GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0029 in Pseudomonas putida KT2440

Align TM0029, component of β-glucoside porter (Conners et al., 2005). Binds cellobiose, laminaribiose (Nanavati et al. 2006). Regulated by cellobiose-responsive repressor BglR (characterized)
to candidate PP_4454 PP_4454 putative Opine ABC transporter, permease protein

Query= TCDB::Q9WXN6
         (280 letters)



>FitnessBrowser__Putida:PP_4454
          Length = 290

 Score =  145 bits (367), Expect = 8e-40
 Identities = 85/281 (30%), Positives = 158/281 (56%), Gaps = 10/281 (3%)

Query: 4   TMIRPLFKNKKFIIGFSIFLFFLFLGIFGPMFYRVDPTEMTWDYE-QPPSSAHPLGTDTY 62
           T+ + LF+N+   IG  + +  + + +F P+    DP +    Y  +PPS+   LGTDTY
Sbjct: 14  TLWQALFQNRLSWIGIGLLVMIVLVALFAPLIAPYDPLQQNIAYRLEPPSAEFWLGTDTY 73

Query: 63  GRDVLAQLLHGIRSSLYIGFLAAIISLVIGTIIGSFSAVKRGIVDDVLMGITNIVLTTPS 122
           GRDVL++L++G R SL +GF+A +I++V+G+ +G  +    GI D ++ G  +++L+ P+
Sbjct: 74  GRDVLSRLIYGTRVSLLVGFVAVMIAMVVGSALGVIAGYVGGITDRLITGFVDVLLSFPT 133

Query: 123 ILIAILIASYLKVRSVEMVAVILGLFQWPWFARAIRAQLMSVMSREYVYLSVMAGYSDLR 182
           +L+ +++A+ L   S+E + + + + +   F R  RA  +++  R++V      GY   R
Sbjct: 134 LLLGLMVAAMLGA-SLENLIIAIAITEIAPFVRIARAPTIALKQRDFVEAGRSLGYGPGR 192

Query: 183 LVIEDLIPTIATYAFMSFVLFINGGIMGEAGLSLIGLG-PTQGISLGIMLQ--WAVLMEA 239
           L+   ++P + +   +   L++   I  EA LS IGLG P    + G M++  +  +++A
Sbjct: 193 LMTVHILPNMISEVLVLGALWMATAIRTEASLSFIGLGVPPPAPTWGSMIREGFENILDA 252

Query: 240 VRRGLWWWFVPPGLAIVAVTASLLVISTAMDEVFNPRLREE 280
                WW  V P LAI+    +L ++  A+ +  +P+ R E
Sbjct: 253 -----WWLTVFPSLAILLTVLALSLLGDALRDANDPKTRSE 288


Lambda     K      H
   0.330    0.144    0.441 

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: 196
Number of extensions: 12
Number of successful extensions: 4
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: 280
Length of database: 290
Length adjustment: 26
Effective length of query: 254
Effective length of database: 264
Effective search space:    67056
Effective search space used:    67056
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 47 (22.7 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