GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Acidovorax sp. GW101-3H11

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate Ac3H11_2941 Various polyols ABC transporter, ATP-binding component

Query= uniprot:D4GP39
         (383 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_2941
          Length = 350

 Score =  275 bits (702), Expect = 2e-78
 Identities = 158/359 (44%), Positives = 213/359 (59%), Gaps = 20/359 (5%)

Query: 1   MARLTLDDVTKVYTDEGGGDIVAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETV 60
           MA L L  + K +     G+  A++ I L I  GEF+V VGPSGCGKST LR++AGLE +
Sbjct: 1   MAYLQLRGIEKFF-----GEHRAIKGIDLTIQQGEFIVFVGPSGCGKSTLLRLIAGLEAI 55

Query: 61  TEGELRLEDRVLNGVSAQDRDIAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRV 120
             G L L+ R +    +  RD+AMVFQSYALYPH SV  NMSF L+ +  +    I ++V
Sbjct: 56  DGGSLMLDGRDITDQPSSKRDLAMVFQSYALYPHMSVYENMSFALKLAK-VDKQVIDEKV 114

Query: 121 EETTDMLGISDLLDRKPGQLSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRT 180
           +    +L ++  L R P +LSGGQ+QRVA+GRAIVR P+VFL DEPLSNLDA LR + R 
Sbjct: 115 QNAARILNLTQYLQRTPKELSGGQRQRVAIGRAIVRAPKVFLFDEPLSNLDAALRGQTRV 174

Query: 181 ELQRLQGELGVTTVYVTHDQTEAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFI 240
           E+ +L  +LG TT+YVTHDQ EAMT+ DRV VL DG ++QVGTPL+ Y +P N FVA FI
Sbjct: 175 EIAKLHRDLGATTIYVTHDQVEAMTLADRVVVLRDGIIEQVGTPLELYDKPANQFVAQFI 234

Query: 241 GEPSMNLFDGSLSGDTFRGDGFDYPLSGATRDQLGGASGLTLGIRPEDVTVGERRSGQRT 300
           G P MN+            D    P+         GA+   +G+RPE++TV  R +G   
Sbjct: 235 GTPQMNVVP---------VDKLPQPVQQQAPAAPAGAAVGAIGLRPENITV--RTTGATP 283

Query: 301 FDAEVVVVEPQGNENAVHLRFVDGDEGTQFTATTTGQSRVEAGDRTTVSFPEDAIHLFD 359
              +V ++E  G E  +   +V    G QF +    ++ +  GD  ++       H FD
Sbjct: 284 VGGQVDLIEALGAETLI---YVTTPGGAQFVSRQNDRTDLRVGDAVSLDIDASQAHWFD 339


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: 399
Number of extensions: 19
Number of successful extensions: 4
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: 350
Length adjustment: 30
Effective length of query: 353
Effective length of database: 320
Effective search space:   112960
Effective search space used:   112960
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: 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