GapMind for Amino acid biosynthesis

 

L-arginine biosynthesis in Herbaspirillum seropedicae SmR1

Best path

argA, argB, argC, argD, argE, carA, carB, argI, argG, argH

Also see fitness data for the top candidates

Rules

Overview: Arginine biosynthesis in GapMind is based on MetaCyc pathways L-arginine biosynthesis I via L-acetyl-ornithine (link), II (acetyl cycle) (link), III via N-acetyl-L-citrulline (link), or IV via LysW-ornithine (link). GapMind also includes L-arginine biosynthesis with succinylated intermediates, as in Bacteroidetes (PMC5764234). These pathways all involve the activation of glutamate (by aceylation, succinylation, or attachment of LysW), followed by phosphorylation, reduction and transamination, to activated ornithine. In most pathways, this intermediate is cleaved to ornithine before transcarbamoylation, but in the N-acetylcitrulline or succinylated pathways, transcarbamoylation occurs before hydrolysis. In the final two steps, citrulline is converted to arginine by ArgG and ArgH.

21 steps (16 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
argA N-acylglutamate synthase HSERO_RS17320 HSERO_RS01730
argB N-acylglutamate kinase HSERO_RS21495 HSERO_RS08035
argC N-acylglutamylphosphate reductase HSERO_RS19210 HSERO_RS14025
argD N-acetylornithine aminotransferase HSERO_RS16670 HSERO_RS05420
argE N-acetylornithine deacetylase HSERO_RS13940 HSERO_RS16100
carA carbamoyl phosphate synthase subunit alpha HSERO_RS06920
carB carbamoyl phosphate synthase subunit beta HSERO_RS06925
argI ornithine carbamoyltransferase HSERO_RS07185
argG arginosuccinate synthetase HSERO_RS07180
argH arginosuccinate lyase HSERO_RS14685
Alternative steps:
argD'B N-succinylornithine aminotransferase HSERO_RS16670 HSERO_RS17580
argE'B N-succinylcitrulline desuccinylase
argF' acetylornithine transcarbamoylase HSERO_RS07185
argF'B N-succinylornithine carbamoyltransferase
argJ ornithine acetyltransferase HSERO_RS01730
argX glutamate--LysW ligase
lysJ [LysW]-2-aminoadipate semialdehyde transaminase / [LysW]-glutamate semialdehyde transaminase HSERO_RS16670 HSERO_RS05420
lysK [LysW]-lysine hydrolase / [LysW]-ornithine hydrolase
lysW 2-aminoadipate/glutamate carrier protein
lysY [LysW]-2-aminoadipate 6-phosphate reductase / [LysW]-glutamylphosphate reductase HSERO_RS19210
lysZ [LysW]-2-aminoadipate 6-kinase / [LysW]-glutamate kinase HSERO_RS21495

Confidence: high confidence medium confidence low confidence
? – known gap: despite the lack of a good candidate for this step, this organism (or a related organism) performs the pathway

This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 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