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Saro_1957 protein (Novosphingobium aromaticivorans) - STRING interaction network
"Saro_1957" - Inositol-1(or 4)-monophosphatase in Novosphingobium aromaticivorans
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query proteins and first shell of interactors
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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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Neighborhood
Gene Fusion
Cooccurence
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Experiments
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Textmining
[Homology]
Score
Saro_1957Inositol-1(or 4)-monophosphatase (274 aa)    
Predicted Functional Partners:
Saro_0101
Myo-inositol-1-phosphate synthase (366 aa)
   
 
  0.972
Saro_3171
Inositol monophosphatase (258 aa)
   
   
    0.954
efp
Elongation factor P; Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase (187 aa)
   
        0.910
Saro_0102
Nucleotidyl transferase (249 aa)
       
    0.901
Saro_1552
Twin-arginine translocation pathway signal protein (702 aa)
     
 
    0.900
thiE
Thiamine-phosphate pyrophosphorylase; Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) (213 aa)
   
 
    0.731
hisH
Imidazole glycerol phosphate synthase subunit HisH; IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR (209 aa)
   
 
  0.682
Saro_1964
Fructose-1,6-bisphosphate aldolase (301 aa)
   
    0.646
Saro_1959
Hypothetical protein (129 aa)
              0.632
hisD
Histidinol dehydrogenase; Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (429 aa)
   
 
  0.625
Your Current Organism:
Novosphingobium aromaticivorans
NCBI taxonomy Id: 279238
Other names: N. aromaticivorans, N. aromaticivorans DSM 12444, Novosphingobium aromaticivorans, Novosphingobium aromaticivorans DSM 12444, Novosphingobium aromaticivorans str. DSM 12444, Novosphingobium aromaticivorans strain DSM 12444, Novosphingobium aromaticivorum, Sphingomonas aromaticivorans
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