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 A4FG06

Entry ID Method Resolution Chain Position Source
AF-A4FG06-F1 Predicted AlphaFoldDB

No variants for A4FG06

Variant ID(s) Position Change Description Diseaes Association Provenance
No variants for A4FG06

No associated diseases with A4FG06

5 regional properties for A4FG06

Type Name Position InterPro Accession
domain Aminoacyl-tRNA synthetase, class II (D/K/N) 155 - 492 IPR004364
domain OB-fold nucleic acid binding domain, AA-tRNA synthetase-type 55 - 131 IPR004365
domain Aminoacyl-tRNA synthetase, class II 179 - 494 IPR006195
domain Lysyl-tRNA synthetase, class II, C-terminal 169 - 494 IPR018149
domain Lysine-tRNA ligase, class II, N-terminal 53 - 166 IPR044136

Functions

Description
EC Number
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

1 GO annotations of molecular function

Name Definition
double-stranded DNA binding Binding to double-stranded DNA.

2 GO annotations of biological process

Name Definition
DNA recombination Any process in which a new genotype is formed by reassortment of genes resulting in gene combinations different from those that were present in the parents. In eukaryotes genetic recombination can occur by chromosome assortment, intrachromosomal recombination, or nonreciprocal interchromosomal recombination. Interchromosomal recombination occurs by crossing over. In bacteria it may occur by genetic transformation, conjugation, transduction, or F-duction.
double-strand break repair via nonhomologous end joining The repair of a double-strand break in DNA in which the two broken ends are rejoined with little or no sequence complementarity. Information at the DNA ends may be lost due to the modification of broken DNA ends. This term covers instances of separate pathways, called classical (or canonical) and alternative nonhomologous end joining (C-NHEJ and A-NHEJ). These in turn may further branch into sub-pathways, but evidence is still unclear.

No homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
No homologous proteins
10 20 30 40 50 60
MINSPPIGYL PGMRTMWRGA ISFGLVNIGV RLYAATADHD YQFHQVHRQD HGRIHHKRVC
70 80 90 100 110 120
EECGREIDYD DIVKGYETSD GELVVLDSQD LRKLPIRTDR AIDLLECVPA EQVDPTYFQK
130 140 150 160 170 180
TYYLEPEKSA RRPYVLLREA LRRTDLLAVV KITMRQRETL ATIRPAGDVL VLHTMLWPDE
190 200 210 220 230 240
IRRPDFDFLT DDAGDTEVSK QEIDMATSLV ENMTEDFDPT EFTDDYQRAL AELIDAKTKG
250 260 270 280 290 300
TKPPRKRPEP ADEGEVVDLM GALERSVDQA RTSRTSRRKT TASASRRRSS SNREKTGSRD
KTRKRA