GapMind for catabolism of small carbon sources

 

Alignments for a candidate for araH in Pseudomonas fluorescens FW300-N2E2

Align L-arabinose ABC transporter, permease protein AraH (characterized)
to candidate Pf6N2E2_163 Ribose ABC transport system, permease protein RbsC (TC 3.A.1.2.1)

Query= CharProtDB::CH_014278
         (328 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_163
          Length = 325

 Score =  152 bits (385), Expect = 8e-42
 Identities = 104/325 (32%), Positives = 163/325 (50%), Gaps = 9/325 (2%)

Query: 7   SGSGAPKSSFSF---GRIWDQYGMLVVFAVLFIACAIFVPNFATFINMKGLGLAISMSGM 63
           + S   KSS +F   G      G L+    LF A +    ++ TF  +      I    +
Sbjct: 3   TASAVGKSSGNFYGLGTYLGLAGALLAMVALFSALSSHFLSYDTFSTLAN---QIPDLMV 59

Query: 64  VACGMLFCLASGDFDLSVASVIACAGVTTAV-VINLTESLWIGVAAGLLLGVLCGLVNGF 122
           +A GM F L  G  DLSV SV+A A  T +V V+    S+W     G+ +  L G V G 
Sbjct: 60  LAVGMTFILIIGGIDLSVGSVLALAASTVSVAVLGWGWSVWPSALLGMAVAALAGTVTGS 119

Query: 123 VIAKLKINALITTLATMQIVRGLAYIISDGKAVGIEDESFFALGYANWFGLPAPIWLTVA 182
           +    +I + I +L  +++ RGLAY ++  +   I D SF  L     FG+     + + 
Sbjct: 120 ITVAWRIPSFIVSLGVLEMARGLAYQMTGSRTAYIGD-SFAWLSNPIAFGISPSFIIALL 178

Query: 183 CLIIFGLLLNKTTFGRNTLAIGGNEEAARLAGVPVVRTKIIIFVLSGLVSAIAGIILASR 242
            + I   +L +T FGR  + IG NEEA RLAG+     KI++F L GL++ +A +   SR
Sbjct: 179 VIFIAQAVLTRTVFGRYLIGIGTNEEAVRLAGINPKPYKILVFSLMGLLAGVAALFQISR 238

Query: 243 MTSGQPMTSIGYELIVISACVLGGVSLKGGIGKISYVVAGILILGTVENAMNLLNISPFA 302
           + +  P    G EL VI+A V+GG SL GG G +     G+LI+  +   +  +  +   
Sbjct: 239 LEAADPNAGSGLELQVIAAVVIGGTSLMGGRGSVISTFFGVLIISVLAAGLAQIGATEPT 298

Query: 303 QYVVRGLILLAAVIFDRYK-QKAKR 326
           + ++ G +++ AV+ D Y+ Q+A R
Sbjct: 299 KRIITGAVIVVAVVLDTYRSQRASR 323


Lambda     K      H
   0.327    0.141    0.414 

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: 289
Number of extensions: 19
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: 328
Length of database: 325
Length adjustment: 28
Effective length of query: 300
Effective length of database: 297
Effective search space:    89100
Effective search space used:    89100
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: 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:

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