GapMind for catabolism of small carbon sources

 

L-tyrosine catabolism in Brucella inopinata BO1

Best path

aroP, HPD, hmgA, maiA, fahA, aacS, atoB

Rules

Overview: Tyrosine utilization in GapMind is based on MetaCyc pathway tyrosine degradation I, via homogentisate (link). This pathway requires oxygen. Another pathway via 4-hydroxyphenylacetate is known (link), but the 4-hydroxyphenylpyruvate oxidase has not been linked to sequence. The other MetaCyc pathways do not yield fixed carbon or are not reported in prokaryotes.

19 steps (12 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
aroP L-tyrosine transporter (AroP/FywP) BIBO1_RS14845
HPD 4-hydroxyphenylpyruvate dioxygenase
hmgA homogentisate dioxygenase
maiA maleylacetoacetate isomerase BIBO1_RS08965 BIBO1_RS10995
fahA fumarylacetoacetate hydrolase BIBO1_RS12805
aacS acetoacetyl-CoA synthetase BIBO1_RS06845 BIBO1_RS13010
atoB acetyl-CoA C-acetyltransferase BIBO1_RS17190 BIBO1_RS16830
Alternative steps:
Ac3H11_1692 L-tyrosine ABC transporter, ATPase component 2 BIBO1_RS12235 BIBO1_RS14990
Ac3H11_1693 L-tyrosine ABC transporter, ATPase component 1 BIBO1_RS12240 BIBO1_RS19765
Ac3H11_1694 L-tyrosine ABC transporter, permease component 2 BIBO1_RS12245
Ac3H11_1695 L-tyrosine ABC transporter, permease component 1 BIBO1_RS12250
Ac3H11_2396 L-tyrosine ABC transporter, substrate-binding component component BIBO1_RS12225 BIBO1_RS12220
atoA acetoacetyl-CoA transferase, A subunit BIBO1_RS16820
atoD acetoacetyl-CoA transferase, B subunit BIBO1_RS16825
CAT L-tyrosine transporter CAT
MCT10 L-tyrosine transporter MCT10
TAT1 L-tyrosine permease TAT1
tyrP Tyrosine permease
tyt1 L-tyrosine:Na+ symporter Tyt1

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.

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