GapMind for catabolism of small carbon sources

 

Aligments for a candidate for TM1748 in Pseudomonas fluorescens GW456-L13

Align TM1748, component of Probable mannose/mannoside porter. Induced by beta-mannan (Conners et al., 2005). Regulated by mannose-responsive regulator manR (characterized)
to candidate PfGW456L13_3345 Oligopeptide transport system permease protein OppC (TC 3.A.1.5.1)

Query= TCDB::Q9X270
         (289 letters)



>lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3345 Oligopeptide
           transport system permease protein OppC (TC 3.A.1.5.1)
          Length = 339

 Score =  121 bits (304), Expect = 2e-32
 Identities = 76/241 (31%), Positives = 118/241 (48%), Gaps = 4/241 (1%)

Query: 48  PYPYDEPHY---IRAFEGPSKDFIFGTDALGRDLFSRILYSLRNACIIGFGSQFVVLIIG 104
           PY Y   +Y   + A   PS D + GTD  GRD+ +R++Y  R + +       +  IIG
Sbjct: 99  PYSYQSINYDLKVPAPAPPSTDNLLGTDDQGRDVLARVIYGFRISVLFALTLTVLSSIIG 158

Query: 105 GILGAVAGFKGGWIDKFIMSIVDIMFAFPTFLFNVILVTALGRGLFTIFLAIGLTGWAGM 164
            I GA+ GF GGW+D      ++I    P     +IL + +    + +   + L  W  +
Sbjct: 159 VIAGALQGFYGGWVDLAGQRFLEIWSGLPVLYLLIILASFVQPNFWWLLGIMLLFSWMSL 218

Query: 165 ARLVRGQVLYLKNSEFVEAAKAAGASTFYIIRKHILPNMIGPILVNLAFGVPGAMMTESG 224
             +VR + L  +N E+V AA+A G     I+ +HILPN +   +  + F + GA+ T + 
Sbjct: 219 VDVVRAEFLRGRNLEYVRAARALGMQNGAIMFRHILPNAMVSTMTFMPFILTGAIGTLTA 278

Query: 225 LAVIGMGVRPPMPSWGNLIGEGIGMMMAFPHLLIFPAVTFAFTLISFTFLADGLRDAFNP 284
           L  +G G+    PS G L+ +G   + A P L I      A  L    F+ +  RDAF+P
Sbjct: 279 LDFLGFGLPAGSPSLGELVAQGKSNLQA-PWLGISAFAVLALMLSLLVFIGESARDAFDP 337

Query: 285 R 285
           R
Sbjct: 338 R 338


Lambda     K      H
   0.331    0.147    0.457 

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: 252
Number of extensions: 10
Number of successful extensions: 2
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: 289
Length of database: 339
Length adjustment: 27
Effective length of query: 262
Effective length of database: 312
Effective search space:    81744
Effective search space used:    81744
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 48 (23.1 bits)

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 (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:

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. 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:

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 preprint 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