Aligments for a candidate for bkdC in Pseudomonas fluorescens FW300-N2E3

GapMind for catabolism of small carbon sources

Aligments for a candidate for bkdC in Pseudomonas fluorescens FW300-N2E3

Align Dihydrolipoyllysine-residue (2-methylpropanoyl)transferase (EC 2.3.1.168) (characterized)
to candidate AO353_26645 AO353_26645 branched-chain alpha-keto acid dehydrogenase subunit E2

Query= reanno::pseudo13_GW456_L13:PfGW456L13_3542
         (425 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_26645
          Length = 425

 Score =  739 bits (1907), Expect = 0.0
 Identities = 389/428 (90%), Positives = 402/428 (93%), Gaps = 6/428 (1%)

Query: 1   MGTHVIKMPDIGEGIAEVELSVWHVKVGDMVVEDQVLADVMTDKAMVDIPSPVHGKVIAL 60
           MGTHVIKMPDIGEGIAEVELSVWHVKVGDMVVEDQVLADVMTDKAMVDIPSPVHGKVI+L
Sbjct: 1   MGTHVIKMPDIGEGIAEVELSVWHVKVGDMVVEDQVLADVMTDKAMVDIPSPVHGKVISL 60

Query: 61  GGQPGEVMAVGSVLISIEVEGAGNVKESAQPAPVV---KEAPVAATKVETVVESKPVAAP 117
           GG+PGEVMAVGS+LISIEVEG GNVK S+QPAP     K APVAA KVE  +ESK     
Sbjct: 61  GGEPGEVMAVGSILISIEVEGEGNVKASSQPAPAAPAPKPAPVAAPKVEAAIESKSAVPA 120

Query: 118 APKAAVCQGPMVAREADERPLASPAVRKHALDLGIQLRLVRGTGPAGRVLHEDLDAYLAQ 177
            P A   QGPM+AREADERPLASPAVRKHALD GIQLRLVRGTGPAGR+LHEDL+AYLAQ
Sbjct: 121 RPVAP--QGPMIAREADERPLASPAVRKHALDAGIQLRLVRGTGPAGRILHEDLEAYLAQ 178

Query: 178 GQSNASAPVAAAYAQRTDEQQIPVIGMRRKIAQRMQDATQRAAHFSYVEEIDVTAVEELR 237
           GQSNAS+ VAA YA+R DEQQIPVIGMRRKIAQRMQDATQRAAHFSYVEEIDVTAVEELR
Sbjct: 179 GQSNASSTVAA-YAERNDEQQIPVIGMRRKIAQRMQDATQRAAHFSYVEEIDVTAVEELR 237

Query: 238 AHLNEKHGATRGKLTLLPFLVRALVVALRDFPQINARYDDEAQVITRLGAVHVGIATQAD 297
           AHLNEKHGATRGKLTLLPFLVRA+VVALRDFPQINARYDDEAQVITRLGAVHVG+ATQ+D
Sbjct: 238 AHLNEKHGATRGKLTLLPFLVRAMVVALRDFPQINARYDDEAQVITRLGAVHVGVATQSD 297

Query: 298 IGLMVPVVRHAEARSLWDSAAEISRLATAARNGKASRDELSGSTITLTSLGALGGIVSTP 357
           IGLMVPVVRHAEARSLWDSAAEISRLATAARNGKASRDELSGSTITLTSLGALGGIVSTP
Sbjct: 298 IGLMVPVVRHAEARSLWDSAAEISRLATAARNGKASRDELSGSTITLTSLGALGGIVSTP 357

Query: 358 VLNLPEVAIVGVNKIVERPMVIKGQIVIRKMMNLSSSFDHRVVDGMDAALFIQAIRGLLE 417
           VLNLPEVAIVGVNKIVERPMVIKGQIVIRKMMNLSSSFDHRVVDGMDAA FIQAIRGLLE
Sbjct: 358 VLNLPEVAIVGVNKIVERPMVIKGQIVIRKMMNLSSSFDHRVVDGMDAAQFIQAIRGLLE 417

Query: 418 QPATLFVE 425
           QPATLFVE
Sbjct: 418 QPATLFVE 425


Lambda     K      H
   0.318    0.133    0.368 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 659
Number of extensions: 12
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 425
Length of database: 425
Length adjustment: 32
Effective length of query: 393
Effective length of database: 393
Effective search space:   154449
Effective search space used:   154449
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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Protein sequences (fasta format)
Organisms (tab-delimited)
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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:

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, 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

GapMind for catabolism of small carbon sources