Q54WH2
Gene name |
forA |
Protein name |
Formin-A |
Names |
|
Species |
Dictyostelium discoideum (Slime mold) |
KEGG Pathway |
ddi:DDB_G0279607 |
EC number |
|
Protein Class |
|
Descriptions
Autoinhibitory domains (AIDs)
Target domain |
759-1199 (FH2 domain) |
Relief mechanism |
Partner binding |
Assay |
|
Target domain |
759-1199 (FH2 domain) |
Relief mechanism |
Partner binding |
Assay |
|
Accessory elements
No accessory elements
Autoinhibited structure
Activated structure
1 structures for Q54WH2
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q54WH2-F1 | Predicted | AlphaFoldDB |
No variants for Q54WH2
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| No variants for Q54WH2 | |||||
No associated diseases with Q54WH2
6 regional properties for Q54WH2
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | C2 domain | 1 - 108 | IPR000008 |
| domain | Formin, FH3 domain | 352 - 553 | IPR010472 |
| domain | Formin, GTPase-binding domain | 139 - 347 | IPR010473 |
| domain | Diaphanous autoregulatory (DAD) domain | 1174 - 1209 | IPR014767 |
| domain | Rho GTPase-binding/formin homology 3 (GBD/FH3) domain | 139 - 539 | IPR014768 |
| domain | Formin, FH2 domain | 759 - 1199 | IPR015425 |
4 GO annotations of cellular component
| Name | Definition |
|---|---|
| actin cytoskeleton | The part of the cytoskeleton (the internal framework of a cell) composed of actin and associated proteins. Includes actin cytoskeleton-associated complexes. |
| cell cortex | The region of a cell that lies just beneath the plasma membrane and often, but not always, contains a network of actin filaments and associated proteins. |
| cell trailing edge | The area of a motile cell opposite to the direction of movement. |
| cleavage furrow | The cleavage furrow is a plasma membrane invagination at the cell division site. The cleavage furrow begins as a shallow groove and eventually deepens to divide the cytoplasm. |
4 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. |
| phosphatidylinositol binding | Binding to an inositol-containing glycerophospholipid, i.e. phosphatidylinositol (PtdIns) and its phosphorylated derivatives. |
| profilin binding | Binding to profilin, an actin-binding protein that forms a complex with G-actin and prevents it from polymerizing to form F-actin. |
| small GTPase binding | Binding to a small monomeric GTPase. |
6 GO annotations of biological process
| Name | Definition |
|---|---|
| 'de novo' actin filament nucleation | The actin nucleation process in which actin monomers combine in the absence of any existing actin filaments; elongation of the actin oligomer formed by nucleation leads to the formation of an unbranched filament. |
| actin filament polymerization | Assembly of actin filaments by the addition of actin monomers to a filament. |
| actin nucleation | The initial step in the formation of an actin filament, in which actin monomers combine to form a new filament. Nucleation is slow relative to the subsequent addition of more monomers to extend the filament. |
| cell migration | The controlled self-propelled movement of a cell from one site to a destination guided by molecular cues. Cell migration is a central process in the development and maintenance of multicellular organisms. |
| 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. |
| negative regulation of bleb assembly | Any process that stops, prevents or reduces the frequency, rate or extent of bleb assembly. |
No homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| No homologous proteins | ||||
| 10 | 20 | 30 | 40 | 50 | 60 |
| MADKLYQIKL | DIKKGKNIVG | SDGSVCSPYL | RVTWGGKKQQ | KTKVITKSAE | PEWNFSCLLE |
| 70 | 80 | 90 | 100 | 110 | 120 |
| IKKEKNPQKP | GLEFELIEHK | QFSEKEISST | TYQLPESLIL | GEACNYSVPM | SIATSKGDQK |
| 130 | 140 | 150 | 160 | 170 | 180 |
| CEILIAITAI | NFGKDKQDEE | KKRHDEIQKK | FAQLVEQLAT | DSKAREGMMK | LPYEARAQLV |
| 190 | 200 | 210 | 220 | 230 | 240 |
| EQHRDKLANE | KHPDEYVVLL | IKEITRKNIQ | LAGGLQKSHS | ASNASLGSLS | PVTPRVDDGL |
| 250 | 260 | 270 | 280 | 290 | 300 |
| SVAELKNISV | ALRSRGLDWI | HQFHKLGATT | RLVELLSLYV | NKKSHTEESL | QKQLECLNCI |
| 310 | 320 | 330 | 340 | 350 | 360 |
| KNLMNNNVGI | GYIFGIKDSF | KTIVLCLGSE | YEKVNELAIG | LLNTICFLPK | INGHKLLIEL |
| 370 | 380 | 390 | 400 | 410 | 420 |
| LNYFKEEKKE | SRRFISIVKS | LKSKAGVIET | KETLKTKSIY | LSFINIIVNT | PAEIDLRLAL |
| 430 | 440 | 450 | 460 | 470 | 480 |
| RQEFYWLGIK | EILVKLSNYT | YDESPELDTQ | ITVFEEEESK | DNKEMSERFQ | EFKGLNLDNV |
| 490 | 500 | 510 | 520 | 530 | 540 |
| DDVLKTLMDR | IRPKGLVDCM | REISKDLLLL | PIDDDVGIRN | WVLASRIIKQ | ISLRDKNIGI |
| 550 | 560 | 570 | 580 | 590 | 600 |
| DEDILPLENL | LLMCEQEAKE | VPLKSQIESL | KKDAQDLAKK | ITTQDIELKE | KVEIIKKNEE |
| 610 | 620 | 630 | 640 | 650 | 660 |
| LTTKQLEEQI | NIAKKKDEEI | NQLKALVEQL | KLTQGTAKPD | SAAASTSVAP | PPPPPPMTGG |
| 670 | 680 | 690 | 700 | 710 | 720 |
| GAPPPPPPPP | PMTGGGGPPP | PPPPPPMTGG | GPPPPPPPPP | MTGGGPPPPP | PPPGGGPPPP |
| 730 | 740 | 750 | 760 | 770 | 780 |
| PPPPGAKAGG | PPPPPPPFGK | GPPPPPGGFG | MKKAAAPPRK | EVPVPALKMK | GLQWVSLNDK |
| 790 | 800 | 810 | 820 | 830 | 840 |
| KIQGTIFSKF | NLDTSKDINL | DYKDIEGVFA | AKVIEKKEST | APKKTGPVSI | IDPKTSQNLS |
| 850 | 860 | 870 | 880 | 890 | 900 |
| IFLSQFKGKS | YDDICGAISK | GDETVFQPNH | IDALIGFLPS | EDDINNINEF | LREEKDITKL |
| 910 | 920 | 930 | 940 | 950 | 960 |
| GPPEQFSMKI | HSVPQVKARL | QAMKFKYAYE | SKKSDLKVDI | DNFKQGTQEI | KGSEKIPKLL |
| 970 | 980 | 990 | 1000 | 1010 | 1020 |
| EVILILGNFI | NGGTARGNAY | GFKLNTITKL | ADTKSTDNKL | SLVNYLTRVV | IKDFPHLNSF |
| 1030 | 1040 | 1050 | 1060 | 1070 | 1080 |
| AQDLGHVEAA | GRVSLSQVQA | EVATLRKEFV | QVQKSIETLN | SGTGEEAVDP | FKVKYEEFCT |
| 1090 | 1100 | 1110 | 1120 | 1130 | 1140 |
| QTAEDIDLIT | SSSQQIETDY | KDLLAMFGED | SKSEPSEFFG | MFTKFMDQYD | KATKENEQLS |
| 1150 | 1160 | 1170 | 1180 | 1190 | 1200 |
| IQAEKIAKRE | AAKKLKEEED | AKKKQLAEER | KQKGETVEVK | ESVVDDLLDT | IASGDAFKNR |
| 1210 | |||||
| RRRARKTDQD | STIEPIDL |