| Type | Description |
|---|---|
| Definition | HXXXD-type acyl-transferase family protein |
| Date | Results | Publications |
|---|---|---|
| 2013-03-23 11:09:00 | Overexpression of a novel BAHD family acyltransferase gene, ABS1/At4g15400, was the cause of the dwarf phenotype. | 22956280 |
| 2012-10-13 11:21:00 | BIA1 is strongly expressed in the root elongation zone and encodes a cytosolic acyltransferase-like protein. | 22544867 |
| Type | IDs |
|---|---|
| Synonymous | ABNORMAL SHOOT 1, ABS1, BRASSINOSTEROID INACTIVATOR1, DL3745C, FCAALL.284 |
| Gene |
UniProtKB-ID:
BIA1_ARATH,
A0A654FPI7_ARATH
UniprotKB:
O23393,
A0A654FPI7
UniParc:
UPI0000039702
EMBL:
CP002687,
CACRSJ010000109,
Z97338,
AL161541,
BT023456
EnsemblGenome:
AT4G15400
KO:
ath:AT4G15400
|
| Nucleutide sequences |
EMBL-CDS:
CAB10319.1,
CAB78582.1,
AEE83596.1,
AAY56447.1,
VYS62782.1
Gene_ORFName:
Dl3745c,
FCAALL.284,
AN1_LOCUS18205
EnsemblGenome_TRS:
AT4G15400.1
|
| Protein sequencees |
EnsemblGenome_PRO:
AT4G15400.1
RefSeq:
NP_193275.1
|
| Others |
UniRef100:
UniRef100_O23393
UniRef90:
UniRef90_O23393
UniRef50:
UniRef50_O23393
UniGene:
At.4342
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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