GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kguD in Salinicoccus carnicancri Crm

Align 2-ketogluconate 6-phosphate reductase (EC 1.1.1.43) (characterized)
to candidate WP_017547969.1 C792_RS0103040 D-glycerate dehydrogenase

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



>NCBI__GCF_000330705.1:WP_017547969.1
          Length = 318

 Score =  204 bits (520), Expect = 2e-57
 Identities = 126/312 (40%), Positives = 176/312 (56%), Gaps = 7/312 (2%)

Query: 1   MKKIVAWKSLPEDVLAYLQQHAQVVQVDATQ----HDAFVAALKDADGGIGS-SVKITPA 55
           MKKIV  +++  D++  L++  +V   +  Q     + F+   +DA   +   S K+   
Sbjct: 1   MKKIVITRNINPDIVDKLRKDFEVSVWEEDQKPMPREKFLEETRDAHAVLTMLSDKVDEE 60

Query: 56  MLEGATRLKALSTISVGFDQFDVADLTRRGIVLANTPDVLTESTADTVFSLILASARRVV 115
            L  A  LK ++ ++VGFD  D+    R  +V+ NTPDVLTE+TA+  F+L+L SAR+V+
Sbjct: 61  FLSNAPELKVVANLAVGFDNIDLDAARRHEVVITNTPDVLTETTAELAFTLMLVSARKVL 120

Query: 116 ELAEWVKAGHWQHSIGPALFGVDVQGKTLGIVGLGRIGGAVARRAALGFNMKVLYTNRSA 175
                +  G+W       + G DV GKT+GI G+G IG A ARR A GF   +LY NRS 
Sbjct: 121 AANNELMEGNWSGWSPYHMAGTDVFGKTVGIFGMGSIGAAFARRLA-GFRSNILYHNRSE 179

Query: 176 NPQAEEAYGARRVELAELLATADFVCLQVPLTPETKHLIGAAELKSMKKSAILINASRGA 235
           +  A +  GA+ V   ELL+ +DFV    PLT ETKH   A     MK +A  IN  RGA
Sbjct: 180 SEAANDL-GAKLVSFDELLSQSDFVLCAAPLTEETKHKFDAEAFGKMKDTAHFINIGRGA 238

Query: 236 TVDEKALIEALQNGTIHGAGLDVFETEPLPSDSPLLKLANVVALPHIGSATHETRHAMAR 295
            V E  L EA+ +G I GA LDVFE EP+ +D   + L N+  LPHIGSA+  TR+ M  
Sbjct: 239 HVVEDDLAEAVSSGVIAGAALDVFENEPIGADHQFVGLDNMTLLPHIGSASVATRNNMMN 298

Query: 296 NAAENLVAALDG 307
               N++  L+G
Sbjct: 299 LCVNNIMEVLNG 310


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: 235
Number of extensions: 11
Number of successful extensions: 3
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: 318
Length adjustment: 28
Effective length of query: 293
Effective length of database: 290
Effective search space:    84970
Effective search space used:    84970
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 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