Z)/14:0(3-OH))
PS(18:1(9Z)/19:iso)
PS(19:0cycv8c/10:0(3-OH))
PS(19:0cycv8c/12:0(3-OH))
PS(19:0cycv8c/14:0(3-OH))
PS(19:0cycv8c/19:iso)
PS(19:iso/10:0)
PS(19:iso/10:0(3-OH))
PS(19:iso/12:0)
PS(19:iso/12:0(3-OH))
PS(19:iso/14:0)
PS(19:iso/14:0(3-OH))
PS(19:iso/15:0)
PS(19:iso/15:0cyclo)
PS(19:iso/16:0)
PS(19:iso/16:1(9Z))
PS(19:iso/17:0cycw7c)
PS(19:iso/18:1(9Z))
PS(19:iso/19:0cycv8c)
PS(19:iso/19:iso)
PG(10:0(3-OH)/10:0)
PG(10:0(3-OH)/10:0(3-OH))
PG(10:0(3-OH)/12:0)
PG(10:0(3-OH)/12:0(3-OH))
PG(10:0(3-OH)/14:0)
PG(10:0(3-OH)/14:0(3-OH))
PG(10:0(3-OH)/15:0)
PG(10:0(3-OH)/15:0cyclo)
PG(10:0(3-OH)/16:0)
PG(10:0(3-OH)/16:1(9Z))
PG(10:0(3-OH)/17:0cycw7c)
PG(10:0(3-OH)/18:1(9Z))
PG(10:0(3-OH)/19:0cycv8c)
PG(10:0(3-OH)/19:iso)
PG(10:0/10:0(3-OH))
PG(10:0/12:0(3-OH))
PG(10:0/14:0(3-OH))
PG(10:0/19:iso)
PG(12:0(3-OH)/10:0)
PG(12:0(3-OH)/10:0(3-OH))
PG(12:0(3-OH)/12:0)
PG(12:0(3-OH)/12:0(3-OH))
PG(12:0(3-OH)/14:0)
PG(12:0(3-OH)/14:0(3-OH))
PG(12:0(3-OH)/15:0)
PG(12:0(3-OH)/15:0cyclo)
PG(12:0(3-OH)/16:0)
PG(12:0(3-OH)/16:1(9Z))
PG(12:0(3-OH)/17:0cycw7c)
PG(12:0(3-OH)/18:1(9Z))
PG(12:0(3-OH)/19:0cycv8c)
PG(12:0(3-OH)/19:iso)
PG(12:0/10:0(3-OH))
PG(12:0/12:0(3-OH))
PG(12:0/14:0(3-OH))
PG(12:0/19:iso)
PG(14:0(3-OH)/10:0)
PG(14:0(3-OH)/10:0(3-OH))
PG(14:0(3-OH)/12:0)
PG(14:0(3-OH)/12:0(3-OH))
PG(14:0(3-OH)/14:0)
PG(14:0(3-OH)/14:0(3-OH))
PG(14:0(3-OH)/15:0)
PG(14:0(3-OH)/15:0cyclo)
PG(14:0(3-OH)/16:0)
PG(14:0(3-OH)/16:1(9Z))
PG(14:0(3-OH)/17:0cycw7c)
PG(14:0(3-OH)/18:1(9Z))
PG(14:0(3-OH)/19:0cycv8c)
PG(14:0(3-OH)/19:iso)
PG(14:0/10:0(3-OH))
PG(14:0/12:0(3-OH))
PG(14:0/14:0(3-OH))
PG(14:0/19:iso)
PG(15:0/10:0(3-OH))
PG(15:0/12:0(3-OH))
PG(15:0/14:0(3-OH))
PG(15:0/19:iso)
PG(15:0cyclo/10:0(3-OH))
PG(15:0cyclo/12:0(3-OH))
PG(15:0cyclo/14:0(3-OH))
PG(15:0cyclo/19:iso)
PG(16:0/10:0(3-OH))
PG(16:0/12:0(3-OH))
PG(16:0/14:0(3-OH))
PG(16:0/19:iso)
PG(16:1(9Z)/10:0(3-OH))
PG(16:1(9Z)/12:0(3-OH))
PG(16:1(9Z)/14:0(3-OH))
PG(16:1(9Z)/19:iso)
PG(17:0cycw7c/10:0(3-OH))
PG(17:0cycw7c/12:0(3-OH))
PG(17:0cycw7c/14:0(3-OH))
PG(17:0cycw7c/19:iso)
PG(18:1(9Z)/10:0(3-OH))
PG(18:1(9Z)/12:0(3-OH))
PG(18:1(9Z)/14:0(3-OH))
PG(18:1(9Z)/19:iso)
PG(19:0cycv8c/10:0(3-OH))
PG(19:0cycv8c/12:0(3-OH))
PG(19:0cycv8c/14:0(3-OH))
PG(19:0cycv8c/19:iso)
PG(19:iso/10:0)
PG(19:iso/10:0(3-OH))
PG(19:iso/12:0)
PG(19:iso/12:0(3-OH))
PG(19:iso/14:0)
PG(19:iso/14:0(3-OH))
PG(19:iso/15:0)
PG(19:iso/15:0cyclo)
PG(19:iso/16:0)
PG(19:iso/16:1(9Z))
PG(19:iso/17:0cycw7c)
PG(19:iso/18:1(9Z))
PG(19:iso/19:0cycv8c)
PG(19:iso/19:iso)
More...
P63386
Details
mlaF
Probable phospholipid import ATP-binding protein MlaF
Enzyme
P0A935
Details
mltA
Membrane-bound lytic murein transglycosylase A
Enzyme
N-Acetyl-D-glucosamine(anhydrous)N-Acetylmuramyl-tripeptide
N-Acetyl-D-glucosamine(anhydrous)N-Acetylmuramyl-tetrapeptide
P41052
Details
mltB
Membrane-bound lytic murein transglycosylase B
Enzyme
N-Acetyl-D-glucosamine(anhydrous)N-Acetylmuramyl-tripeptide
N-Acetyl-D-glucosamine(anhydrous)N-Acetylmuramyl-tetrapeptide
P0C066
Details
mltC
Membrane-bound lytic murein transglycosylase C
Enzyme
N-Acetyl-D-glucosamine(anhydrous)N-Acetylmuramyl-tripeptide
N-Acetyl-D-glucosamine(anhydrous)N-Acetylmuramyl-tetrapeptide
P0AEZ7
Details
mltD
Membrane-bound lytic murein transglycosylase D
Enzyme
P0AGC5
Details
mltF
Membrane-bound lytic murein transglycosylase F
Enzyme
N-Acetyl-D-glucosamine(anhydrous)N-Acetylmuramyl-tripeptide
N-Acetyl-D-glucosamine(anhydrous)N-Acetylmuramyl-tetrapeptide
P52045
Details
mmcD
Methylmalonyl-CoA decarboxylase
Enzyme
(S)-Methylmalonyl-CoA
Carbon dioxide
Propionyl-CoA
Hydrogen ion
Methylmalonyl-CoA
More...
Q47690
Details
mmuM
Homocysteine S-methyltransferase
Enzyme
L-Homocysteine
S-Methylmethionine
L-Methionine
S-Adenosylmethionine
S-Adenosylhomocysteine
Hydrogen ion
Homocysteine
More...
Q47689
Details
mmuP
Probable S-methylmethionine permease
Enzyme
S-Methylmethionine
Hydrogen ion
P54746
Details
mngB
Alpha-mannosidase mngB
Enzyme
Water
2(alpha-D-Mannosyl-6-phosphate)-D-glycerate
Glyceric acid
Mannose 6-phosphate
2-O-(6-Phospho-alpha-D-mannosyl)-D-glycerate
More...
P13669
Details
mngR
Mannosyl-D-glycerate transport/metabolism system repressor MngR
Enzyme
2(alpha-D-Mannosyl)-D-glycerate
2(alpha-D-Mannosyl-6-phosphate)-D-glycerate
2-O-(6-Phospho-alpha-D-mannosyl)-D-glycerate
P25745
Details
mnmA
tRNA-specific 2-thiouridylase mnmA
Enzyme
Adenosine triphosphate
Adenosine monophosphate
Pyrophosphate
P77182
Details
mnmC
tRNA 5-methylaminomethyl-2-thiouridine biosynthesis bifunctional protein mnmC
Enzyme
S-Adenosylhomocysteine
P0A769
Details
mntH
Manganese transport protein mntH
Enzyme
Iron
Manganese
Hydrogen ion
P0A9F1
Details
mntR
Transcriptional regulator MntR
Enzyme
P30745
Details
moaA
Molybdenum cofactor biosynthesis protein A
Enzyme
Guanosine triphosphate
Water
Cyclic pyranopterin monophosphate
Pyrophosphate
More...
P0A738
Details
moaC
Molybdenum cofactor biosynthesis protein C
Enzyme
Guanosine triphosphate
Water
Cyclic pyranopterin monophosphate
Pyrophosphate
More...
P30748
Details
moaD
Molybdopterin synthase sulfur carrier subunit
Enzyme
Cyclic pyranopterin monophosphate
Copper
Molybdopterin
NADH
Adenosine monophosphate
NAD
Hydrogen ion
Water
More...
P30749
Details
moaE
Molybdopterin synthase catalytic subunit
Enzyme
Cyclic pyranopterin monophosphate
Copper
Molybdopterin
Hydrogen ion
Water
More...
P32173
Details
mobA
Molybdopterin-guanine dinucleotide biosynthesis protein A
Enzyme
Guanosine triphosphate
Pyrophosphate
Molybdopterin
Molybdopterin guanine dinucleotide
Bis-molybdopterin guanine dinucleotide
Hydrogen ion
More...
P32125
Details
mobB
Molybdopterin-guanine dinucleotide biosynthesis protein B
Enzyme
Guanosine triphosphate
Pyrophosphate
Molybdopterin
Molybdopterin guanine dinucleotide
Bis-molybdopterin guanine dinucleotide
Hydrogen ion
More...
P37329
Details
modA
Molybdate-binding periplasmic protein
Enzyme
Adenosine triphosphate
Water
Molybdate
ADP
Phosphate
Sulfate
Hydrogen ion
More...
P0AF01
Details
modB
Molybdenum transport system permease protein modB
Enzyme
Molybdenum
Adenosine triphosphate
Water
Molybdate
ADP
Phosphate
Sulfate
Hydrogen ion
More...
Displaying proteins
1026 - 1050
of
2133
in total
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