GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Pseudomonas fluorescens FW300-N2C3

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate AO356_27685 AO356_27685 ABC transporter ATP-binding protein

Query= uniprot:D4GP39
         (383 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_27685
          Length = 367

 Score =  293 bits (751), Expect = 4e-84
 Identities = 162/346 (46%), Positives = 220/346 (63%), Gaps = 17/346 (4%)

Query: 24  VEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETVTEGELRLEDRVLNGVSAQDRDIA 83
           ++ I L+++D EF+V VGPSGCGKST LR++AGLE V++G + L+ R +  VS   RD+A
Sbjct: 19  IKGIDLEVNDREFVVFVGPSGCGKSTLLRLIAGLEEVSDGTIELDGRDITEVSPAKRDLA 78

Query: 84  MVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRVEETTDMLGISDLLDRKPGQLSGG 143
           MVFQ+YALYPH SVR NMSF L+ + G+P  E+ ++V E   +L +  +L+RKP QLSGG
Sbjct: 79  MVFQTYALYPHMSVRKNMSFALDLA-GVPKAEVEKKVNEAARILELGPMLERKPKQLSGG 137

Query: 144 QQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQRLQGELGVTTVYVTHDQTEA 203
           Q+QRVA+GRAIVR+P++FL DEPLSNLDA LR +MR EL RL  EL  T +YVTHDQ EA
Sbjct: 138 QRQRVAIGRAIVRNPKIFLFDEPLSNLDAALRVQMRLELARLHKELQATMIYVTHDQVEA 197

Query: 204 MTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFIGEPSMNLFDGSLSGDTFR----- 258
           MT+ D+V VL+ G ++QVG+PL+ YH+P NLFVAGF+G P M    G ++    +     
Sbjct: 198 MTLADKVVVLNGGRIEQVGSPLELYHQPANLFVAGFLGTPKMGFLKGKVTALDSQGCEVL 257

Query: 259 ---GDGFDYPLSGATRDQLGGASGLTLGIRPEDVTVGERRSGQRTFDAEVVVVEPQGNEN 315
              G   + P SGA    +GGA  +TLGIRPE + + +   G  T      V E  G++ 
Sbjct: 258 LDAGTRINLPRSGANL-SVGGA--VTLGIRPEHLNLAQ--PGDCTLQVTADVSERLGSDT 312

Query: 316 AVHLRFVDGDEGTQFTATTTGQSRVEAGDRTTVSFPEDAIHLFDGE 361
             H+    G+     T    G      G++  +    +  HLFD E
Sbjct: 313 FCHVVTTSGE---ALTMRVRGDLASRFGEQLNLHLDAEHCHLFDAE 355


Lambda     K      H
   0.316    0.136    0.384 

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: 420
Number of extensions: 21
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: 383
Length of database: 367
Length adjustment: 30
Effective length of query: 353
Effective length of database: 337
Effective search space:   118961
Effective search space used:   118961
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 50 (23.9 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