STRINGSTRING
bx7 protein (Zea mays) - STRING interaction network
"bx7" - O-methyltransferase BX7 in Zea mays
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second shell of interactors
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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
bx7O-methyltransferase BX7 (Bx7), mRNA (288 aa)    
Predicted Functional Partners:
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)
           
  0.721
CYP71C4
Cytochrome P450 71C4 (EC 1.14.-.-)(Protein benzoxazineless 2); Catalyzes the conversion of indole to indolin-2-one (542 aa)
           
  0.721
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)
           
  0.721
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)
           
  0.721
CYP71C3
Cytochrome P450 71C3 (EC 1.14.-.-)(Protein benzoxazineless 5); Catalyzes the conversion of 2-hydroxy-1,4-benzoxazin-3- one (HBOA) to 2,4-dihydroxy-1,4-benzoxazin-3-one (DIBOA) (534 aa)
           
  0.721
CYP71C1
Cytochrome P450 71C1 (EC 1.14.-.-)(Protein benzoxazineless 4); Catalyzes the conversion of 3-hydroxyindolin-2-one to 2- hydroxy-1,4-benzoxazin-3-one (HBOA) (530 aa)
           
  0.720
CYP71C2
Cytochrome P450 71C2 (EC 1.14.-.-)(Protein benzoxazineless 3); Catalyzes the conversion of indolin-2-one to 3- hydroxyindolin-2-one (536 aa)
           
  0.567
tsa1
Tryptophan synthase alpha (319 aa)
           
  0.566
Zm.84405
Hydroquinone glucosyltransferase (491 aa)
           
  0.524
Zm.122470
Uncharacterized protein (85 aa)
           
  0.524
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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