Protein Info for PP_2012 in Pseudomonas putida KT2440

Annotation: Probable inorganic polyphosphate/ATP-NAD kinase

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 50 100 150 200 250 315 PF01513: NAD_kinase" amino acids 26 to 139 (114 residues), 82 bits, see alignment E=5e-27 PF20143: NAD_kinase_C" amino acids 164 to 290 (127 residues), 137.6 bits, see alignment E=2e-44

Best Hits

Swiss-Prot: 100% identical to NADK_PSEP1: NAD kinase (nadK) from Pseudomonas putida (strain ATCC 700007 / DSM 6899 / BCRC 17059 / F1)

KEGG orthology group: K00858, NAD+ kinase [EC: 2.7.1.23] (inferred from 100% identity to ppu:PP_2012)

Predicted SEED Role

"NAD kinase (EC 2.7.1.23)" in subsystem NAD and NADP cofactor biosynthesis global (EC 2.7.1.23)

MetaCyc Pathways

KEGG Metabolic Maps

Isozymes

No predicted isozymes

Use Curated BLAST to search for 2.7.1.23

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

See Q88LC3 at UniProt or InterPro

Protein Sequence (315 amino acids)

>PP_2012 Probable inorganic polyphosphate/ATP-NAD kinase (Pseudomonas putida KT2440)
MVSPIIGASSPAAEPCRSPMEQFRNIGIIGRLGSSQVLDTIRRLKKFLLDRHLHVILEDT
IAEVLPGHGLQTSTRKLLGEVCDLVIVVGGDGSLLGAARALARHNIPVLGINRGNLGFLT
DIRPDELEQKVAEVLDGHYLVENRFLLQAEVRRHHEAIGQGDALNDVVLHPGKSTRMIEF
EIYIDGQFVCSQKADGLIVATPTGSTAYALSAGGPIMHPKLDAIVIVPMYPHTLSGRPIV
VDGNSELKIVVSKDLQIYPQVSCDGQNHFTCAPGDTITVSKKPQKLRLIHPLDHNYYEVC
RTKLGWGSRLGSSDD