GapMind for catabolism of small carbon sources

 

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

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

Query= uniprot:D4GP38
         (383 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_2941
          Length = 350

 Score =  246 bits (628), Expect = 7e-70
 Identities = 145/362 (40%), Positives = 203/362 (56%), Gaps = 25/362 (6%)

Query: 1   MGQIQLTDLTKRFGDTVAVDDLSLDIDDEEFLVLVGPSGCGKSTTLRMLAGLETPTSGDI 60
           M  +QL  + K FG+  A+  + L I   EF+V VGPSGCGKST LR++AGLE    G +
Sbjct: 1   MAYLQLRGIEKFFGEHRAIKGIDLTIQQGEFIVFVGPSGCGKSTLLRLIAGLEAIDGGSL 60

Query: 61  YIGGDHMNYRVPQNRDIAMVFQDYALYPHMTVRQNIRFGLEEEEGYTSAERDERVVEVAE 120
            + G  +  +    RD+AMVFQ YALYPHM+V +N+ F L+  +       DE+V   A 
Sbjct: 61  MLDGRDITDQPSSKRDLAMVFQSYALYPHMSVYENMSFALKLAK-VDKQVIDEKVQNAAR 119

Query: 121 TLGIADLLDRKPDELSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQNL 180
            L +   L R P ELSGGQ+QRVA+GRAIVR P+VFL DEPLSNLDA LR + R E+  L
Sbjct: 120 ILNLTQYLQRTPKELSGGQRQRVAIGRAIVRAPKVFLFDEPLSNLDAALRGQTRVEIAKL 179

Query: 181 QDQLAVTTVYVTHNQTEAMTMADRIAVMDDGELQQVASPFECYHEPNNLFVAEFIGEPMI 240
              L  TT+YVTH+Q EAMT+ADR+ V+ DG ++QV +P E Y +P N FVA+FIG P +
Sbjct: 180 HRDLGATTIYVTHDQVEAMTLADRVVVLRDGIIEQVGTPLELYDKPANQFVAQFIGTPQM 239

Query: 241 NLVRGTRSESTFVGEHFSYPLDEDVMESVDDRDDFVLGVRPEDIEV--ADAAPDDAALDD 298
           N+V           +    P+ +    +        +G+RPE+I V    A P    +D 
Sbjct: 240 NVV---------PVDKLPQPVQQQAPAAPAGAAVGAIGLRPENITVRTTGATPVGGQVD- 289

Query: 299 HDLQMDVTVVEPHGDQNVLHLSHPDQPSADDALQAVTEGMHLVTRGDRVTVTIPPDKIHL 358
                   ++E  G + +++++ P            T+    +  GD V++ I   + H 
Sbjct: 290 --------LIEALGAETLIYVTTPGGAQFVSRQNDRTD----LRVGDAVSLDIDASQAHW 337

Query: 359 FD 360
           FD
Sbjct: 338 FD 339


Lambda     K      H
   0.317    0.135    0.386 

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: 320
Number of extensions: 14
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: 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: 41 (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.

Links

Downloads

Related tools

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