blastp_kegg |
lcl|csv:101222356
|
3 |
192 |
+ |
190 |
Gaps:17 |
48.10 |
422 |
57.14 |
3e-63 |
ammonium transporter 1 member 2-like
|
blastp_kegg |
lcl|cic:CICLE_v10019808mg
|
3 |
192 |
+ |
190 |
Gaps:17 |
40.28 |
504 |
57.64 |
9e-63 |
hypothetical protein
|
blastp_kegg |
lcl|cmo:103485853
|
3 |
192 |
+ |
190 |
Gaps:17 |
39.73 |
511 |
56.65 |
3e-62 |
ammonium transporter 1 member 2-like
|
blastp_kegg |
lcl|cit:102627368
|
31 |
192 |
+ |
162 |
Gaps:17 |
21.53 |
813 |
64.57 |
4e-62 |
ammonium transporter 1 member 2-like
|
blastp_kegg |
lcl|mdm:103414323
|
3 |
192 |
+ |
190 |
Gaps:17 |
40.28 |
504 |
56.65 |
2e-61 |
ammonium transporter 1 member 2-like
|
blastp_kegg |
lcl|cmo:103485850
|
31 |
192 |
+ |
162 |
Gaps:17 |
34.25 |
511 |
61.14 |
1e-60 |
ammonium transporter 1 member 2
|
blastp_kegg |
lcl|csv:101227720
|
3 |
192 |
+ |
190 |
Gaps:17 |
39.73 |
511 |
54.19 |
2e-60 |
ammonium transporter 1 member 2-like
|
blastp_kegg |
lcl|csv:101217871
|
3 |
192 |
+ |
190 |
Gaps:17 |
39.73 |
511 |
54.19 |
3e-60 |
ammonium transporter 1 member 2-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa004450mg
|
3 |
192 |
+ |
190 |
Gaps:17 |
39.88 |
509 |
55.17 |
1e-59 |
hypothetical protein
|
blastp_kegg |
lcl|rcu:RCOM_0610260
|
3 |
192 |
+ |
190 |
Gaps:18 |
40.00 |
510 |
55.88 |
8e-59 |
ammonium transporter putative
|
blastp_pdb |
2b2j_A
|
1 |
189 |
+ |
189 |
Gaps:23 |
43.61 |
399 |
29.31 |
2e-07 |
mol:protein length:399 ammonium transporter
|
blastp_pdb |
2b2i_A
|
1 |
189 |
+ |
189 |
Gaps:23 |
43.61 |
399 |
29.31 |
2e-07 |
mol:protein length:399 ammonium transporter
|
blastp_pdb |
2b2h_A
|
1 |
189 |
+ |
189 |
Gaps:23 |
43.61 |
399 |
29.31 |
2e-07 |
mol:protein length:399 ammonium transporter
|
blastp_pdb |
2b2f_A
|
1 |
189 |
+ |
189 |
Gaps:23 |
43.61 |
399 |
29.31 |
2e-07 |
mol:protein length:399 ammonium transporter
|
blastp_uniprot_sprot |
sp|Q6K9G1|AMT12_ORYSJ
|
3 |
192 |
+ |
190 |
Gaps:18 |
41.13 |
496 |
53.43 |
9e-57 |
Ammonium transporter 1 member 2 OS Oryza sativa subsp. japonica GN AMT1-2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O04161|AMT12_SOLLC
|
3 |
192 |
+ |
190 |
Gaps:24 |
40.08 |
514 |
53.88 |
5e-56 |
Ammonium transporter 1 member 2 OS Solanum lycopersicum GN AMT1-2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9ZPJ8|AMT12_ARATH
|
3 |
192 |
+ |
190 |
Gaps:18 |
39.69 |
514 |
51.96 |
4e-54 |
Ammonium transporter 1 member 2 OS Arabidopsis thaliana GN AMT1-2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q7XQ12|AMT11_ORYSJ
|
3 |
192 |
+ |
190 |
Gaps:18 |
40.96 |
498 |
50.98 |
5e-54 |
Ammonium transporter 1 member 1 OS Oryza sativa subsp. japonica GN AMT1-1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9SVT8|AMT14_ARATH
|
3 |
192 |
+ |
190 |
Gaps:19 |
40.67 |
504 |
50.24 |
2e-53 |
Ammonium transporter 1 member 4 OS Arabidopsis thaliana GN AMT1-4 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|P58905|AMT11_SOLLC
|
3 |
192 |
+ |
190 |
Gaps:18 |
41.39 |
488 |
51.49 |
3e-53 |
Ammonium transporter 1 member 1 OS Solanum lycopersicum GN AMT1-1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P54144|AMT11_ARATH
|
31 |
192 |
+ |
162 |
Gaps:17 |
34.93 |
501 |
57.71 |
4e-53 |
Ammonium transporter 1 member 1 OS Arabidopsis thaliana GN AMT1-1 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q6K9G3|AMT13_ORYSJ
|
31 |
192 |
+ |
162 |
Gaps:18 |
35.34 |
498 |
56.25 |
1e-52 |
Ammonium transporter 1 member 3 OS Oryza sativa subsp. japonica GN AMT1-3 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9LK16|AMT15_ARATH
|
31 |
192 |
+ |
162 |
Gaps:16 |
35.08 |
496 |
56.32 |
2e-52 |
Putative ammonium transporter 1 member 5 OS Arabidopsis thaliana GN AMT1-5 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q9SQH9|AMT13_ARATH
|
3 |
192 |
+ |
190 |
Gaps:17 |
40.76 |
498 |
51.23 |
2e-52 |
Ammonium transporter 1 member 3 OS Arabidopsis thaliana GN AMT1-3 PE 2 SV 2
|
rpsblast_cdd |
gnl|CDD|162060
|
31 |
189 |
+ |
159 |
Gaps:23 |
36.72 |
403 |
39.19 |
5e-27 |
TIGR00836 amt ammonium transporter. The Ammonium Transporter (Amt) Family (TC 2.A.49) All functionally characterized members of the Amt family are ammonia or ammonium uptake transporters. Some but not others also transport methylammonium. The mechanism of energy coupling if any to methyl-NH2 or NH3 uptake by the AmtB protein of E. coli is not entirely clear. NH4+ uniport driven by the pmf energy independent NH3 facilitation and NH4+/K+ antiport have been proposed as possible transport mechanisms. In Corynebacterium glutamicum and Arabidopsis thaliana uptake via the Amt1 homologues of AmtB has been reported to be driven by the pmf.
|
rpsblast_cdd |
gnl|CDD|201500
|
31 |
192 |
+ |
162 |
Gaps:15 |
38.35 |
399 |
37.91 |
9e-23 |
pfam00909 Ammonium_transp Ammonium Transporter Family.
|
rpsblast_cdd |
gnl|CDD|30353
|
33 |
189 |
+ |
157 |
Gaps:23 |
35.21 |
409 |
34.72 |
4e-17 |
COG0004 AmtB Ammonia permease [Inorganic ion transport and metabolism].
|
rpsblast_cdd |
gnl|CDD|163373
|
31 |
184 |
+ |
154 |
Gaps:18 |
37.13 |
404 |
33.33 |
5e-12 |
TIGR03644 marine_trans_1 probable ammonium transporter marine subtype. Members of this protein family are well conserved subclass of putative ammonimum transporters belonging to the much broader set of ammonium/methylammonium transporter described by TIGR00836. Species with this transporter tend to be marine bacteria. Partial phylogenetic profiling (PPP) picks a member of this protein family as the single best-scoring protein vs. a reference profile for the marine environment Genome Property for a large number of different query genomes. This finding by PPP suggests that this transporter family represents an important adaptation to the marine environment.
|
rpsblast_kog |
gnl|CDD|35901
|
31 |
189 |
+ |
159 |
Gaps:15 |
30.00 |
500 |
42.67 |
3e-31 |
KOG0682 KOG0682 KOG0682 Ammonia permease [Inorganic ion transport and metabolism].
|