Q94A28
Gene name |
ACO2 |
Protein name |
Aconitate hydratase 2, mitochondrial |
Names |
Aconitase 2, mACO2, Citrate hydro-lyase 2 |
Species |
Arabidopsis thaliana (Mouse-ear cress) |
KEGG Pathway |
ath:AT4G26970 |
EC number |
4.2.1.3: Hydro-lyases |
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 Q94A28
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-Q94A28-F1 | Predicted | AlphaFoldDB |
48 variants for Q94A28
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| ENSVATH14300608 | 5 | A>S | No | 1000Genomes | |
| tmp_4_13543119_A_T | 15 | R>W | No | 1000Genomes | |
| tmp_4_13543146_G_A | 24 | A>T | No | 1000Genomes | |
| tmp_4_13543150_C_T | 25 | S>F | No | 1000Genomes | |
| ENSVATH00540379 | 25 | S>T | No | 1000Genomes | |
| ENSVATH12251899 | 27 | E>D | No | 1000Genomes | |
| tmp_4_13543159_C_A | 28 | T>K | No | 1000Genomes | |
| tmp_4_13543165_C_T | 30 | S>L | No | 1000Genomes | |
| ENSVATH02929038 | 35 | S>P | No | 1000Genomes | |
| ENSVATH06782515 | 36 | A>S | No | 1000Genomes | |
| ENSVATH02929039 | 40 | R>L | No | 1000Genomes | |
| ENSVATH00540381 | 43 | T>S | No | 1000Genomes | |
| ENSVATH02929042 | 57 | R>Q | No | 1000Genomes | |
| tmp_4_13543263_A_C | 63 | T>P | No | 1000Genomes | |
| tmp_4_13543264_C_G | 63 | T>R | No | 1000Genomes | |
| ENSVATH00540383 | 75 | A>T | No | 1000Genomes | |
| tmp_4_13543336_T_G | 87 | V>G | No | 1000Genomes | |
| tmp_4_13543369_T_G | 98 | M>R | No | 1000Genomes | |
| ENSVATH00540385 | 107 | I>L | No | 1000Genomes | |
| ENSVATH00540386 | 126 | P>T | No | 1000Genomes | |
| ENSVATH06782529 | 159 | D>N | No | 1000Genomes | |
| tmp_4_13543969_T_A | 169 | N>K | No | 1000Genomes | |
| tmp_4_13543971_C_G | 170 | T>R | No | 1000Genomes | |
| tmp_4_13544477_G_A | 278 | V>I | No | 1000Genomes | |
| tmp_4_13545036_G_A | 365 | V>M | No | 1000Genomes | |
| ENSVATH00540404 | 439 | R>G | No | 1000Genomes | |
| ENSVATH12252035 | 488 | A>T | No | 1000Genomes | |
| tmp_4_13546125_C_T | 506 | P>S | No | 1000Genomes | |
| tmp_4_13546145_A_T | 512 | E>D | No | 1000Genomes | |
| tmp_4_13546443_C_T | 585 | R>* | No | 1000Genomes | |
| tmp_4_13546616_G_A | 615 | D>N | No | 1000Genomes | |
| tmp_4_13546635_C_A | 621 | A>D | No | 1000Genomes | |
| ENSVATH06782574 | 624 | G>E | No | 1000Genomes | |
| ENSVATH02929119 | 676 | I>L | No | 1000Genomes | |
| ENSVATH00540413 | 679 | R>G | No | 1000Genomes | |
| ENSVATH02929120 | 680 | S>R | No | 1000Genomes | |
| ENSVATH02929122 | 683 | K>E | No | 1000Genomes | |
| tmp_4_13547341_G_A | 715 | E>K | No | 1000Genomes | |
| ENSVATH12252040 | 720 | G>E | No | 1000Genomes | |
| ENSVATH14300652 | 722 | P>H | No | 1000Genomes | |
| ENSVATH00540415 | 740 | N>S | No | 1000Genomes | |
| ENSVATH06782586 | 800 | R>L | No | 1000Genomes | |
| tmp_4_13547712_A_T | 838 | E>D | No | 1000Genomes | |
| tmp_4_13548136_A_G | 927 | E>G | No | 1000Genomes | |
| tmp_4_13548195_G_A | 947 | D>N | No | 1000Genomes | |
| ENSVATH14300654 | 970 | F>S | No | 1000Genomes | |
| ENSVATH12252097 | 994 | A>T | No | 1000Genomes | |
| ENSVATH12252098 | 994 | A>V | No | 1000Genomes |
No associated diseases with Q94A28
No regional properties for Q94A28
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| No domain, repeats, and functional sites for Q94A28 | |||
Functions
| Description | ||
|---|---|---|
| EC Number | 4.2.1.3 | Hydro-lyases |
| Subcellular Localization |
|
|
| PANTHER Family | ||
| PANTHER Subfamily | ||
| PANTHER Protein Class | ||
| PANTHER Pathway Category | No pathway information available | |
3 GO annotations of cellular component
| Name | Definition |
|---|---|
| chloroplast | A chlorophyll-containing plastid with thylakoids organized into grana and frets, or stroma thylakoids, and embedded in a stroma. |
| cytosol | The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes. |
| mitochondrion | A semiautonomous, self replicating organelle that occurs in varying numbers, shapes, and sizes in the cytoplasm of virtually all eukaryotic cells. It is notably the site of tissue respiration. |
5 GO annotations of molecular function
| Name | Definition |
|---|---|
| 4 iron, 4 sulfur cluster binding | Binding to a 4 iron, 4 sulfur (4Fe-4S) cluster; this cluster consists of four iron atoms, with the inorganic sulfur atoms found between the irons and acting as bridging ligands. |
| aconitate hydratase activity | Catalysis of the reaction: citrate = isocitrate. The reaction occurs in two steps: (1) citrate = cis-aconitate + H2O, (2) cis-aconitate + H2O = isocitrate. This reaction is the interconversion of citrate and isocitrate via the labile, enzyme-bound intermediate cis-aconitate. Water is removed from one part of the citrate molecule and added back to a different atom to form isocitrate. |
| citrate dehydratase activity | Catalysis of the reaction: citrate = cis-aconitate + H2O. |
| copper ion binding | Binding to a copper (Cu) ion. |
| iron-responsive element binding | Binding to an iron-responsive element, a regulatory sequence found in the 5'- and 3'-untranslated regions of mRNAs encoding many iron-binding proteins. |
6 GO annotations of biological process
| Name | Definition |
|---|---|
| citrate metabolic process | The chemical reactions and pathways involving citrate, 2-hydroxy-1,2,3-propanetricarboyxlate. Citrate is widely distributed in nature and is an important intermediate in the TCA cycle and the glyoxylate cycle. |
| glyoxylate cycle | A modification of the TCA cycle occurring in some plants and microorganisms, in which isocitrate is cleaved to glyoxylate and succinate. Glyoxylate can then react with acetyl-CoA to form malate. |
| isocitrate metabolic process | The chemical reactions and pathways involving isocitrate, the anion of isocitric acid, 1-hydroxy-1,2,3-propanetricarboxylic acid. Isocitrate is an important intermediate in the TCA cycle and the glycoxylate cycle. |
| response to iron ion starvation | 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 starvation stimulus, deprivation of iron ion. |
| response to oxidative stress | 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 oxidative stress, a state often resulting from exposure to high levels of reactive oxygen species, e.g. superoxide anions, hydrogen peroxide (H2O2), and hydroxyl radicals. |
| tricarboxylic acid cycle | A nearly universal metabolic pathway in which the acetyl group of acetyl coenzyme A is effectively oxidized to two CO2 and four pairs of electrons are transferred to coenzymes. The acetyl group combines with oxaloacetate to form citrate, which undergoes successive transformations to isocitrate, 2-oxoglutarate, succinyl-CoA, succinate, fumarate, malate, and oxaloacetate again, thus completing the cycle. In eukaryotes the tricarboxylic acid is confined to the mitochondria. See also glyoxylate cycle. |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MYRRATSGVR | SASARLSSSL | SRIASSETAS | VSAPSASSLR | NQTNRSKSFS | SALRSFRVCS |
| 70 | 80 | 90 | 100 | 110 | 120 |
| ASTRWSHGGS | WGSPASLRAQ | ARNSTPVMEK | FERKYATMAS | EHSYKDILTS | LPKPGGGEYG |
| 130 | 140 | 150 | 160 | 170 | 180 |
| KYYSLPALND | PRIDKLPFSV | RILLESAIRN | CDNYQVTKDD | VEKILDWENT | STKQVEIAFK |
| 190 | 200 | 210 | 220 | 230 | 240 |
| PARVILQDFT | GVPVLVDLAS | MRDAVKNLGS | DPSKINPLVP | VDLVVDHSIQ | VDFARSEDAA |
| 250 | 260 | 270 | 280 | 290 | 300 |
| QKNLELEFKR | NKERFTFLKW | GSTAFQNMLV | VPPGSGIVHQ | VNLEYLGRVV | FNSKGFLYPD |
| 310 | 320 | 330 | 340 | 350 | 360 |
| SVVGTDSHTT | MIDGLGVAGW | GVGGIEAEAA | MLGQPMSMVL | PGVVGFKLDG | KLKEGVTATD |
| 370 | 380 | 390 | 400 | 410 | 420 |
| LVLTVTQILR | KHGVVGKFVE | FYGEGMSELS | LADRATIANM | SPEYGATMGF | FPVDHVTLEY |
| 430 | 440 | 450 | 460 | 470 | 480 |
| LKLTGRSDET | VSMIESYLRA | NNMFVDYNEP | QQERAYTSYL | QLDLGHVEPC | ISGPKRPHDR |
| 490 | 500 | 510 | 520 | 530 | 540 |
| VPLKDMKADW | HACLDNPVGF | KGFAVPKEKQ | EEVVKFSYNG | QPAEIKHGSV | VIAAITSCTN |
| 550 | 560 | 570 | 580 | 590 | 600 |
| TSNPSVMIGA | ALVAKKASDL | GLKVKPWVKT | SLAPGSRVVE | KYLDRSGLRE | SLTKQGFEIV |
| 610 | 620 | 630 | 640 | 650 | 660 |
| GYGCTTCIGN | SGNLDPEVAS | AIEGTDIIPA | AVLSGNRNFE | GRVHPQTRAN | YLASPPLVVA |
| 670 | 680 | 690 | 700 | 710 | 720 |
| YALAGTVDID | FEKEPIGTRS | DGKSVYLRDV | WPSNEEVAQV | VQYSVLPSMF | KSSYETITEG |
| 730 | 740 | 750 | 760 | 770 | 780 |
| NPLWNELSAP | SSTLYSWDPN | STYIHEPPYF | KNMTANPPGP | REVKDAYCLL | NFGDSVTTDH |
| 790 | 800 | 810 | 820 | 830 | 840 |
| ISPAGNIQKT | SPAAKFLMDR | GVISEDFNSY | GSRRGNDEVM | ARGTFANIRI | VNKLLKGEVG |
| 850 | 860 | 870 | 880 | 890 | 900 |
| PNTVHIPTGE | KLSVFDAASK | YKTAEQDTII | LAGAEYGSGS | SRDWAAKGPL | LLGVKAVIAK |
| 910 | 920 | 930 | 940 | 950 | 960 |
| SFERIHRSNL | AGMGIIPLCF | KAGEDAETLG | LTGHERYTVH | LPTKVSDIRP | GQDVTVTTDS |
| 970 | 980 | 990 | |||
| GKSFVCTLRF | DTEVELAYYD | HGGILPYVIR | SLSAK |