GapMind for catabolism of small carbon sources

 

Protein Pf1N1B4_2417 in Pseudomonas fluorescens FW300-N1B4

Annotation: FitnessBrowser__pseudo1_N1B4:Pf1N1B4_2417

Length: 490 amino acids

Source: pseudo1_N1B4 in FitnessBrowser

Candidate for 27 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-arginine catabolism patD med 4-trimethylammoniobutyraldehyde dehydrogenase (EC 1.2.1.47) (characterized) 51% 98% 486.1 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-citrulline catabolism patD med 4-trimethylammoniobutyraldehyde dehydrogenase (EC 1.2.1.47) (characterized) 51% 98% 486.1 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
putrescine catabolism patD med 4-trimethylammoniobutyraldehyde dehydrogenase (EC 1.2.1.47) (characterized) 51% 98% 486.1 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-phenylalanine catabolism pad-dh med aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized) 43% 92% 394.8 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
4-hydroxybenzoate catabolism praB med 2-hydroxymuconate-6-semialdehyde dehydrogenase (EC 1.2.1.85) (characterized) 42% 97% 381.3 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-tryptophan catabolism praB med 2-hydroxymuconate-6-semialdehyde dehydrogenase (EC 1.2.1.85) (characterized) 42% 97% 381.3 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-tryptophan catabolism nbaE med aminomuconate-semialdehyde dehydrogenase (EC 1.2.1.32) (characterized) 40% 95% 339.7 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-arginine catabolism kauB lo 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized) 40% 96% 365.9 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-arginine catabolism puuC lo 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized) 40% 96% 365.9 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-citrulline catabolism puuC lo 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized) 40% 96% 365.9 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
putrescine catabolism puuC lo 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized) 40% 96% 365.9 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-lysine catabolism patD lo aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized) 37% 99% 327 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-arginine catabolism davD lo Glutarate-semialdehyde dehydrogenase (EC 1.2.1.20) (characterized) 37% 97% 325.9 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-citrulline catabolism davD lo Glutarate-semialdehyde dehydrogenase (EC 1.2.1.20) (characterized) 37% 97% 325.9 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-lysine catabolism davD lo Glutarate-semialdehyde dehydrogenase (EC 1.2.1.20) (characterized) 37% 97% 325.9 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-proline catabolism davD lo Glutarate-semialdehyde dehydrogenase (EC 1.2.1.20) (characterized) 37% 97% 325.9 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-arginine catabolism putA lo L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized) 32% 91% 237.3 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-arginine catabolism rocA lo L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized) 32% 91% 237.3 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-citrulline catabolism putA lo L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized) 32% 91% 237.3 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-citrulline catabolism rocA lo L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized) 32% 91% 237.3 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-proline catabolism putA lo L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized) 32% 91% 237.3 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-isoleucine catabolism iolA lo Methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial; MMSDH; Malonate-semialdehyde dehydrogenase [acylating]; Aldehyde dehydrogenase family 6 member A1; EC 1.2.1.18; EC 1.2.1.27 (characterized) 30% 88% 233.8 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
myo-inositol catabolism mmsA lo Methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial; MMSDH; Malonate-semialdehyde dehydrogenase [acylating]; Aldehyde dehydrogenase family 6 member A1; EC 1.2.1.18; EC 1.2.1.27 (characterized) 30% 88% 233.8 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
propionate catabolism iolA lo Methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial; MMSDH; Malonate-semialdehyde dehydrogenase [acylating]; Aldehyde dehydrogenase family 6 member A1; EC 1.2.1.18; EC 1.2.1.27 (characterized) 30% 88% 233.8 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-threonine catabolism iolA lo Methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial; MMSDH; Malonate-semialdehyde dehydrogenase [acylating]; Aldehyde dehydrogenase family 6 member A1; EC 1.2.1.18; EC 1.2.1.27 (characterized) 30% 88% 233.8 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-valine catabolism iolA lo Methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial; MMSDH; Malonate-semialdehyde dehydrogenase [acylating]; Aldehyde dehydrogenase family 6 member A1; EC 1.2.1.18; EC 1.2.1.27 (characterized) 30% 88% 233.8 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1
L-lysine catabolism amaB lo aldehyde dehydrogenase (NAD+) (EC 1.2.1.3); L-aminoadipate-semialdehyde dehydrogenase (EC 1.2.1.31) (characterized) 32% 83% 226.5 betaine-aldehyde dehydrogenase (EC 1.2.1.8) 84% 818.1

Sequence Analysis Tools

View Pf1N1B4_2417 at FitnessBrowser

Find papers: PaperBLAST

Find functional residues: SitesBLAST

Search for conserved domains

Find the best match in UniProt

Compare to protein structures

Predict transmenbrane helices: Phobius

Predict protein localization: PSORTb

Find homologs in fast.genomics

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Sequence

MARFELQKLYIDGGYSDASSDATFEAINPANGEVLATVQRATKEDVERAVVSAEKGQKIW
AAMTAMERSRILRRAVDILRERNDELAALETLDTGKAYSETRYVDIVTGADVLEYYAGLV
PAIEGEQIPLRTTSFVYTRREPLGIVAGIGAWNYPIQIALWKSAPALAAGNAMIFKPSEV
TSLTTLKLAEIYTEAGLPAGVFNVLTGSGREVGTWLTEHPRIEKISFTGGTDTGKKVMAS
ASGSSLKDVTMELGGKSPLIIFDDADLDRAADTAMMANFYSSGQVCTNGTRVFVPSHLKA
AFEAKIVERVARIRVGNPEDENTNFGPLVSFAHMESVLGYIAKGKEEGARLLCGGDRLTD
GEFAKGAFVAPTVFTDCTDEMTIVREEIFGPVMSILTYETEEEVIRRANDTEFGLAAGVV
TKDLNRAHRVIHQLEAGICWINAWGESDAKMPVGGYKQSGVGRENGISSLNNFTRIKSVQ
VELGDYASVF

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory