Aligments for a candidate for Dshi_1194 in Pseudomonas fluorescens FW300-N2E2

GapMind for catabolism of small carbon sources

Aligments for a candidate for Dshi_1194 in Pseudomonas fluorescens FW300-N2E2

Align TRAP transporter (characterized, see rationale)
to candidate Pf6N2E2_320 TRAP transporter, 4TM/12TM fusion protein, unknown substrate 1

Query= uniprot:A8LI82
         (743 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_320
          Length = 675

 Score =  338 bits (867), Expect = 5e-97
 Identities = 200/526 (38%), Positives = 289/526 (54%), Gaps = 60/526 (11%)

Query: 187 VLAICGVAVATYLITIYGTLMRNSTGTPFAPIGISIAAVAGTALIMELTRRVAGMALIVI 246
           VL++ GVA A Y       L++ S       + + I  V    L+ E  RRV G+AL +I
Sbjct: 75  VLSLGGVATALYQWVFESDLIQRSGDLTTTDMIMGIVLVV---LVFEAARRVMGIALPII 131

Query: 247 AGIFLAYVFVGQYLPGFLNAPAVTWQRFFSQV-YTDAGILGPTTAVSSTYIILFIIFAAF 305
            G+FLAY   G+YLPG L        +  +Q+ +   G+ G  T VS+TYI LFI+F AF
Sbjct: 132 CGLFLAYGLFGEYLPGDLAHRGYGLDQIINQLSFGTEGLYGTPTYVSATYIFLFILFGAF 191

Query: 306 LQASKVGDYFVNFAFAAAGQSRGGPAKVAIFASGLMGMINGTSAGNVVATGSLTIPLMKK 365
           L+ + +   F +FA    G   GGPAKVA+ +S LMG I G+   NVV TG  TIPLMK+
Sbjct: 192 LEKAGMIKLFTDFAMGLFGHKLGGPAKVAVVSSALMGTITGSGIANVVTTGQFTIPLMKR 251

Query: 366 VGYHKKTAGAVEAAASTGGQIMPPIMGAGAFIMAEITGIPYTEIALAAIIPAILYFVSVY 425
            GY    AG VEA +S G QIMPP+MGA AFIMAE   +P+ EIA AA+IPA LYF SV+
Sbjct: 252 FGYKAAFAGGVEATSSMGSQIMPPVMGAVAFIMAETINVPFVEIAKAALIPACLYFGSVF 311

Query: 426 FMVDLEAAKLGMRGMSRDELPKFNKMVRQV-YLFLPIIILIYALFMGYSVIRAGTLATVA 484
           +MV LEA +  ++G+ +D+ P     V+   +L +P+ +L+Y LF G + + +G +    
Sbjct: 312 WMVHLEAKRSDLKGLPKDQCPSAWGAVKDSWFLLIPLGVLVYLLFSGRTPLFSGMVGLAL 371

Query: 485 AAVV------------------SWFTP-------FRMGPRSIAKAFEIAGTM-------- 511
            A+V                   W          FR+G   I   F + G +        
Sbjct: 372 TAIVILGSAIILKVSNYALRCAFWIALGLLCVGFFRLG---IGVVFAVIGVLVVACWFMQ 428

Query: 512 -------------------SVQIIAVCACAGIIVGVISLTGVGARFSAVLLGIADTSQLL 552
                              +V +   CA  G I+ V+SLTGV + F+  +L I   + LL
Sbjct: 429 GTRETLVICLHALVDGARHAVPVGIACALVGSIIAVVSLTGVASTFAGYILAIGRDNLLL 488

Query: 553 ALFFAMCIAILLGMGMPTTAAYAVAASVVAPGLVQLGIPLLTAHFFVFYFAVLSAITPPV 612
           +L   M   ++LGMG+PT   Y + +S+ AP L++LG+PL+ +H FVFYF +L+ +TPPV
Sbjct: 489 SLILTMLTCLVLGMGIPTIPNYIITSSIAAPALLELGVPLIVSHMFVFYFGILADLTPPV 548

Query: 613 ALASYAAAGISGANPMETSVTSFKIGIAAFIVPFMFFYNSAILMDG 658
           ALA +AAA I+  + ++ S  + +I +A F++PFM  YN A+++ G
Sbjct: 549 ALACFAAAPIARESGLKISFWAVRIALAGFVIPFMTVYNPALMLQG 594


Lambda     K      H
   0.327    0.140    0.419 

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: 1252
Number of extensions: 82
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 743
Length of database: 675
Length adjustment: 39
Effective length of query: 704
Effective length of database: 636
Effective search space:   447744
Effective search space used:   447744
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 55 (25.8 bits)

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

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Steps (tab-delimited)
Rules (tab-delimited)
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