GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xylF_Tm in Pseudomonas fluorescens FW300-N2E3

Align ABC-type transporter, integral membrane subunit, component of Xylose porter (Nanavati et al. 2006). Regulated by xylose-responsive regulator XylR (characterized)
to candidate AO353_20825 AO353_20825 ABC transporter permease

Query= TCDB::Q9WXW7
         (317 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_20825
          Length = 325

 Score =  162 bits (411), Expect = 8e-45
 Identities = 110/306 (35%), Positives = 162/306 (52%), Gaps = 4/306 (1%)

Query: 13  LGPLVALVSLAVFTAILNPRFLTAFNLQALGRQIAIFGLLAIGETFVIISGGGAIDLSPG 72
           LG   AL+++    ++L+  FL+      L  QI    +LA+G TFV+I GG  IDLS G
Sbjct: 21  LGLAGALLAMIALFSVLSSHFLSYDTFSTLANQIPDLMVLAVGMTFVLIIGG--IDLSVG 78

Query: 73  SMVALTGVMVAW-LMTHGVPVWISVILILLFSIGAGAWHGLFVTKLRVPAFIITLGTLTI 131
           S++AL G  V+  ++  G  V  + +L +  +  AG   G      R+P+FI++LG L +
Sbjct: 79  SVLALAGSTVSVAILGWGWSVLPAALLGMAAAAVAGTITGSITVAWRIPSFIVSLGVLEM 138

Query: 132 ARGMAAVITKGWPIIGLPSSFLKIGQGEFLKIPIPVWILLAVALVADFFLRKTVYGKHLR 191
           ARG+A  +T G     +  +F  +       I     I L V  +A   L +TV+G++L 
Sbjct: 139 ARGVAYQMT-GSRTAYIGDAFAWLSNPITFGISPSFIIALLVIFIAQAVLTRTVFGRYLI 197

Query: 192 ASGGNEVAARFSGVNVDRVRMIAFMVSGFLAGVVGIIIAARLSQGQPGVGSMYELYAIAS 251
             G NE A R +G+N    +++ F + G LAG+  +   +RL    P  GS  EL  IA+
Sbjct: 198 GIGTNEEAVRLAGINPKPYKILVFSLMGLLAGIAALFQISRLEAADPNAGSGLELQVIAA 257

Query: 252 TVIGGTSLTGGEGSVLGAIVGASIISLLWNALVLLNVSTYWHNVVIGIVIVVAVTLDILR 311
            VIGGTSL GG GSV+    G  IIS+L   L  +  +     ++ G VIVVAV LD  R
Sbjct: 258 VVIGGTSLMGGRGSVISTFFGVLIISVLAAGLAQIGATEPTKRIITGAVIVVAVVLDTYR 317

Query: 312 RRLASK 317
            + AS+
Sbjct: 318 SQRASR 323


Lambda     K      H
   0.328    0.143    0.424 

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: 306
Number of extensions: 20
Number of successful extensions: 6
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: 317
Length of database: 325
Length adjustment: 28
Effective length of query: 289
Effective length of database: 297
Effective search space:    85833
Effective search space used:    85833
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