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anmK protein (Methylobacter tundripaludum) - STRING interaction network
"anmK" - Anhydro-N-acetylmuramic acid kinase in Methylobacter tundripaludum
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second shell of interactors
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Known Interactions
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experimentally determined
Predicted Interactions
gene neighborhood
gene fusions
gene co-occurrence
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textmining
co-expression
protein homology
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anmKAnhydro-N-acetylmuramic acid kinase; Catalyzes the specific phosphorylation of 1,6-anhydro-N- acetylmuramic acid (anhMurNAc) with the simultaneous cleavage of the 1,6-anhydro ring, generating MurNAc-6-P. Is required for the utilization of anhMurNAc either imported from the medium or derived from its own cell wall murein, and thus plays a role in cell wall recycling; Belongs to the anhydro-N-acetylmuramic acid kinase family (385 aa)    
Predicted Functional Partners:
nagZ
Beta-hexosaminidase; Plays a role in peptidoglycan recycling by cleaving the terminal beta-1,4-linked N-acetylglucosamine (GlcNAc) from peptide-linked peptidoglycan fragments, giving rise to free GlcNAc, anhydro-N-acetylmuramic acid and anhydro-N-acetylmuramic acid-linked peptides; Belongs to the glycosyl hydrolase 3 family. NagZ subfamily (336 aa)
 
 
  0.993
Mettu_3558
PFAM- Peptidase M23; KEGG- nhl-Nhal_1103 peptidase M23 (490 aa)
 
          0.897
Mettu_1551
N-acetylmuramyl-L-alanine amidase, negative regulator of AmpC, AmpD; KEGG- efe-EFER_0130 N-acetyl-anhydromuranmyl-L-alanine amidase; PFAM- N-acetylmuramoyl-L-alanine amidase, family 2; SMART- N-acetylmuramoyl-L-alanine amidase, family 2 (180 aa)
 
 
  0.791
tyrS
Tyrosine--tRNA ligase; Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction- tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr); Belongs to the class-I aminoacyl-tRNA synthetase family. TyrS type 2 subfamily (398 aa)
              0.676
murB
UDP-N-acetylenolpyruvoylglucosamine reductase; Cell wall formation (304 aa)
     
   
  0.623
glmU
Bifunctional protein GlmU; Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain (488 aa)
         
  0.621
murA
UDP-N-acetylglucosamine 1-carboxyvinyltransferase; Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine; Belongs to the EPSP synthase family. MurA subfamily (421 aa)
         
  0.621
glmM
Phosphoglucosamine mutase; Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate; Belongs to the phosphohexose mutase family (446 aa)
           
  0.618
Mettu_4338
Beta-glucosidase; KEGG- cps-CPS_2365 xylosidase/arabinosidase; PFAM- Glycoside hydrolase, family 3, N-terminal; Glycoside hydrolase, family 3, C-terminal; Belongs to the glycosyl hydrolase 3 family (733 aa)
 
 
  0.592
rpsI
PFAM- Ribosomal protein S9; KEGG- mca-MCA0905 ribosomal protein S9; Belongs to the universal ribosomal protein uS9 family (131 aa)
           
  0.455
Your Current Organism:
Methylobacter tundripaludum
NCBI taxonomy Id: 697282
Other names: M. tundripaludum SV96, Methylobacter sp. SV96, Methylobacter tundripaludum, Methylobacter tundripaludum DSM 17260, Methylobacter tundripaludum SV96, Methylobacter tundripaludum str. SV96, Methylobacter tundripaludum strain SV96
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