GapMind for catabolism of small carbon sources

 

Aligments for a candidate for natA in Pseudomonas fluorescens FW300-N1B4

Align NatA aka BRAF aka SLR0467, component of Leucine/proline/alanine/serine/glycine (and possibly histidine) porter, NatABCDE (characterized)
to candidate Pf1N1B4_1346 Urea ABC transporter, ATPase protein UrtD

Query= TCDB::Q55164
         (267 letters)



>lcl|FitnessBrowser__pseudo1_N1B4:Pf1N1B4_1346 Urea ABC transporter,
           ATPase protein UrtD
          Length = 289

 Score =  135 bits (339), Expect = 1e-36
 Identities = 87/269 (32%), Positives = 148/269 (55%), Gaps = 17/269 (6%)

Query: 1   MSDRITPAENLGSPESSLLLAQGLSKSFGGLRAVDHADIVVKEGSITGLIGPNGAGKTTL 60
           +  R+ P   L +   ++L  + +S SF G +A++  ++ +  G +  +IGPNGAGKTTL
Sbjct: 33  LGQRVGPG--LNTRHGTILTLEDISVSFDGFKALNDLNLYIGVGELRCIIGPNGAGKTTL 90

Query: 61  FNLLSNFIRPDQGEVLFNGD-SIGQLAPHQIALRGSVRTFQVAKVLSRLTVLENMLLADQ 119
            ++++   RP  G+  F     + Q++  QIA  G  R FQ   V   L+V EN+ LA  
Sbjct: 91  MDVITGKTRPSHGKAWFGETLDLTQMSEVQIAQAGIGRKFQKPTVFEALSVFENLELA-- 148

Query: 120 HQTGEKFLPRLINFRRVQKEERANREKAMAMLESVGLGAKAQDYAGALSGGQRKLLEMAR 179
            Q  +K +   +  R   ++    +++   +LE++ L A     AG LS GQ++ LE+  
Sbjct: 149 -QKTDKSVWASLRARLSGEQ----KDRISEVLETIRLTASVNRPAGMLSHGQKQFLEIGM 203

Query: 180 ALMSNPKLILLDEPAAGVNPT---LIGQICEHIVNWNRQGITFLVIEHNMDVIMTLCHHV 236
            LM +P+L+LLDEP AG+         ++ + +   +    + +V+EH+M  + ++  HV
Sbjct: 204 LLMQDPQLLLLDEPVAGMTDAETEFTAELFKSLAGKH----SLMVVEHDMGFVGSIADHV 259

Query: 237 WVLAEGRNLADGTPEQIQSDPRVLEAYLG 265
            VL +G  LA+G+ EQ+Q + RV+E YLG
Sbjct: 260 TVLHQGSVLAEGSLEQVQDNERVIEVYLG 288


Lambda     K      H
   0.319    0.136    0.389 

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: 190
Number of extensions: 9
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: 267
Length of database: 289
Length adjustment: 25
Effective length of query: 242
Effective length of database: 264
Effective search space:    63888
Effective search space used:    63888
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 (21.7 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 the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.

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