GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacK in Marinobacter adhaerens HP15

Align Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale)
to candidate GFF960 HP15_939 spermidine/putrescine ABC transporter ATPase subunit

Query= uniprot:D4GP39
         (383 letters)



>FitnessBrowser__Marino:GFF960
          Length = 372

 Score =  204 bits (518), Expect = 4e-57
 Identities = 126/341 (36%), Positives = 189/341 (55%), Gaps = 18/341 (5%)

Query: 22  VAVEEISLDIDDGEFLVLVGPSGCGKSTTLRMMAGLETVTEGELRLEDRVLNGVSAQDRD 81
           +AV+ ++LDI  GE   L+G SG GKST LRM+AG ET   G + L+ + +  +    R 
Sbjct: 28  LAVDNVNLDIHKGEIFALLGGSGSGKSTLLRMLAGFETPNAGSIMLDGQDVTALPPFLRP 87

Query: 82  IAMVFQSYALYPHKSVRGNMSFGLEESTGLPDDEIRQRVEETTDMLGISDLLDRKPGQLS 141
             M+FQSYAL+PH +V  N++ GL++   LP  EIR RV     ++ +     RKP QLS
Sbjct: 88  TNMMFQSYALFPHMTVEQNIAMGLKQDK-LPKSEIRDRVAAMLKLVKMEPYARRKPQQLS 146

Query: 142 GGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQRLQGELGVTTVYVTHDQT 201
           GGQQQRVAL R++ + P++ L+DEP+  LD KLR EM+ EL  +   +G T + VTHDQ 
Sbjct: 147 GGQQQRVALARSLAKRPKLLLLDEPMGALDKKLRTEMQLELVEILENVGATCLMVTHDQE 206

Query: 202 EAMTMGDRVAVLDDGELQQVGTPLDCYHRPNNLFVAGFIGEPSMNLFDGSLSGD-----T 256
           EAMTM  R+A++  G + Q+G+P+D Y  PN+   A FIG  S+N+F+  +  D     T
Sbjct: 207 EAMTMASRIAIMAQGRIAQIGSPIDIYESPNSRMTAEFIG--SVNIFEAHIREDEADSVT 264

Query: 257 FRGDGFDYPL---SGATRDQLGGASGLTLGIRPEDV-TVGERRSGQRTFDAEVV-VVEPQ 311
              D  D P+    G T      ++   + +RPE +    ++  G+  +    V  +   
Sbjct: 265 LTSDLLDAPVFIDRGVTTP--AESTATLVALRPEKIYLTPDKPDGENNWSCGTVDNIAYL 322

Query: 312 GNENAVHLRFVDGD--EGTQFTATTTGQSRVEAGDRTTVSF 350
           G+  + +++   G   + T       G+ R   GDR  VS+
Sbjct: 323 GDITSYYVKLASGKRVQATMANVERRGE-RPTWGDRVFVSW 362


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: 368
Number of extensions: 16
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: 372
Length adjustment: 30
Effective length of query: 353
Effective length of database: 342
Effective search space:   120726
Effective search space used:   120726
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