Protein Info for B158DRAFT_1992 in Kangiella aquimarina DSM 16071

Annotation: biotin-dependent carboxylase uncharacterized domain

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

1 50 100 150 200 250 309 TIGR00724: biotin-dependent carboxylase uncharacterized domain" amino acids 3 to 306 (304 residues), 274.4 bits, see alignment E=5.4e-86 PF02626: CT_A_B" amino acids 25 to 285 (261 residues), 279.5 bits, see alignment E=1.6e-87

Best Hits

KEGG orthology group: None (inferred from 83% identity to kko:Kkor_0560)

Predicted SEED Role

"Allophanate hydrolase 2 subunit 2 (EC 3.5.1.54)" (EC 3.5.1.54)

MetaCyc Pathways

KEGG Metabolic Maps

Isozymes

Compare fitness of predicted isozymes for: 3.5.1.54

Use Curated BLAST to search for 3.5.1.54

Sequence Analysis Tools

PaperBLAST (search for papers about homologs of this protein)

Search CDD (the Conserved Domains Database, which includes COG and superfam)

Search 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 (309 amino acids)

>B158DRAFT_1992 biotin-dependent carboxylase uncharacterized domain (Kangiella aquimarina DSM 16071)
MSINFIKAGLQTSLQDLGRPGFRRFGIPNNGALDPVSLQIANWLVSKPLNSACLEITQAG
PVIEFTQDMAIAVTGAHFELSIDDLPVDMHQTLLVNKGERLTFGKLVNGARAYLAFSAEP
DMPKIMESYSTNLMAQFGGYEGKALKNNDTIPLTNIVIPKTRKTPKGLQLQFSDNYQIRF
NEGREWSCFSKDMKQQFLQTAYQVTSQSNRMGMRLKGEAIKTEMPLSMTTVPITPGTIQI
PPDGQPIVTLADGQTTGGYPRIGQVITADLPILGQLKANDSISFQKIDVEDAIDLFKAKT
NLMKQLLGV