GapMind for catabolism of small carbon sources

 

Protein WP_089301742.1 in Haloechinothrix alba DSM 45207

Annotation: NCBI__GCF_900188115.1:WP_089301742.1

Length: 477 amino acids

Source: GCF_900188115.1 in NCBI

Candidate for 26 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 aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized) 41% 96% 343.2 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
L-citrulline catabolism patD med aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized) 41% 96% 343.2 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
putrescine catabolism patD med aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized) 41% 96% 343.2 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
4-hydroxybenzoate catabolism praB med aminomuconate-semialdehyde dehydrogenase (EC 1.2.1.32) (characterized) 40% 94% 307 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
L-tryptophan catabolism nbaE med aminomuconate-semialdehyde dehydrogenase (EC 1.2.1.32) (characterized) 40% 94% 307 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
L-tryptophan catabolism praB med aminomuconate-semialdehyde dehydrogenase (EC 1.2.1.32) (characterized) 40% 94% 307 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
L-arginine catabolism puuC lo 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized) 38% 94% 312.8 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
L-citrulline catabolism puuC lo 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized) 38% 94% 312.8 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
putrescine catabolism puuC lo 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized) 38% 94% 312.8 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
L-valine catabolism mmsA lo methylmalonate-semialdehyde dehydrogenase (CoA-acylating) (EC 1.2.1.27) (characterized) 34% 95% 250 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
L-arginine catabolism putA lo L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized) 35% 89% 247.7 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
L-arginine catabolism rocA lo L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized) 35% 89% 247.7 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
L-citrulline catabolism putA lo L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized) 35% 89% 247.7 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
L-citrulline catabolism rocA lo L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized) 35% 89% 247.7 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
L-proline catabolism putA lo L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized) 35% 89% 247.7 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
L-isoleucine catabolism iolA lo malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized) 33% 96% 228.4 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
myo-inositol catabolism mmsA lo malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized) 33% 96% 228.4 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
propionate catabolism iolA lo malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized) 33% 96% 228.4 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
L-threonine catabolism iolA lo malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized) 33% 96% 228.4 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
L-valine catabolism iolA lo malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized) 33% 96% 228.4 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
L-arginine catabolism astD lo N-succinylglutamate 5-semialdehyde dehydrogenase; Succinylglutamic semialdehyde dehydrogenase; SGSD; EC 1.2.1.71 (characterized) 34% 94% 216.1 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
L-citrulline catabolism astD lo N-succinylglutamate 5-semialdehyde dehydrogenase; Succinylglutamic semialdehyde dehydrogenase; SGSD; EC 1.2.1.71 (characterized) 34% 94% 216.1 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
L-arabinose catabolism xacF lo Alpha-ketoglutaric semialdehyde dehydrogenase 2; alphaKGSA dehydrogenase 2; 2,5-dioxovalerate dehydrogenase 2; KGSADH-II; EC 1.2.1.26 (characterized) 30% 61% 100.5 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
D-galacturonate catabolism dopDH lo Alpha-ketoglutaric semialdehyde dehydrogenase 2; alphaKGSA dehydrogenase 2; 2,5-dioxovalerate dehydrogenase 2; KGSADH-II; EC 1.2.1.26 (characterized) 30% 61% 100.5 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
D-glucuronate catabolism dopDH lo Alpha-ketoglutaric semialdehyde dehydrogenase 2; alphaKGSA dehydrogenase 2; 2,5-dioxovalerate dehydrogenase 2; KGSADH-II; EC 1.2.1.26 (characterized) 30% 61% 100.5 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5
D-xylose catabolism dopDH lo Alpha-ketoglutaric semialdehyde dehydrogenase 2; alphaKGSA dehydrogenase 2; 2,5-dioxovalerate dehydrogenase 2; KGSADH-II; EC 1.2.1.26 (characterized) 30% 61% 100.5 3-succinoylsemialdehyde-pyridine dehydrogenase; SAPD; EC 1.2.1.83 52% 464.5

Sequence Analysis Tools

View WP_089301742.1 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

MAAPATTRIGHFVDGQTRYESSESIDVFDPASEEVIGSVPAGTRAEVDSAVAAARRAFPE
WSARPVAERAEVVRAISNGIAARRDAIAADITADVGAPITFATKVQAVLPAATSEAVADL
LSSGEFSFREEIGNSLVEREPVGVVAAITPWNYPLHQIMAKIAPALAAGCTVVLKPSEVA
PLCTRHLVDVLTEAGVPAGVVNIVHGTGPEVGAALAGHEDVDMVSFTGSTRGGRAVSAAA
ADTIKRVALELGGKSANVVLDDADLGKAVKLGVANAFLNGGQSCNAWTRMLVPESLHDEA
VSLACEAAAKYEPGDPTDGSTRLGPLVSETQRDKVVGFIRSGVESGATLAFGGPERPDDR
DTGYFVRPTVFAGVRPDVTVAQEEIFGPVLCVIPYSDEDDAVRIANSTVYGLAGAVFSGS
DERALSVARRMRTGQVDINGGAFNPLAPFGGYKQSGTGREFGKYGIEEFCEVKSIQR

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