Curated BLAST
Searching in Phaeobacter inhibens BS107 (Phaeo)
Found 18 curated entries in PaperBLAST's database that match '3.5.3.12'.
These curated entries have 14 distinct sequences.
Running ublast with E ≤ 0.01
Found 1 relevant proteins in Phaeobacter inhibens BS107, or try another query
PGA1_c26490: putative agmatine deiminase
is similar to: | PaperBLAST |
A0A0H2Z743: agmatine deiminase (EC 3.5.3.12) from Pseudomonas aeruginosa | 39% id,
99% cov |
A0A0H2Z8C6: agmatine deiminase (EC 3.5.3.12) from Pseudomonas aeruginosa | 38% id,
97% cov |
A0A0H3G8U9: agmatine deiminase (EC 3.5.3.12) from Listeria monocytogenes | 33% id,
97% cov |
S0F349: agmatine deiminase (EC 3.5.3.12) from Lactococcus cremoris | 31% id,
99% cov |
AGUA_ARATH / Q8GWW7: Agmatine deiminase; Agmatine iminohydrolase; Protein EMBRYO DEFECTIVE 1873; EC 3.5.3.12 from Arabidopsis thaliana
At5g08170 / Q8GWW7: agmatine iminohydrolase (EC 3.5.3.12) from Arabidopsis thaliana | 32% id,
95% cov |
AGUA_ENTFA / Q837U5: Putative agmatine deiminase; Agmatine iminohydrolase; EC 3.5.3.12 from Enterococcus faecalis
Q837U5: agmatine deiminase (EC 3.5.3.12) from Enterococcus faecalis | 30% id,
99% cov |
AO356_10030: Agmatine deiminase (EC 3.5.3.12) from Pseudomonas fluorescens | 34% id,
68% cov |
AGUA_PSEAE / Q9I6J9: Agmatine deiminase; Agmatine iminohydrolase; EC 3.5.3.12 from Pseudomonas aeruginosa
aguA / Q9I6J9: agmatine deiminase subunit (EC 3.5.3.12) from Pseudomonas aeruginosa
Q9I6J9: agmatine deiminase (EC 3.5.3.12) from Pseudomonas aeruginosa | 36% id,
65% cov |
Q5KR05: agmatine deiminase (EC 3.5.3.12) from Selenomonas ruminantium | 31% id,
68% cov |
AGUA_MEDTR / G7JT50: Agmatine deiminase; Agmatine iminohydrolase; MtAIH; EC 3.5.3.12 from Medicago truncatula | 33% id,
63% cov |
Q5KR05: agmatine deiminase (EC 3.5.3.12) from Selenomonas ruminantium | 42% id,
21% cov |
More... |
The hits are sorted by %identity * %coverage (highest first)
Running ublast against the 6-frame translation. All reading frames of at least 30 codons are included.
Found hits to 1 reading frames. These were all redundant with annotated proteins.
by Morgan Price,
Arkin group
Lawrence Berkeley National Laboratory