GapMind for catabolism of small carbon sources

 

Protein WP_034527751.1 in Lactobacillus oryzae SG293

Annotation: NCBI__GCF_000740055.1:WP_034527751.1

Length: 473 amino acids

Source: GCF_000740055.1 in NCBI

Candidate for 25 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-arginine catabolism gabD hi succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) (characterized) 56% 99% 520.8
L-citrulline catabolism gabD hi succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) (characterized) 56% 99% 520.8
putrescine catabolism gabD hi succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) (characterized) 56% 99% 520.8
4-hydroxybenzoate catabolism adh lo Aldehyde dehydrogenase; NAD/NADP-dependent aldehyde dehydrogenase; EC 1.2.1.3; EC 1.2.1.4 (characterized) 37% 100% 312.4 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
2'-deoxyinosine catabolism adh lo Aldehyde dehydrogenase; NAD/NADP-dependent aldehyde dehydrogenase; EC 1.2.1.3; EC 1.2.1.4 (characterized) 37% 100% 312.4 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
2-deoxy-D-ribose catabolism adh lo Aldehyde dehydrogenase; NAD/NADP-dependent aldehyde dehydrogenase; EC 1.2.1.3; EC 1.2.1.4 (characterized) 37% 100% 312.4 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
ethanol catabolism adh lo Aldehyde dehydrogenase; NAD/NADP-dependent aldehyde dehydrogenase; EC 1.2.1.3; EC 1.2.1.4 (characterized) 37% 100% 312.4 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
L-threonine catabolism adh lo Aldehyde dehydrogenase; NAD/NADP-dependent aldehyde dehydrogenase; EC 1.2.1.3; EC 1.2.1.4 (characterized) 37% 100% 312.4 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
thymidine catabolism adh lo Aldehyde dehydrogenase; NAD/NADP-dependent aldehyde dehydrogenase; EC 1.2.1.3; EC 1.2.1.4 (characterized) 37% 100% 312.4 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
L-tryptophan catabolism adh lo Aldehyde dehydrogenase; NAD/NADP-dependent aldehyde dehydrogenase; EC 1.2.1.3; EC 1.2.1.4 (characterized) 37% 100% 312.4 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
L-arginine catabolism davD lo Glutarate-semialdehyde dehydrogenase (EC 1.2.1.20) (characterized) 35% 93% 267.3 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
L-citrulline catabolism davD lo Glutarate-semialdehyde dehydrogenase (EC 1.2.1.20) (characterized) 35% 93% 267.3 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
L-lysine catabolism davD lo Glutarate-semialdehyde dehydrogenase (EC 1.2.1.20) (characterized) 35% 93% 267.3 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
L-proline catabolism davD lo Glutarate-semialdehyde dehydrogenase (EC 1.2.1.20) (characterized) 35% 93% 267.3 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
L-fucose catabolism aldA lo NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized) 32% 92% 245.7 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
L-rhamnose catabolism aldA lo NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized) 32% 92% 245.7 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
L-threonine catabolism aldA lo NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized) 32% 92% 245.7 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
L-arginine catabolism patD lo aminobutyraldehyde dehydrogenase (EC 1.2.1.19); betaine-aldehyde dehydrogenase (EC 1.2.1.8) (characterized) 31% 93% 233.4 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
L-citrulline catabolism patD lo aminobutyraldehyde dehydrogenase (EC 1.2.1.19); betaine-aldehyde dehydrogenase (EC 1.2.1.8) (characterized) 31% 93% 233.4 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
putrescine catabolism patD lo aminobutyraldehyde dehydrogenase (EC 1.2.1.19); betaine-aldehyde dehydrogenase (EC 1.2.1.8) (characterized) 31% 93% 233.4 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
L-arabinose catabolism xacF lo Alpha-ketoglutaric semialdehyde dehydrogenase 1; alphaKGSA dehydrogenase 1; 2,5-dioxovalerate dehydrogenase 1; 2-oxoglutarate semialdehyde dehydrogenase 1; KGSADH-I; Succinate-semialdehyde dehydrogenase [NAD(+)]; SSDH; EC 1.2.1.26; EC 1.2.1.24 (characterized) 33% 90% 230.3 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
D-galacturonate catabolism dopDH lo Alpha-ketoglutaric semialdehyde dehydrogenase 1; alphaKGSA dehydrogenase 1; 2,5-dioxovalerate dehydrogenase 1; 2-oxoglutarate semialdehyde dehydrogenase 1; KGSADH-I; Succinate-semialdehyde dehydrogenase [NAD(+)]; SSDH; EC 1.2.1.26; EC 1.2.1.24 (characterized) 33% 90% 230.3 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
D-glucuronate catabolism dopDH lo Alpha-ketoglutaric semialdehyde dehydrogenase 1; alphaKGSA dehydrogenase 1; 2,5-dioxovalerate dehydrogenase 1; 2-oxoglutarate semialdehyde dehydrogenase 1; KGSADH-I; Succinate-semialdehyde dehydrogenase [NAD(+)]; SSDH; EC 1.2.1.26; EC 1.2.1.24 (characterized) 33% 90% 230.3 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
D-xylose catabolism dopDH lo Alpha-ketoglutaric semialdehyde dehydrogenase 1; alphaKGSA dehydrogenase 1; 2,5-dioxovalerate dehydrogenase 1; 2-oxoglutarate semialdehyde dehydrogenase 1; KGSADH-I; Succinate-semialdehyde dehydrogenase [NAD(+)]; SSDH; EC 1.2.1.26; EC 1.2.1.24 (characterized) 33% 90% 230.3 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8
L-lysine catabolism patD lo aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized) 31% 93% 222.2 succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) 56% 520.8

Sequence Analysis Tools

View WP_034527751.1 at NCBI

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

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Sequence

MAYKTVNPFTNEVVKTYPDATSEQVENALQATHKLFKQWELEGPETRADQLHEIARLMRE
DSDHLAEVMVTDMGKLFREAKGEVELCAIIADYFADHGADLLKPTTIDTIATGTAKVLKH
PTGVLMMVEPWNFPYYQIMRVFAPNFMVGNPMILKHASNTPGSAVAFENVVKQSSAPDAS
LINLFVNYDQVSDIIADPRVQGVALTGSERGGRSVATEAGKNLKKNTMELGGTDAFIVLD
DTDIDTVSEIAWRARLYNAGQVCTSSKRFIVADNLYDQFVAKLKENFASVKPGDPMAANT
TLAPMNTKRAKDKLQSQVDEAIASGATLVYGNEPIDLPGQFFQPTILTDIKPDNPAYSEE
MFGPVAEVYKVHSDQEAIDLANDSQLGLGGIVFSGNPKRGEKVAAQIETGMVFVNNFMVS
LPELPFGGVKESGYGREMSAIGINAFVNEQLIVTADAPDMSNLAGGLVATDPE

This GapMind analysis is from Sep 24 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