GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuK in Pseudomonas fluorescens FW300-N2E3

Align ABC transporter (characterized, see rationale)
to candidate AO353_07265 AO353_07265 spermidine/putrescine ABC transporter ATP-binding protein

Query= uniprot:A0A166QFW2
         (381 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_07265
          Length = 374

 Score =  244 bits (623), Expect = 3e-69
 Identities = 137/342 (40%), Positives = 209/342 (61%), Gaps = 11/342 (3%)

Query: 18  ILRDVSLEIAAGEFVVFVGPSGCGKSTLLRLIAGLDSICGGDLLIDGRRVNDLEPRERGV 77
           I++D++LEI  GEF+  +GPSG GK+T L ++AG ++   G++L+ GR +N++ P +R +
Sbjct: 30  IVKDLNLEIRKGEFLTLLGPSGSGKTTSLMMLAGFETPTAGEILLAGRAINNVPPHKRDI 89

Query: 78  GMVFQSYALYPHMSVYDNISFGLKLAKTDKTSLRERVLKTAQILQLDKLLQRKPKELSGG 137
           GMVFQ+YAL+PHM+V +N++F L +   +K+ + +RV +   ++QLD   QR P +LSGG
Sbjct: 90  GMVFQNYALFPHMTVAENLAFPLTVRGLNKSDVSDRVKRVLSMVQLDAFAQRYPAQLSGG 149

Query: 138 QRQRVAMGRAMAREPDILLFDEPLSNLDASLRVQMRNEIARLHDRLGSTMIYVTHDQVEA 197
           Q+QRVA+ RA+  EP ++L DEPL  LD  LR  M+ EI  LH RLG T++YVTHDQ EA
Sbjct: 150 QQQRVALARALVFEPQLVLMDEPLGALDKQLREHMQMEIKHLHQRLGVTVVYVTHDQGEA 209

Query: 198 MTLADKIVVLNGGRVEQVGSPRELYERPASRFVAGFLGSPRMNFLSARLQTPGETSLVDT 257
           +T++D++ V + G ++Q+  PRELYE+P + FVA F+G    N L+ RL +      V  
Sbjct: 210 LTMSDRVAVFHQGEIQQIAPPRELYEKPKNTFVANFIG--ENNRLNGRLHSHTGDRCVVE 267

Query: 258 LVWGITSLPFDSSNLAAGTPLSLGIRPEHVSLKAADGT-----AGVVVTAVEYLGSETYV 312
           L  G        +    G P++L IRPE VSL  +  +     +G V   + YLG    V
Sbjct: 268 LGRGEKVEALAVNVGKTGEPVTLSIRPERVSLNGSSESCVNRFSGRVAEFI-YLGDHVRV 326

Query: 313 HLET-GQDEPLICR--CEVSAGWQAGDRVELLLDLDNLHLFD 351
            LE  G+ +  + +   E+      GD V L   ++++   D
Sbjct: 327 RLEVCGKTDFFVKQPIAELDPALAVGDVVPLGWQVEHVRALD 368


Lambda     K      H
   0.320    0.137    0.394 

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: 338
Number of extensions: 17
Number of successful extensions: 2
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: 381
Length of database: 374
Length adjustment: 30
Effective length of query: 351
Effective length of database: 344
Effective search space:   120744
Effective search space used:   120744
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: 50 (23.9 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