GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kguD in Cupriavidus basilensis 4G11

Align 2-ketogluconate 6-phosphate reductase (EC 1.1.1.43) (characterized)
to candidate RR42_RS14190 RR42_RS14190 2-hydroxyacid dehydrogenase

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



>FitnessBrowser__Cup4G11:RR42_RS14190
          Length = 332

 Score =  230 bits (586), Expect = 4e-65
 Identities = 142/312 (45%), Positives = 190/312 (60%), Gaps = 14/312 (4%)

Query: 22  AQVVQVDATQHDAFV--AALKDADGG-----IGSSVKITPAMLEGATRLKALSTISVGFD 74
           AQ   VD  Q D  +  AALK    G       ++ +I   ++ G   L+A+  ++VG++
Sbjct: 21  AQYFDVDDNQPDVALDGAALKARLAGKAGVLANAADRIDAGLVAGLPALRAVCNMAVGYN 80

Query: 75  QFDVADLTRRGIVLANTPDVLTESTADTVFSLILASARRVVELAEWVKAGHWQHSIGPAL 134
             DV  LT  GIV  NTPDVLTE+TAD  ++L++A+ARRV E   W++AG W+       
Sbjct: 81  NLDVPALTAAGIVATNTPDVLTETTADFGWALLMATARRVTESEHWLRAGKWERWSYDMF 140

Query: 135 FGVDVQGKTLGIVGLGRIGGAVARRAALGFNMKVLYTNRSANPQ-AEEAYGARRVELAEL 193
            G+D+   TLGI+G+GRIG A+ARRAA GF M VLY NRS  P+  E    AR V  AEL
Sbjct: 141 LGMDLYRSTLGILGMGRIGQALARRAA-GFGMSVLYHNRSRLPEDTERVLNARYVSKAEL 199

Query: 194 LATADFVCLQVPLTPETKHLIGAAELKSMKKSAILINASRGATVDEKALIEALQNGTIHG 253
           LA +D + L +P + ++ H IGAAEL  MK SA L+N +RG  VD+ AL  AL+ G I  
Sbjct: 200 LAQSDHLLLVLPYSAQSHHSIGAAELAQMKPSATLVNLARGGVVDDAALARALREGRIFA 259

Query: 254 AGLDVFETEPLPSDSPLLKLANVVALPHIGSATHETRHAMARNAAENLVAAL----DGTL 309
           AGLDVFE EP      LL + NVV  PHI SA+ +TR AMA  AA+NL+AAL        
Sbjct: 260 AGLDVFEAEP-QVHPDLLTVPNVVLTPHIASASEKTRRAMADLAADNLIAALGVGPQAGQ 318

Query: 310 TSNIVNREVLSK 321
             +++N EV+++
Sbjct: 319 PPSVINPEVMAR 330


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: 252
Number of extensions: 11
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: 332
Length adjustment: 28
Effective length of query: 293
Effective length of database: 304
Effective search space:    89072
Effective search space used:    89072
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: 48 (23.1 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