STRINGSTRING
bx10 protein (Zea mays) - STRING interaction network
"bx10" - Putative uncharacterized protein in Zea mays
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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
bx10Putative uncharacterized protein (375 aa)    
Predicted Functional Partners:
Zm.2685
Indole-3-glycerol phosphate lyase1 (274 aa)
           
  0.721
GRMZM2G046163_P01
Hypothetical protein LOC100273163 (336 aa)
           
  0.626
BX1
Indole-3-glycerol phosphate lyase, chloroplastic Precursor (EC 4.1.2.8)(Indole synthase)(Tryptophan synthase alpha chain)(EC 4.2.1.20)(Benzoxazineless 1); The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate. In bacteria, tryptophan synthase alpha (TSA) activity is almost completely dependent on formation of an active alpha2beta2 complex with tryptophan synthase beta (TSB), and indole is usually not released during tryptophan synthesis. In maize, the TSA homolog BX1 catalyzes the formation of free indole from indo [...] (351 aa)
           
  0.624
GRMZM2G310739_P01
Glucan endo-1,3-beta-glucosidase 5 (481 aa)
           
  0.546
GRMZM2G005798_P01
Putative uncharacterized protein (488 aa)
           
  0.546
BX9
Benzoxazinone synthesis9 ; Glucosyltransferase involved in the last step of benzoxazinoid glucoside biosynthesis. Catalyzes the glucosylation of hydroxamic acids utilizing UDP-glucose as glucose doner, reducing the toxicity of these natural insecticides for storage. Can use DIMBOA and DIBOA as substrates, HMBOA (2-hydroxy-7- methoxy-2H-1,4-benzoxazin-3(4H)-one) and HBOA (2-hydroxy-2H-1,4- benzoxazin-3(4H)-one) with a lower efficiency, but not indole acetic acid or quercitin (462 aa)
           
  0.529
Bx8
Benzoxazinone synthesis8 (bx8), mRNA; Glucosyltransferase involved in the last step of benzoxazinoid glucoside biosynthesis. Catalyzes the glucosylation of hydroxamic acids utilizing UDP-glucose as glucose doner, reducing the toxicity of these natural insecticides for storage. Can use DIMBOA and DIBOA as substrates, HMBOA (2-hydroxy-7- methoxy-2H-1,4-benzoxazin-3(4H)-one) and HBOA (2-hydroxy-2H-1,4- benzoxazin-3(4H)-one) with a lower efficiency, but not indole acetic acid or quercitin (481 aa)
           
  0.529
GRMZM2G423331_P01
Naringenin 7-O-methyltransferase-like (247 aa)
   
          0.507
prh2
Hypothetical protein LOC100383928 (956 aa)
         
  0.487
GRMZM2G429873_P01
Hypothetical protein LOC100192780 (344 aa)
           
  0.483
Your Current Organism:
Zea mays
NCBI taxonomy Id: 4577
Other names: Euchlaena, Z. mays, Zea, Zea L., Zea mays, Zea mays L., Zea mays var. japonica, maize
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