GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livM in Cupriavidus basilensis 4G11

Align ABC transporter ATP-binding protein (characterized, see rationale)
to candidate RR42_RS16970 RR42_RS16970 ABC transporter ATP-binding protein

Query= uniprot:A0A165KER0
         (358 letters)



>FitnessBrowser__Cup4G11:RR42_RS16970
          Length = 386

 Score =  452 bits (1164), Expect = e-132
 Identities = 225/339 (66%), Positives = 270/339 (79%), Gaps = 3/339 (0%)

Query: 13  VALLVLPLILQSFG-NAWVRIADLALLYVLLALGLNIVVGYAGLLDLGYVAFYAVGAYLF 71
           +  L  P ++Q+ G N WVR+ D AL+Y++LALGLNIVVG+AGLLDLGY+AFYAVGAY+ 
Sbjct: 31  IIALCAPFLVQTLGGNYWVRVLDFALIYIMLALGLNIVVGFAGLLDLGYIAFYAVGAYMM 90

Query: 72  ALMASPHLADNFAAFAAMFPNGLHTSLWIVIPVAALLAAFFGAMLGAPTLKLRGDYLAIV 131
           AL+ SPHLA+ F     +FPNGLH S+W V+P+A L+AA FG +LGAPTLKLRGDYLAIV
Sbjct: 91  ALLGSPHLANQFEWIHQLFPNGLHLSMWFVLPLAVLVAATFGVLLGAPTLKLRGDYLAIV 150

Query: 132 TLGFGEIIRIFLNNLDHPVNLTNGPKGLGQIDSVKVFGLDLGKRLEVFGFDINSVTLYYY 191
           TLGFGEIIRIFLNNLD P+N+TNGPKG+  +D V +FG D  K  E+FG     V +YYY
Sbjct: 151 TLGFGEIIRIFLNNLDRPLNITNGPKGITAVDPVHIFGFDFSKSHEIFGLKFTPVFMYYY 210

Query: 192 LFLVLVVVSVIICYRLQDSRIGRAWMAIREDEIAAKAMGINTRNMKLLAFGMGASFGGVS 251
           L +VLV+  V IC RLQ+SRIGRA++AIREDEIAAKAMGINTRN+KLLAF MGASFGG S
Sbjct: 211 LLVVLVIAIVFICLRLQNSRIGRAFVAIREDEIAAKAMGINTRNIKLLAFAMGASFGGAS 270

Query: 252 GAMFGAFQGFVSPESFSLMESVMIVAMVVLGGIGHIPGVILGAVLLSALPEVLRYVAGPL 311
           GA+FGAFQGFVSPESF L ES+ I+A+VVLGG+GHIPGVILG +LL    E+LR VA P 
Sbjct: 271 GAVFGAFQGFVSPESFVLWESIYILAIVVLGGMGHIPGVILGGILLVGFQELLRAVAEPA 330

Query: 312 QAMTDGR--LDSAILRQLLIALAMIIIMLLRPRGLWPSP 348
           Q M  G   +D+ +LRQLL  LA++ +ML RP GLWPSP
Sbjct: 331 QNMIFGHTIVDAEVLRQLLFGLALVGVMLYRPAGLWPSP 369


Lambda     K      H
   0.328    0.144    0.430 

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: 19
Number of successful extensions: 2
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: 358
Length of database: 386
Length adjustment: 30
Effective length of query: 328
Effective length of database: 356
Effective search space:   116768
Effective search space used:   116768
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 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