GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacJ in Stenotrophomonas chelatiphaga DSM 21508

Align Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale)
to candidate WP_057507764.1 ABB28_RS05960 polyamine ABC transporter ATP-binding protein

Query= uniprot:D4GP38
         (383 letters)



>NCBI__GCF_001431535.1:WP_057507764.1
          Length = 378

 Score =  223 bits (568), Expect = 7e-63
 Identities = 135/326 (41%), Positives = 180/326 (55%), Gaps = 11/326 (3%)

Query: 2   GQIQLTDLTKRFGDTVAVDDLSLDIDDEEFLVLVGPSGCGKSTTLRMLAGLETPTSGDIY 61
           G + + DL K F   VAVDD++LD+   E   L+G SG GKST LR L G ETPT G I 
Sbjct: 19  GYLSIRDLRKEFDGFVAVDDVNLDVRKGEIFALLGGSGSGKSTLLRCLGGFETPTRGSIV 78

Query: 62  IGGDHMNYRVPQNRDIAMVFQDYALYPHMTVRQNIRFGLEEEEGYTSAERDERVVEVAET 121
           + G  +    P  R + M+FQ YAL+PHM+V QNI FGL+++ G        RV E+ E 
Sbjct: 79  LDGQPLVALPPYKRPVNMMFQSYALFPHMSVEQNIAFGLKQD-GLAGDAIRRRVGEMLEL 137

Query: 122 LGIADLLDRKPDELSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQNLQ 181
           + +  L  R+P +LSGGQQQRVAL R++ + P++ L+DEP+  LD KLR++M+ EL N+ 
Sbjct: 138 VHMTSLAKRRPHQLSGGQQQRVALARSLAKGPKLLLLDEPMGALDKKLRSQMQLELVNII 197

Query: 182 DQLAVTTVYVTHNQTEAMTMADRIAVMDDGELQQVASPFECYHEPNNLFVAEFIGEPMIN 241
           +   VT V VTH+Q EAMTMA RIAVMD G +QQV  P E Y +P N FVA FIG   +N
Sbjct: 198 ETSGVTCVMVTHDQEEAMTMATRIAVMDAGWIQQVGKPDEVYEQPANRFVAGFIGS--VN 255

Query: 242 LVRGTRSES-----TFVGEHFSYPLDEDVMESVDDRDDFVLGVRPEDIEVADAAPDDAAL 296
              G   E      T     F  P+      +  +       VRPE I +    P+    
Sbjct: 256 SFEGVIDEDLPEYVTVRSPAFPAPIYIGHGITCYEGQPVAFAVRPEKIIIGKDEPEGHTN 315

Query: 297 DDHDLQMDVTVVEPHGDQNVLHLSHP 322
               +  D+      G  +V H+  P
Sbjct: 316 KAQGVIEDIAY---FGSHSVYHVRLP 338


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: 344
Number of extensions: 18
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: 378
Length adjustment: 30
Effective length of query: 353
Effective length of database: 348
Effective search space:   122844
Effective search space used:   122844
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: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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