GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Dshi_0546 in Stutzerimonas stutzeri A1501

Align ABC transporter for Xylitol, ATPase component (characterized)
to candidate WP_011913323.1 PST_RS11065 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= reanno::Dino:3607124
         (338 letters)



>NCBI__GCF_000013785.1:WP_011913323.1
          Length = 371

 Score =  353 bits (907), Expect = e-102
 Identities = 192/363 (52%), Positives = 240/363 (66%), Gaps = 25/363 (6%)

Query: 1   MAGIKIDKINKFYGTTQALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEGVSSGRI 60
           MA +KI  + K +   + +  I+LDI D EFVVFVGPSGCGKSTLLR +AGLE VSSGRI
Sbjct: 1   MADLKIHNLKKGFDGNEIIKGIDLDIRDREFVVFVGPSGCGKSTLLRLIAGLEEVSSGRI 60

Query: 61  EIGGRDVTTVEPADRDLAMVFQSYALYPHMTVRENMEFGMKVNGFEPDLRKERIAEAARV 120
           E+ GRD+T V PA RDLAMVFQ+YALYPHMTVR+NM F + + G +      +I  AAR 
Sbjct: 61  ELDGRDITDVSPAKRDLAMVFQTYALYPHMTVRKNMSFALDLAGADKQEVARKIEAAART 120

Query: 121 LQLEDYLDRKPGQLSGGQRQRV----AIGRAIVKNPSVFLFDEPLSNLDAKLRVQMRVEL 176
           L+LE  L+RKP QLSGGQRQRV    AIGRAIV+NP VFLFDEPLSNLDA LRVQMR+EL
Sbjct: 121 LELEPLLERKPRQLSGGQRQRVAIGRAIGRAIVRNPKVFLFDEPLSNLDAALRVQMRLEL 180

Query: 177 EGLHKQLGATMIYVTHDQVEAMTMADKIVVLNRGRIEQVGSPMDLYHKPNSRFVAEFIGS 236
             LH++L ATMIYVTHDQVEAMT+ADK+VVLN GRIEQVGSPM+LYH P + FVA F+G+
Sbjct: 181 SRLHQELQATMIYVTHDQVEAMTLADKVVVLNGGRIEQVGSPMELYHHPANLFVAGFLGT 240

Query: 237 PAMNVFSS-----DVGLQDISLDASAAF----------------VGCRPEHIEIVPDGDG 275
           P M          +    ++ LDA                    +G RPEH+    +G+ 
Sbjct: 241 PKMGFLKGHASRVEASGCEVELDAGCRLFLPVSGATLKAGDPVTLGIRPEHLNRGSEGNC 300

Query: 276 HIAATVHVKERLGGESLLYLGLKGGGQIVARVGGDDETKVGAAVSLRFSRHRLHQFDEAG 335
            +     V ERLG ++  ++  + G Q+  R+ GD   + G ++SL       H FD +G
Sbjct: 301 QLTVKADVSERLGSDTYCHVVTRNGEQLTMRIRGDFTPRYGESLSLTLEAAHCHLFDSSG 360

Query: 336 RAI 338
           +A+
Sbjct: 361 QAV 363


Lambda     K      H
   0.320    0.139    0.396 

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: 416
Number of extensions: 14
Number of successful extensions: 3
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: 338
Length of database: 371
Length adjustment: 29
Effective length of query: 309
Effective length of database: 342
Effective search space:   105678
Effective search space used:   105678
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 49 (23.5 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