GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Pseudomonas simiae WCS417

Align ABC transporter for D-Sorbitol, ATPase component (characterized)
to candidate GFF2270 PS417_11575 spermidine/putrescine ABC transporter ATPase

Query= reanno::acidovorax_3H11:Ac3H11_2941
         (350 letters)



>FitnessBrowser__WCS417:GFF2270
          Length = 342

 Score =  256 bits (653), Expect = 8e-73
 Identities = 142/334 (42%), Positives = 202/334 (60%), Gaps = 5/334 (1%)

Query: 1   MAYLQLRGIEKFFGEHRAIKGIDLTIQQGEFIVFVGPSGCGKSTLLRLIAGLEAIDGGSL 60
           MA+LQL  + K +G   A+   DL +++GEF+  +GPSGCGK+T L++IAG   + GG +
Sbjct: 1   MAFLQLNALSKRYGAVDAVVATDLAVEKGEFVSLLGPSGCGKTTTLQMIAGFVDVSGGQI 60

Query: 61  MLDGRDITDQPSSKRDLAMVFQSYALYPHMSVYENMSFALKLAKVDKQVIDEKVQNAARI 120
           +LDGRDIT    + R L +VFQSYAL+PHMSV +N++F LK+ KV    I  KV+    +
Sbjct: 61  LLDGRDITHAKPASRGLGVVFQSYALFPHMSVRDNVAFGLKMRKVPAAEIASKVKTVLEL 120

Query: 121 LNLTQYLQRTPKELSGGQRQRVAIGRAIVRAPKVFLFDEPLSNLDAALRGQTRVEIAKLH 180
           + L  +  R P+ELSGGQRQRVA+ RA+V  P V L DEPLSNLDA LR + + EI ++ 
Sbjct: 121 VRLAPHADRYPRELSGGQRQRVALARALVIEPPVLLLDEPLSNLDANLREEMQFEIRRIQ 180

Query: 181 RDLGATTIYVTHDQVEAMTLADRVVVLRDGIIEQVGTPLELYDKPANQFVAQFIGTPQMN 240
             +G TT+ VTHDQ EA++++DRVVV++ G + Q+  P +LY+ P  +F++ F+G   + 
Sbjct: 181 CAVGITTLMVTHDQAEALSISDRVVVMQAGRVTQIDAPYKLYEHPRTRFISDFVGKANLL 240

Query: 241 VVPVDKLPQPVQQQAPAAPAGAAVGAIGLRPENITVRTTGATPVGGQVDLIEALGAETLI 300
               D L  P  +      +G     + LRPE I +   G+  + G+V      G++ L 
Sbjct: 241 PGDYDLLGSPQVRH----ESGDGELTLSLRPEKIQLVDAGSGRLQGKVLDSYFFGSQWLY 296

Query: 301 YVTTPGGAQFVSRQND-RTDLRVGDAVSLDIDAS 333
            + T  G   V R ND    L  G AV LD  AS
Sbjct: 297 RIHTSLGEITVVRSNDGSAPLGYGAAVGLDWQAS 330


Lambda     K      H
   0.320    0.137    0.388 

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: 291
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: 350
Length of database: 342
Length adjustment: 29
Effective length of query: 321
Effective length of database: 313
Effective search space:   100473
Effective search space used:   100473
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 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