Type | Description |
---|---|
Definition | Ras GTPase activating protein 1 |
Date | Results | Publications |
---|---|---|
2015-08-01 10:53:00 | the Ras/MEK/MAPK pathway regulates regional-fate specification via HSPGs during development | 25848695 |
2012-06-23 10:10:00 | the PlexA GAP domain is phosphorylated by the cAMP-dependent protein kinase This PlexA phosphorylation generates a specific binding site for 14-3-3epsilon, a phospho-binding protein that we find to be necessary for axon guidance | 22500634 |
2010-01-21 00:00:00 | Neurofibromatosis type 1 (NF1) is among the most common genetic disorders of humans and is caused by loss of neurofibromin, a large and highly conserved protein whose only known function is to serve as a GTPase-Activating Protein (GAP) for Ras. | 17114577 |
Type | IDs |
---|---|
Synonymous | CG6721, Dmel\CG6721, FBpp0076097, GAP, GAP1, Gap, Gap 1, Gap1, Ras-GAP, RasGAP, RasGap1, gap, gap1, mip, rI533, rasGAP, sxt |
Gene |
UniProtKB-ID:
GAP1_DROME,
M9PF62_DROME
UniprotKB:
P48423,
M9PF62
UniParc:
UPI0002941191,
UPI0000081179
EMBL:
M86655,
BT011114,
AY051747,
AE014296
EnsemblGenome:
FBgn0004390
KO:
dme:Dmel_CG6721
|
Nucleutide sequences |
EMBL-CDS:
AAK93171.1,
AAN11935.1,
AAA28595.1,
AAF50196.1,
AAR82781.1,
AGB94359.1
Gene_ORFName:
CG6721,
CG6721,
Dmel_CG6721
EnsemblGenome_TRS:
FBtr0076367,
FBtr0076368,
FBtr0330168
|
Protein sequencees |
EnsemblGenome_PRO:
FBpp0076096,
FBpp0076097,
FBpp0303201
RefSeq:
NP_001261664.1,
NP_729562.1,
NP_524014.2
|
Others |
UniRef100:
UniRef100_P48423
UniRef90:
UniRef90_P48423
UniRef50:
UniRef50_P48423
UniGene:
Dm.919
|
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Conserved domain | Region: {{conservedDomain.region == '' || conservedDomain.region == null ? "-": conservedDomain.region}} GFID: {{conservedDomain.gfid == '' || conservedDomain.gfid == null ? "-": conservedDomain.gfid}} Family: {{conservedDomain.family == '' || conservedDomain.family == null ? "-": conservedDomain.family}} CDD: {{conservedDomain.cdd}} - |
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