GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglK in Dinoroseobacter shibae DFL-12

Align ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized)
to candidate 3607949 Dshi_1357 ABC transporter related (RefSeq)

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



>FitnessBrowser__Dino:3607949
          Length = 349

 Score =  343 bits (879), Expect = 5e-99
 Identities = 196/361 (54%), Positives = 237/361 (65%), Gaps = 12/361 (3%)

Query: 1   MTGLLLKDIRKSYGAVDVIHGIDLDIKEGEFVVFVGPSGCGKSTLLRMIAGLEEITGGDM 60
           M  + L  + K +G V VI G+DL+I++GEFVVFVGPSGCGKSTLLRMI GLE+ + G M
Sbjct: 1   MGAITLSKVEKWFGDVQVIKGVDLEIRDGEFVVFVGPSGCGKSTLLRMIGGLEDTSRGAM 60

Query: 61  FIDGERVNDVPPSKRGIAMVFQSYALYPHMTVYDNMAFGMRIARESKEEIDRRVRGAADM 120
            IDG  V D PP+KRG+ MVFQSYALYPHM+V +NM F ++ A     EI  +V  AA +
Sbjct: 61  LIDGVDVTDHPPAKRGLTMVFQSYALYPHMSVRENMGFSLKTAGAPAAEIAEKVEAAAAV 120

Query: 121 LQLTPYLDRLPKALSGGQRQRVAIGRAICRNPKVFLFDEPLSNLDAALRVATRIEIAKLS 180
           L+L PYLDR PK LSGGQRQRVAIGR+I R P  FLFDEPLSNLDAALRV  R EIAKL 
Sbjct: 121 LKLEPYLDRRPKDLSGGQRQRVAIGRSIVRAPTAFLFDEPLSNLDAALRVEMRYEIAKLH 180

Query: 181 ERMSDTTMIYVTHDQVEAMTLADRIVVLSAGHIEQVGAPLELYERPANLFVARFIGSPAM 240
           + + DTTMIYVTHDQVEAMTLADRIVVL  G I QVG P ELYE PANLFVA+FIGSP M
Sbjct: 181 QSL-DTTMIYVTHDQVEAMTLADRIVVLEFGKIAQVGTPRELYETPANLFVAQFIGSPKM 239

Query: 241 NVIPATITATGQQTAVSLAGGKSVTLDVPTNASENGKTASFGVRPEDLRVTEADDFLFEG 300
           NV+P T T  G+    +  GG           S +      G+RPE +          +G
Sbjct: 240 NVMPCT-TDAGRYRLSAGRGGV---------FSGDRPAVQLGIRPEHITPGAPGTGACDG 289

Query: 301 TVSIVEALGEVTLLYIEGLVENEPIIAKMPGIARVGRGDKVRFTADKAKLHLFDTNGQSY 360
            V +VE LG  TLL ++   E   +  ++ G   +  GD V  + +  +L  FDT+G + 
Sbjct: 290 RVDVVEYLGADTLLVLDCGPEGR-VTVRVIGDTDLTPGDAVGLSFNPDRLSFFDTDGLAI 348

Query: 361 R 361
           R
Sbjct: 349 R 349


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: 378
Number of extensions: 11
Number of successful extensions: 4
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: 349
Length adjustment: 29
Effective length of query: 333
Effective length of database: 320
Effective search space:   106560
Effective search space used:   106560
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.

Links

Downloads

Related tools

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