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 A4Z012

Entry ID Method Resolution Chain Position Source
AF-A4Z012-F1 Predicted AlphaFoldDB

No variants for A4Z012

Variant ID(s) Position Change Description Diseaes Association Provenance
No variants for A4Z012

No associated diseases with A4Z012

5 regional properties for A4Z012

Type Name Position InterPro Accession
domain Aminoacyl-tRNA synthetase, class II (D/K/N) 162 - 501 IPR004364
domain OB-fold nucleic acid binding domain, AA-tRNA synthetase-type 68 - 146 IPR004365
domain Aminoacyl-tRNA synthetase, class II 184 - 503 IPR006195
domain Lysyl-tRNA synthetase, class II, C-terminal 177 - 503 IPR018149
domain Lysine-tRNA ligase, class II, N-terminal 67 - 174 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
MAPRAYWKGS LKLSLVTCPV VLYPASTSVE KTRFHLINRE TGNRLKQQMI DAETGDLVEG
70 80 90 100 110 120
DQKGRGYELS KGQYVEIEPE ELEAVQIESN HTIDIDSFVP REEIDQRYLN HPYYIAPDGK
130 140 150 160 170 180
AAVDAFAVIR DAMKDQDRVA LARIVLTHRE HVIAIEPMGK GMLGTTLRFP YELRDEAEFF
190 200 210 220 230 240
DDIKAPKITK DMVELAGHIL QTKAAHFKPS EFKDQYETAL KALVKRKASG KPIKLPEPEE
250 260 270 280 290
RSGNVVSLMD ALKQSLGKGD KKAAPAPSRR APAHRRPAKK AHRSAARQRK AG