Q54KF1
Gene name |
forC |
Protein name |
Formin-C |
Names |
|
Species |
Dictyostelium discoideum (Slime mold) |
KEGG Pathway |
ddi:DDB_G0287295 |
EC number |
|
Protein Class |
|

Descriptions
Autoinhibitory domains (AIDs)
Target domain |
601-1077 (FH2 domain) |
Relief mechanism |
Partner binding |
Assay |
|
Target domain |
601-1077 (FH2 domain) |
Relief mechanism |
Partner binding |
Assay |
|
Accessory elements
No accessory elements
Autoinhibited structure

Activated structure

2 structures for Q54KF1
Entry ID | Method | Resolution | Chain | Position | Source |
---|---|---|---|---|---|
2L1A | NMR | - | A | 1-100 | PDB |
AF-Q54KF1-F1 | Predicted | AlphaFoldDB |
No variants for Q54KF1
Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
---|---|---|---|---|---|
No variants for Q54KF1 |
No associated diseases with Q54KF1
5 GO annotations of cellular component
Name | Definition |
---|---|
cell-cell junction | A cell junction that forms a connection between two or more cells of an organism; excludes direct cytoplasmic intercellular bridges, such as ring canals in insects. |
cytoplasm | The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures. |
cytoskeleton | A cellular structure that forms the internal framework of eukaryotic and prokaryotic cells. The cytoskeleton includes intermediate filaments, microfilaments, microtubules, the microtrabecular lattice, and other structures characterized by a polymeric filamentous nature and long-range order within the cell. The various elements of the cytoskeleton not only serve in the maintenance of cellular shape but also have roles in other cellular functions, including cellular movement, cell division, endocytosis, and movement of organelles. |
cytosol | The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes. |
macropinosome | A membrane-bounded, uncoated intracellular vesicle formed by the process of macropinocytosis. |
1 GO annotations of molecular function
Name | Definition |
---|---|
actin filament binding | Binding to an actin filament, also known as F-actin, a helical filamentous polymer of globular G-actin subunits. |
6 GO annotations of biological process
Name | Definition |
---|---|
actin filament bundle assembly | The assembly of actin filament bundles; actin filaments are on the same axis but may be oriented with the same or opposite polarities and may be packed with different levels of tightness. |
actin filament network formation | The assembly of a network of actin filaments; actin filaments on different axes and with differing orientations are crosslinked together to form a mesh of filaments. |
cortical actin cytoskeleton organization | A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of actin-based cytoskeletal structures in the cell cortex, i.e. just beneath the plasma membrane. |
culmination involved in sorocarp development | The process whose specific outcome is the progression of the culminant over time, from its formation to the mature structure. Culmination begins with a morphogenetic change of the finger-like or migratory slug giving rise to an organized structure containing a stalk and a sorus. This process is the final stage of sorocarp development. |
gene expression | The process in which a gene's sequence is converted into a mature gene product (protein or RNA). This includes the production of an RNA transcript and its processing, translation and maturation for protein-coding genes. |
sorocarp spore cell differentiation | The process in which a relatively unspecialized cell acquires specialized features of a sorocarp spore cell, a cell of the sorocarp sorus. A sorocarp is the fruiting body characteristic of certain cellular slime moulds (e.g., Dictyosteliida) and consists of both stalk and a sorus (spore mass). |
No homologous proteins in AiPD
UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
---|---|---|---|---|
No homologous proteins |
10 | 20 | 30 | 40 | 50 | 60 |
MKIRVELING | NEHRTSSTPQ | QPQQNPSVSH | IFDGETAVKD | HIKVLLTHFK | IPVDKVSSYA |
70 | 80 | 90 | 100 | 110 | 120 |
LQNPFTLAYV | EDSFLTPERL | VEAEKSYFIL | RMKPHAIADR | VVDQLTKIEP | TSPHIKDTIF |
130 | 140 | 150 | 160 | 170 | 180 |
NIRYQMKDVE | YVEEFIIKGG | INQLLAVIIK | SRGNTQSYAL | TALRCFMGYN | SGLEEVMSRP |
190 | 200 | 210 | 220 | 230 | 240 |
QLIDKLYSLV | CSVGVLPSVC | RQAIELLFCV | CNFDGFQLVH | RSAKNHAQET | STPAYSNLIT |
250 | 260 | 270 | 280 | 290 | 300 |
LLSSGDMETQ | LNTLTLFNCL | LDNAPNPRKS | EKLLSRWQQL | GIIKILKSQE | HVTHSDFRTQ |
310 | 320 | 330 | 340 | 350 | 360 |
IARFQANSGF | GIDGSGRKRT | LTRQLSTQEL | EFQLHQFREQ | QPLISLLTSE | LKFLRNAIKS |
370 | 380 | 390 | 400 | 410 | 420 |
AIENGSYINY | RAPTERYDEY | SQRKLEMIGD | SPTNLQFLKR | NDKFTNAFRK | SMYVRSPNTS |
430 | 440 | 450 | 460 | 470 | 480 |
DLFDSSTLED | TYDGNNDTNS | CTSISTSSTP | IHISQPTTLI | VPSTTPNHPP | QQSQQTPPLQ |
490 | 500 | 510 | 520 | 530 | 540 |
LQKEKEKEKE | KEKEKEKEKE | KEQQQQQQQS | NKQSTPKPNL | SCLLSPITIS | NTLNNNNNNN |
550 | 560 | 570 | 580 | 590 | 600 |
NNTNNNIIKS | NNNNNNNNCT | IKDLSPIVKS | EKSNEDEIHE | ISLNGASSNH | EEPIKYKLQP |
610 | 620 | 630 | 640 | 650 | 660 |
TKSPITPSKR | MKPLHWTRIL | NSQFEGKKTI | WNSYLPEVTF | EEELFVDLFS | LYTERIVSFS |
670 | 680 | 690 | 700 | 710 | 720 |
GSPVGSGTSI | SGGGPIKSKP | IQKVISVLSQ | KRSNAIIVMC | GKLPSDDILI | RAIRNLDSNK |
730 | 740 | 750 | 760 | 770 | 780 |
LSLDGVSSII | SNFPTSEELA | SIHELHSNEV | ILDKPERWCL | MIDGFPMIKH | RLRCWEFMLK |
790 | 800 | 810 | 820 | 830 | 840 |
IEDSLKSIIE | SIDTVLLACK | ELRTSITINC | LFSLLLQLGN | YLNGGHLYRG | QSDGFNLESL |
850 | 860 | 870 | 880 | 890 | 900 |
SKMIEIKDNS | NSGSLLDFAI | KTLYQQSPMK | GNSNTSIHLE | LAHVPNASLI | NFTDVGTSVS |
910 | 920 | 930 | 940 | 950 | 960 |
KLLQDYSEIV | LMSDEIQQTT | DKDDPFLDIV | PKFMGTILLI | LKNLQTKFLE | TEKYLFETID |
970 | 980 | 990 | 1000 | 1010 | 1020 |
YFNPTNQTLQ | QYQQQQYQQY | QQQQFQQNII | NNNNNNNNNN | SNNNNNNISG | NTTTTTTTTT |
1030 | 1040 | 1050 | 1060 | 1070 | 1080 |
TTTTGSIINN | NNNNNNNNNN | SNNNIINNNN | SQSNLQSLLH | PQYYLSNSSS | SSSSSYKITP |
1090 | 1100 | 1110 | 1120 | 1130 | 1140 |
PLSSSLSITS | QEWNQQKFTC | EKFFTLFSTI | TTAFKKSPSK | RLSQKGFGLK | ISNSDDPMAV |
1150 | |||||
IIEALKTGSP | NDMVKRAF |