GapMind for catabolism of small carbon sources

 

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

Align Xylose/arabinose import permease protein XylH (characterized, see rationale)
to candidate Pf1N1B4_4287 Inositol transport system permease protein

Query= uniprot:Q4J711
         (356 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_4287
          Length = 340

 Score =  133 bits (335), Expect = 6e-36
 Identities = 96/326 (29%), Positives = 160/326 (49%), Gaps = 18/326 (5%)

Query: 8   RRF--EFQLFLVNVIIALFFYF------ENSAYFSSNNITTIFQYLAEIGIIAIGEAMLM 59
           RRF  E  +FLV + I L F        + S   +S  +  +   ++ IG++AIG   ++
Sbjct: 18  RRFPTELSIFLVLIGIGLVFEMFGWIVRDQSFLMNSQRLVLMILQVSIIGLLAIGVTQVI 77

Query: 60  LCGEIDLSPPALANFVPLITLTIYNS------IYQAISPTPAIVVSILLSLGLASLIGLM 113
           +   IDLS  ++     +I  ++  +      ++ +++  P + + +++ LG+  L G +
Sbjct: 78  ITTGIDLSSGSVLALSAMIAASLAQTSDFARAVFPSLTDLP-VWIPVIVGLGVGLLAGAI 136

Query: 114 NGLITTKAKVNSLITTVGTLFLFNGIALIYSGGYPESFPYFRFLGGTVSILPVPFIWSLG 173
           NG I     +   I T+G +    G+A  Y+ G P S     +       +PV  I+ + 
Sbjct: 137 NGSIIAITGIPPFIATLGMMVSARGLARYYTEGQPVSMLSDSYTAIGHGAMPV-IIFLVV 195

Query: 174 ALVFLILLLHYTKIGVWTIAAGSNPTGASEVGVPVDRVKIINFIIMANIGALVGIIQGSR 233
           A++F I L  YTK G +T A G N   A   G+ V R  +I + I   +  L G++  +R
Sbjct: 196 AVIFHIAL-RYTKYGKYTYAIGGNMQAARTSGINVKRHLVIVYSIAGLLAGLAGVVASAR 254

Query: 234 VLTIGATNFTADVVLEGIAAAVIGGTSLVGGKGSLVGAFLGSVFISELLNGFNILGINAY 293
             T G         L+ IAAAVIGGTSL GG G + G  +G++ +  + +GF  +G++AY
Sbjct: 255 AAT-GQAGMGMSYELDAIAAAVIGGTSLAGGVGRITGTVIGALILGVMASGFTFVGVDAY 313

Query: 294 EFDAILGGAIVVVMVLSYYAKRASYK 319
             D I G  IVV +V+  Y  +   K
Sbjct: 314 IQDIIKGLIIVVAVVIDQYRNKRKLK 339


Lambda     K      H
   0.325    0.143    0.404 

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: 307
Number of extensions: 25
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: 356
Length of database: 340
Length adjustment: 29
Effective length of query: 327
Effective length of database: 311
Effective search space:   101697
Effective search space used:   101697
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 49 (23.5 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