GapMind for catabolism of small carbon sources

 

L-tyrosine catabolism in Klebsiella michiganensis M5al

Best path

Ac3H11_2396, Ac3H11_1695, Ac3H11_1694, Ac3H11_1693, Ac3H11_1692, HPD, hmgA, maiA, fahA, atoA, atoD, atoB

Also see fitness data for the top candidates

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 (15 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
Ac3H11_2396 L-tyrosine ABC transporter, substrate-binding component component BWI76_RS07260 BWI76_RS26350
Ac3H11_1695 L-tyrosine ABC transporter, permease component 1 BWI76_RS07280 BWI76_RS26345
Ac3H11_1694 L-tyrosine ABC transporter, permease component 2 BWI76_RS07275 BWI76_RS26340
Ac3H11_1693 L-tyrosine ABC transporter, ATPase component 1 BWI76_RS07270 BWI76_RS05980
Ac3H11_1692 L-tyrosine ABC transporter, ATPase component 2 BWI76_RS07265 BWI76_RS05975
HPD 4-hydroxyphenylpyruvate dioxygenase BWI76_RS16945
hmgA homogentisate dioxygenase
maiA maleylacetoacetate isomerase BWI76_RS19575 BWI76_RS25335
fahA fumarylacetoacetate hydrolase BWI76_RS03870
atoA acetoacetyl-CoA transferase, A subunit BWI76_RS16145
atoD acetoacetyl-CoA transferase, B subunit BWI76_RS16140
atoB acetyl-CoA C-acetyltransferase BWI76_RS23445 BWI76_RS01360
Alternative steps:
aacS acetoacetyl-CoA synthetase BWI76_RS17800 BWI76_RS23695
aroP L-tyrosine transporter (AroP/FywP) BWI76_RS04870 BWI76_RS07360
CAT L-tyrosine transporter CAT
MCT10 L-tyrosine transporter MCT10
TAT1 L-tyrosine permease TAT1 BWI76_RS06025 BWI76_RS07360
tyrP Tyrosine permease BWI76_RS18295 BWI76_RS25050
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 17 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 against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer. 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. 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 the paper from 2019 on GapMind for amino acid biosynthesis, or view the source code.

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