GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctA in Paraburkholderia atlantica CCGE1002

Align aerobic C4-dicarboxylate transport protein (characterized)
to candidate WP_013093576.1 BC1002_RS29195 dicarboxylate/amino acid:cation symporter

Query= CharProtDB::CH_014038
         (428 letters)



>NCBI__GCF_000092885.1:WP_013093576.1
          Length = 443

 Score =  268 bits (685), Expect = 2e-76
 Identities = 148/367 (40%), Positives = 226/367 (61%), Gaps = 8/367 (2%)

Query: 41  FVKLIKMIIAPVIFCTVVTGIAGMESMKAVGRTGAVALLYFEIVSTIALIIGLIIVNVVQ 100
           F++L+KMIIAP++F T+V+GI+ M+S K++GR GA  + +F + S I+L IGL+ VN+ +
Sbjct: 48  FLRLVKMIIAPLVFATLVSGISSMDSGKSIGRIGAKTIGWFVVASLISLTIGLLFVNIAR 107

Query: 101 PGAGMNVDPATLDAKA-VAVYADQAKDQGIVAFIMDVIPASVIGAFASGNILQVLLFAVL 159
           PGA +N+     D    +   A   KD     F+  + P+SVI A A+  I+Q+L+F++ 
Sbjct: 108 PGAHLNLQLPAADVHPNLQTSALNFKD-----FLTHMFPSSVIEAMANNQIMQILVFSLF 162

Query: 160 FGFALHRL-GSKGQLIFNVIESFSQVIFGIINMIMRLAPIGAFGAMAFTIGKYGVGTLVQ 218
           FG AL ++ G  G+ +   I+    V+    N +M  AP+G F A+A  +   G+G +  
Sbjct: 163 FGIALGKVPGLPGEFLKRSIDGLMDVMLRATNAVMLFAPVGVFAAIAGAVTSQGLGIIFT 222

Query: 219 LGQLIICFYITCILFVVLVLGSIAKATGFSIFKFIRYIREELLIVLGTSSSESALPRMLD 278
            G+LI  FY+        +  +   A G  + +  R IRE ++I   T+SSE+A P++ +
Sbjct: 223 YGKLIGWFYVALFTLWGALYFAGRAALGCRMGQLFRSIREPMIIAFSTASSEAAYPKLTE 282

Query: 279 KMEKLGCRKSVVGLVIPTGYSFNLDGTSIYLTMAAVFIAQATNSQMDIVHQITLLIVLLL 338
            +++ G RK +VG V+P GYSFNLDG+ +Y   AA+FIAQA    M I  QIT+L++L++
Sbjct: 283 VLQEFGVRKRLVGFVLPLGYSFNLDGSMVYQAFAAIFIAQAFGVDMPIGIQITMLLILMV 342

Query: 339 SSKGAAGVTGSGFIVLAATLSAVGHLPVAGLALILGIDRFMSEARALTNLVGNGVATIVV 398
           SSKG A V     +V+AA L  + HLP AGL L++GID+ +   R  TN++GN +AT VV
Sbjct: 343 SSKGMAAVPRGSLVVVAAIL-PMFHLPEAGLLLVMGIDQILDMGRTATNVLGNSIATAVV 401

Query: 399 AKWVKEL 405
           AKW  EL
Sbjct: 402 AKWEGEL 408


Lambda     K      H
   0.327    0.142    0.401 

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: 476
Number of extensions: 27
Number of successful extensions: 4
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: 428
Length of database: 443
Length adjustment: 32
Effective length of query: 396
Effective length of database: 411
Effective search space:   162756
Effective search space used:   162756
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: 51 (24.3 bits)

This GapMind analysis is from Apr 09 2024. 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