GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21106 in Pseudomonas stutzeri RCH2

Align ABC transporter for L-Fucose, ATPase component (characterized)
to candidate GFF857 Psest_0871 ABC-type sugar transport systems, ATPase components

Query= reanno::Smeli:SM_b21106
         (365 letters)



>FitnessBrowser__psRCH2:GFF857
          Length = 371

 Score =  312 bits (799), Expect = 1e-89
 Identities = 179/369 (48%), Positives = 227/369 (61%), Gaps = 17/369 (4%)

Query: 1   MAPVTLKKLVKRYGALEVVHGIDLEVKDREFIALVGPSGCGKSTTLRMIAGLEEVSGGAI 60
           MA VTL+ + K Y    +   IDL+++D EF+  VGPSGCGKST LR+IAGLE+++ G +
Sbjct: 1   MASVTLRDICKSYDGTPITRHIDLDIEDGEFVVFVGPSGCGKSTLLRLIAGLEDITSGDL 60

Query: 61  EIGGRKVNDLPPRARNISMVFQSYALYPHMTVAENMGFSLKIAGRPAEEIKTRVAEAAAI 120
            I  ++VNDLPP+ R++ MVFQSYALYPHMTVAENM F LK+A     EIK RV   A I
Sbjct: 61  LIDNQRVNDLPPKDRSVGMVFQSYALYPHMTVAENMAFGLKLASVDKREIKRRVEAVAEI 120

Query: 121 LDLAHLLERRPSQLSGGQRQRVAMGRAIVRQPDVFLFDEPLSNLDAKLRTQVRTEIKKLH 180
           L L  LLER+P  LSGGQRQRVA+GR +VR+P VFLFDEPLSNLDA LR Q+R EI +LH
Sbjct: 121 LQLDKLLERKPKDLSGGQRQRVAIGRTMVREPKVFLFDEPLSNLDAFLRVQMRIEIARLH 180

Query: 181 ARMQATMIYVTHDQVEAMTLSDRIVIMRDGHIEQVGTPEDVFRRPATKFVAGFIGSPPMN 240
            R+++TMIYVTHDQVEAMTL+D+IV++  G I QVG P  ++  P  +FVAGF+GSP MN
Sbjct: 181 QRIRSTMIYVTHDQVEAMTLADKIVVLNAGEIAQVGQPLHLYHYPKNRFVAGFLGSPQMN 240

Query: 241 MEEAVLTDGK-----LAFASGATLPLPPRFRSLVREGQKVTFGLRPDDVYPSGHGLHAGD 295
             E            +   SG  L LP    S V  G  +T G+RP+      H +   +
Sbjct: 241 FVEVRAISASPETVTIELPSGYPLTLPVD-GSAVSPGDPLTLGIRPE------HFVMPDE 293

Query: 296 ADAVHEIELPVTITEPLGNETLVFTQFNGRDWVSRMLNPRPLR--PGEAVPMSFDLARAH 353
           AD     +  +T+ E LG   L++        V  +     LR   GE         + H
Sbjct: 294 ADFTFHGQ--ITVAERLGQYNLLYLTLERLQDVITLCVDGNLRVTEGETFAAGLKADKCH 351

Query: 354 LFDGETGRA 362
           LF  E G A
Sbjct: 352 LF-RENGEA 359


Lambda     K      H
   0.320    0.137    0.397 

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: 411
Number of extensions: 22
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: 365
Length of database: 371
Length adjustment: 30
Effective length of query: 335
Effective length of database: 341
Effective search space:   114235
Effective search space used:   114235
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