GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kguD in Stenotrophomonas chelatiphaga DSM 21508

Align 2-ketogluconate 6-phosphate reductase (EC 1.1.1.43) (characterized)
to candidate WP_057687229.1 ABB28_RS15235 D-glycerate dehydrogenase

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



>NCBI__GCF_001431535.1:WP_057687229.1
          Length = 345

 Score =  232 bits (592), Expect = 9e-66
 Identities = 136/308 (44%), Positives = 188/308 (61%), Gaps = 8/308 (2%)

Query: 5   VAWKSLP--EDVLAYLQQHAQVVQVDATQ---HDAFVAALKDADGGIGS-SVKITPAMLE 58
           V W S P  + V+  L+   +++  DA      +     L+  DG I + + +I  A L 
Sbjct: 7   VVWVSQPLIDAVIEPLRAQVELITTDAVTAWTQEQLAERLRGVDGAIITLNERIGAAQLA 66

Query: 59  GATRLKALSTISVGFDQFDVADLTRRGIVLANTPDVLTESTADTVFSLILASARRVVELA 118
           GA RL+ ++ + VG++  DV  L+  G++ +NTPDVLTE+TAD  F+L++A+ARR+ E  
Sbjct: 67  GADRLQVIANVGVGYNNLDVDALSAAGVLASNTPDVLTETTADLGFALLMAAARRITESE 126

Query: 119 EWVKAGHWQHSIGPALFGVDVQGKTLGIVGLGRIGGAVARRAALGFNMKVLYTNRSANPQ 178
            W++ G W       + G D+ G TLGI+G+GRIG  +ARR A GF M+VLY NRS  P 
Sbjct: 127 RWLRDGQWGQWSFQTMLGADIHGSTLGILGMGRIGQGIARRGAHGFGMRVLYHNRSRLPA 186

Query: 179 AEEA-YGARRVELAELLATADFVCLQVPLTPETKHLIGAAELKSMKKSAILINASRGATV 237
           A EA  GA+  EL  LLA +D + L +P T  + HLI A+ L  MK +A L+N +RG  V
Sbjct: 187 ATEAEVGAQYAELDALLAQSDHLVLVLPYTAASHHLINASALAKMKPTATLVNIARGGIV 246

Query: 238 DEKALIEALQNGTIHGAGLDVFETEPLPSDSPLLKLANVVALPHIGSATHETRHAMARNA 297
           DE AL +AL +G +  AGLDV+E EP      LL L NVV  PHIGSA+  TR AM + A
Sbjct: 247 DELALADALAHGRLAAAGLDVYEGEPQVRPE-LLALRNVVLTPHIGSASLGTRKAMVQLA 305

Query: 298 AENLVAAL 305
            +NL+AAL
Sbjct: 306 VDNLLAAL 313


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: 239
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: 345
Length adjustment: 28
Effective length of query: 293
Effective length of database: 317
Effective search space:    92881
Effective search space used:    92881
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