GapMind for catabolism of small carbon sources

 

Aligments for a candidate for kguK in Pseudomonas simiae WCS417

Align 2-ketogluconokinase (EC 2.7.1.13) (characterized)
to candidate GFF2464 PS417_12565 2-dehydro-3-deoxygluconokinase

Query= metacyc::MONOMER-12748
         (320 letters)



>lcl|FitnessBrowser__WCS417:GFF2464 PS417_12565
           2-dehydro-3-deoxygluconokinase
          Length = 313

 Score =  475 bits (1223), Expect = e-139
 Identities = 242/308 (78%), Positives = 260/308 (84%)

Query: 1   MPDIDILSFGETMAMFVAEHGGDLAQVQHFHKRIAGADSNVAIGLARLGFKVAWLSRVGN 60
           M +IDILSFGETMAMFVAE  GDLA V  FHKRIAGADSNVAIGL+RLGFKVAWLSRVGN
Sbjct: 1   MSEIDILSFGETMAMFVAEQTGDLAHVAQFHKRIAGADSNVAIGLSRLGFKVAWLSRVGN 60

Query: 61  DSLGRFVLDTLRAEGLDCRFVRCDPIHPTGFQLKSREDGGDDPRVEYFRRGSAASHLAIS 120
           DSLGRFV+DTL  EGLDCR V  DP HPTGFQLKSRE+ GDDP+VEYFR+GSAASHL+I+
Sbjct: 61  DSLGRFVVDTLTQEGLDCRHVAVDPAHPTGFQLKSREETGDDPQVEYFRKGSAASHLSIA 120

Query: 121 DLDPALLRARHLHATGIPPALSDSARELSGHLMHTQRSAGHSVSFDPNLRPALWPSEALM 180
            + PALL+ARHLHATGIPPALS++ RELS  LM   R AG SVSFDPNLRP+LW ++  M
Sbjct: 121 AISPALLQARHLHATGIPPALSEATRELSVELMTQMRKAGRSVSFDPNLRPSLWANQQTM 180

Query: 181 IREINRLAALAHWVLPGLAEGRLLTGRDDPADIAAFYLDQGAEAVVIKLGAHGAYYRTQL 240
           IREIN LA LA WVLPGL EGR LTG DDPADIAAFYLDQGAEAV IKLG  GAYYRT L
Sbjct: 181 IREINALAGLADWVLPGLGEGRQLTGFDDPADIAAFYLDQGAEAVAIKLGPDGAYYRTHL 240

Query: 241 DAGFVEGVPVAQVVDTVGAGDGFAVGLISALLESRGILEAVQRANWIGSRAVQSRGDMEG 300
           D GFV  V V +VVDTVGAGDGFAVG+ISALLE+    EAVQR NWIGSRAVQSRGDMEG
Sbjct: 241 DQGFVAAVRVDKVVDTVGAGDGFAVGMISALLENLSFPEAVQRGNWIGSRAVQSRGDMEG 300

Query: 301 LPLRHELP 308
           LP R ELP
Sbjct: 301 LPARSELP 308


Lambda     K      H
   0.321    0.138    0.414 

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: 447
Number of extensions: 17
Number of successful extensions: 1
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: 320
Length of database: 313
Length adjustment: 27
Effective length of query: 293
Effective length of database: 286
Effective search space:    83798
Effective search space used:    83798
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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