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 A9WFT9

Entry ID Method Resolution Chain Position Source
AF-A9WFT9-F1 Predicted AlphaFoldDB

No variants for A9WFT9

Variant ID(s) Position Change Description Diseaes Association Provenance
No variants for A9WFT9

No associated diseases with A9WFT9

1 regional properties for A9WFT9

Type Name Position InterPro Accession
domain PdxS/SNZ N-terminal domain 9 - 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
MEKSTWTTKV GLAQMLKGGV IMDVVTPEQA RIAEEAGAVA VMALERVPAD IRAQGGVARM
70 80 90 100 110 120
SDPELILAIK QAVTIPVMAK ARIGHFVEAQ VLEAIGVDYI DESEVLTPAD EEHHINKHKF
130 140 150 160 170 180
RVPFVCGCRN LGEALRRVAE GAAMLRTKGE AGTGNVVEAV RHARAVYSEI RRLQSMNEDE
190 200 210 220 230 240
LFTYAKQIQA PYELVKQVAT EGKLPVVNFA AGGIATPADA ALLMQLGVDG IFVGSGIFKS
250 260 270 280 290
GDPVKRARAI VEATTHYNDP EIIAEVSKGL GEAMVGINID QIPADQLMAR RGW