GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Dshi_0546 in Pseudomonas stutzeri RCH2

Align ABC transporter for Xylitol, ATPase component (characterized)
to candidate GFF1860 Psest_1899 ABC-type sugar transport systems, ATPase components

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



>FitnessBrowser__psRCH2:GFF1860
          Length = 390

 Score =  292 bits (748), Expect = 8e-84
 Identities = 159/361 (44%), Positives = 228/361 (63%), Gaps = 32/361 (8%)

Query: 1   MAGIKIDKINKFYGTTQ--ALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEGVSSG 58
           MA +++  + K YG +Q   L DI L I+ GEF++ VGPSGCGKSTL+  +AGLE ++ G
Sbjct: 1   MASLELRNVQKSYGNSQIATLKDIALKIDAGEFLILVGPSGCGKSTLMNCIAGLENITGG 60

Query: 59  RIEIGGRDVTTVEPADRDLAMVFQSYALYPHMTVRENMEFGMKVNGFEPDLRKERIAEAA 118
            I + G D++   P DRD+AMVFQSYALYP M+VR+N+ FG+K+        +E +A  A
Sbjct: 61  EILVDGEDISQASPKDRDIAMVFQSYALYPTMSVRDNIAFGLKMRKVPAAKIEEEVARVA 120

Query: 119 RVLQLEDYLDRKPGQLSGGQRQRVAIGRAIVKNPSVFLFDEPLSNLDAKLRVQMRVELEG 178
           ++LQ+E  L+RKP QLSGGQ+QRVA+GRA+ + P ++LFDEPLSNLDAKLRV+MR E++ 
Sbjct: 121 KLLQIEPLLERKPSQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEIKL 180

Query: 179 LHKQLGATMIYVTHDQVEAMTMADKIVVLNRGRIEQVGSPMDLYHKPNSRFVAEFIGSPA 238
           +H++L  T +YVTHDQ+EAMT+ DK+ V+  G I+Q G+P ++Y+ P + FVA FIGSP 
Sbjct: 181 MHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGVIQQFGTPHEIYNNPANLFVASFIGSPP 240

Query: 239 MN---------------VFSSDVGLQDISLDASA--------AFVGCRPEHIEIVPDG-- 273
           MN               V +S+ G  ++ L  ++          +G RPE I + P G  
Sbjct: 241 MNFVPLRIRQRDGRWVGVLNSEQGSCELPLPITSDDGLRDRELILGIRPEQIGLAPAGSA 300

Query: 274 DGHIAATVHVKERLGGESLLYLGLKGGGQIVA--RVGGDDETKVGAAVSLRFSRHRLHQF 331
           D  +A  + V E  G ++L+   L    Q+ A  R+  D   +VG  ++L+F   R   F
Sbjct: 301 DFSLAVDIEVVEPTGPDTLVVFTL---NQVKACCRLAPDQAPRVGETLNLQFDPRRALLF 357

Query: 332 D 332
           D
Sbjct: 358 D 358


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: 385
Number of extensions: 16
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: 390
Length adjustment: 29
Effective length of query: 309
Effective length of database: 361
Effective search space:   111549
Effective search space used:   111549
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