GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuK in Pseudomonas fluorescens FW300-N1B4

Align ABC transporter (characterized, see rationale)
to candidate Pf1N1B4_4847 Various polyols ABC transporter, ATP-binding component

Query= uniprot:A0A166QFW2
         (381 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_4847
          Length = 367

 Score =  371 bits (953), Expect = e-107
 Identities = 195/361 (54%), Positives = 253/361 (70%), Gaps = 2/361 (0%)

Query: 1   MIKLKLDNVNKQLGGMRILRDVSLEIAAGEFVVFVGPSGCGKSTLLRLIAGLDSICGGDL 60
           M  LK+ N+ K   G  I++ + LE+   EFVVFVGPSGCGKSTLLRLIAGL+ + GG +
Sbjct: 1   MANLKIKNLQKGFEGFSIIKGIDLEVNDKEFVVFVGPSGCGKSTLLRLIAGLEEVSGGTI 60

Query: 61  LIDGRRVNDLEPRERGVGMVFQSYALYPHMSVYDNISFGLKLAKTDKTSLRERVLKTAQI 120
            +DGR + ++ P +R + MVFQ+YALYPHMSV  N+SF L LA   K  + ++V + A+I
Sbjct: 61  ELDGRDITEVSPAKRDLAMVFQTYALYPHMSVRKNMSFALDLAGVAKAEVEKKVGEAARI 120

Query: 121 LQLDKLLQRKPKELSGGQRQRVAMGRAMAREPDILLFDEPLSNLDASLRVQMRNEIARLH 180
           L+L  +L+RKPK+LSGGQRQRVA+GRA+ R P I LFDEPLSNLDA+LRVQMR E+ RLH
Sbjct: 121 LELGPMLERKPKQLSGGQRQRVAIGRAIVRNPKIFLFDEPLSNLDAALRVQMRLELLRLH 180

Query: 181 DRLGSTMIYVTHDQVEAMTLADKIVVLNGGRVEQVGSPRELYERPASRFVAGFLGSPRMN 240
             L +TMIYVTHDQVEAMT+ADK+VVLNGG++EQVGSP +LY +PA+ FVAGFLG+P+M 
Sbjct: 181 KELQATMIYVTHDQVEAMTMADKVVVLNGGKIEQVGSPLDLYHQPANLFVAGFLGTPKMG 240

Query: 241 FLSARLQTPGETSLVDTLVWGI-TSLPFDSSNLAAGTPLSLGIRPEHVSL-KAADGTAGV 298
           FL  ++      S    L  G   +LP   +NL+ G  ++LGIRPEH+ L +  D T  V
Sbjct: 241 FLKGKVTRVNGQSCEVLLDAGTRITLPLSGANLSVGGAVTLGIRPEHLELAQPGDCTLQV 300

Query: 299 VVTAVEYLGSETYVHLETGQDEPLICRCEVSAGWQAGDRVELLLDLDNLHLFDADGVALS 358
                E LGS+T+ H+ T   E L  R       + G+ + L LD ++ HLFDADGVAL+
Sbjct: 301 TADVSERLGSDTFCHVLTSSGEALTMRVRGDLASRYGETLSLHLDAEHCHLFDADGVALT 360

Query: 359 R 359
           R
Sbjct: 361 R 361


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: 388
Number of extensions: 12
Number of successful extensions: 3
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: 367
Length adjustment: 30
Effective length of query: 351
Effective length of database: 337
Effective search space:   118287
Effective search space used:   118287
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