GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kguD in Collimonas pratensis Ter91

Align 2-ketogluconate 6-phosphate reductase (EC 1.1.1.43) (characterized)
to candidate WP_061938723.1 CPter91_RS06895 D-glycerate dehydrogenase

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



>NCBI__GCF_001584185.1:WP_061938723.1
          Length = 336

 Score =  242 bits (618), Expect = 8e-69
 Identities = 151/332 (45%), Positives = 210/332 (63%), Gaps = 18/332 (5%)

Query: 3   KIVAWKSLPEDVLAYLQQHAQVVQVDATQHDAFVAA------LKDADGGIGS-SVKITPA 55
           KI+  +++  +V+A +   AQ  +V++ Q D   +A      L+D DG I + S +I+  
Sbjct: 4   KILMARAVFPEVIARM---AQYFEVESNQEDRIFSAAELAQKLQDKDGVIATASERISAE 60

Query: 56  MLEGATRLKALSTISVGFDQFDVADLTRRGIVLANTPDVLTESTADTVFSLILASARRVV 115
           +L+ + RLKA+   +VG++  DVA  T+ G+++ NTPDVL E+TAD  ++L++A+ARRV 
Sbjct: 61  LLQASPRLKAVCNQAVGYNNIDVAAATKAGVMVTNTPDVLNETTADFGWALLMATARRVT 120

Query: 116 ELAEWVKAGHWQHSIGPALFGVDVQGKTLGIVGLGRIGGAVARRAALGFNMKVLYTNRS- 174
           E   W++AGHW+     +  G DV G TLGI+G+GRIG A+ARR ++GF+M+VLY NRS 
Sbjct: 121 EAEHWLRAGHWKQWRYDSFLGADVHGSTLGIIGMGRIGQAIARR-SMGFDMQVLYHNRSR 179

Query: 175 ANPQAE-EAYGARRVELAELLATADFVCLQVPLTPETKHLIGAAELKSMKKSAILINASR 233
             P+ E  A  AR V   ELL  AD V L +P + E+ H IG+AEL  MK  A L+N +R
Sbjct: 180 LAPELETRANQARYVSKEELLGAADHVILVLPYSKESHHTIGSAELALMKPGATLVNLAR 239

Query: 234 GATVDEKALIEALQNGTIHGAGLDVFETEPLPSDSPLLKLANVVALPHIGSATHETRHAM 293
           G  VD+ ALI AL++  I  AGLDVFE EP       L L+NVV  PHI SA+  TR AM
Sbjct: 240 GGIVDDLALIAALRDKKIAAAGLDVFENEP-ALHPDFLGLSNVVLTPHIASASEPTRRAM 298

Query: 294 ARNAAENLVAAL----DGTLTSNIVNREVLSK 321
           A  AA+NL+AAL    D     N++N EVL K
Sbjct: 299 ADCAADNLLAALLPGKDRMYPPNLLNPEVLGK 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: 242
Number of extensions: 12
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 Sep 24 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