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

GapMind for catabolism of small carbon sources

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

Align Benzoyl-CoA reductase electron transfer protein, putative (characterized, see rationale)
to candidate Pf6N2E2_1468 NAD-dependent formate dehydrogenase beta subunit

Query= uniprot:Q39TW5
         (635 letters)



>lcl|FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1468 NAD-dependent formate
           dehydrogenase beta subunit
          Length = 519

 Score =  335 bits (860), Expect = 2e-96
 Identities = 194/511 (37%), Positives = 289/511 (56%), Gaps = 21/511 (4%)

Query: 38  ASGAAEVIAAFKTELEFHGLTTEVNTKGTGCPGFCERGPIVMIYPEGIC--YLKVKPEDV 95
           A GA +V  A   E E   L   V    T   G     P+V +   G+   +  V P DV
Sbjct: 14  AVGADKVADALALEAERRQLPLTVLR--TSSRGLYWLEPLVELESAGVRLGFGPVTPADV 71

Query: 96  PEIVSHTIKEKKVVDRLLYEDPATGTRALRESD-IPFYKNQQRNILSENLRLDSKSMDDY 154
           P ++             L  DP +   AL   + IP+ K+QQR + +        S+DDY
Sbjct: 72  PGLLD-----------ALTGDPGSHPLALGPVEAIPYLKSQQRLLFARAGITQPLSLDDY 120

Query: 155 LAIGGYSALSKVLFQMTPEDVMGEIKKSNLRGRGGGGFPAWRKWEESRNAPDPIKYVIVN 214
            A GG+  L++ + QM   DV+  +  S LRGRGG  FPA  KW   R+A    KYV+ N
Sbjct: 121 RAQGGFQGLARSI-QMDGADVVASVLDSGLRGRGGAAFPAGIKWRTVRDAVGAQKYVVCN 179

Query: 215 ADEGDPGAFMDRALIEGNPHSILEGLIIGAYAVGAHEGFIYVRQEYPLAVENINLAIRQA 274
           ADEGD G F DR L+EG+P  ++EG+II   AVGA  G+IYVR EYP A+  +N A+R A
Sbjct: 180 ADEGDSGTFADRMLMEGDPFLLIEGMIIAGLAVGATMGYIYVRSEYPAAISTLNDALRIA 239

Query: 275 SERGFVGKDILGSGFDFTVKVHMGAGAFVCGESSALMTALEGRAGEPRPKYIHTAVKGVW 334
            + G++G ++ GSG  F ++V +GAGA++CGE +AL+ +LEG+ G  R K    A++G++
Sbjct: 240 RDAGYLGANVSGSGRTFDIEVRVGAGAYICGEETALLESLEGKRGTVRAKPPLPAIQGLF 299

Query: 335 DHPSVLNNVETWANVTQIITKGADWFTSYGTAGSTGTKIFSLVGKITNTGLVEVPMGVTL 394
             P++++NV T A+V  I+ KGA ++  +G   S GT  F L G +   GLVE   G++L
Sbjct: 300 GLPTLVHNVVTLASVPIILEKGAQFYRDFGMGRSLGTMPFQLAGNVRQGGLVERAFGLSL 359

Query: 395 RDIITKVGGGIPGGKKFKAVQTGGPSGGCIPEAMLDLPVDFDELTKAGSMMGSGGMIVMD 454
           R+++   GGG   G+  KA Q GGP G  +P +  D P+D++     G+M+G GG++V D
Sbjct: 360 RELVEGYGGGTASGRPLKAAQVGGPLGAWVPPSQFDTPLDYEAFAAMGAMLGHGGVVVAD 419

Query: 455 EDTCMVDIARYFIDFLKDESCGKCTPCREGIRQMLAVLTRI---TVGKGKEGDIELLEEL 511
           +   M  +AR+ + F  +ESCGKCTPCR G  + + V+ R+   T    ++    LL++L
Sbjct: 420 DSLDMAQMARFALQFCAEESCGKCTPCRIGSTRGVEVVDRLIASTEAGARQEQALLLQDL 479

Query: 512 AESTG-AALCALGKSAPNPVLSTIRYFRDEY 541
            ++    +LCALG     PV S +++F  ++
Sbjct: 480 CDTLQYGSLCALGGMTSYPVASALKHFPADF 510


Lambda     K      H
   0.319    0.138    0.420 

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: 790
Number of extensions: 44
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: 635
Length of database: 519
Length adjustment: 36
Effective length of query: 599
Effective length of database: 483
Effective search space:   289317
Effective search space used:   289317
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 53 (25.0 bits)

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

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

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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