F4J4P8
Gene name |
At3g58220 (F9D24.130) |
Protein name |
MATH domain and coiled-coil domain-containing protein At3g58220 |
Names |
RTM3-like protein At3g58220 |
Species |
Arabidopsis thaliana (Mouse-ear cress) |
KEGG Pathway |
ath:AT3G58220 |
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 F4J4P8
Entry ID | Method | Resolution | Chain | Position | Source |
---|---|---|---|---|---|
AF-F4J4P8-F1 | Predicted | AlphaFoldDB |
49 variants for F4J4P8
Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
---|---|---|---|---|---|
ENSVATH12817727 | 8 | L>F | No | 1000Genomes | |
ENSVATH12817726 | 15 | W>R | No | 1000Genomes | |
ENSVATH06337379 | 17 | I>F | No | 1000Genomes | |
ENSVATH12817725 | 24 | G>* | No | 1000Genomes | |
ENSVATH12817725 | 24 | G>R | No | 1000Genomes | |
ENSVATH06337378 | 31 | D>E | No | 1000Genomes | |
ENSVATH06337373 | 40 | W>* | No | 1000Genomes | |
ENSVATH00425794 | 41 | R>H | No | 1000Genomes | |
tmp_3_21566214_G_T | 44 | A>D | No | 1000Genomes | |
tmp_3_21566215_C_T | 44 | A>T | No | 1000Genomes | |
tmp_3_21566212_A_G | 45 | Y>H | No | 1000Genomes | |
ENSVATH12817714 | 48 | G>E | No | 1000Genomes | |
tmp_3_21566196_C_A | 50 | R>M | No | 1000Genomes | |
ENSVATH06337372 | 68 | P>L | No | 1000Genomes | |
ENSVATH00425793 | 85 | N>D | No | 1000Genomes | |
tmp_3_21566090_A_C | 85 | N>K | No | 1000Genomes | |
tmp_3_21566074_G_A | 91 | Q>* | No | 1000Genomes | |
tmp_3_21565938_A_T | 97 | N>K | No | 1000Genomes | |
tmp_3_21565918_G_T | 104 | T>N | No | 1000Genomes | |
ENSVATH12817710 | 112 | M>I | No | 1000Genomes | |
tmp_3_21565889_G_A | 114 | R>C | No | 1000Genomes | |
ENSVATH02520906 | 114 | R>P | No | 1000Genomes | |
ENSVATH06337370 | 126 | V>L | No | 1000Genomes | |
tmp_3_21565334_T_C | 159 | N>D | No | 1000Genomes | |
ENSVATH06337363 | 167 | T>I | No | 1000Genomes | |
ENSVATH00425790 | 170 | I>V | No | 1000Genomes | |
ENSVATH09450244 | 181 | T>A | No | 1000Genomes | |
ENSVATH09450243 | 181 | T>K | No | 1000Genomes | |
ENSVATH09450242 | 182 | L>F | No | 1000Genomes | |
ENSVATH06337361 | 184 | S>R | No | 1000Genomes | |
ENSVATH06337360 | 186 | I>M | No | 1000Genomes | |
ENSVATH06337359 | 187 | L>* | No | 1000Genomes | |
ENSVATH09450241 | 193 | I>T | No | 1000Genomes | |
ENSVATH09450239 | 195 | L>I | No | 1000Genomes | |
ENSVATH09450237 | 198 | N>H | No | 1000Genomes | |
ENSVATH12817669 | 198 | N>S | No | 1000Genomes | |
ENSVATH06337356 | 202 | R>* | No | 1000Genomes | |
ENSVATH02520899 | 202 | R>Q | No | 1000Genomes | |
ENSVATH02520897 | 213 | I>L | No | 1000Genomes | |
ENSVATH02520895 | 234 | A>E | No | 1000Genomes | |
ENSVATH02520894 | 235 | D>G | No | 1000Genomes | |
ENSVATH12817667 | 245 | G>S | No | 1000Genomes | |
ENSVATH02520891 | 252 | D>E | No | 1000Genomes | |
ENSVATH02520890 | 258 | V>E | No | 1000Genomes | |
ENSVATH02520888 | 263 | V>L | No | 1000Genomes | |
tmp_3_21564829_C_T | 264 | V>I | No | 1000Genomes | |
ENSVATH02520887 | 269 | K>E | No | 1000Genomes | |
ENSVATH02520885 | 292 | L>M | No | 1000Genomes | |
ENSVATH02520879 | 311 | D>G | No | 1000Genomes |
No associated diseases with F4J4P8
1 regional properties for F4J4P8
Type | Name | Position | InterPro Accession |
---|---|---|---|
domain | MATH/TRAF domain | 10 - 137 | IPR002083 |
No GO annotations of cellular component
Name | Definition |
---|---|
No GO annotations for cellular component |
No GO annotations of molecular function
Name | Definition |
---|---|
No GO annotations for molecular function |
No GO annotations of biological process
Name | Definition |
---|---|
No GO annotations for biological process |
15 homologous proteins in AiPD
UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
---|---|---|---|---|
Q6IQ16 | SPOPL | Speckle-type POZ protein-like | Homo sapiens (Human) | PR |
Q6YCH2 | Tdpoz4 | TD and POZ domain-containing protein 4 | Mus musculus (Mouse) | PR |
Q2M2N2 | Spopl | Speckle-type POZ protein-like | Mus musculus (Mouse) | PR |
P34371 | bath-42 | BTB and MATH domain-containing protein 42 | Caenorhabditis elegans | PR |
F4IN32 | At2g42460 | MATH domain and coiled-coil domain-containing protein At2g42460 | Arabidopsis thaliana (Mouse-ear cress) | PR |
F4J4A0 | At3g44790 | MATH domain and coiled-coil domain-containing protein At3g44790 | Arabidopsis thaliana (Mouse-ear cress) | PR |
F4J4A1 | At3g44800 | MATH domain and coiled-coil domain-containing protein At3g44800 | Arabidopsis thaliana (Mouse-ear cress) | PR |
P0DKG7 | At2g42480 | MATH domain and coiled-coil domain-containing protein At2g42480 | Arabidopsis thaliana (Mouse-ear cress) | PR |
Q9LSD2 | At3g27040 | MATH domain and coiled-coil domain-containing protein At3g27040 | Arabidopsis thaliana (Mouse-ear cress) | PR |
Q9M2I2 | At3g58340 | MATH domain and coiled-coil domain-containing protein At3g58340 | Arabidopsis thaliana (Mouse-ear cress) | PR |
Q9M2J0 | At3g58260 | MATH domain and coiled-coil domain-containing protein At3g58260 | Arabidopsis thaliana (Mouse-ear cress) | PR |
Q9M2J5 | At3g58210 | MATH domain and coiled-coil domain-containing protein At3g58210 | Arabidopsis thaliana (Mouse-ear cress) | PR |
Q9ZUA7 | At2g01790 | MATH domain and coiled-coil domain-containing protein At2g01790 | Arabidopsis thaliana (Mouse-ear cress) | PR |
P0DKG4 | At2g42465 | MATH domain and coiled-coil domain-containing protein At2g42465 | Arabidopsis thaliana (Mouse-ear cress) | PR |
Q9SHT3 | At2g05410 | MATH domain and coiled-coil domain-containing protein At2g05410 | Arabidopsis thaliana (Mouse-ear cress) | PR |
10 | 20 | 30 | 40 | 50 | 60 |
MGRIGSPLGK | NEFSWVIKDF | SSLGVRAIYS | DEFVIGGCKW | RLIAYPMGNR | IKKYMSLYVE |
70 | 80 | 90 | 100 | 110 | 120 |
VADSKHLPSG | WSINTELRME | VVNHNLYKPS | QQKYRKNLWF | DQKTPSWGYK | TMIRHSKLSG |
130 | 140 | 150 | 160 | 170 | 180 |
EEGFLVSGEV | TIVVKIDVYR | VFGKIKRNDD | GVKSNDSVNK | TQQVKETMDI | NGFQVLPSQV |
190 | 200 | 210 | 220 | 230 | 240 |
TLVSRILKKY | PDIALGFNAK | NRHLRTACMN | VLISLIETLC | QSPQELSDED | MDEADNALVY |
250 | 260 | 270 | 280 | 290 | 300 |
VQDAGFKVDW | LDKKLKEVKE | KKVVEQTGKT | RIQELEEELK | EFKQKCLDRE | ALLEKEKAKV |
310 | |||||
LAARASLTLD | DFV |