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trpA protein (Pedobacter sp. BAL39) - STRING interaction network
"trpA" - Tryptophan synthase alpha chain in Pedobacter sp. BAL39
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second shell of interactors
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proteins of unknown 3D structure
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some 3D structure is known or predicted
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Known Interactions
from curated databases
experimentally determined
Predicted Interactions
gene neighborhood
gene fusions
gene co-occurrence
Others
textmining
co-expression
protein homology
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[Homology]
Score
trpATryptophan synthase alpha chain ; The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (255 aa)    
Predicted Functional Partners:
trpB
Tryptophan synthase beta chain ; The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (393 aa)
  0.999
trpF
N-(5’-phosphoribosyl)anthranilate isomerase (224 aa)
 
 
  0.995
PBAL39_12342
Indole-3-glycerol phosphate synthase (132 aa)
 
  0.991
trpD
Anthranilate phosphoribosyltransferase ; Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5’-phosphoribosyl)-anthranilate (PRA) (329 aa)
 
  0.981
PBAL39_12332
Anthranilate synthase component II (190 aa)
 
 
  0.980
PBAL39_12327
Anthranilate synthase component I (468 aa)
 
 
  0.959
PBAL39_06041
P-aminobenzoate synthetase, component I (444 aa)
 
 
  0.954
ilvA
Threonine deaminase ; Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine/imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA (416 aa)
     
 
  0.876
glyA
Serine hydroxymethyltransferase ; Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism (423 aa)
     
 
  0.866
PBAL39_13647
Cystathionine beta-synthase (453 aa)
         
  0.851
Your Current Organism:
Pedobacter sp. BAL39
NCBI taxonomy Id: 391596
Other names: P. sp. BAL39, Pedobacter BAL39, Pedobacter sp. BAL39
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