Q7YXU4
Gene name |
cpnA (DDB_G0293008) |
Protein name |
Copine-A |
Names |
|
Species |
Dictyostelium discoideum (Slime mold) |
KEGG Pathway |
ddi:DDB_G0293008 |
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 Q7YXU4
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q7YXU4-F1 | Predicted | AlphaFoldDB |
No variants for Q7YXU4
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| No variants for Q7YXU4 | |||||
No associated diseases with Q7YXU4
5 regional properties for Q7YXU4
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | C2 domain | 1 - 111 | IPR000008-1 |
| domain | C2 domain | 116 - 246 | IPR000008-2 |
| domain | von Willebrand factor, type A | 284 - 484 | IPR002035 |
| domain | Copine, C-terminal | 305 - 518 | IPR010734 |
| domain | Copine, C2B domain | 136 - 246 | IPR037768 |
Functions
6 GO annotations of cellular component
| Name | Definition |
|---|---|
| contractile vacuolar membrane | The lipid bilayer surrounding the contractile vacuole. |
| cytosol | The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes. |
| early endosome membrane | The lipid bilayer surrounding an early endosome. |
| late endosome membrane | The lipid bilayer surrounding a late endosome. |
| phagocytic vesicle membrane | The lipid bilayer surrounding a phagocytic vesicle. |
| plasma membrane | The membrane surrounding a cell that separates the cell from its external environment. It consists of a phospholipid bilayer and associated proteins. |
3 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. |
| calcium-dependent phospholipid binding | Binding to a phospholipid, a class of lipids containing phosphoric acid as a mono- or diester, in the presence of calcium. |
| metal ion binding | Binding to a metal ion. |
15 GO annotations of biological process
| Name | Definition |
|---|---|
| cellular response to calcium ion | Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a calcium ion stimulus. |
| contractile vacuole discharge | The regulated release of water from a contractile vacuole to the outside of a cell by fusion of the contractile vacuole membrane with the plasma membrane. |
| contractile vacuole organization | A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of a contractile vacuole. A specialized vacuole that fills with water from the cytoplasm and then discharges this externally by the opening of contractile vacuole pores. |
| 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. |
| hypotonic response | Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of detection of, or exposure to, a hypotonic environment, i.e. an environment with a lower concentration of solutes than the organism or cell. |
| mitotic cytokinesis | A cell cycle process that results in the division of the cytoplasm of a cell after mitosis, resulting in the separation of the original cell into two daughter cells. |
| negative regulation of exocytosis | Any process that stops, prevents, or reduces the frequency, rate or extent of exocytosis. |
| positive phototaxis | The directed movement of a cell or organism towards a source of light. |
| regulation of actin cytoskeleton organization | Any process that modulates the frequency, rate or extent of the formation, arrangement of constituent parts, or disassembly of cytoskeletal structures comprising actin filaments and their associated proteins. |
| regulation of aggregate size involved in sorocarp development | Any process that modulates the size of the aggregate formed during sorocarp formation. |
| regulation of post-lysosomal vacuole size | Any process that modulates the volume of a post-lysosomal vacuole, a membrane-bounded intracellular vesicle formed late in the endocytic pathway when the pH in the vacuole becomes neutral prior to exocytosis. |
| response to ammonium ion | Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an ammonium stimulus. |
| response to calcium ion | Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a calcium ion stimulus. |
| sorocarp stalk cell differentiation | The process in which a relatively unspecialized cell acquires specialized features of a sorocarp stalk cell, any of the cellulose-covered cells that form the stalk of a sorocarp. An example of this process is found in Dictyostelium discoideum. |
| thermotaxis | The directed movement of a motile cell or organism in response to a temperature gradient. Movement may be towards either a higher or lower temperature. |
No homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| No homologous proteins | ||||
| 10 | 20 | 30 | 40 | 50 | 60 |
| MNLKPPTSKV | ELRIKCHKIL | DKDTLSKSDP | RASVYEKDRA | GQFRLIGKTE | TIQNQLNPEF |
| 70 | 80 | 90 | 100 | 110 | 120 |
| KTPIVIDYRF | EEIQVLKFEI | HDVDKNDEDF | IGDASCTLTS | ILSKPGQTVC | LQLLTKSGKH |
| 130 | 140 | 150 | 160 | 170 | 180 |
| AGSMTVIAEE | IKNTLQTIKF | NLIGKKFDKK | DLFGAGCDPY | LIISRKVPST | NTFVKIYESQ |
| 190 | 200 | 210 | 220 | 230 | 240 |
| VQKGTLNPVF | SGIEMKLEEL | CGGDMQREIK | FEFYDWDRIG | KHDYIGEFHT | NAQELLQPNQ |
| 250 | 260 | 270 | 280 | 290 | 300 |
| AFNVINSHKQ | EKKSGYKNSG | TVSVSDAVIE | REYNFLEYIM | GGCQMNLIVG | IDCTASNGDS |
| 310 | 320 | 330 | 340 | 350 | 360 |
| NDPNSLHYKN | AQGLNQYANA | ICSVGNVIVP | YTTTPLIPVY | GFGGIMPGQS | EVSHCFPMTL |
| 370 | 380 | 390 | 400 | 410 | 420 |
| NASNTLCCGV | NGVLDCYYDN | ISKIQLHGPT | YFAPLINMAA | RYASQGQSQS | NQKYTILMII |
| 430 | 440 | 450 | 460 | 470 | 480 |
| TDGEILDADN | TIDAIVKSSG | LPLSIIIVGV | GNANFTNMNI | LDGDDAALQS | GGVRAERDIV |
| 490 | 500 | 510 | 520 | 530 | 540 |
| QFVAMRDYLN | RPNELAAEVL | REIPTQFLSF | MKKYKFRPNP | PPPPPPVIIG | APPQYDNPTT |
| 550 | 560 | 570 | 580 | 590 | |
| TTTATSPSTG | IDLNKGSNVG | LNLTKTESSP | SPSGGAGIDL | NKGSVVDITK | GVSNVSLEKN |