P50531
Gene name |
rad17 (SPAC14C4.13) |
Protein name |
Checkpoint protein rad17 |
Names |
|
Species |
Schizosaccharomyces pombe (strain 972 / ATCC 24843) (Fission yeast) |
KEGG Pathway |
spo:SPAC14C4.13 |
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 P50531
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-P50531-F1 | Predicted | AlphaFoldDB |
18 variants for P50531
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| I_5253411_G_T | 18 | K>N | No | Jeffares_SNPs | |
| I_5253553_G_C | 66 | E>Q | No | Jeffares_SNPs | |
| I_5253565_C_A | 70 | Q>K | No | Jeffares_SNPs | |
| I_5253677_G_A | 93 | A>T | No | Jeffares_SNPs | |
| I_5253906_C_T | 150 | S>L | No | Jeffares_SNPs | |
| I_5253980_A_G | 175 | M>V | No | Jeffares_SNPs | |
| I_5254015_T_A | 186 | N>K | No | Jeffares_SNPs | |
| I_5254079_T_A | 208 | S>T | No | Jeffares_SNPs | |
| I_5254457_A_G | 334 | T>A | No | Jeffares_SNPs | |
| I_5254733_G_A | 426 | G>S | No | Jeffares_SNPs | |
| I_5254776_A_C | 440 | Q>P | No | Jeffares_SNPs | |
| I_5254782_A_C | 442 | N>T | No | Jeffares_SNPs | |
| I_5254854_A_G | 466 | K>R | No | Jeffares_SNPs | |
| I_5254905_G_A | 483 | S>N | No | Jeffares_SNPs | |
| I_5255060_T_G | 535 | F>V | No | Jeffares_SNPs | |
| I_5255163_T_G | 569 | I>S | No | Jeffares_SNPs | |
| I_5255223_C_T | 589 | A>V | No | Jeffares_SNPs | |
| I_5255225_C_T | 590 | H>Y | No | Jeffares_SNPs |
No associated diseases with P50531
1 regional properties for P50531
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | AAA+ ATPase domain | 104 - 241 | IPR003593 |
4 GO annotations of cellular component
| Name | Definition |
|---|---|
| chromatin | The ordered and organized complex of DNA, protein, and sometimes RNA, that forms the chromosome. |
| 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. |
| nucleus | A membrane-bounded organelle of eukaryotic cells in which chromosomes are housed and replicated. In most cells, the nucleus contains all of the cell's chromosomes except the organellar chromosomes, and is the site of RNA synthesis and processing. In some species, or in specialized cell types, RNA metabolism or DNA replication may be absent. |
| Rad17 RFC-like complex | A pentameric protein complex related to replication factor C, which loads a trimeric complex of checkpoint proteins (known as the checkpoint clamp or 9-1-1 complex) onto DNA at damage sites; functions in DNA damage cell cycle checkpoints. In Schizosaccharomyces pombe the subunits are known as Rad17, Rfc2, Rfc3, Rfc4, and Rfc5, while in Saccharomyces cerevisiae the subunits are known as Rad24p, Rfc2p, Rfc3p, Rfc4p, and Rfc5p. |
3 GO annotations of molecular function
| Name | Definition |
|---|---|
| ATP binding | Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator. |
| chromatin binding | Binding to chromatin, the network of fibers of DNA, protein, and sometimes RNA, that make up the chromosomes of the eukaryotic nucleus during interphase. |
| DNA clamp loader activity | Facilitating the opening of the ring structure of the PCNA complex, or any of the related sliding clamp complexes, and their closing around the DNA duplex, driven by ATP hydrolysis. |
6 GO annotations of biological process
| Name | Definition |
|---|---|
| DNA damage checkpoint signaling | A signal transduction process that contributes to a DNA damage checkpoint. |
| DNA repair | The process of restoring DNA after damage. Genomes are subject to damage by chemical and physical agents in the environment (e.g. UV and ionizing radiations, chemical mutagens, fungal and bacterial toxins, etc.) and by free radicals or alkylating agents endogenously generated in metabolism. DNA is also damaged because of errors during its replication. A variety of different DNA repair pathways have been reported that include direct reversal, base excision repair, nucleotide excision repair, photoreactivation, bypass, double-strand break repair pathway, and mismatch repair pathway. |
| mitotic DNA replication checkpoint signaling | A signal transduction process that contributes to a mitotic DNA replication checkpoint. |
| mitotic G2 DNA damage checkpoint signaling | A mitotic cell cycle checkpoint that detects and negatively regulates progression through the G2/M transition of the cell cycle in response to DNA damage. |
| mitotic intra-S DNA damage checkpoint signaling | A mitotic cell cycle checkpoint that slows DNA synthesis in response to DNA damage by the prevention of new origin firing and the stabilization of slow replication fork progression. |
| 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 |
| MRRQLSFHES | TKRSLKKKKI | RKIEKPSLVS | KTSRDKNASI | TDIHEEDIEA | FSDEENKIVH |
| 70 | 80 | 90 | 100 | 110 | 120 |
| LNNLKEDRFQ | LWFEKYIPQK | AADLAVHKSK | ISAIKQWMLT | DSLESRLLLI | CGPSGCGKST |
| 130 | 140 | 150 | 160 | 170 | 180 |
| AVQVLAKELG | YSLIEWLNPM | NLKEPSNQES | DTLSLTEKFS | RFMSLCETYP | ELELMDSNNI |
| 190 | 200 | 210 | 220 | 230 | 240 |
| QKRGKNAQGK | KKFIFLDEIP | HLSKFNGSLD | AFRNVIRTAL | TSRGAFSIIM | VLTEIQLNNL |
| 250 | 260 | 270 | 280 | 290 | 300 |
| EGINSQDRNS | FNSVQIMGND | LLQDPRVTVL | QFNPIAPTYM | KKCLGSILRK | EGVPKSPKLL |
| 310 | 320 | 330 | 340 | 350 | 360 |
| SLVENICSAS | EGDLRSAINS | LQLSISQSFE | KKGTKNIREV | KEGKGKGNDF | SLEAAQVLER |
| 370 | 380 | 390 | 400 | 410 | 420 |
| LSKSDSEAYA | RFKNYKSAYI | PKSDKNENSF | FKKDVGLGMM | HAIGKVVWNK | REGDDEVLKA |
| 430 | 440 | 450 | 460 | 470 | 480 |
| SSQQTGNSER | IKGVKVSKSQ | ENKNCISLKS | DQRERMLNVD | QCFTSKRRSL | VDIESTINQS |
| 490 | 500 | 510 | 520 | 530 | 540 |
| GLSGSVFRYG | LFENYVDSCV | TTDEAFNVCD | LLSISDCLSH | DFPYSYTGDE | ISTWFSVQGT |
| 550 | 560 | 570 | 580 | 590 | 600 |
| LFYLPSPVPR | KWRQLRFQQW | NNEGIVRGIF | DDYMVIYGKR | SVSDPVIEAH | EDQVLEDIDD |
| PIEDED |