GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glt in Dyella japonica UNC79MFTsu3.2

Align Sodium:dicarboxylate symporter (characterized, see rationale)
to candidate N515DRAFT_1080 N515DRAFT_1080 Na+/H+-dicarboxylate symporter

Query= uniprot:A1S570
         (437 letters)



>FitnessBrowser__Dyella79:N515DRAFT_1080
          Length = 422

 Score =  265 bits (677), Expect = 2e-75
 Identities = 144/397 (36%), Positives = 229/397 (57%), Gaps = 6/397 (1%)

Query: 23  ILIGLLLRNFFGGSEWVQDYITEGFFHVIGTIFINSLKMLVVPLVFISLVCGTCSLSEPS 82
           +L G +L    G   W+    +  +F  +G +++  +KM+ VPLVF ++V    SL    
Sbjct: 16  VLAGFVLGALAG---WLCGPGSVAWFQPLGDVYVALIKMIAVPLVFFAVVNSVSSLHGVQ 72

Query: 83  KLGRLGGKTLAFYLFTTAIALVVAISAAVLVQPG-NASLASESMQYSAKEAPSLADVLIN 141
           ++  LGG+T  ++  T A+A+ V +    L  PG      + +  Y  +E PS   VL++
Sbjct: 73  RMAALGGRTFLWFALTAALAVGVGLLVGHLTDPGLGVGQLTMAGDYKVREVPSAVKVLLD 132

Query: 142 IVPSNPMKALSEGNMLQIIIFAVIFGFAISHIGERGRRVAALFDDLNEVIMRVVTLIMQL 201
           +VP+NP +ALSEG +LQ+I FA + G A+  IGE+  R+  LF + N+ +++V   ++++
Sbjct: 133 VVPTNPFRALSEGKILQVIFFAGLLGLALVKIGEKSARLRELFGEANDAMIQVTRFVLEM 192

Query: 202 APYGVFALMGKLALTLGMETLESVIKYFMLVLVVLLFHGFVVYPTLLKLFSGLSPLMFIR 261
            P G F L+  L    G E L  + K+ + +         VVY  LL L  GLSP  F R
Sbjct: 193 TPIGTFGLIAALVAGYGFEKLLPLGKFVLALYAACAVQIVVVYGGLL-LAHGLSPRRFFR 251

Query: 262 KMRDVQLFAFSTASSNATLPVTMEASEHRLGADNKVASFTLPLGATINMDGT-AIMQGVA 320
            +      AF+++SS A++PV + +    LG     ASF +PLGA+I MDG  AI   ++
Sbjct: 252 GVLPAMQVAFTSSSSFASMPVALRSVTQNLGVSPAYASFAVPLGASIKMDGCGAIYPAIS 311

Query: 321 TVFIAQVFGIDLTITDYAMVVMTATLASIGTAGVPGVGLVMLAMVLNQVGLPVEGIALIL 380
           ++F+AQ FG+ L    Y ++++ + L S GTAGVPG   VM+ +VL+  GLPVEGI  ++
Sbjct: 312 SIFVAQYFGLQLEPAQYFVILLASVLGSFGTAGVPGTATVMVTLVLSSAGLPVEGIGYLV 371

Query: 381 GVDRMLDMVRTAVNVTGDTVATVVIAKSEGALNEAVF 417
            +DR+LDM+RT  NVTG  +  V++A+ +G L+  V+
Sbjct: 372 AIDRVLDMMRTMTNVTGQMLVPVLVAREQGLLDMDVY 408


Lambda     K      H
   0.325    0.139    0.388 

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: 369
Number of extensions: 17
Number of successful extensions: 5
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: 437
Length of database: 422
Length adjustment: 32
Effective length of query: 405
Effective length of database: 390
Effective search space:   157950
Effective search space used:   157950
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 51 (24.3 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