GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc04256 in Pseudomonas fluorescens GW456-L13

Align ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized)
to candidate PfGW456L13_2830 Putrescine transport ATP-binding protein PotA (TC 3.A.1.11.1)

Query= reanno::Smeli:SMc04256
         (361 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_2830
          Length = 361

 Score =  222 bits (566), Expect = 1e-62
 Identities = 133/297 (44%), Positives = 183/297 (61%), Gaps = 12/297 (4%)

Query: 2   TSVSVRDLSLNF----GAVTVLDRLNLDIDHGEFLVLLGSSGCGKSTLLNCIAGLLDVSD 57
           T++ VR++S  +    G    LD +++DI   EF  LLG SGCGK+TLL  IAG   VSD
Sbjct: 5   TAIEVRNVSKRYSDDPGLAPALDNVSVDIADNEFFTLLGPSGCGKTTLLRTIAGFEHVSD 64

Query: 58  GQIFIKDRNVTWEEPKDRGIGMVFQSYALYPQMTVEKNLSFGLKVAKIPPAEIEKRVKRA 117
           G+I +    V    P  R +  VFQSYAL+P M+V +N++FGL++  +    I +RV   
Sbjct: 65  GEIRLAGEPVNDLPPFKRRVNTVFQSYALFPHMSVAQNIAFGLEMQGLDRKLIPQRVDEM 124

Query: 118 SEILQIQPLLKRKPSELSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRSELRVEIK 177
             ++Q+Q L KRKP+ELSGGQ+QRVA+ RAL     V L DEPLS LD KLR E++VE+K
Sbjct: 125 LALVQMQHLAKRKPAELSGGQQQRVALARALAPKPKVLLLDEPLSALDLKLRKEMQVELK 184

Query: 178 RLHQSLKNTMIYVTHDQIEALTLADRIAVMKSGVIQQLADPMTIYNAPENLFVAGFIGSP 237
           R+ +    T I+VTHDQ EALTL+DRIAVM +G I Q+  P  IY  P++ FVA FIG  
Sbjct: 185 RVQKEAGITFIFVTHDQEEALTLSDRIAVMSAGKILQIGSPNEIYERPQHQFVAQFIG-- 242

Query: 238 SMNFFRGEVE--PKDGRSFVRAGGIAFDVTAYPAHTRLQPGQKVVLGLRPEHVKVDE 292
            +NF  G ++   ++ + FV   G+  ++   P   +   G KV L  RPE  ++ E
Sbjct: 243 DINFLPGHIKRGQQNEKLFV-PNGMPVEI---PCPAQGFDGSKVQLAFRPERSQLVE 295


Lambda     K      H
   0.320    0.137    0.392 

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: 360
Number of extensions: 24
Number of successful extensions: 1
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: 361
Length of database: 361
Length adjustment: 29
Effective length of query: 332
Effective length of database: 332
Effective search space:   110224
Effective search space used:   110224
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