Protein WP_245258013.1 in Rhodomicrobium vannielii ATCC 17100

GapMind for catabolism of small carbon sources

Protein WP_245258013.1 in Rhodomicrobium vannielii ATCC 17100

Annotation: NCBI__GCF_000166055.1:WP_245258013.1

Length: 658 amino acids

Source: GCF_000166055.1 in NCBI

Candidate for 15 steps in catabolism of small carbon sources

Pathway	Step	Score	Similar to	Id.	Cov.	Bits	Other hit	Other id.	Other bits
4-hydroxybenzoate catabolism	acs	hi	Acetyl-coenzyme A synthetase (EC 6.2.1.1) (characterized)	57%	99%	776.2
4-hydroxybenzoate catabolism	acs	hi	acs: acetate--CoA ligase (EC 6.2.1.1) (TIGR02188)		99%	907.7
L-lactate catabolism	acs	hi	Acetyl-coenzyme A synthetase (EC 6.2.1.1) (characterized)	57%	99%	776.2
L-lactate catabolism	acs	hi	acs: acetate--CoA ligase (EC 6.2.1.1) (TIGR02188)		99%	907.7
acetate catabolism	acs	hi	Acetyl-coenzyme A synthetase (EC 6.2.1.1) (characterized)	57%	99%	776.2
acetate catabolism	acs	hi	acs: acetate--CoA ligase (EC 6.2.1.1) (TIGR02188)		99%	907.7
2'-deoxyinosine catabolism	acs	hi	Acetyl-coenzyme A synthetase (EC 6.2.1.1) (characterized)	57%	99%	776.2
2'-deoxyinosine catabolism	acs	hi	acs: acetate--CoA ligase (EC 6.2.1.1) (TIGR02188)		99%	907.7
2-deoxy-D-ribose catabolism	acs	hi	Acetyl-coenzyme A synthetase (EC 6.2.1.1) (characterized)	57%	99%	776.2
2-deoxy-D-ribose catabolism	acs	hi	acs: acetate--CoA ligase (EC 6.2.1.1) (TIGR02188)		99%	907.7
ethanol catabolism	acs	hi	Acetyl-coenzyme A synthetase (EC 6.2.1.1) (characterized)	57%	99%	776.2
ethanol catabolism	acs	hi	acs: acetate--CoA ligase (EC 6.2.1.1) (TIGR02188)		99%	907.7
L-threonine catabolism	acs	hi	Acetyl-coenzyme A synthetase (EC 6.2.1.1) (characterized)	57%	99%	776.2
L-threonine catabolism	acs	hi	acs: acetate--CoA ligase (EC 6.2.1.1) (TIGR02188)		99%	907.7
thymidine catabolism	acs	hi	Acetyl-coenzyme A synthetase (EC 6.2.1.1) (characterized)	57%	99%	776.2
thymidine catabolism	acs	hi	acs: acetate--CoA ligase (EC 6.2.1.1) (TIGR02188)		99%	907.7
L-tryptophan catabolism	acs	hi	Acetyl-coenzyme A synthetase (EC 6.2.1.1) (characterized)	57%	99%	776.2
L-tryptophan catabolism	acs	hi	acs: acetate--CoA ligase (EC 6.2.1.1) (TIGR02188)		99%	907.7
propionate catabolism	prpE	hi	Acetyl-coenzyme A synthetase; AcCoA synthetase; Acs; Acetate--CoA ligase; Acyl-activating enzyme; EC 6.2.1.1 (characterized)	54%	99%	760.8
2-deoxy-D-ribonate catabolism	aacS	lo	acetoacetate-CoA ligase (EC 6.2.1.16) (characterized)	31%	90%	248.4	Acetyl-coenzyme A synthetase (EC 6.2.1.1)	57%	776.2
2-deoxy-D-ribose catabolism	aacS	lo	acetoacetate-CoA ligase (EC 6.2.1.16) (characterized)	31%	90%	248.4	Acetyl-coenzyme A synthetase (EC 6.2.1.1)	57%	776.2
L-leucine catabolism	aacS	lo	acetoacetate-CoA ligase (EC 6.2.1.16) (characterized)	31%	90%	248.4	Acetyl-coenzyme A synthetase (EC 6.2.1.1)	57%	776.2
L-phenylalanine catabolism	aacS	lo	acetoacetate-CoA ligase (EC 6.2.1.16) (characterized)	31%	90%	248.4	Acetyl-coenzyme A synthetase (EC 6.2.1.1)	57%	776.2
L-tyrosine catabolism	aacS	lo	acetoacetate-CoA ligase (EC 6.2.1.16) (characterized)	31%	90%	248.4	Acetyl-coenzyme A synthetase (EC 6.2.1.1)	57%	776.2

Sequence Analysis Tools

View WP_245258013.1 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

MRQMVQSEVYPVPPEFAARAHVDAAAYERLYRWSIEDPDGFWKKEAAFLDWIKPFTEVSD
TSFDVNNFRVRWFADGTLNGSVNCIDRHLAAKADKPAVFWEGDTPGESRVVTWGELADKV
NRLANVLKSLGVGKGDVVAIYLPVIPEVMVAMMATIRIGAVHTVVFSGFSAESLENRIAD
SKAKVLITADEGFRGGRISPLKRNADDAVRNQPSIEHVIVVRRSGAEVPFTPGRDLWYDE
ATEAADPWCEPVEVGAEDPLFILYTSGSTGKPKGLVHTTAGYLVHAGTSWRIIFDWHEGD
VFWSTADVGWVTAHSYKLYGPLLNGATTVMFEGVPSWPDASRWWSIIEKHRVNIFYTAPT
ALRSLMREGEAPVRKHDLSSLRVLGSVGEPINPEAWRWFHSVIGGGRCPIVDNYWQTETG
AVTLVPIPGAIPNKPGMAAKPYFGIRPEVVSPEGVTLEGPAEGNMCFRGSWPGQARTILH
DHERFLKTYFAPFPGRFFSGDGVTRDEDGYYRIAGRVDDVINVSGHRLGTVELESAIASH
PAVAEAAVVGYNHDVKGQGVFAYVTLKADMPETEELRAEIRQWVRARISPIASPDIVQWA
PALPKNRAGKILRRILLKIANNDFSDFGDTSTLADASVVEDIIARRKAELAKLTRENA

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.

Downloads

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 2024 update 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