GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Pseudomonas simiae WCS417

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate GFF2490 PS417_12700 ABC transporter ATP-binding protein

Query= uniprot:D4GP39
         (383 letters)



>FitnessBrowser__WCS417:GFF2490
          Length = 367

 Score =  290 bits (741), Expect = 6e-83
 Identities = 163/344 (47%), Positives = 214/344 (62%), Gaps = 17/344 (4%)

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

Query: 84  MVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRVEETTDMLGISDLLDRKPGQLSGG 143
           MVFQ+YALYPH SVR NMSF L+ + G+    +  +V E   +L +  LL+RKP QLSGG
Sbjct: 79  MVFQTYALYPHMSVRKNMSFALDLA-GVDKKLVESKVSEAARILELGPLLERKPKQLSGG 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 MTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFIGEPSMNLFDG--------SLSGD 255
           MT+ D+V VL+ G ++QVG+PL+ YH+P NLFVAGF+G P M    G        S    
Sbjct: 198 MTLADKVVVLNSGRIEQVGSPLELYHQPANLFVAGFLGTPKMGFLKGKVTRVESQSCEVQ 257

Query: 256 TFRGDGFDYPLSGATRDQLGGASGLTLGIRPEDVTVGERRSGQRTFDAEVVVVEPQGNEN 315
              G   + PLSGAT   L   S +TLGIRPE + +     GQ T      V E  G++ 
Sbjct: 258 LDAGTLINLPLSGAT---LSVGSAVTLGIRPEHLEIAS--PGQTTLTVTADVGERLGSDT 312

Query: 316 AVHLRFVDGDEGTQFTATTTGQSRVEAGDRTTVSFPEDAIHLFD 359
             H+   +G+     T    G    + G+   +       HLFD
Sbjct: 313 FCHVITANGE---PLTMRIRGDMASQYGETLHLHLDPAHCHLFD 353


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: 393
Number of extensions: 16
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: 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