Q2QN30
Gene name |
NRAMP6 (Os12g0581600, LOC_Os12g39180, OsJ_36661) |
Protein name |
Metal transporter Nramp6 |
Names |
|
Species |
Oryza sativa subsp japonica (Rice) |
KEGG Pathway |
osa:4352640 |
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 Q2QN30
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q2QN30-F1 | Predicted | AlphaFoldDB |
No variants for Q2QN30
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| No variants for Q2QN30 | |||||
No associated diseases with Q2QN30
No regional properties for Q2QN30
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| No domain, repeats, and functional sites for Q2QN30 | |||
1 GO annotations of cellular component
| Name | Definition |
|---|---|
| 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. |
2 GO annotations of molecular function
| Name | Definition |
|---|---|
| cadmium ion transmembrane transporter activity | Enables the transfer of cadmium (Cd) ions from one side of a membrane to the other. |
| manganese ion transmembrane transporter activity | Enables the transfer of manganese (Mn) ions from one side of a membrane to the other. |
1 GO annotations of biological process
| Name | Definition |
|---|---|
| iron ion homeostasis | Any process involved in the maintenance of an internal steady state of iron ions within an organism or cell. |
12 homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| Q27981 | SLC11A1 | Natural resistance-associated macrophage protein 1 | Bos taurus (Bovine) | PR |
| P49279 | SLC11A1 | Natural resistance-associated macrophage protein 1 | Homo sapiens (Human) | PR |
| P49281 | SLC11A2 | Natural resistance-associated macrophage protein 2 | Homo sapiens (Human) | PR |
| P41251 | Slc11a1 | Natural resistance-associated macrophage protein 1 | Mus musculus (Mouse) | PR |
| P49282 | Slc11a2 | Natural resistance-associated macrophage protein 2 | Mus musculus (Mouse) | PR |
| O77741 | SLC11A1 | Natural resistance-associated macrophage protein 1 | Sus scrofa (Pig) | PR |
| P70553 | Slc11a1 | Natural resistance-associated macrophage protein 1 | Rattus norvegicus (Rat) | PR |
| O54902 | Slc11a2 | Natural resistance-associated macrophage protein 2 | Rattus norvegicus (Rat) | PR |
| Q6ZG85 | NRAT1 | Metal transporter NRAT1 | Oryza sativa subsp japonica (Rice) | PR |
| Q9C6B2 | NRAMP2 | Metal transporter Nramp2 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| Q9SN36 | NRAMP5 | Metal transporter Nramp5 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| Q9SNV9 | NRAMP3 | Metal transporter Nramp3 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MAPLPAAATA | TASSAATPAD | DEAHSLLPST | PSNEEDDDDL | EERAYEATEK | VIVSISDFPD |
| 70 | 80 | 90 | 100 | 110 | 120 |
| ADDDEEESGL | ATSTAASGIP | PFSWRKLWLF | TGPGFLMSIA | FLDPGNLEGD | LQAGAVAGDT |
| 130 | 140 | 150 | 160 | 170 | 180 |
| LLWLLLWATS | MGLLVQLLAA | RVGVATGRHL | AELCRDEYPS | WARRALWLMA | EVAMVGADIQ |
| 190 | 200 | 210 | 220 | 230 | 240 |
| EVIGSAIAIK | ILSRGFLPLW | AGVVITALDC | FIFLSLENYG | VRKLEAVFAI | LIATMAVSFA |
| 250 | 260 | 270 | 280 | 290 | 300 |
| WMFTDTKPNM | KNLFIGILVP | KLSSRTIRQA | VGVVGCVIMP | HNVFLHSALV | QSRKIDPNKE |
| 310 | 320 | 330 | 340 | 350 | 360 |
| HQVREALRYY | SIESTIALAV | SFMINLFVTT | VFAKGFYGTK | EAGNIGLENA | GQYLQEKFGG |
| 370 | 380 | 390 | 400 | 410 | 420 |
| GFFPILYIWG | IGLLAAGQSS | TITGTYAGQF | IMGGFLNLKL | KKWIRSLITR | SFAIVPTIIV |
| 430 | 440 | 450 | 460 | 470 | 480 |
| ALFFDKSDSL | DVLNEWLNVL | QSIQIPFALI | PLITLVSKEK | VMGVFKIGRN | TQAVTWTVAT |
| 490 | 500 | 510 | 520 | 530 | 540 |
| LLITINGYLL | LDFFSSEIRG | LLSGSILCVA | VLAYASFVLY | LILRGTELPN | QIITTIRKSF |
| S |