Q9LZA4
Gene name |
At5g04060 (F21E1.1, F8F6.270) |
Protein name |
Probable methyltransferase PMT7 |
Names |
|
Species |
Arabidopsis thaliana (Mouse-ear cress) |
KEGG Pathway |
ath:AT5G04060 |
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 Q9LZA4
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q9LZA4-F1 | Predicted | AlphaFoldDB |
45 variants for Q9LZA4
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| tmp_5_1099277_G_C | 3 | G>R | No | 1000Genomes | |
| ENSVATH03019499 | 8 | F>L | No | 1000Genomes | |
| tmp_5_1099308_C_T | 13 | S>L | No | 1000Genomes | |
| ENSVATH10555242 | 58 | S>F | No | 1000Genomes | |
| ENSVATH10555345 | 108 | S>I | No | 1000Genomes | |
| ENSVATH06919244 | 125 | E>K | No | 1000Genomes | |
| ENSVATH00605595 | 128 | L>V | No | 1000Genomes | |
| ENSVATH00605597 | 173 | E>D | No | 1000Genomes | |
| tmp_5_1100094_C_T | 192 | P>L | No | 1000Genomes | |
| ENSVATH03019523 | 210 | L>R | No | 1000Genomes | |
| tmp_5_1100279_G_A | 213 | G>R | No | 1000Genomes | |
| tmp_5_1100384_G_C | 248 | E>Q | No | 1000Genomes | |
| ENSVATH00605601 | 260 | R>G | No | 1000Genomes | |
| ENSVATH10555351 | 281 | V>I | No | 1000Genomes | |
| ENSVATH03019526 | 289 | D>E | No | 1000Genomes | |
| tmp_5_1100513_C_T | 291 | H>Y | No | 1000Genomes | |
| ENSVATH06919252 | 296 | V>I | No | 1000Genomes | |
| ENSVATH03019529 | 298 | M>I | No | 1000Genomes | |
| ENSVATH10555352 | 318 | A>T | No | 1000Genomes | |
| ENSVATH10555353 | 354 | V>I | No | 1000Genomes | |
| ENSVATH00605606 | 358 | D>A | No | 1000Genomes | |
| ENSVATH00605607 | 375 | G>D | No | 1000Genomes | |
| ENSVATH03019530 | 375 | G>S | No | 1000Genomes | |
| ENSVATH06919254 | 379 | V>L | No | 1000Genomes | |
| tmp_5_1100875_T_C | 380 | S>P | No | 1000Genomes | |
| ENSVATH10555354 | 380 | S>W | No | 1000Genomes | |
| tmp_5_1100933_A_T | 399 | Q>L | No | 1000Genomes | |
| ENSVATH03019532 | 406 | T>I | No | 1000Genomes | |
| ENSVATH03019533 | 407 | D>E | No | 1000Genomes | |
| tmp_5_1100994_A_T | 419 | K>N | No | 1000Genomes | |
| ENSVATH06919257 | 423 | E>K | No | 1000Genomes | |
| tmp_5_1101098_C_T | 430 | T>I | No | 1000Genomes | |
| ENSVATH10555438 | 461 | I>F | No | 1000Genomes | |
| tmp_5_1101247_C_A | 480 | P>T | No | 1000Genomes | |
| tmp_5_1101309_T_A | 500 | H>Q | No | 1000Genomes | |
| tmp_5_1101438_T_A | 516 | L>Q | No | 1000Genomes | |
| ENSVATH00605611 | 528 | Y>H | No | 1000Genomes | |
| tmp_5_1101495_A_G | 535 | E>G | No | 1000Genomes | |
| tmp_5_1101664_A_T | 553 | I>F | No | 1000Genomes | |
| ENSVATH00605615 | 562 | R>S | No | 1000Genomes | |
| tmp_5_1101713_A_T | 569 | K>M | No | 1000Genomes | |
| ENSVATH00605617 | 576 | A>T | No | 1000Genomes | |
| ENSVATH06919264 | 592 | C>G | No | 1000Genomes | |
| ENSVATH10555441 | 599 | I>N | No | 1000Genomes | |
| ENSVATH03019540 | 600 | L>V | No | 1000Genomes |
No associated diseases with Q9LZA4
1 regional properties for Q9LZA4
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | BTB/POZ domain | 99 - 172 | IPR000210 |
6 GO annotations of cellular component
| Name | Definition |
|---|---|
| cytoplasm | The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures. |
| endosome | A vacuole to which materials ingested by endocytosis are delivered. |
| Golgi apparatus | A membrane-bound cytoplasmic organelle of the endomembrane system that further processes the core oligosaccharides (e.g. N-glycans) added to proteins in the endoplasmic reticulum and packages them into membrane-bound vesicles. The Golgi apparatus operates at the intersection of the secretory, lysosomal, and endocytic pathways. |
| Golgi membrane | The lipid bilayer surrounding any of the compartments of the Golgi apparatus. |
| 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. |
| trans-Golgi network | The network of interconnected tubular and cisternal structures located within the Golgi apparatus on the side distal to the endoplasmic reticulum, from which secretory vesicles emerge. The trans-Golgi network is important in the later stages of protein secretion where it is thought to play a key role in the sorting and targeting of secreted proteins to the correct destination. |
1 GO annotations of molecular function
| Name | Definition |
|---|---|
| methyltransferase activity | Catalysis of the transfer of a methyl group to an acceptor molecule. |
1 GO annotations of biological process
| Name | Definition |
|---|---|
| methylation | The process in which a methyl group is covalently attached to a molecule. |
5 homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| Q84TJ0 | At3g10200 | Probable methyltransferase PMT6 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| Q9C884 | At1g33170 | Probable methyltransferase PMT18 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| Q9SIZ3 | At2g40280 | Probable methyltransferase PMT23 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| Q9ZW75 | At2g43200 | Probable methyltransferase PMT19 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| Q9SZX8 | At4g10440 | Probable methyltransferase PMT17 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MGGGYVLFGS | ARSGQMIMVA | LVLMVGSFYA | GSIFGNNSPI | YISQPSSSNS | SSSSPSQSGP |
| 70 | 80 | 90 | 100 | 110 | 120 |
| SNFANKIELT | YRRTSVSIPE | SGVNVCPLKF | NEYIPCHNVT | YVQQLLPSLN | LSRREELERH |
| 130 | 140 | 150 | 160 | 170 | 180 |
| CPPLEQRLFC | LVPPPKDYKI | PIRWPTSRDY | VWRSNVNHTH | LAEVKGGQNW | VHEQGQLWWF |
| 190 | 200 | 210 | 220 | 230 | 240 |
| PGGGTHFKHG | APEYIQRLGN | MTTNETGDLL | SAGVEQVLDV | GCGVASFAAY | LLPLGIKTMS |
| 250 | 260 | 270 | 280 | 290 | 300 |
| FAPKDGHENQ | IQFALERGIR | AMISAIATKQ | MPYPAASFDM | VHCSRCRVDW | HENDGVLMKE |
| 310 | 320 | 330 | 340 | 350 | 360 |
| VNRLLRPNGY | FVYSAPPAYR | KDKDFPVIWD | KLVNLTSAMC | WKLISRKVQT | AIWVKEDDEA |
| 370 | 380 | 390 | 400 | 410 | 420 |
| CLRKNAELEL | ITICGVEDVS | KASWKVPLRD | CVDISENRQQ | KPSSLTDRLS | SYPTSLREKG |
| 430 | 440 | 450 | 460 | 470 | 480 |
| ISEDEFTLDT | NFWREQVNQY | WELMNVNKTE | VRNVMDTNAF | IGGFAAAMNS | YPLWVMNVVP |
| 490 | 500 | 510 | 520 | 530 | 540 |
| ATMNDTLSGI | YQRGLTGAYH | DWCEPFSTYP | RTYDLLHADH | LFTHYKIYGE | GCLLEDIMLE |
| 550 | 560 | 570 | 580 | 590 | |
| MDRIIRPQGF | IIIRDEESIV | SRVRDLAPKF | LWEVEAHELQ | DKYKKTETVL | FCRKKFWAIL |