GapMind for Amino acid biosynthesis

 

L-arginine biosynthesis in Chlorobium phaeobacteroides BS1

Best path

argJ, argB, argC, argD, carA, carB*, argI, argG, argH

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 (17 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
argJ ornithine acetyltransferase Cphamn1_1336
argB N-acylglutamate kinase Cphamn1_1335
argC N-acylglutamylphosphate reductase Cphamn1_1337
argD N-acetylornithine aminotransferase Cphamn1_0638 Cphamn1_0202
carA carbamoyl phosphate synthase subunit alpha Cphamn1_2349
carB* carbamoyl phosphate synthase subunit beta Cphamn1_0534 with Cphamn1_0628
argI ornithine carbamoyltransferase Cphamn1_1334 Cphamn1_1767
argG arginosuccinate synthetase Cphamn1_1332
argH argininosuccinate lyase Cphamn1_1327
Alternative steps:
argA N-acylglutamate synthase Cphamn1_1336 Cphamn1_2308
argD'B N-succinylornithine aminotransferase Cphamn1_0638 Cphamn1_2453
argE N-acetylornithine deacetylase Cphamn1_1324
argE'B N-succinylcitrulline desuccinylase
argF' acetylornithine transcarbamoylase Cphamn1_1334
argF'B N-succinylornithine carbamoyltransferase Cphamn1_1334
argX glutamate--LysW ligase
lysJ [LysW]-glutamate-semialdehyde aminotransferase Cphamn1_0202 Cphamn1_0638
lysK [LysW]-ornithine hydrolase
lysW 2-aminoadipate/glutamate carrier protein
lysY [LysW]-glutamate-6-phosphate reductase Cphamn1_1337
lysZ [LysW]-glutamate kinase Cphamn1_1335

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 Apr 09 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

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:

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