GapMind for catabolism of small carbon sources

 

Protein WP_099619149.1 in Marinobacter guineae M3B

Annotation: NCBI__GCF_002744735.1:WP_099619149.1

Length: 505 amino acids

Source: GCF_002744735.1 in NCBI

Candidate for 19 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-arginine catabolism kauB hi 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized) 70% 100% 725.7 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) 57% 568.5
L-arginine catabolism puuC hi 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized) 70% 100% 725.7 aldehyde dehydrogenase 55% 547.7
L-citrulline catabolism puuC hi 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized) 70% 100% 725.7 aldehyde dehydrogenase 55% 547.7
putrescine catabolism puuC hi 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized) 70% 100% 725.7 aldehyde dehydrogenase 55% 547.7
L-arginine catabolism gabD med 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized) 57% 99% 568.5 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) 70% 725.7
L-arginine catabolism patD med 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized) 57% 99% 568.5 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) 70% 725.7
L-citrulline catabolism gabD med 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized) 57% 99% 568.5 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) 70% 725.7
L-citrulline catabolism patD med 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized) 57% 99% 568.5 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) 70% 725.7
putrescine catabolism gabD med 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized) 57% 99% 568.5 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) 70% 725.7
putrescine catabolism patD med 4-(gamma-glutamylamino)butanal dehydrogenase (EC 1.2.1.99) (characterized) 57% 99% 568.5 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) 70% 725.7
L-phenylalanine catabolism pad-dh med aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized) 43% 92% 390.6 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) 70% 725.7
L-fucose catabolism aldA med NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized) 42% 94% 376.3 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) 70% 725.7
L-rhamnose catabolism aldA med NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized) 42% 94% 376.3 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) 70% 725.7
L-threonine catabolism aldA med NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized) 42% 94% 376.3 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) 70% 725.7
L-arginine catabolism putA lo L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized) 30% 84% 154.8 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) 70% 725.7
L-arginine catabolism rocA lo L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized) 30% 84% 154.8 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) 70% 725.7
L-citrulline catabolism putA lo L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized) 30% 84% 154.8 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) 70% 725.7
L-citrulline catabolism rocA lo L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized) 30% 84% 154.8 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) 70% 725.7
L-proline catabolism putA lo L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized) 30% 84% 154.8 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) 70% 725.7

Sequence Analysis Tools

View WP_099619149.1 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

Find homologs in fast.genomics

Fitness BLAST: loading...

Sequence

MNQSTYSTTPTDQAGWQALADQLTLEGRAYVDGAYQWASNNETFACISPVDGRELAQIAS
CDQADAELAVAAARKAFESGAWSHLAPTKRKAVLLRFADLIDAHGDELALLETLDMGKPI
GHARAVDVPATVRAIRWTAEAIDKVYGELAATPHDQIGMISREPIGVVAAIVPWNFPMIM
ASWKIAPALAAGNSVILKPSEKSPLTAIRLAALAEEAGIPNGVFNVLPGYGHTVGKALAL
HMDVDCLVFTGSTNVAKQLMIYAGQSNMKRVWLEAGGKSPNIVFADAPDLKKAAAEAASA
IAFNQGEVCTAGSRLLVEESIRTEFLGLIREALTTWRPGHPLDPATTCGAIVDQAQLDRI
IEYIGIGKSEGATLVEGGKRVMEETGGLFVQPTVFDGVNNRMRIASEEIFGPVLSVIGFN
TAEEAITIANDSIYGLAAAVWTSNINTAHKVAKALKAGSVWINHYDGGDMTAPFGGFKQS
GNGRDKSLHAFDKYTEIKATWLVIE

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