P46551
Gene name |
cdk-12 |
Protein name |
Cyclin-dependent kinase 12 |
Names |
Cell division cycle 2-related protein kinase 7, Cell division protein kinase 12 |
Species |
Caenorhabditis elegans |
KEGG Pathway |
|
EC number |
2.7.11.22: Protein-serine/threonine kinases |
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
461-484 (Activation loop from InterPro)
Target domain |
311-605 (Protein kinase domain) |
Relief mechanism |
|
Assay |
|
Autoinhibited structure

Activated structure

1 structures for P46551
Entry ID | Method | Resolution | Chain | Position | Source |
---|---|---|---|---|---|
AF-P46551-F1 | Predicted | AlphaFoldDB |
No variants for P46551
Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
---|---|---|---|---|---|
No variants for P46551 |
No associated diseases with P46551
Functions
Description | ||
---|---|---|
EC Number | 2.7.11.22 | Protein-serine/threonine kinases |
Subcellular Localization |
|
|
PANTHER Family | ||
PANTHER Subfamily | ||
PANTHER Protein Class | ||
PANTHER Pathway Category | No pathway information available |
4 GO annotations of cellular component
Name | Definition |
---|---|
cyclin-dependent protein kinase holoenzyme complex | Cyclin-dependent protein kinases (CDKs) are enzyme complexes that contain a kinase catalytic subunit associated with a regulatory cyclin partner. |
cyclin/CDK positive transcription elongation factor complex | A transcription elongation factor complex that facilitates the transition from abortive to productive elongation by phosphorylating the CTD domain of the large subunit of DNA-directed RNA polymerase II, holoenzyme. Contains a cyclin and a cyclin-dependent protein kinase catalytic subunit. |
euchromatin | A dispersed and relatively uncompacted form of chromatin that is in a transcription-competent conformation. |
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. |
5 GO annotations of molecular function
Name | Definition |
---|---|
ATP binding | Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator. |
cyclin binding | Binding to cyclins, proteins whose levels in a cell varies markedly during the cell cycle, rising steadily until mitosis, then falling abruptly to zero. As cyclins reach a threshold level, they are thought to drive cells into G2 phase and thus to mitosis. |
cyclin-dependent protein serine/threonine kinase activity | Cyclin-dependent catalysis of the reactions: ATP + protein serine = ADP + protein serine phosphate, and ATP + protein threonine = ADP + protein threonine phosphate. |
protein serine kinase activity | Catalysis of the reactions: ATP + protein serine = ADP + protein serine phosphate. |
RNA polymerase II CTD heptapeptide repeat kinase activity | Catalysis of the reaction: ATP + RNA polymerase II large subunit CTD heptapeptide repeat (YSPTSPS) = ADP + H+ + phosphorylated RNA polymerase II. |
5 GO annotations of biological process
Name | Definition |
---|---|
nematode larval development | The process whose specific outcome is the progression of the nematode larva over time, from its formation to the mature structure. Nematode larval development begins with the newly hatched first-stage larva (L1) and ends with the end of the last larval stage (for example the fourth larval stage (L4) in C. elegans). Each stage of nematode larval development is characterized by proliferation of specific cell lineages and an increase in body size without alteration of the basic body plan. Nematode larval stages are separated by molts in which each stage-specific exoskeleton, or cuticle, is shed and replaced anew. |
phosphorylation of RNA polymerase II C-terminal domain | The process of introducing a phosphate group on to an amino acid residue in the C-terminal domain of RNA polymerase II. Typically, this occurs during the transcription cycle and results in production of an RNA polymerase II enzyme where the carboxy-terminal domain (CTD) of the largest subunit is extensively phosphorylated, often referred to as hyperphosphorylated or the II(0) form. Specific types of phosphorylation within the CTD are usually associated with specific regions of genes, though there are exceptions. The phosphorylation state regulates the association of specific complexes such as the capping enzyme or 3'-RNA processing machinery to the elongating RNA polymerase complex. |
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. |
protein phosphorylation | The process of introducing a phosphate group on to a protein. |
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. |
3 homologous proteins in AiPD
UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
---|---|---|---|---|
Q09437 | cdk-11.1 | Cyclin-dependent kinase 11.1 | Caenorhabditis elegans | PR |
F4I114 | At1g09600 | Probable serine/threonine-protein kinase At1g09600 | Arabidopsis thaliana (Mouse-ear cress) | PR |
Q9ZVM9 | At1g54610 | Probable serine/threonine-protein kinase At1g54610 | Arabidopsis thaliana (Mouse-ear cress) | PR |
10 | 20 | 30 | 40 | 50 | 60 |
MEISPGSSTH | ERDRKGSYGH | RERTRSHSGS | PSRFYSKDKR | GSSRQGVRPR | DRDSKDSISP |
70 | 80 | 90 | 100 | 110 | 120 |
QYKQRNWSRG | GGGGGRDRGR | NDFSYRKKGK | DYNKRRDKRS | RSRSRHRSPK | RSGSSKKSKR |
130 | 140 | 150 | 160 | 170 | 180 |
RNSSGSSSSD | LMDTSLMSEL | KKHGDYGSSS | KSKKKSRKRR | KHSSSSSSSS | GEAMDLPVSS |
190 | 200 | 210 | 220 | 230 | 240 |
NGMNVTAIPP | PPSFNINPFQ | PMFSQPPPPP | LPPNSQFMTP | PPRPPPAPFS | IPPPSVDIHF |
250 | 260 | 270 | 280 | 290 | 300 |
AATASFSLSS | IPPPPPQTDG | GASSSKRQDP | LPMPPDSKRI | ATRPVITTRR | GHATNRPSDS |
310 | 320 | 330 | 340 | 350 | 360 |
DSWYKTNLTH | YTMLDQIGEG | TYGQVYKAVN | NLTGEQVALK | RVRLENEKEG | FPITAIREIK |
370 | 380 | 390 | 400 | 410 | 420 |
ILRQLHHKNI | VRLMDIVIDD | ISMDELKRTR | ANFYLVFEYV | DHDLIGLLES | KELVDFNKDQ |
430 | 440 | 450 | 460 | 470 | 480 |
ICSLFKQLLE | GLAYIHNTGF | LHRDIKCSNI | LVNNKGELKI | ADLGLARLWE | KESRLYTNRV |
490 | 500 | 510 | 520 | 530 | 540 |
ITLWYRPPEL | LLGDERYGPA | IDVWSTGCML | GELFTRKPLF | NGNNEFGQLE | LISKVCGSPN |
550 | 560 | 570 | 580 | 590 | 600 |
VDNWPELTEL | VGWNTFRMKR | TYQRRIREEF | EHIMPREAVD | LLDKMLTLNP | EKRISAKEAL |
610 | 620 | 630 | 640 | 650 | 660 |
NHPWIRSLEH | TTVQPLKLPQ | HQDCHEMWSK | KQKKSARLGR | QAEGSSGSGH | SIRATSHPRA |
670 | 680 | 690 | 700 | 710 | 720 |
PTQPSTTTTK | SNGSSNHHHH | HHHSHHHASS | LPPSGGHAPP | PPPPPTQASS | TSHNNHQPVP |
QSQYQSVFFK |