GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c12650 in Halostagnicola larsenii XH-48

Align D-lactate transporter, permease component 1 (characterized)
to candidate WP_049954224.1 HALLA_RS14495 branched-chain amino acid ABC transporter permease

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



>NCBI__GCF_000517625.1:WP_049954224.1
          Length = 359

 Score =  171 bits (432), Expect = 4e-47
 Identities = 108/361 (29%), Positives = 177/361 (49%), Gaps = 61/361 (16%)

Query: 11  LLLVVAILTLFAPFILNPFPTGSALAQFNAGYPDLMQRFVIFGIFAIGFNILFGLTGYLS 70
           L++ +A L + AP +           Q +  + +L+ R +IF +FA+  + +FG  G LS
Sbjct: 29  LVIAIAALAVAAPIV----------EQIHPFWLNLLVRMMIFALFALSLDFVFGYAGLLS 78

Query: 71  FGHAAFLGVGSYSAVWMFKLLSMNVVPAIVLSVIVAGLFALVIGYVSLRRSGIYFSILTL 130
           FGHAA  G G Y+A  +    + +    + ++VI   + A +IG++S+R  GIYF++LTL
Sbjct: 79  FGHAAMFGAGGYAAAILLTDGTSHAFVVLPVAVIAGVVVAALIGWLSVRARGIYFAMLTL 138

Query: 131 AFAQMSFNLAYSVLTPITNGETGLQLTLDDPRVLGVSATADGSIPVTSLFGLEMRSTFEM 190
           AFAQM + +A++ L     G+  +  T  D  + G+         +  LFG++   T   
Sbjct: 139 AFAQMFYVIAFTDLPATVLGQESV--TGGDNGLYGIG--------MYELFGIDFTETLMY 188

Query: 191 VVGPWAFQFNAGYYLCALILLAAFYLSIRIFRSPFGLMLKAVKSNQQRMNYTGLNTRPYT 250
                       +YL   ++  +  + +R+  S FG +L+ ++ N++R+ + G + R Y 
Sbjct: 189 ------------FYLTLALVALSLAVLVRLANSQFGRVLQGIRENEERVEFIGYDVRRYK 236

Query: 251 LAAFVISGMYAGLAGGLMASMDPLAGAERMQWTASGEVVLMTILGGAGTLIGPVLGAGFI 310
           +  F ISG +AGLAGGL      +A    + W  SGE+++M +LGG GTL GP+LGAG +
Sbjct: 237 VVGFAISGGFAGLAGGLYVPFQSVAHPGNLHWMISGELIVMLLLGGMGTLWGPMLGAGLV 296

Query: 311 KYFENIFSKINDNVLHSWFSFMPDGIEDAMVFIVHPFIGKGWHLTLGILFMLVVIFLPGG 370
              E   +                                 W + LG +F+ VVIF P G
Sbjct: 297 VLLEEQLAGF-----------------------------ASWEVILGSIFVGVVIFAPRG 327

Query: 371 L 371
           L
Sbjct: 328 L 328


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: 458
Number of extensions: 30
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 400
Length of database: 359
Length adjustment: 30
Effective length of query: 370
Effective length of database: 329
Effective search space:   121730
Effective search space used:   121730
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: 50 (23.9 bits)

This GapMind analysis is from Sep 24 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