GapMind for catabolism of small carbon sources

 

L-arginine catabolism in Dyella jiangningensis SBZ3-12

Best path

rocE, rocF, rocD, PRO3, put1, putA

Rules

Overview: Arginine utilization in GapMind is based on MetaCyc pathways L-arginine degradation I via arginase (link); II via arginine succinyltransferase (link), III via arginine decarboxylase and agmatinase (link), IV via arginine decarboxylase and agmatine deiminase (link), V via arginine deiminase (link), VI (arginase 2, link), VII (arginase 3, link), VIII via arginase oxidase (link), IX via arginine:pyruvate transaminase (link), X via arginine monooxygenase (link), XIII via proline (link), and XIV via D-ornithine (link). Common intermediates are L-ornithine or L-proline. GapMind does not include pathways XI (link), which is poorly understood, or XII (link), which is not reported in prokaryotes.

71 steps (35 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
rocE L-arginine permease BLQ78_RS08805 BLQ78_RS03050
rocF arginase BLQ78_RS12020
rocD ornithine aminotransferase BLQ78_RS08910 BLQ78_RS10980
PRO3 pyrroline-5-carboxylate reductase BLQ78_RS09780
put1 proline dehydrogenase BLQ78_RS22330
putA L-glutamate 5-semialdeyde dehydrogenase BLQ78_RS22330 BLQ78_RS22185
Alternative steps:
AAP3 L-arginine transporter AAP3
adiA arginine decarboxylase (AdiA/SpeA) BLQ78_RS19965 BLQ78_RS20800
aguA agmatine deiminase BLQ78_RS03965
aguB N-carbamoylputrescine hydrolase BLQ78_RS03970
arcA arginine deiminase
arcB ornithine carbamoyltransferase BLQ78_RS15265 BLQ78_RS09745
arcC carbamate kinase
arg-monooxygenase arginine 2-monooxygenase
aroD L-arginine oxidase
artJ L-arginine ABC transporter, periplasmic substrate-binding component ArtJ/HisJ/ArtI/AotJ/ArgT
artM L-arginine ABC transporter, permease component 1 (ArtM/HisM/AotM)
artP L-arginine ABC transporter, ATPase component ArtP/HisP/AotP/BgtA BLQ78_RS18995 BLQ78_RS06240
artQ L-arginine ABC transporter, permease component 2 (ArtQ/HisQ/AotQ)
aruF ornithine/arginine N-succinyltransferase subunit AruAI (AruF)
aruG ornithine/arginine N-succinyltransferase subunit AruAII (AruG)
aruH L-arginine:pyruvate transaminase BLQ78_RS03865 BLQ78_RS00200
aruI 2-ketoarginine decarboxylase BLQ78_RS07905
astA arginine N-succinyltransferase
astB N-succinylarginine dihydrolase
astC succinylornithine transaminase BLQ78_RS10980 BLQ78_RS09675
astD succinylglutamate semialdehyde dehydrogenase BLQ78_RS04710 BLQ78_RS22185
astE succinylglutamate desuccinylase
atoB acetyl-CoA C-acetyltransferase BLQ78_RS14970 BLQ78_RS03030
bgtB L-arginine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
braC ABC transporter for glutamate, histidine, arginine, and other amino acids, substrate-binding component BraC
braD ABC transporter for glutamate, histidine, arginine, and other amino acids, permease component 1 (BraD)
braE ABC transporter for glutamate, histidine, arginine, and other amino acids, permease component 2 (BraE)
braF ABC transporter for glutamate, histidine, arginine, and other amino acids, ATPase component 1 (BraF) BLQ78_RS20900 BLQ78_RS07820
braG ABC transporter for glutamate, histidine, arginine, and other amino acids, ATPase component 2 (BraG) BLQ78_RS16735 BLQ78_RS09090
Can1 L-arginine transporter Can1
CAT1 L-arginine transporter CAT1 BLQ78_RS06275 BLQ78_RS06270
davD glutarate semialdehyde dehydrogenase BLQ78_RS02465 BLQ78_RS22185
davT 5-aminovalerate aminotransferase BLQ78_RS10980 BLQ78_RS10985
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase BLQ78_RS19345 BLQ78_RS07700
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase BLQ78_RS03025 BLQ78_RS14055
gabD succinate semialdehyde dehydrogenase BLQ78_RS22185 BLQ78_RS18940
gabT gamma-aminobutyrate transaminase BLQ78_RS09675 BLQ78_RS10980
gbamidase guanidinobutyramidase
gbuA guanidinobutyrase
gcdG succinyl-CoA:glutarate CoA-transferase
gcdH glutaryl-CoA dehydrogenase BLQ78_RS04735 BLQ78_RS04630
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
kauB 4-guanidinobutyraldehyde dehydrogenase BLQ78_RS22185 BLQ78_RS02465
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO)
ocd ornithine cyclodeaminase
odc L-ornithine decarboxylase BLQ78_RS20800
oraE D-ornithine 4,5-aminomutase, beta (E) subunit
oraS D-ornithine 4,5-aminomutase, alpha (S) subunit
ord 2,4-diaminopentanoate dehydrogenase
orr ornithine racemase
ortA 2-amino-4-oxopentanoate thiolase, alpha subunit
ortB 2-amino-4-oxopentanoate thiolase, beta subunit
patA putrescine aminotransferase (PatA/SpuC) BLQ78_RS09675 BLQ78_RS10980
patD gamma-aminobutyraldehyde dehydrogenase BLQ78_RS22185 BLQ78_RS02465
prdA D-proline reductase, prdA component
prdB D-proline reductase, prdB component
prdC D-proline reductase, electron transfer component PrdC
prdF proline racemase BLQ78_RS14870
puo putrescine oxidase
puuA glutamate-putrescine ligase BLQ78_RS13685
puuB gamma-glutamylputrescine oxidase BLQ78_RS04065
puuC gamma-glutamyl-gamma-aminobutyraldehyde dehydrogenase BLQ78_RS22185 BLQ78_RS02465
puuD gamma-glutamyl-gamma-aminobutyrate hydrolase
rocA 1-pyrroline-5-carboxylate dehydrogenase BLQ78_RS22330 BLQ78_RS22185
speB agmatinase

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 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