blastp_kegg |
lcl|tcc:TCM_007928
|
11 |
237 |
+ |
227 |
Gaps:29 |
41.39 |
488 |
81.19 |
9e-109 |
Diacylglycerol kinase 5 isoform 1
|
blastp_kegg |
lcl|sot:102590752
|
9 |
237 |
+ |
229 |
Gaps:27 |
40.64 |
502 |
78.92 |
7e-106 |
diacylglycerol kinase 5-like
|
blastp_kegg |
lcl|eus:EUTSA_v10001971mg
|
11 |
237 |
+ |
227 |
Gaps:29 |
41.22 |
490 |
80.20 |
2e-105 |
hypothetical protein
|
blastp_kegg |
lcl|aly:ARALYDRAFT_480938
|
11 |
237 |
+ |
227 |
Gaps:30 |
41.60 |
488 |
79.31 |
3e-104 |
hypothetical protein
|
blastp_kegg |
lcl|pop:POPTR_0013s14470g
|
9 |
237 |
+ |
229 |
Gaps:30 |
41.18 |
493 |
80.79 |
4e-104 |
POPTRDRAFT_663551 hypothetical protein
|
blastp_kegg |
lcl|brp:103838018
|
11 |
237 |
+ |
227 |
Gaps:30 |
41.51 |
489 |
79.31 |
8e-103 |
diacylglycerol kinase 5
|
blastp_kegg |
lcl|sot:102588823
|
9 |
237 |
+ |
229 |
Gaps:27 |
38.70 |
522 |
78.71 |
1e-102 |
diacylglycerol kinase 5-like
|
blastp_kegg |
lcl|pda:103717315
|
9 |
237 |
+ |
229 |
Gaps:29 |
41.96 |
491 |
76.21 |
4e-102 |
diacylglycerol kinase 5-like
|
blastp_kegg |
lcl|cam:101510741
|
11 |
237 |
+ |
227 |
Gaps:27 |
40.90 |
489 |
76.50 |
9e-102 |
diacylglycerol kinase delta-like
|
blastp_kegg |
lcl|rcu:RCOM_1176580
|
9 |
237 |
+ |
229 |
Gaps:26 |
41.43 |
490 |
76.85 |
4e-101 |
diacylglycerol kinase alpha putative (EC:2.7.1.107)
|
blastp_uniprot_sprot |
sp|Q9C5E5|DGK5_ARATH
|
11 |
230 |
+ |
220 |
Gaps:30 |
38.51 |
509 |
79.08 |
3e-101 |
Diacylglycerol kinase 5 OS Arabidopsis thaliana GN DGK5 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|F4JKI3|DGK6_ARATH
|
9 |
216 |
+ |
208 |
Gaps:29 |
38.41 |
466 |
68.16 |
4e-79 |
Diacylglycerol kinase 6 OS Arabidopsis thaliana GN DGK6 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|F4JQ95|DGK7_ARATH
|
11 |
167 |
+ |
157 |
Gaps:27 |
26.83 |
492 |
37.12 |
4e-19 |
Diacylglycerol kinase 7 OS Arabidopsis thaliana GN DGK7 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q8VZG1|DGK3_ARATH
|
11 |
167 |
+ |
157 |
Gaps:27 |
27.05 |
488 |
34.85 |
1e-16 |
Diacylglycerol kinase 3 OS Arabidopsis thaliana GN DGK3 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q1PDI2|DGK4_ARATH
|
28 |
167 |
+ |
140 |
Gaps:26 |
23.41 |
487 |
37.72 |
1e-15 |
Diacylglycerol kinase 4 OS Arabidopsis thaliana GN DGK4 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q03603|DGK3_CAEEL
|
1 |
188 |
+ |
188 |
Gaps:68 |
18.87 |
795 |
35.33 |
1e-06 |
Probable diacylglycerol kinase 3 OS Caenorhabditis elegans GN dgk-3 PE 3 SV 3
|
rpsblast_cdd |
gnl|CDD|201338
|
28 |
154 |
+ |
127 |
Gaps:34 |
59.24 |
157 |
39.78 |
1e-19 |
pfam00609 DAGK_acc Diacylglycerol kinase accessory domain. Diacylglycerol (DAG) is a second messenger that acts as a protein kinase C activator. This domain is assumed to be an accessory domain: its function is unknown.
|
rpsblast_cdd |
gnl|CDD|128360
|
29 |
154 |
+ |
126 |
Gaps:33 |
59.38 |
160 |
36.84 |
3e-12 |
smart00045 DAGKa Diacylglycerol kinase accessory domain (presumed). Diacylglycerol (DAG) is a second messenger that acts as a protein kinase C activator. DAG can be produced from the hydrolysis of phosphatidylinositol 4 5-bisphosphate (PIP2) by a phosphoinositide-specific phospholipase C and by the degradation of phosphatidylcholine (PC) by a phospholipase C or the concerted actions of phospholipase D and phosphatidate phosphohydrolase. This domain might either be an accessory domain or else contribute to the catalytic domain. Bacterial homologues are known.
|
rpsblast_kog |
gnl|CDD|36384
|
26 |
188 |
+ |
163 |
Gaps:32 |
20.66 |
634 |
35.88 |
5e-35 |
KOG1169 KOG1169 KOG1169 Diacylglycerol kinase [Lipid transport and metabolism Signal transduction mechanisms].
|
rpsblast_kog |
gnl|CDD|36385
|
36 |
237 |
+ |
202 |
Gaps:47 |
15.38 |
1099 |
28.40 |
1e-09 |
KOG1170 KOG1170 KOG1170 Diacylglycerol kinase [Lipid transport and metabolism].
|