Protein Info for B158DRAFT_2288 in Kangiella aquimarina DSM 16071
Annotation: haloacid dehalogenase superfamily, subfamily IA, variant 1 with third motif having Dx(3-4)D or Dx(3-4)E
These analyses and tools can help you predict a protein's function, but be skeptical. For enzymes, over 10% of annotations from KEGG or SEED are probably incorrect. For other types of proteins, the error rates may be much higher. MetaCyc and Swiss-Prot have low error rates, but the best hits in these databases are often quite distant, so this protein's function may not be the same. TIGRFam has low error rates. Finally, many experimentally-characterized proteins are not in any of these databases. To find relevant papers, use PaperBLAST.
Protein Families and Features
Best Hits
KEGG orthology group: K00817, histidinol-phosphate aminotransferase [EC: 2.6.1.9] (inferred from 86% identity to kko:Kkor_0855)Predicted SEED Role
"Histidinol-phosphate aminotransferase (EC 2.6.1.9)" in subsystem Histidine Biosynthesis (EC 2.6.1.9)
MetaCyc Pathways
- superpathway of histidine, purine, and pyrimidine biosynthesis (42/46 steps found)
- superpathway of aromatic amino acid biosynthesis (17/18 steps found)
- superpathway of L-phenylalanine biosynthesis (10/10 steps found)
- superpathway of L-tyrosine biosynthesis (9/10 steps found)
- L-phenylalanine biosynthesis I (3/3 steps found)
- L-histidine biosynthesis (8/10 steps found)
- L-tyrosine degradation I (4/5 steps found)
- 3-(4-hydroxyphenyl)pyruvate biosynthesis (1/1 steps found)
- L-tyrosine biosynthesis I (2/3 steps found)
- L-tyrosine degradation II (1/2 steps found)
- atromentin biosynthesis (1/2 steps found)
- L-phenylalanine degradation III (2/4 steps found)
- L-tyrosine degradation III (2/4 steps found)
- L-phenylalanine degradation II (anaerobic) (1/3 steps found)
- L-tyrosine degradation IV (to 4-methylphenol) (1/3 steps found)
- superpathway of chorismate metabolism (41/59 steps found)
- superpathway of plastoquinol biosynthesis (2/5 steps found)
- 4-hydroxybenzoate biosynthesis I (eukaryotes) (1/5 steps found)
- L-phenylalanine degradation VI (reductive Stickland reaction) (1/5 steps found)
- L-tyrosine degradation V (reductive Stickland reaction) (1/5 steps found)
- L-phenylalanine degradation IV (mammalian, via side chain) (2/9 steps found)
- rosmarinic acid biosynthesis I (1/10 steps found)
- (S)-reticuline biosynthesis I (1/11 steps found)
- superpathway of rosmarinic acid biosynthesis (1/14 steps found)
- anaerobic aromatic compound degradation (Thauera aromatica) (1/27 steps found)
KEGG Metabolic Maps
- Alkaloid biosynthesis II
- Biosynthesis of alkaloids derived from histidine and purine
- Biosynthesis of alkaloids derived from ornithine, lysine and nicotinic acid
- Biosynthesis of phenylpropanoids
- Histidine metabolism
- Novobiocin biosynthesis
- Phenylalanine metabolism
- Phenylalanine, tyrosine and tryptophan biosynthesis
- Tyrosine metabolism
Isozymes
Compare fitness of predicted isozymes for: 2.6.1.9
Use Curated BLAST to search for 2.6.1.9
Sequence Analysis Tools
PaperBLAST (search for papers about homologs of this protein)
Search CDD (the Conserved Domains Database, which includes COG and superfam)
Compare to protein structures
Predict protein localization: PSORTb (Gram-negative bacteria)
Predict transmembrane helices and signal peptides: Phobius
Check the current SEED with FIGfam search
Find homologs in fast.genomics or the ENIGMA genome browser
Find the best match in UniProt
Protein Sequence (565 amino acids)
>B158DRAFT_2288 haloacid dehalogenase superfamily, subfamily IA, variant 1 with third motif having Dx(3-4)D or Dx(3-4)E (Kangiella aquimarina DSM 16071) MNMQETRIEPLKLDFNERADRFPAWLDMTKLTPQNYWRYPDQTELKQQMSNQFGLLPEQI MVTNGGDEAIEIMFKVASLEQKELIIPMPAFSQYLSGIKVWNSKAQLIPAQDNQSIDLES SLRALTKNSILVLTSPNNPTGETLALDVIRDACRKAKEKGAEVFLDQAYIEFTGQAEQSL SLLEEFDNLILLRTLSKAYGLAGIRCGYLLGSESLIKRFADRKMPFNVPRPTLEIARQAF SPEAQNDVADFCQQIAQNRDQLVQLLRQRGLNVLDSEANFILIIDAPDRLKLIKAACELN NIQIKTDLVGLELNKQGLPEQSAIRIAIPYELQPLRQALSLALQPELICFDMDGVLIDTS KSYDAAIKQTVEYFVGTQPAQQAIDTLRSQGGFNNDWVLTYELIKQNTNDAVPEYEQVVE QFQTLYLGSNGDAGLNQLEEGILSSELCTQIFVQNSKSIKTAVVTGRPRGEAEIGLGLLG IRNTFLVSDCDVIESKPAPEGINQCKAYYGATICWMLGDTPDDIQAAKAAGALAIGVSNK ENEQNLYQAGADLVVASVNELERLL