A2XL32
Gene name |
ERS1 (OSERS) |
Protein name |
Probable ethylene response sensor 1 |
Names |
|
Species |
Oryza sativa subsp indica (Rice) |
KEGG Pathway |
|
EC number |
2.7.13.3: Protein-histidine 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
No accessory elements
Autoinhibited structure
Activated structure
1 structures for A2XL32
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-A2XL32-F1 | Predicted | AlphaFoldDB |
No variants for A2XL32
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| No variants for A2XL32 | |||||
No associated diseases with A2XL32
13 regional properties for A2XL32
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | Protein kinase domain | 613 - 875 | IPR000719 |
| domain | Ephrin receptor ligand binding domain | 28 - 206 | IPR001090 |
| domain | Serine-threonine/tyrosine-protein kinase, catalytic domain | 614 - 871 | IPR001245 |
| conserved_site | Tyrosine-protein kinase, receptor class V, conserved site | 182 - 202 | IPR001426-1 |
| conserved_site | Tyrosine-protein kinase, receptor class V, conserved site | 247 - 267 | IPR001426-2 |
| domain | Sterile alpha motif domain | 901 - 968 | IPR001660 |
| domain | Fibronectin type III | 328 - 432 | IPR003961-1 |
| domain | Fibronectin type III | 436 - 529 | IPR003961-2 |
| active_site | Tyrosine-protein kinase, active site | 735 - 747 | IPR008266 |
| binding_site | Protein kinase, ATP binding site | 619 - 646 | IPR017441 |
| domain | Tyrosine-protein kinase, catalytic domain | 613 - 871 | IPR020635 |
| domain | Ephrin receptor, transmembrane domain | 538 - 610 | IPR027936 |
| domain | Ephrin type-A receptor 2, ligand binding domain | 28 - 201 | IPR034263 |
Functions
| Description | ||
|---|---|---|
| EC Number | 2.7.13.3 | Protein-histidine kinases |
| Subcellular Localization |
|
|
| PANTHER Family | ||
| PANTHER Subfamily | ||
| PANTHER Protein Class | ||
| PANTHER Pathway Category | No pathway information available | |
2 GO annotations of cellular component
| Name | Definition |
|---|---|
| endoplasmic reticulum membrane | The lipid bilayer surrounding the endoplasmic reticulum. |
| integral component of membrane | The component of a membrane consisting of the gene products and protein complexes having at least some part of their peptide sequence embedded in the hydrophobic region of the membrane. |
3 GO annotations of molecular function
| Name | Definition |
|---|---|
| ATP binding | Binding to ATP, adenosine 5'-triphosphate, a universally important coenzyme and enzyme regulator. |
| metal ion binding | Binding to a metal ion. |
| phosphorelay sensor kinase activity | Catalysis of the phosphorylation of a histidine residue in response to detection of an extracellular signal such as a chemical ligand or change in environment, to initiate a change in cell state or activity. The two-component sensor is a histidine kinase that autophosphorylates a histidine residue in its active site. The phosphate is then transferred to an aspartate residue in a downstream response regulator, to trigger a response. |
1 GO annotations of biological process
| Name | Definition |
|---|---|
| ethylene-activated signaling pathway | The series of molecular signals generated by the reception of ethylene (ethene, C2H4) by a receptor and ending with modulation of a cellular process, e.g. transcription. |
No homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| No homologous proteins | ||||
| 10 | 20 | 30 | 40 | 50 | 60 |
| MDGCDCIEPL | WPTDELLIKY | QYISDFFIAL | AYFSIPLELI | YFVKKSSFFP | YRWVLIQFGA |
| 70 | 80 | 90 | 100 | 110 | 120 |
| FIVLCGATHL | INLWTFTTHT | KTVAMVMTVA | KVSTAVVSCA | TALMLVHIIP | DLLSVKTREL |
| 130 | 140 | 150 | 160 | 170 | 180 |
| FLKNKAEQLD | REMGLIRTQE | ETGRHVRMLT | HEIRSTLDRH | TILKTTLVEL | GGTLGLEECA |
| 190 | 200 | 210 | 220 | 230 | 240 |
| LWMPSRSGSS | LQLSHTLRHQ | ITVGSTVSIN | LPVVNQVFSS | NRAIIIPHTS | PLARIRPLAG |
| 250 | 260 | 270 | 280 | 290 | 300 |
| RYVPPEVAAV | RVPLLHLSNF | QINDWPELSA | KSYAIMVLML | PSDSARKWHV | HELELVEVVA |
| 310 | 320 | 330 | 340 | 350 | 360 |
| DQVAVALSHA | AILEESMRAR | DLLMEQNVAL | DLARREAEMA | IRARNDFLAV | MNHEMRTPMN |
| 370 | 380 | 390 | 400 | 410 | 420 |
| AIIALSSLLL | ETELTPEQRL | MVETVLKSSN | LLATLINDVL | DLSKLEDGSL | ELEIKAFNLH |
| 430 | 440 | 450 | 460 | 470 | 480 |
| AVFKEVMSFI | KPIAAIKRLS | VSVMLAPDLP | LCAIGDEKRL | MQTILNISGN | AVKFTKEGHI |
| 490 | 500 | 510 | 520 | 530 | 540 |
| TLVASVVKAD | SLREFRTPDF | HPTASDDNFY | LKVQIKDTGC | GISPQDLPQV | FTKFAQSQPG |
| 550 | 560 | 570 | 580 | 590 | 600 |
| GNRGYSGSGL | GLAICKRFVT | LMGGHIWLDS | EGTGRGCTVT | FVIQLGICDN | TNAYQQKLIP |
| 610 | 620 | 630 | |||
| LVWPSSGDAD | FVGPVPNAPN | EEKGQASLKS | RYQRSI |