Descriptions

The autoinhibited protein was predicted that may have potential autoinhibitory elements via cis-regPred.

Autoinhibitory domains (AIDs)

Target domain

Relief mechanism

Assay

cis-regPred

Accessory elements

No accessory elements

Autoinhibited structure

Activated structure

1 structures for Q8Y5G2

Entry ID Method Resolution Chain Position Source
AF-Q8Y5G2-F1 Predicted AlphaFoldDB

No variants for Q8Y5G2

Variant ID(s) Position Change Description Diseaes Association Provenance
No variants for Q8Y5G2

No associated diseases with Q8Y5G2

1 regional properties for Q8Y5G2

Type Name Position InterPro Accession
domain PdxS/SNZ N-terminal domain 8 - 213 IPR033755

Functions

Description
EC Number 4.3.3.6 Amine-lyases
Subcellular Localization
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

No GO annotations of cellular component

Name Definition
No GO annotations for cellular component

2 GO annotations of molecular function

Name Definition
amine-lyase activity Catalysis of the release of amines by the cleavage of a carbon-nitrogen bond or the reverse reaction with an amine as a substrate.
pyridoxal 5'-phosphate synthase (glutamine hydrolysing) activity Catalysis of the reaction: D-ribose 5-phosphate + D-glyceraldehyde 3-phosphate + L-glutamine = pyridoxal 5'-phosphate + L-glutamate + 3 H2O + phosphate. The reaction occurs in two steps: L-glutamine + H2O = L-glutamate + NH3, and subsequently D-ribose 5-phosphate + D-glyceraldehyde 3-phosphate + NH3 = pyridoxal 5'-phosphate + 4 H2O + phosphate.

3 GO annotations of biological process

Name Definition
cellular amino acid metabolic process The chemical reactions and pathways involving amino acids, carboxylic acids containing one or more amino groups, as carried out by individual cells.
pyridoxal phosphate biosynthetic process The chemical reactions and pathways resulting in the formation of pyridoxal phosphate, pyridoxal phosphorylated at the hydroxymethyl group of C-5, the active form of vitamin B6.
pyridoxine biosynthetic process The chemical reactions and pathways resulting in the formation of pyridoxine, 2-methyl-3-hydroxy-4,5-bis(hydroxymethyl)pyridine, one of the vitamin B6 compounds.

No homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
No homologous proteins
10 20 30 40 50 60
MEKKVGTDRV KRGMAQMQKG GVIMDVVNAE QAKIAEEAGA VAVMALERVP SDIRAAGGVA
70 80 90 100 110 120
RMADPRIVEE VMKAVSIPVM AKARIGHITE ARVLEAMGVD YIDESEVLTP ADDEFHLLKS
130 140 150 160 170 180
DFTVPFVCGC RDIGEALRRI GEGAAMLRTK GEPGTGNIVE AVRHMRQVNG QIRQIAGMTD
190 200 210 220 230 240
DELMVAAKNF GAPYELIKEI KTLGKLPVVN FAAGGVATPA DAALMMELGA DGVFVGSGIF
250 260 270 280 290
KSDNPAKFAS AIVQATTYYT DYELIGKLSK ELGSPMKGIE MSRLNPEDRM QDRSF