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 Q7SA95

Entry ID Method Resolution Chain Position Source
AF-Q7SA95-F1 Predicted AlphaFoldDB

No variants for Q7SA95

Variant ID(s) Position Change Description Diseaes Association Provenance
No variants for Q7SA95

No associated diseases with Q7SA95

3 regional properties for Q7SA95

Type Name Position InterPro Accession
domain DNA mismatch repair protein, S5 domain 2-like 209 - 327 IPR013507
conserved_site DNA mismatch repair, conserved site 94 - 100 IPR014762
domain MutL, C-terminal, dimerisation 450 - 593 IPR014790

Functions

Description
EC Number 3.6.4.12 Acting on ATP; involved in cellular and subcellular movement
Subcellular Localization
  • Nucleus
  • Chromosome, telomere
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

5 GO annotations of cellular component

Name Definition
chromosome, subtelomeric region A region of the chromosome, adjacent to the telomere (on the centromeric side) that contains repetitive DNA and sometimes genes. This region is usually heterochromatin.
chromosome, telomeric repeat region A complex of DNA and protein that seals the end of a chromosome. The telomeric repeat DNA consists of simple tandemly repeated sequences specific for each species. Typically one strand is G-rich and the other C-rich. The G-rich strand forms a 3'-terminal overhang, the length of which varies with species. The single strand overhang is bound by a variety of proteins, including telomere capping proteins that bind to the single-stranded DNA and seal the telomeric loop.
Ku70:Ku80 complex Heterodimeric protein complex composed of a 70 kDa and a 80 kDa subunit, binds DNA through a channel formed by the heterodimer. Functions in DNA double stranded break repair, chromosome maintenance, transcription regulation, V(D)J recombination, and activation of DNA-PK.
pericentric heterochromatin Heterochromatin that is located adjacent to the CENP-A rich centromere 'central core' and characterized by methylated H3 histone at lysine 9 (H3K9me2/H3K9me3).
site of double-strand break A region of a chromosome at which a DNA double-strand break has occurred. DNA damage signaling and repair proteins accumulate at the lesion to respond to the damage and repair the DNA to form a continuous DNA helix.

6 GO annotations of molecular function

Name Definition
ATP binding Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator.
ATP hydrolysis activity Catalysis of the reaction: ATP + H2O = ADP + H+ phosphate. ATP hydrolysis is used in some reactions as an energy source, for example to catalyze a reaction or drive transport against a concentration gradient.
damaged DNA binding Binding to damaged DNA.
DNA helicase activity Unwinding of a DNA helix, driven by ATP hydrolysis.
RNA binding Binding to an RNA molecule or a portion thereof.
telomeric DNA binding Binding to a telomere, a specific structure at the end of a linear chromosome required for the integrity and maintenance of the end.

7 GO annotations of biological process

Name Definition
cellular response to gamma radiation Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a gamma radiation stimulus. Gamma radiation is a form of electromagnetic radiation (EMR) or light emission of a specific frequency produced from sub-atomic particle interaction, such as electron-positron annihilation and radioactive decay. Gamma rays are generally characterized as EMR having the highest frequency and energy, and also the shortest wavelength, within the electromagnetic radiation spectrum.
cellular response to X-ray Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of X-ray radiation. An X-ray is a form of electromagnetic radiation with a wavelength in the range of 10 nanometers to 100 picometers (corresponding to frequencies in the range 30 PHz to 3 EHz).
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.
negative regulation of telomere maintenance via recombination Any process that stops, prevents, or reduces the frequency, rate or extent of a recombinational process involved in the maintenance of proper telomeric length.
stalled replication fork localization to nuclear periphery A cellular localization process where a DNA replication fork that has stalled is signaled to relocate and anchor to the nuclear periphery for the time necessary to complete recombination-dependent replication.
telomere maintenance Any process that contributes to the maintenance of proper telomeric length and structure by affecting and monitoring the activity of telomeric proteins, the length of telomeric DNA and the replication and repair of the DNA. These processes includes those that shorten, lengthen, replicate and repair the telomeric DNA sequences.

No homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
No homologous proteins
10 20 30 40 50 60
MSWRKDQDER LDGDEGDEEL DENDYKTQKD AVLFAIDVSK SMLKPPQNTG DKKADKDSAL
70 80 90 100 110 120
TAALTCAYQI MQQRIISQPK DMMGVLLFGT EKSKFRDDSG NGTGYPHCYL LSDLDIPGAE
130 140 150 160 170 180
DVKKLKALIE DGDDEDEIMV PSKEPVIMSN MLFCANQVFT TNAANFGSRR LFIVTDNDDP
190 200 210 220 230 240
HAGDKQAKSS AAVRAKDLYD LGVVIELFPI SREDKKFDLS KFYDDIIYRN PAAEAGQSES
250 260 270 280 290 300
PKTSKSGDGL TLLNSLISNI NSKQTPKRSY FSNLPFELAP GLTISIKGYM PLNRQTPTRS
310 320 330 340 350 360
CYVYEGEEQA QVVQSETAQV DFAARTVEKS ELRKGYKFGG EHICFKPEEL AELKQMGKKT
370 380 390 400 410 420
LRIIGFKKRS KIPSWASVKK SIFIFPSEEQ YVGSTRVFSA LWQKLLKDDK VGIAWFVARE
430 440 450 460 470 480
NAHPVMVAIF PSGNPDDEEA NTPYLPAGLW LYPLPFADDV RSVDHVTAPP RPADELTDQM
490 500 510 520 530 540
RQVIQNLQLP KAMYDPRKYP NPSLQWHYKI LQAKALDEET PDAMDDVTLP KYRQIDKRVG
550 560 570 580 590 600
GYLAEWKEML AKKANDLQNT RAFKREFEED DERPAKRAKP SKKAASGGGG PANSNADLKK
610 620 630 640
AFEQGTLGKM TVAELKDIMA SKGISTAGRK AELVERLEQW VEENL