GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c12650 in Marinobacter algicola DG893

Align D-lactate transporter, permease component 1 (characterized)
to candidate WP_007154551.1 MDG893_RS14445 branched-chain amino acid ABC transporter permease

Query= reanno::Phaeo:GFF1249
         (400 letters)



>NCBI__GCF_000170835.1:WP_007154551.1
          Length = 331

 Score =  178 bits (451), Expect = 2e-49
 Identities = 112/311 (36%), Positives = 157/311 (50%), Gaps = 48/311 (15%)

Query: 6   KKDKTLLLVVAILTLFAPFILNPFPTGSALAQFNAGYPDLMQRFVIFGIFAIGFNILFGL 65
           +K + L LV+ +L L AP ++               YP  + + + F +FA+ FN+L G 
Sbjct: 23  RKKQILNLVLLVLLLLAPAVM---------------YPVFLMKILCFALFAVAFNLLLGY 67

Query: 66  TGYLSFGHAAFLGVGSYSAVWMFKLLS-MNVVPAIVLSVIVAGLFALVIGYVSLRRSGIY 124
           TG LSFGHAAFL  GSY+  ++    S +     I+     A +  L  G V++RR GIY
Sbjct: 68  TGLLSFGHAAFLAAGSYTTGYLLSNFSGLTTEMGIIAGTAAATVLGLGFGVVAIRRQGIY 127

Query: 125 FSILTLAFAQMSFNLAYSVLTPITNGETGLQLTLDDPRVLGVSATADGSIPVTSLFGL-E 183
           F+++TLA AQ+ +   + V  P T GE G+                   +P   LFGL +
Sbjct: 128 FAMITLALAQLVY--FFFVQAPFTGGEDGMH-----------------GVPRGHLFGLVD 168

Query: 184 MRSTFEMVVGPWAFQFNAGYYLCALILLAAFYLSIRIFRSPFGLMLKAVKSNQQRMNYTG 243
           + + + M            YY    + L  + +  RI  SPFG +LKA+K N+ R    G
Sbjct: 169 LSNNYAM------------YYFVLAVFLGGYLVVQRIVGSPFGQVLKAIKQNEPRAVSLG 216

Query: 244 LNTRPYTLAAFVISGMYAGLAGGLMASMDPLAGAERMQWTASGEVVLMTILGGAGTLIGP 303
            N   Y L AFVIS   AGLAG +   +  LA      W  SGEV+LMT+LGG GTL+GP
Sbjct: 217 YNVDRYKLLAFVISASLAGLAGSVKTVVFQLASLNDAHWHMSGEVILMTLLGGTGTLLGP 276

Query: 304 VLGAGFIKYFE 314
           V+GA F+   E
Sbjct: 277 VVGATFVVNLE 287


Lambda     K      H
   0.327    0.143    0.435 

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: 441
Number of extensions: 40
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: 400
Length of database: 331
Length adjustment: 29
Effective length of query: 371
Effective length of database: 302
Effective search space:   112042
Effective search space used:   112042
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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