SuCComBase

Sulfur Containing Compound Database

SCC Gene Description

Gene name CYP82G1
AGI ID AT3G25180
Gene length 515
Uniprot ID Q9LSF8
Protein Name Cytochrome P450 82G1
Synonym MJL12.5
EC number EC 1.14.-.-
Entrez Gene 822110
Refseq mrna NM_113423
Refseq protein NP_189154
Function Camalexin originates from tryptophan and its biosynthesis involves the cytochrome P450 enzymes CYP79B2 and CYP71B15 (PAD3). Camalexin induction is a complex process, for which triggering by reactive oxygen species (ROS), salicylic acid signalling, and the glutathione status are important. Targets of the signalling cascade are the tryptophan and camalexin biosynthetic genes, which are strongly transcriptionally upregulated at the sites of pathogen infection (Glawischnig et al. 2004) .
Group Camalexin biosynthesis
Reference Glawischnig et al. (2004)
Organism AGI ID Gene Name Protein Name Identity E-Value Description

Papaya

AT3G25180

CYP82G1

Cytochrome P450 82G1

54.049

9.66E-166

Broccoli

AT3G25180

CYP82G1

Cytochrome P450 82G1

83.036

0

Broccoli

AT3G25180

CYP82G1

Cytochrome P450 82G1

42.612

4.23E-119

Broccoli

AT3G25180

CYP82G1

Cytochrome P450 82G1

44.727

1.34E-57

Cabbage

AT3G25180

CYP82G1

Cytochrome P450 82G1

83.133

0

Cabbage

AT3G25180

CYP82G1

Cytochrome P450 82G1

43.75

2.36E-116

Cabbage

AT3G25180

CYP82G1

Cytochrome P450 82G1

43.437

2.87E-104

Cabbage

AT3G25180

CYP82G1

Cytochrome P450 82G1

40.135

9.27E-91

Cabbage

AT3G25180

CYP82G1

Cytochrome P450 82G1

41.471

3.56E-59

GO ID Ontology GO Term Description

GO:0005506

MF

iron ion binding

Interacting selectively and non-covalently with iron (Fe) ions.

GO:0006952

BP

defense response

Reactions, triggered in response to the presence of a foreign body or the occurrence of an injury, which result in restriction of damage to the organism attacked or prevention/recovery from the infection caused by the attack.

GO:0009507

CC

chloroplast

A chlorophyll-containing plastid with thylakoids organized into grana and frets, or stroma thylakoids, and embedded in a stroma.

GO:0016020

CC

membrane

A lipid bilayer along with all the proteins and protein complexes embedded in it an attached to it.

GO:0016021

CC

integral component of membrane

The component of a membrane consisting of the gene products and protein complexes having at least some part of their peptide sequence embedded in the hydrophobic region of the membrane.

GO:0016114

BP

terpenoid biosynthetic process

The chemical reactions and pathways resulting in the formation of terpenoids, any member of a class of compounds characterized by an isoprenoid chemical structure.

GO:0019825

MF

oxygen binding

Interacting selectively and non-covalently with oxygen (O2).

GO:0020037

MF

heme binding

Interacting selectively and non-covalently with heme, any compound of iron complexed in a porphyrin (tetrapyrrole) ring.

GO:0044550

BP

secondary metabolite biosynthetic process

The chemical reactions and pathways resulting in the formation of secondary metabolites, the compounds that are not necessarily required for growth and maintenance of cells, and are often unique to a taxon.

GO:0046246

BP

terpene biosynthetic process

The chemical reactions and pathways resulting in the formation of terpenes, any of a large group of hydrocarbons made up of isoprene units.

GO:0055114

BP

oxidation-reduction process

A metabolic process that results in the removal or addition of one or more electrons to or from a substance, with or without the concomitant removal or addition of a proton or protons.

GO:0097007

MF

4,8,12-trimethyltrideca-1,3,7,11-tetraene synthase activity

Catalysis of the reaction: (EE)-geranyllinalool + NADPH + O2 = 4,8,12-trimethyl-1,3,7,11-tridecatetraene + NADP+ + 2 H2O. It is unknown whether this reaction proceeds by the direct release of the 4-carbon compound but-1-en-3-one, or whether the substrate

GO:0097008

MF

(3E)-4,8-dimethyl-1,3,7-nonatriene synthase activity

Catalysis of the reaction: (E)-nerolidol + NADPH + O2 = (3E)-4,8-dimethylnona-1,3,7-triene + NADP+ + 2 H2O. It is unknown whether this reaction proceeds by the direct release of the 4-carbon compound but-1-en-3-one, or whether the substrate is first degra

No references found.