GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c12650 in Thioclava dalianensis DLFJ1-1

Align D-lactate transporter, permease component 1 (characterized)
to candidate WP_038066401.1 DL1_RS11905 branched-chain amino acid ABC transporter permease

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



>NCBI__GCF_000715505.1:WP_038066401.1
          Length = 323

 Score =  148 bits (373), Expect = 3e-40
 Identities = 108/367 (29%), Positives = 170/367 (46%), Gaps = 69/367 (18%)

Query: 15  VAILTLFAPFILNPFPTGSALAQFNAGYPDLMQRFVIFGIFAIGFNILFGLTGYLSFGHA 74
           V I    A  +L PF   S +         L    +I+ +     N+L G TG LSFG  
Sbjct: 9   VQICLALATVLLLPFVLNSGI---------LATEILIYAMVVAACNLLLGYTGLLSFGQG 59

Query: 75  AFLGVGSYSAVWMFKLLSMNVVPAIVLSVIVAGLFALVIGYVSLRRSGIYFSILTLAFAQ 134
            F G+G+Y A  +    ++ +   ++++V++ GL A  +G+ S+RR G+YF +LTLAFAQ
Sbjct: 60  IFFGLGTYVAGVLTTRWAVPIPLVLLVAVVLGGLVATAVGWFSIRRQGVYFVMLTLAFAQ 119

Query: 135 MSFNLAYSVLTPITNGETGLQLTLDDPRVLGVSATADGSIPVTSLFGLEMRSTFEMVVGP 194
           M + LAY+  + IT G+ GL L +  P+++G                        ++ GP
Sbjct: 120 MFYFLAYT-FSDITGGDNGL-LGVPRPQIMG-----------------------HVLDGP 154

Query: 195 WAFQFNAGYYLCALILLAAFYLSIRIFRSPFGLMLKAVKSNQQRMNYTGLNTRPYTLAAF 254
           W +     Y   A+  L  F + + + RS FG  L A++ N+ R    G   R + + AF
Sbjct: 155 WGY-----YSFVAIFFLVIFAVLLVVTRSTFGRTLLAIRENEGRAAAIGFPVRLFKIEAF 209

Query: 255 VISGMYAGLAGGLMASMDPLAGAERMQWTASGEVVLMTILGGAGTLIGPVLGAGFIKYFE 314
            ISG    L G L A +  +A  E + +  S  +++MTI+GG+ +L G V+GAGF     
Sbjct: 210 AISGAITALGGALHALLIGIAPLESINYHTSEMILVMTIIGGSTSLFGSVMGAGF----- 264

Query: 315 NIFSKINDNVLHSWFSFMPDGIEDAMVFIVHPFIGKGWHLTLGILFMLVVIFLPGGLVEG 374
             +  ++D +   W                       W L LG++ + V +F   GL   
Sbjct: 265 --YLLLSDTLSVIW---------------------PRWLLLLGLVLVTVALFFQRGL--W 299

Query: 375 GQKLRGW 381
           G   RGW
Sbjct: 300 GLVERGW 306


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: 410
Number of extensions: 32
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: 323
Length adjustment: 29
Effective length of query: 371
Effective length of database: 294
Effective search space:   109074
Effective search space used:   109074
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.

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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