P32558
Gene name |
SPT16 (CDC68, SSF1, YGL207W) |
Protein name |
FACT complex subunit SPT16 |
Names |
Cell division control protein 68, Facilitates chromatin transcription complex subunit SPT16, Suppressor of Ty protein 16 |
Species |
Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) |
KEGG Pathway |
sce:YGL207W |
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
8 structures for P32558
11 variants for P32558
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| s07-99174 | 68 | V>I | No | SGRP | |
| s07-99262 | 97 | K>R | No | SGRP | |
| s07-99286 | 105 | R>K | No | SGRP | |
| s07-99307 | 112 | L>H | No | SGRP | |
| s07-99330 | 120 | V>I | No | SGRP | |
| s07-100020 | 350 | E>K | No | SGRP | |
| s07-100114 | 381 | V>A | No | SGRP | |
| s07-100366 | 465 | V>A | No | SGRP | |
| s07-100533 | 521 | A>T | No | SGRP | |
| s07-100672 | 567 | Y>C | No | SGRP | |
| s07-101891 | 973 | E>D | No | SGRP |
No associated diseases with P32558
5 regional properties for P32558
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | Peptidase M24 | 200 - 422 | IPR000994 |
| domain | Histone chaperone RTT106/FACT complex subunit SPT16-like, middle domain | 834 - 924 | IPR013719 |
| domain | FACT complex subunit Spt16 domain | 553 - 707 | IPR013953 |
| domain | FACT complex subunit Spt16, N-terminal lobe domain | 6 - 169 | IPR029148 |
| domain | FACT complex subunit Spt16, peptidase M24-like domain | 184 - 435 | IPR033825 |
Functions
3 GO annotations of cellular component
| Name | Definition |
|---|---|
| chromatin | The ordered and organized complex of DNA, protein, and sometimes RNA, that forms the chromosome. |
| FACT complex | A histone chaperone complex that facilitates nucleosome disassembly and reassembly upon DNA or RNA polymerase passage. |
| replication fork protection complex | A protein complex conserved in eukaryotes and associated with the replication fork; the complex stabilizes stalled replication forks and is thought to be involved in coordinating leading- and lagging-strand synthesis and in replication checkpoint signaling. |
No GO annotations of molecular function
| Name | Definition |
|---|---|
| No GO annotations for molecular function |
10 GO annotations of biological process
| Name | Definition |
|---|---|
| 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. |
| DNA-templated DNA replication | A DNA replication process that uses parental DNA as a template for the DNA-dependent DNA polymerases that synthesize the new strands. |
| nucleosome assembly | The aggregation, arrangement and bonding together of a nucleosome, the beadlike structural units of eukaryotic chromatin composed of histones and DNA. |
| nucleosome organization | A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of one or more nucleosomes. |
| positive regulation of RNA polymerase II transcription preinitiation complex assembly | Any process that activates or increases the frequency, rate or extent of RNA polymerase II transcriptional preinitiation complex assembly. |
| positive regulation of transcription elongation by RNA polymerase II | Any process that activates or increases the frequency, rate or extent of transcription elongation, the extension of an RNA molecule after transcription initiation and promoter clearance by the addition of ribonucleotides, catalyzed by RNA polymerase II. |
| positive regulation of transcription initiation by RNA polymerase II | Any process that increases the rate, frequency or extent of a process involved in starting transcription from an RNA polymerase II promoter. |
| regulation of chromatin organization | Any process that modulates the frequency, rate or extent of chromatin organization. |
| regulation of sister chromatid cohesion | Any process that modulates the frequency, rate or extent of sister chromatid cohesion. |
| transcription elongation by RNA polymerase II promoter | The extension of an RNA molecule after transcription initiation and promoter clearance at an RNA polymerase II promoter by the addition of ribonucleotides catalyzed by RNA polymerase II. |
4 homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| Q9Y5B9 | SUPT16H | FACT complex subunit SPT16 | Homo sapiens (Human) | PR |
| Q8H6B1 | SPT16 | FACT complex subunit SPT16 | Zea mays (Maize) | PR |
| Q7X923 | SPT16 | FACT complex subunit SPT16 | Oryza sativa subsp japonica (Rice) | PR |
| O82491 | SPT16 | FACT complex subunit SPT16 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MEELNIDFDV | FKKRIELLYS | KYNEFEGSPN | SLLFVLGSSN | AENPYQKTTI | LHNWLLSYEF |
| 70 | 80 | 90 | 100 | 110 | 120 |
| PATLIALVPG | KVIIITSSAK | AKHLQKAIDL | FKDPESKITL | ELWQRNNKEP | ELNKKLFDDV |
| 130 | 140 | 150 | 160 | 170 | 180 |
| IALINSAGKT | VGIPEKDSYQ | GKFMTEWNPV | WEAAVKENEF | NVIDISLGLS | KVWEVKDVNE |
| 190 | 200 | 210 | 220 | 230 | 240 |
| QAFLSVSSKG | SDKFMDLLSN | EMVRAVDEEL | KITNAKLSDK | IENKIDDVKF | LKQLSPDLSA |
| 250 | 260 | 270 | 280 | 290 | 300 |
| LCPPNYKFNF | DLLDWTYSPI | IQSGKKFDLR | VSARSTNDQL | YGNGCILASC | GIRYNNYCSN |
| 310 | 320 | 330 | 340 | 350 | 360 |
| ITRTFLIDPS | EEMANNYDFL | LTLQKEIVTN | ILKPGRTPKE | VYESVIEYIE | KTKPELVPNF |
| 370 | 380 | 390 | 400 | 410 | 420 |
| TKNIGSLIGL | EFRDSNFILN | VKNDYRKIQR | GDCFNISFGF | NNLKDSQSAN | NYALQLADTV |
| 430 | 440 | 450 | 460 | 470 | 480 |
| QIPLDETEPP | RFLTNYTKAK | SQISFYFNNE | EEDNNKKKSS | PATKVPSKPD | RNSKILRTKL |
| 490 | 500 | 510 | 520 | 530 | 540 |
| RGEARGGAED | AQKEQIRKEN | QKKLHEKLEK | NGLLRFSAAD | ANGPDSEPRQ | YFKKYESYVR |
| 550 | 560 | 570 | 580 | 590 | 600 |
| DSQLPTNIRD | LRIHVDWKSQ | TIILPIYGRP | VPFHINSYKN | GSKNEEGEYT | YLRLNFNSPG |
| 610 | 620 | 630 | 640 | 650 | 660 |
| SSGGISKKVE | ELPYEESADN | QFVRSITLRS | KDGDRMSETF | KQIADLKKEA | TKREQERKAL |
| 670 | 680 | 690 | 700 | 710 | 720 |
| ADVVQQDKLI | ENKTGRTKRL | DQIFVRPNPD | TKRVPSTVFI | HENGIRFQSP | LRTDSRIDIL |
| 730 | 740 | 750 | 760 | 770 | 780 |
| FSNIKNLIFQ | SCKGELIVVI | HIHLKNPILM | GKKKIQDVQF | YREASDMSVD | ETGGGRRGQS |
| 790 | 800 | 810 | 820 | 830 | 840 |
| RFRRYGDEDE | LEQEQEERRK | RAALDKEFKY | FADAIAEASN | GLLTVENTFR | DLGFQGVPNR |
| 850 | 860 | 870 | 880 | 890 | 900 |
| SAVFCMPTTD | CLVQLIEPPF | LVINLEEVEI | CILERVQFGL | KNFDMVFVYK | DFNKPVTHIN |
| 910 | 920 | 930 | 940 | 950 | 960 |
| TVPIESLDFL | KQWLTDMDIP | YTVSTINLNW | ATIMKSLQDD | PYQFFLDGGW | NFLATGSDDE |
| 970 | 980 | 990 | 1000 | 1010 | 1020 |
| ASDESEEEVS | EYEASEDDVS | DESAFSEDEE | GSEVDDDISG | DESEDYTGDE | SEEGEDWDEL |
| 1030 | |||||
| EKKAARADRG | ANFRD |