GapMind for catabolism of small carbon sources

 

Aligments 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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