GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc02869 in Pseudomonas fluorescens GW456-L13

Align N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized)
to candidate PfGW456L13_1799 Putrescine transport ATP-binding protein PotA (TC 3.A.1.11.1)

Query= reanno::Phaeo:GFF2754
         (331 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1799
          Length = 351

 Score =  237 bits (605), Expect = 3e-67
 Identities = 138/323 (42%), Positives = 192/323 (59%), Gaps = 28/323 (8%)

Query: 1   MTALQLTNVCKSFGPVEVLKDINLTVEDGEFVVFVGPSGCGKSTLLRVISGLEDATAGEI 60
           M+ L L NV K +G    +KD+NL + +G+ V F+GPSGCGK+TLLR+I+GLE  + GEI
Sbjct: 1   MSGLILENVEKHYGSACAVKDVNLHLPEGKLVCFLGPSGCGKTTLLRMIAGLETLSGGEI 60

Query: 61  SIGGQTVTTTPPAKRGIAMVFQSYALYPHLSVRENMALALKQERQPKEEIAARVAEASRM 120
            + G+ +  TP   R   MVFQS AL+PH++V EN+A  LK     K +  ARV E   +
Sbjct: 61  RLDGEDIGHTPAHLRNFGMVFQSLALFPHMTVGENIAYPLKLRGVSKADQQARVVELLEL 120

Query: 121 LSLEDYLDRRPSELSGGQRQRVAIGRAVVREPKLFLFDEPLSNLDAALRMNTRLEIARLH 180
           + L+  ++R  ++LSGGQRQRVAI RA+   PK+ L DEPLS LDA LR + ++EI +L 
Sbjct: 121 IQLQAMINRPVAKLSGGQRQRVAIARAIANHPKILLLDEPLSALDAKLRESMQVEIRQLQ 180

Query: 181 RQLSASMIYVTHDQIEAMTLADKIVVLRDGRIEQVGTPMELYNNPANRFVAEFIGAPAMN 240
           ++L+ + I VTHDQ EAMT+AD +VVL + +++QVGTP+E+Y +PAN FVA+FIG+   N
Sbjct: 181 QRLNITTIMVTHDQREAMTMADIVVVLGEHKVQQVGTPIEIYRHPANEFVADFIGSG--N 238

Query: 241 FVPAQRLGGNPGQFIG---------------------IRPEYARISPVGPLAGEVIHVEK 279
             PA  LG       G                     IRPE  ++S     AG      +
Sbjct: 239 IFPATVLGNGKVSLPGGDALQVPICSSIVVGEKVKMLIRPEDLQLSAPQATAG-----NR 293

Query: 280 LGGDTNILVDMGEDLTFTARLFG 302
           L G    + D+G  +  T    G
Sbjct: 294 LLGKVTFVRDIGATIETTVECSG 316


Lambda     K      H
   0.320    0.137    0.391 

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: 314
Number of extensions: 14
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: 331
Length of database: 351
Length adjustment: 28
Effective length of query: 303
Effective length of database: 323
Effective search space:    97869
Effective search space used:    97869
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