catabolism of small carbon sources in Sphingomonas koreensis DSMZ 15582

GapMind for catabolism of small carbon sources

catabolism of small carbon sources in Sphingomonas koreensis DSMZ 15582

Pathways are sorted by completeness. Sort by name instead.

Pathway	Steps
histidine	Ga0059261_1577, hutH, hutU, hutI, hutF, hutG'
xylose	xylT, xdh, xylC, xad, kdaD, dopDH
NAG	nagF, nagEcb, nagA, nagB
cellobiose	bgl, MFS-glucose, glk
maltose	malI, susB, glk
proline	CCNA_00435, put1, putA
sucrose	ams, MFS-glucose, glk
trehalose	treF, MFS-glucose, glk
acetate	deh, acs
fructose	glcP, scrK
glucose	MFS-glucose, glk
glutamate	gltP, gdhA
aspartate	glt
fumarate	dctA
L-malate	dctA
2-oxoglutarate	kgtP
succinate	dctA
threonine	snatA, tdh, kbl, gcvP, gcvT, gcvH, lpd
glucosamine	nagX, nagF, nagEcb, nagA, nagB
ethanol	etoh-dh-nad, adh, acs
glucuronate	exuT, uxaC, uxuB, uxuA, kdgK, eda
asparagine	ans, glt
serine	snatA, sdaB
alanine	snatA
isoleucine	Bap2, bkdA, bkdB, bkdC, lpd, acdH, ech, ivdG, fadA, pccA, pccB, epi, mcm-large, mcm-small
valine	Bap2, bkdA, bkdB, bkdC, lpd, acdH, ech, bch, mmsB, mmsA, pccA, pccB, epi, mcm-large, mcm-small
leucine	leuT, ilvE, bkdA, bkdB, bkdC, lpd, liuA, liuB, liuD, liuC, liuE, atoA, atoD, atoB
4-hydroxybenzoate	pcaK, pobA, ligA, ligB, ligC, ligI, ligU, ligJ, ligK
phenylalanine	aroP, PAH, PCBD, QDPR, HPD, hmgA, maiA, fahA, atoA, atoD, atoB
tyrosine	aroP, HPD, hmgA, maiA, fahA, atoA, atoD, atoB
propionate	putP, prpE, pccA, pccB, epi, mcm-large, mcm-small
gluconate	gntT, gntK, edd, eda
D-lactate	lctP, glcD, glcE, glcF
galactose	HP1174, galdh, galactonolactonase, dgoD, dgoK, dgoA
lactose	lacA', lacC', lacB', klh, MFS-glucose, glk
rhamnose	rhaT, LRA1, LRA2, LRA3, LRA5, LRA6
citrate	SLC13A5, acn, icd
glycerol	glpF, glpK, glpD, tpi
galacturonate	exuT, uxaC, uxaB, uxaA, kdgK, eda
L-lactate	lctP, L-LDH
ribose	rbsU, rbsK
arginine	rocE, astA, astB, astC, astD, astE
mannose	gluP, man-isomerase, scrK
sorbitol	SOT, sdh, scrK
fucose	fucP, fucU, fdh, fuconolactonase, fucD, fucDH, KDF-hydrolase
glucose-6-P	uhpT
pyruvate	SLC5A8
deoxyribose	deoP, deoK, deoC, adh, acs
D-alanine	cycA, dadA
deoxyinosine	nupC, deoD, deoB, deoC, adh, acs
mannitol	PLT5, mt2d, scrK
D-serine	cycA, dsdA
tryptophan	aroP, tnaA
xylitol	fruI, x5p-reductase
arabinose	araE, xacB, xacC, xacD, xacE, xacF
thymidine	nupC, deoA, deoB, deoC, adh, acs
lysine	lysP, davB, davA, davT, davD, gcdG, gcdH, ech, fadB, atoB
deoxyribonate	deoxyribonate-transport, deoxyribonate-dehyd, ketodeoxyribonate-cleavage, garK, atoA, atoD, atoB
putrescine	puuP, patA, patD, gabT, gabD
citrulline	AO353_03055, AO353_03050, AO353_03045, AO353_03040, citrullinase, rocD, PRO3, put1, putA
myoinositol	iolF, iolG, iolM, iolN, iolO, uxaE, uxuB, uxuA, kdgK, eda
phenylacetate	paaT, paaK, paaA, paaB, paaC, paaE, paaG, paaZ1, paaZ2, paaJ1, paaF, paaH, paaJ2

Confidence: high confidence medium confidence low confidence
transporter – transporters and PTS systems are shaded because predicting their specificity is particularly challenging.

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

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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:

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