GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PfGW456L13_1897 in Dinoroseobacter shibae DFL-12

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

Query= reanno::pseudo13_GW456_L13:PfGW456L13_1897
         (386 letters)



>FitnessBrowser__Dino:3607949
          Length = 349

 Score =  295 bits (754), Expect = 2e-84
 Identities = 167/360 (46%), Positives = 221/360 (61%), Gaps = 20/360 (5%)

Query: 1   MATLELRNVNKTYGPGLPDTLKNIELKIDDGEFLILVGPSGCGKSTLMNCIAGLETISGG 60
           M  + L  V K +G      +K ++L+I DGEF++ VGPSGCGKSTL+  I GLE  S G
Sbjct: 1   MGAITLSKVEKWFGD--VQVIKGVDLEIRDGEFVVFVGPSGCGKSTLLRMIGGLEDTSRG 58

Query: 61  AILVDDADISGMSPKDRDIAMVFQSYALYPTMSVRDNIAFGLKIRKMPTAEIDEEVARVS 120
           A+L+D  D++   P  R + MVFQSYALYP MSVR+N+ F LK    P AEI E+V   +
Sbjct: 59  AMLIDGVDVTDHPPAKRGLTMVFQSYALYPHMSVRENMGFSLKTAGAPAAEIAEKVEAAA 118

Query: 121 KLLQIEHLLSRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKL 180
            +L++E  L R+P  LSGGQ+QRVA+GR++ R P  +LFDEPLSNLDA LRVEMR E+  
Sbjct: 119 AVLKLEPYLDRRPKDLSGGQRQRVAIGRSIVRAPTAFLFDEPLSNLDAALRVEMRYEIAK 178

Query: 181 MHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKDIYNNPANLFVASFIGSPP 240
           +HQ L TT +YVTHDQ+EAMTL D++ V++ G I Q GTP+++Y  PANLFVA FIGSP 
Sbjct: 179 LHQSLDTTMIYVTHDQVEAMTLADRIVVLEFGKIAQVGTPRELYETPANLFVAQFIGSPK 238

Query: 241 MNFIPLRLQRKDGRLLALLDSGQARCELPLGMQDAGLEDREVI-LGIRPEQIILANGEAN 299
           MN +P              D+G+ R     G   +G  DR  + LGIRPE I      A 
Sbjct: 239 MNVMP-----------CTTDAGRYRLSAGRGGVFSG--DRPAVQLGIRPEHI---TPGAP 282

Query: 300 GLPTIRAEVQVTEPTGPDTLVFVNLN-DTKVCCRLAPDVAPAVGETLTLQFDPAKVLLFD 358
           G       V V E  G DTL+ ++   + +V  R+  D     G+ + L F+P ++  FD
Sbjct: 283 GTGACDGRVDVVEYLGADTLLVLDCGPEGRVTVRVIGDTDLTPGDAVGLSFNPDRLSFFD 342


Lambda     K      H
   0.319    0.138    0.393 

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: 368
Number of extensions: 12
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: 386
Length of database: 349
Length adjustment: 30
Effective length of query: 356
Effective length of database: 319
Effective search space:   113564
Effective search space used:   113564
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 (21.7 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