GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuK in Pseudomonas stutzeri RCH2

Align ABC transporter (characterized, see rationale)
to candidate GFF857 Psest_0871 ABC-type sugar transport systems, ATPase components

Query= uniprot:A0A166QFW2
         (381 letters)



>FitnessBrowser__psRCH2:GFF857
          Length = 371

 Score =  379 bits (972), Expect = e-109
 Identities = 211/364 (57%), Positives = 251/364 (68%), Gaps = 5/364 (1%)

Query: 1   MIKLKLDNVNKQLGGMRILRDVSLEIAAGEFVVFVGPSGCGKSTLLRLIAGLDSICGGDL 60
           M  + L ++ K   G  I R + L+I  GEFVVFVGPSGCGKSTLLRLIAGL+ I  GDL
Sbjct: 1   MASVTLRDICKSYDGTPITRHIDLDIEDGEFVVFVGPSGCGKSTLLRLIAGLEDITSGDL 60

Query: 61  LIDGRRVNDLEPRERGVGMVFQSYALYPHMSVYDNISFGLKLAKTDKTSLRERVLKTAQI 120
           LID +RVNDL P++R VGMVFQSYALYPHM+V +N++FGLKLA  DK  ++ RV   A+I
Sbjct: 61  LIDNQRVNDLPPKDRSVGMVFQSYALYPHMTVAENMAFGLKLASVDKREIKRRVEAVAEI 120

Query: 121 LQLDKLLQRKPKELSGGQRQRVAMGRAMAREPDILLFDEPLSNLDASLRVQMRNEIARLH 180
           LQLDKLL+RKPK+LSGGQRQRVA+GR M REP + LFDEPLSNLDA LRVQMR EIARLH
Sbjct: 121 LQLDKLLERKPKDLSGGQRQRVAIGRTMVREPKVFLFDEPLSNLDAFLRVQMRIEIARLH 180

Query: 181 DRLGSTMIYVTHDQVEAMTLADKIVVLNGGRVEQVGSPRELYERPASRFVAGFLGSPRMN 240
            R+ STMIYVTHDQVEAMTLADKIVVLN G + QVG P  LY  P +RFVAGFLGSP+MN
Sbjct: 181 QRIRSTMIYVTHDQVEAMTLADKIVVLNAGEIAQVGQPLHLYHYPKNRFVAGFLGSPQMN 240

Query: 241 FLSAR-LQTPGETSLVDTLVWGITSLPFDSSNLAAGTPLSLGIRPEH-VSLKAADGTAGV 298
           F+  R +    ET  ++       +LP D S ++ G PL+LGIRPEH V    AD T   
Sbjct: 241 FVEVRAISASPETVTIELPSGYPLTLPVDGSAVSPGDPLTLGIRPEHFVMPDEADFTFHG 300

Query: 299 VVTAVEYLGSET--YVHLETGQDEPLICRCEVSAGWQAGDRVELLLDLDNLHLFDADGVA 356
            +T  E LG     Y+ LE  QD   +C  + +     G+     L  D  HLF  +G A
Sbjct: 301 QITVAERLGQYNLLYLTLERLQDVITLC-VDGNLRVTEGETFAAGLKADKCHLFRENGEA 359

Query: 357 LSRH 360
            +RH
Sbjct: 360 CTRH 363


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: 13
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: 371
Length adjustment: 30
Effective length of query: 351
Effective length of database: 341
Effective search space:   119691
Effective search space used:   119691
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