GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kguD in Saccharomonospora marina XMU15

Align 2-ketogluconate 6-phosphate reductase (EC 1.1.1.43) (characterized)
to candidate WP_009152937.1 SACMADRAFT_RS06215 phosphoglycerate dehydrogenase

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



>NCBI__GCF_000244955.1:WP_009152937.1
          Length = 531

 Score =  199 bits (505), Expect = 2e-55
 Identities = 117/309 (37%), Positives = 175/309 (56%), Gaps = 6/309 (1%)

Query: 8   KSLPEDVLAYLQQHAQVVQVDATQHDAFVAALKDADGG-IGSSVKITPAMLEGATRLKAL 66
           + L +  ++      +V  VD T   A + A+ DAD   + S+ K+ P +L  A +LK +
Sbjct: 13  EKLAQSAVSVFGDEVEVRHVDGTDRPALLDAVGDADALLVRSATKVDPEVLGAAPKLKVV 72

Query: 67  STISVGFDQFDVADLTRRGIVLANTPDVLTESTADTVFSLILASARRVVELAEWVKAGHW 126
           +   VG D  DV   T+RG+++ N P     S A+   +L+LA ARRV    + ++ G W
Sbjct: 73  ARAGVGLDNVDVPAATQRGVLVVNAPTSNIVSAAEHAVALLLAVARRVSAADQSLRGGEW 132

Query: 127 QHSIGPALFGVDVQGKTLGIVGLGRIGGAVARRAALGFNMKVLYTNRSANPQAEEAYGAR 186
           + S   +  GV++ GKT+G+VG G+IG  VA+R    F   +L  +  A+P      G  
Sbjct: 133 KRS---SFTGVELHGKTVGVVGFGKIGQLVAQRLE-AFGTHLLAYDPYASPARAAQLGVE 188

Query: 187 RVELAELLATADFVCLQVPLTPETKHLIGAAELKSMKKSAILINASRGATVDEKALIEAL 246
            V L ELL  AD + + +P TPETK LI AA L  +K  AI++NA+RG  +DE AL EA+
Sbjct: 189 LVSLDELLQRADAISIHLPKTPETKGLIDAAALSKVKPGAIIVNAARGGLIDEDALAEAV 248

Query: 247 QNGTIHGAGLDVFETEPLPSDSPLLKLANVVALPHIGSATHETRHAMARNAAENLVAALD 306
           + G + GAG+DVF +EP  S SPL +L NVV  PH+G++T E +     + A +++ AL 
Sbjct: 249 REGRVGGAGVDVFASEPTTS-SPLFELPNVVVTPHLGASTVEAQDRAGTDVAHSVLLALR 307

Query: 307 GTLTSNIVN 315
           G    + VN
Sbjct: 308 GDFVPDAVN 316


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: 332
Number of extensions: 17
Number of successful extensions: 5
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: 531
Length adjustment: 31
Effective length of query: 290
Effective length of database: 500
Effective search space:   145000
Effective search space used:   145000
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: 50 (23.9 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