GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1748 in Pseudomonas fluorescens FW300-N1B4

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 Pf1N1B4_5103 Dipeptide transport system permease protein DppC (TC 3.A.1.5.2)

Query= TCDB::Q9X270
         (289 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_5103
          Length = 284

 Score =  154 bits (388), Expect = 3e-42
 Identities = 90/272 (33%), Positives = 150/272 (55%), Gaps = 5/272 (1%)

Query: 18  LRFKKNKMAVIGGVFVLI-LIALAILAPYIAPY-PYDEPHYIRAFEGPSKDFIFGTDALG 75
           L  +  ++A+  G+ +L   + LAI AP+IAP+ P  +   IR    P     FGTD  G
Sbjct: 15  LGLRNPRLAMGLGLTILFGWLVLAIFAPWIAPFDPIAQNTDIRLV-APHLAHPFGTDNFG 73

Query: 76  RDLFSRILYSLRNACIIGFGSQFVVLIIGGILGAVAGFKGGWIDKFIMSIVDIMFAFPTF 135
           RD+ SR+++S R    +         +IG  +GA++G+ GG  D F M ++DI+ AFP  
Sbjct: 74  RDVLSRVIWSARIDLQLAVIGVIFPFLIGTCVGALSGYIGGRFDTFCMRLIDIILAFPFL 133

Query: 136 LFNVILVTALGRGLFTIFLAIGLTGWAGMARLVRGQVLYLKNSEFVEAAKAAGASTFYII 195
           +  + ++  LG GL + ++A+ L GW   ARL+R Q+L LK S+F  AAK+ G     I+
Sbjct: 134 VLMLAIMAILGPGLMSFYIAMALVGWVSYARLIRSQILILKESDFALAAKSLGFGHGRIL 193

Query: 196 RKHILPN-MIGPILVNLAFGVPGAMMTESGLAVIGMGVRPPMPSWGNLIGEGIGMMMAFP 254
            +H+LPN M G I+ +++  V   ++  + ++ +G+GV+PP   WG ++ EG   + +  
Sbjct: 194 FRHLLPNAMFGSIVFSMSDAVL-VLLNGAAVSYLGLGVQPPTAEWGTMVAEGQSFITSAW 252

Query: 255 HLLIFPAVTFAFTLISFTFLADGLRDAFNPRS 286
            +  FP +      + F+ LAD + +    RS
Sbjct: 253 WICTFPGLAIVTLAMGFSLLADAVAEHLGERS 284


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: 267
Number of extensions: 13
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: 289
Length of database: 284
Length adjustment: 26
Effective length of query: 263
Effective length of database: 258
Effective search space:    67854
Effective search space used:    67854
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: 47 (22.7 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:

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