GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kguD in Alicycliphilus denitrificans K601

Align 2-ketogluconate 6-phosphate reductase (EC 1.1.1.43) (characterized)
to candidate WP_009238667.1 ALIDE2_RS09920 phosphonate dehydrogenase

Query= reanno::BFirm:BPHYT_RS11290
         (321 letters)



>NCBI__GCF_000204645.1:WP_009238667.1
          Length = 336

 Score =  178 bits (452), Expect = 1e-49
 Identities = 119/327 (36%), Positives = 170/327 (51%), Gaps = 15/327 (4%)

Query: 3   KIVAWKSLPEDVLAYLQQHAQVVQVDATQ---HDAFVAALKDADGGIGSSV-KITPAMLE 58
           K+V    +  +++  L   A V+     +       +A  KDAD  +      I  A LE
Sbjct: 4   KVVLTHWVHPEIIELLSASADVIPNTTRETLPRSEVIARAKDADALMAFMPDSIDSAFLE 63

Query: 59  GATRLKALSTISVGFDQFDVADLTRRGIVLANTPDVLTESTADTVFSLILASARRVVELA 118
              +L+ +     G+D FDV   TR G+ L   PD+LT  TA+    L+L   R ++E  
Sbjct: 64  ECPKLRVIGAALKGYDNFDVNACTRHGVWLTIVPDLLTIPTAELTIGLLLGLTRHMLEGD 123

Query: 119 EWVKAGHWQHSIGPALFGVDVQGKTLGIVGLGRIGGAVARRAALGFNMKVLYTNR-SANP 177
             +++GH+Q    P L+G  + GKTLGI+G+G +G A+A+R A GF M +LY +    N 
Sbjct: 124 RQIRSGHFQ-GWRPTLYGSGLTGKTLGIIGMGAVGRAIAQRLA-GFEMNLLYCDPIPLNA 181

Query: 178 QAEEAYGARRVELAELLATADFVCLQVPLTPETKHLIGAAELKSMKKSAILINASRGATV 237
           + E+A+  +RV L ELL   D+V   VP+  ET HLI A  L  MK  + LINA RG+ V
Sbjct: 182 EQEKAWHVQRVTLDELLEKCDYVVPMVPMAAETLHLIDATALAKMKTGSYLINACRGSVV 241

Query: 238 DEKALIEALQNGTIHGAGLDVFETEP-LPSDSP-------LLKLANVVALPHIGSATHET 289
           DE A+I AL +G + G   DVFE E  + +D P       L   A     PH+GSA  E 
Sbjct: 242 DENAVIAALASGKLAGYAADVFEMEEWIRADRPQAIPKALLDNTAQTFFTPHLGSAVKEV 301

Query: 290 RHAMARNAAENLVAALDGTLTSNIVNR 316
           R  + R AA N++ AL G      +N+
Sbjct: 302 RLEIERQAAMNIIQALAGEKPMGAINQ 328


Lambda     K      H
   0.317    0.131    0.366 

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: 210
Number of extensions: 7
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: 321
Length of database: 336
Length adjustment: 28
Effective length of query: 293
Effective length of database: 308
Effective search space:    90244
Effective search space used:    90244
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 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