GapMind for catabolism of small carbon sources

 

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

Align ABC transporter for Glycerol, ATPase component 2 (characterized)
to candidate 3607949 Dshi_1357 ABC transporter related (RefSeq)

Query= reanno::acidovorax_3H11:Ac3H11_792
         (358 letters)



>FitnessBrowser__Dino:3607949
          Length = 349

 Score =  207 bits (527), Expect = 3e-58
 Identities = 124/331 (37%), Positives = 186/331 (56%), Gaps = 11/331 (3%)

Query: 29  MEFEDGGAYALLGPSGCGKTTMLNIMSGLLVPSHGKVLFDGRDVTRASPQERNIAQVFQF 88
           +E  DG     +GPSGCGK+T+L ++ GL   S G +L DG DVT   P +R +  VFQ 
Sbjct: 24  LEIRDGEFVVFVGPSGCGKSTLLRMIGGLEDTSRGAMLIDGVDVTDHPPAKRGLTMVFQS 83

Query: 89  PVIYDTMTVAENLAFPLRNRKVPEGQIKQRVGVIAEMLEMSGQLNQRAAGLAADAKQKIS 148
             +Y  M+V EN+ F L+    P  +I ++V   A +L++   L++R   L+   +Q+++
Sbjct: 84  YALYPHMSVRENMGFSLKTAGAPAAEIAEKVEAAAAVLKLEPYLDRRPKDLSGGQRQRVA 143

Query: 149 LGRGLVRADVAAVLFDEPLTVIDPHLKWQLRRKLKQIHHELKLTLIYVTHDQVEALTFAD 208
           +GR +VRA  A  LFDEPL+ +D  L+ ++R ++ ++H  L  T+IYVTHDQVEA+T AD
Sbjct: 144 IGRSIVRAPTA-FLFDEPLSNLDAALRVEMRYEIAKLHQSLDTTMIYVTHDQVEAMTLAD 202

Query: 209 QVVVMTRGKAVQVGSADALFERPAHTFVGHFIGSPGMNFLPAHRDGENLSVAGHRLASPV 268
           ++VV+  GK  QVG+   L+E PA+ FV  FIGSP MN +P   D        +RL++  
Sbjct: 203 RIVVLEFGKIAQVGTPRELYETPANLFVAQFIGSPKMNVMPCTTD-----AGRYRLSAGR 257

Query: 269 GRALPAG--ALQVGIRPEYLALAQPQQAGALPGTVVQVQDIGTYQMLTAKVG-EHTVKAR 325
           G        A+Q+GIRPE++    P   GA  G V  V+ +G   +L    G E  V  R
Sbjct: 258 GGVFSGDRPAVQLGIRPEHITPGAP-GTGACDGRVDVVEYLGADTLLVLDCGPEGRVTVR 316

Query: 326 FTPETRLPSSGDTAWLQVLGEHTCYYKNEEL 356
              +T L + GD   L    +   ++  + L
Sbjct: 317 VIGDTDL-TPGDAVGLSFNPDRLSFFDTDGL 346


Lambda     K      H
   0.320    0.136    0.395 

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: 273
Number of extensions: 13
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: 358
Length of database: 349
Length adjustment: 29
Effective length of query: 329
Effective length of database: 320
Effective search space:   105280
Effective search space used:   105280
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