putrescine catabolism in Mycolicibacterium vanbaalenii PYR-1

GapMind for catabolism of small carbon sources

putrescine catabolism in Mycolicibacterium vanbaalenii PYR-1

Best path

Rules

Overview: Putrescine degradation in GapMind is based on MetaCyc pathways putrescine degradation I via putrescine aminotransferase (link), pathway II with glutamylated intermediates (link), pathway IV via putrescine oxidase (link), or pathway V via putrescine:pyruvate aminotransferase (link). Pathway III is not reported in prokaryotes, so it is not included in GapMind.

all: putrescine-transport and putrescine-degradation
putrescine-degradation: putrescine-to-GABA and GABA-degradation

Comment: Gamma-aminobutyrate is a common intermediate.

putrescine-to-GABA:

patA and patD
or puuA, puuB, puuC and puuD
or puo and patD
Comment: In pathway I or pathway V, putrescine aminotransferase (patA or spuC) forms 4-aminobutanal, and dehydrogenase patD forms GABA. In pathway II, putrescine is converted to GABA with glutamylated intermedates: puuA forms gamma-glutamyl-putrescine, an oxidase forms 4-(gamma-glutaminylamino)butanal, a dehydrogenase forms 4-(gamma-glutamylamino)butanoate, and a hydrolase releases glutamate and GABA. As part of pathway IV, putrescine oxidase (puo) forms 4-aminobutanal, which is probably converted to GABA by dehydrogenase patD.

GABA-degradation: gabT and gabD

Comment: GABA (4-aminobutanoate) is consumed by an aminotransferase (known as gabT or puuE), which forms succinate semialdehyde, and dehydrogenase gabD, which forms succinate.

putrescine-transport:

potA, potB, potC and potD
or puuP
or potE
or TPO1
or UGA4
or POT1
Comment: Transporters were identified using: query: transporter:putrescine

18 steps (12 with candidates)

Or see definitions of steps

Step	Description	Best candidate	2nd candidate
puuP	putrescine:H+ symporter PuuP/PlaP
patA	putrescine aminotransferase (PatA/SpuC)	MVAN_RS16610	MVAN_RS07905
patD	gamma-aminobutyraldehyde dehydrogenase	MVAN_RS12960	MVAN_RS07915
gabT	gamma-aminobutyrate transaminase	MVAN_RS12965	MVAN_RS07905
gabD	succinate semialdehyde dehydrogenase	MVAN_RS24505	MVAN_RS09280
Alternative steps:
POT1	putrescine:H+ symporter POT1
potA	putrescine ABC transporter, ATPase component (PotA/PotG)	MVAN_RS17005	MVAN_RS13165
potB	putrescine ABC transporter, permease component 1 (PotB/PotH)	MVAN_RS17015
potC	putrescine ABC transporter, permease component 2 (PotC/PotI)	MVAN_RS17020
potD	putrescine ABC transporter, substrate-binding component (PotD/PotF)
potE	putrescine:H+ symporter PotE
puo	putrescine oxidase	MVAN_RS28045	MVAN_RS11120
puuA	glutamate-putrescine ligase	MVAN_RS08075	MVAN_RS11420
puuB	gamma-glutamylputrescine oxidase	MVAN_RS15910	MVAN_RS28695
puuC	gamma-glutamyl-gamma-aminobutyraldehyde dehydrogenase	MVAN_RS07400	MVAN_RS01790
puuD	gamma-glutamyl-gamma-aminobutyrate hydrolase	MVAN_RS11425	MVAN_RS03120
TPO1	putrescine transporter TPO1
UGA4	putrescine transporter UGA4

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.

Downloads

Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources