A4SPN7
Gene name |
cmoA |
Protein name |
Carboxy-S-adenosyl-L-methionine synthase |
Names |
Cx-SAM synthase |
Species |
Aeromonas salmonicida (strain A449) |
KEGG Pathway |
asa:ASA_2846 |
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 A4SPN7
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-A4SPN7-F1 | Predicted | AlphaFoldDB |
No variants for A4SPN7
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
| No variants for A4SPN7 | |||||
No associated diseases with A4SPN7
1 regional properties for A4SPN7
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | Methyltransferase domain 25 | 62 - 158 | IPR041698 |
No GO annotations of cellular component
| Name | Definition |
|---|---|
| No GO annotations for cellular component |
2 GO annotations of molecular function
| Name | Definition |
|---|---|
| carboxyl- or carbamoyltransferase activity | Catalysis of the transfer of a carboxyl- or carbamoyl group from one compound (donor) to another (acceptor). |
| S-adenosyl-L-methionine binding | Binding to S-adenosyl-L-methionine. |
1 GO annotations of biological process
| Name | Definition |
|---|---|
| tRNA wobble uridine modification | The process in which a uridine in position 34 of a tRNA is post-transcriptionally modified. |
No homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| No homologous proteins | ||||
| 10 | 20 | 30 | 40 | 50 | 60 |
| MHTKDQIFAA | PIARLGDFCF | DEQVVDVFPD | MIQRSVPGYS | NIISAIGMMA | ARYAQPQSRL |
| 70 | 80 | 90 | 100 | 110 | 120 |
| YDLGCSLGAA | TQAMRRHLTQ | PGCHITAVDL | SHPMIERARA | HLSGFKSEVP | VALVEADICD |
| 130 | 140 | 150 | 160 | 170 | 180 |
| IAIENASVVV | LNFTLQFVDP | EKRMALIQRI | FDGLRPGGIL | ILSEKFRFED | EPVNDLLIEL |
| 190 | 200 | 210 | 220 | 230 | 240 |
| HLDFKRANGY | SELEISQKRN | ALENVMRTDS | LETHRSRLQS | AGFVHQDLWF | QCFNFGSMIA |
| IKSSDAN |