GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xylHsa in Pseudovibrio axinellae Ad2

Align Xylose/arabinose import permease protein XylH (characterized, see rationale)
to candidate WP_068006265.1 PsAD2_RS12365 ABC transporter permease

Query= uniprot:Q4J711
         (356 letters)



>NCBI__GCF_001623255.1:WP_068006265.1
          Length = 368

 Score =  110 bits (274), Expect = 8e-29
 Identities = 100/353 (28%), Positives = 160/353 (45%), Gaps = 59/353 (16%)

Query: 3   ILNVVRRFEFQLFLVNVIIALFFYFE-NSAYFSSNNITTIFQYLAEIGIIAIGEAMLMLC 61
           I  +++R E        ++ +FF F  +   FS           +++GI+AIG A+LM+ 
Sbjct: 19  ISRLMKRPELGALAGLALVTIFFAFTADPKMFSLAGFLNFMTPASQLGILAIGAALLMIG 78

Query: 62  GEIDLSPPALANFVPLI----TLTIYNSIYQAISPTPAIVVSILLSLGLASLIGLMNGLI 117
           GE DLS  ++  F  LI     +T    +Y AI          +++  +A+ +G +NG I
Sbjct: 79  GEFDLSVGSMVAFTGLIFGAAMVTFELPLYAAI----------IVTFMVAAAMGAVNGQI 128

Query: 118 TTKAKVNSLITTVGTLFLFNGIALI------------------YSGGYPESF-------P 152
             +  + S I T+  LF+  G++L+                    G +   F       P
Sbjct: 129 VIRTGLPSFIVTLAFLFILRGLSLVGLKAATGGSTQLRGVREKVEGSWIADFFSGEAFTP 188

Query: 153 YFRFLGGT------------VSILPVPFIW-SLGALVFLILLLHYTKIGVWTIAAGSNPT 199
            F +L               V  +PV  IW +L A V   +LL  ++ G W  A+G + +
Sbjct: 189 LFYWLAENGLVDTFKSGKPKVDGIPVEIIWFTLLAGVATWILLR-SRFGSWIFASGGDSS 247

Query: 200 GASEVGVPVDRVKIINFIIMANIGALVGIIQGSRVLTIGATNFTADVV--LEGIAAAVIG 257
            AS  GVPV RVK+  F+  A   ALV I+    V+  G+T+         E I AAVIG
Sbjct: 248 AASNSGVPVRRVKMYLFMFTACCAALVAILT---VMDAGSTDARRGFQKEFEAIIAAVIG 304

Query: 258 GTSLVGGKGSLVGAFLGSVFISELLNGFNILGINAYEFDAILGGAIVVVMVLS 310
           G+ L GG GS +GAF GS+    +L G +   I+   +   LG  +++ ++ +
Sbjct: 305 GSLLTGGYGSAIGAFFGSIIFGMVLIGLSYTNIDQDWYLVFLGSMLLLAVLFN 357


Lambda     K      H
   0.325    0.143    0.404 

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: 332
Number of extensions: 22
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: 356
Length of database: 368
Length adjustment: 29
Effective length of query: 327
Effective length of database: 339
Effective search space:   110853
Effective search space used:   110853
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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