P73625
Gene name |
mutS2 |
Protein name |
Endonuclease MutS2 |
Names |
|
Species |
Synechocystis sp (strain PCC 6803 / Kazusa) |
KEGG Pathway |
syn:sll1772 |
EC number |
|
Protein Class |
|
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 P73625
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-P73625-F1 | Predicted | AlphaFoldDB |
No variants for P73625
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| No variants for P73625 | |||||
No associated diseases with P73625
4 regional properties for P73625
No GO annotations of cellular component
| Name | Definition |
|---|---|
| No GO annotations for cellular component |
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. |
| ATP-dependent DNA damage sensor activity | A molecule that recognises toxic DNA structures, and initiates a signalling response, driven by ATP hydrolysis. |
| double-stranded DNA binding | Binding to double-stranded DNA. |
| endonuclease activity | Catalysis of the hydrolysis of ester linkages within nucleic acids by creating internal breaks. |
| mismatched DNA binding | Binding to a double-stranded DNA region containing one or more mismatches. |
2 GO annotations of biological process
| Name | Definition |
|---|---|
| mismatch repair | A system for the correction of errors in which an incorrect base, which cannot form hydrogen bonds with the corresponding base in the parent strand, is incorporated into the daughter strand. The mismatch repair system promotes genomic fidelity by repairing base-base mismatches, insertion-deletion loops and heterologies generated during DNA replication and recombination. |
| negative regulation of DNA recombination | Any process that stops, prevents, or reduces the frequency, rate or extent of DNA recombination. |
No homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| No homologous proteins | ||||
| 10 | 20 | 30 | 40 | 50 | 60 |
| MSDSTNLTIA | EETLALLEWP | RLCQHLSTFT | QTPLGAIAAR | YLLPPSQWEE | SRELLAQTQA |
| 70 | 80 | 90 | 100 | 110 | 120 |
| VESIENSPES | NWHFKGIADI | TEPLARVERG | GLVTGLELLA | IAGTLAGVRR | LRRVIEERDD |
| 130 | 140 | 150 | 160 | 170 | 180 |
| LEILQTLVAE | VRTLPELEQA | IHHCLGEDGK | VAERASPKLG | EIRQKLKAVR | EQIQQKLQKI |
| 190 | 200 | 210 | 220 | 230 | 240 |
| IQRQSNALQE | AVITQRGDRF | VLPIKAGYKE | QMPGIVHDSS | ASGNTLYVEP | QAIVELGNKL |
| 250 | 260 | 270 | 280 | 290 | 300 |
| RQARRQEQTE | EERILRQLSD | QVLEVLLDLE | HLLAIATRLD | LATARVRYSF | WLGAHPPQWL |
| 310 | 320 | 330 | 340 | 350 | 360 |
| TPGDEKPITL | RQLRHPLLHW | QAEKEGGPAV | VPITLTIDSQ | IRVIAITGPN | TGGKTVTLKT |
| 370 | 380 | 390 | 400 | 410 | 420 |
| LGLVALMAKV | GLYIPAKETV | EMPWFAQILA | DIGDEQSLQQ | NLSTFSGHIC | RIIRILQALP |
| 430 | 440 | 450 | 460 | 470 | 480 |
| SGVQDVLDPE | IDSPNHPIFP | SLVLLDEVGA | GTDPTEGSAL | AIALLRHLAD | QPCLTVATTH |
| 490 | 500 | 510 | 520 | 530 | 540 |
| YGELKALKYQ | DARFENASVE | FDDQSLSPTY | RLLWGIPGRS | NALAIAQRLG | LPLAIVEQAK |
| 550 | 560 | 570 | 580 | 590 | 600 |
| DKLGGFSEDI | NQVIAGLESQ | RREQEQKAAN | AQKLLQETEI | FYQQVSQKAA | SLQARERELK |
| 610 | 620 | 630 | 640 | 650 | 660 |
| SYQDQEVQQA | IAAAKEEIAK | VIRQLQRGKP | SAQKAQQATE | ILGQIQAEQK | AKVAPKPIGY |
| 670 | 680 | 690 | 700 | 710 | 720 |
| QPTVGERIRI | PSFGQTAEVT | QVNATAQTVN | VTLGLMKMTV | PMADIESLNG | KKVEPPPKSE |
| 730 | 740 | 750 | 760 | 770 | 780 |
| PVPKKVKAEP | PATEAKSPPV | LVRTEKNTLD | CRGDRLERAE | SRLEKALNQA | LDAGVLWIIH |
| 790 | 800 | 810 | 820 | ||
| GKGTGKLRQG | VQEYLSHHPL | VKSYALAPQN | DGGAGVTIAY | LR |