GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuK in Phaeobacter inhibens BS107

Align ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized)
to candidate GFF1645 PGA1_c16680 sugar ABC transporter, ATP-binding protein

Query= reanno::Smeli:SMc03065
         (362 letters)



>FitnessBrowser__Phaeo:GFF1645
          Length = 355

 Score =  360 bits (924), Expect = e-104
 Identities = 198/363 (54%), Positives = 248/363 (68%), Gaps = 13/363 (3%)

Query: 1   MTGLLLKDIRKSYGAVDVIHGIDLDIKEGEFVVFVGPSGCGKSTLLRMIAGLEEITGGDM 60
           M  + L+D+ K YGAV+V+  I+LDI++GEF+V VGPSGCGKSTLLRMIAGLE IT GD 
Sbjct: 1   MARIELRDVAKRYGAVEVLRDINLDIQDGEFIVLVGPSGCGKSTLLRMIAGLEPITSGDF 60

Query: 61  FIDGERVNDVPPSKRGIAMVFQSYALYPHMTVYDNMAFGMRIARESKEEIDRRVRGAADM 120
            IDG+R+NDV P  R IAMVFQSYALYPHM V  NM F M I ++  EE   RV  AA+ 
Sbjct: 61  EIDGQRMNDVRPRDRDIAMVFQSYALYPHMDVARNMGFSMEIRKDPAEERRSRVARAAET 120

Query: 121 LQLTPYLDRLPKALSGGQRQRVAIGRAICRNPKVFLFDEPLSNLDAALRVATRIEIAKLS 180
           L L+  +DRLPKALSGGQRQRVA+GRAI R+P+ FLFDEPLSNLDAALRV  R+EIA+L 
Sbjct: 121 LGLSSLVDRLPKALSGGQRQRVAMGRAIIRDPRAFLFDEPLSNLDAALRVEMRLEIARLH 180

Query: 181 ERMSDTTMIYVTHDQVEAMTLADRIVVLSAGHIEQVGAPLELYERPANLFVARFIGSPAM 240
           +++   TMIYVTHDQVEA+TLADRIVVL+ G I+QVG+PLELYERPAN FVA+FIGSP M
Sbjct: 181 KQLG-ATMIYVTHDQVEALTLADRIVVLNGGDIQQVGSPLELYERPANKFVAQFIGSPTM 239

Query: 241 NVIPATITATGQQTAVSLAGGKSVTLDVPTNASENGKTASFGVRPEDLRVTEADDFLFEG 300
           N++P +  A+G    V    G  +TLD   +  +       G+RPE L V E  +     
Sbjct: 240 NILPVSGAASG----VMATNGMMLTLD---HMHDTAAAVELGIRPEHLDVVEPGEGHLIA 292

Query: 301 TVSIVEALGEVTLLY--IEGLVENEPIIAKMPGIARVGRGDKVRFTADKAKLHLFDTNGQ 358
              +VE LG  T +Y  ++GL    P++ +  G   V  G+++         H+FD  G 
Sbjct: 293 VADVVERLGSDTNIYAKVDGL---GPLMVRKHGNVPVRSGERLGLRVQAQNAHIFDDRGI 349

Query: 359 SYR 361
           + R
Sbjct: 350 ALR 352


Lambda     K      H
   0.320    0.137    0.387 

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: 391
Number of extensions: 14
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: 362
Length of database: 355
Length adjustment: 29
Effective length of query: 333
Effective length of database: 326
Effective search space:   108558
Effective search space used:   108558
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