Protein GFF2285 in Phaeobacter inhibens BS107

GapMind for catabolism of small carbon sources

Protein GFF2285 in Phaeobacter inhibens BS107

Annotation: FitnessBrowser__Phaeo:GFF2285

Length: 474 amino acids

Source: Phaeo in FitnessBrowser

Candidate for 22 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; SsaDH; EC 1.2.1.16 (characterized)	54%	99%	481.1
L-citrulline catabolism	gabD	hi	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16 (characterized)	54%	99%	481.1
putrescine catabolism	gabD	hi	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16 (characterized)	54%	99%	481.1
L-arginine catabolism	davD	med	Glutarate-semialdehyde dehydrogenase; EC 1.2.1.- (characterized)	44%	96%	416.8	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1
L-citrulline catabolism	davD	med	Glutarate-semialdehyde dehydrogenase; EC 1.2.1.- (characterized)	44%	96%	416.8	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1
L-lysine catabolism	davD	med	Glutarate-semialdehyde dehydrogenase; EC 1.2.1.- (characterized)	44%	96%	416.8	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1
L-proline catabolism	davD	med	Glutarate-semialdehyde dehydrogenase; EC 1.2.1.- (characterized)	44%	96%	416.8	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1
4-hydroxybenzoate catabolism	adh	med	aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)	44%	90%	393.7	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1
2'-deoxyinosine catabolism	adh	med	aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)	44%	90%	393.7	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1
2-deoxy-D-ribose catabolism	adh	med	aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)	44%	90%	393.7	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1
ethanol catabolism	adh	med	aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)	44%	90%	393.7	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1
L-threonine catabolism	adh	med	aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)	44%	90%	393.7	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1
thymidine catabolism	adh	med	aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)	44%	90%	393.7	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1
L-tryptophan catabolism	adh	med	aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)	44%	90%	393.7	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1
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)	39%	99%	330.5	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1
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)	39%	99%	330.5	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1
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)	39%	99%	330.5	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1
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)	39%	99%	330.5	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1
L-arabinose catabolism	aldA	lo	lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)	34%	97%	298.9	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1
D-xylose catabolism	aldA	lo	lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)	34%	97%	298.9	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1
L-arginine catabolism	astD	lo	Succinylglutamic semialdehyde dehydrogenase (EC 1.2.1.71) (characterized)	32%	93%	201.1	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1
L-citrulline catabolism	astD	lo	Succinylglutamic semialdehyde dehydrogenase (EC 1.2.1.71) (characterized)	32%	93%	201.1	Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16	54%	481.1

Sequence Analysis Tools

View GFF2285 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

Fitness BLAST: loading...

Sequence

MEYTDLYINGAWHKTSERFDVINPATEEVLASVASADIADADAALDAAEAAMKDWAARTP
RQRSEVLRKAWELMTKRLDYFANLITLENGKAGTDAKGEATYAAEFFRWFAEEAVRADGM
ITHAPASGARIVVQHKPAGLAVLVTPWNYPAAMGTRKIAPALAAGCGVIIKPASETPLTM
LALMPLLEEAGVPAGLVNVLPSRKTGSLVDHMLHDPRIRVVSFTGSTGVGRKLLKGAADQ
VLKPAMELGGNAPVVVFEDADMDVAIEGTMLAKMRNLGEACTAANRIYVHEDIADEFTKR
LSAAMSALKVGDGTDPSVDVGPLVNADTRDKVAAFVADAVAKGAKVECGGTTPNGKGFYY
PPTVLSNVSEDAECVRDEIFGPVAAIQTFTNQDEVIARANDTEYGLVAYVFSEDFKRALQ
VCEQLEYGMVGLNRGLVSDPAAPFGGVKQSGLGREGGHEGMLEFMETQYISASW

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

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Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

Related tools

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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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:

the paper from 2019 on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources