GapMind for catabolism of small carbon sources

 

Aligments for a candidate for kguK in Pseudomonas fluorescens FW300-N2C3

Align 2-ketogluconokinase (EC 2.7.1.13) (characterized)
to candidate AO356_24685 AO356_24685 2-dehydro-3-deoxygluconokinase

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



>lcl|FitnessBrowser__pseudo5_N2C3_1:AO356_24685 AO356_24685
           2-dehydro-3-deoxygluconokinase
          Length = 326

 Score =  463 bits (1192), Expect = e-135
 Identities = 238/307 (77%), Positives = 254/307 (82%)

Query: 1   MPDIDILSFGETMAMFVAEHGGDLAQVQHFHKRIAGADSNVAIGLARLGFKVAWLSRVGN 60
           M + D+LSFGETMAM VA+  GDLA V  FHKRIAGADSNVAIGL+RLGFKVAWLSRVG 
Sbjct: 1   MSEFDVLSFGETMAMLVADQRGDLASVDQFHKRIAGADSNVAIGLSRLGFKVAWLSRVGA 60

Query: 61  DSLGRFVLDTLRAEGLDCRFVRCDPIHPTGFQLKSREDGGDDPRVEYFRRGSAASHLAIS 120
           DSLGRFV  TL  EGLDCR V  DP HPTGFQ KS    G DP+VEYFRR SAASHL++ 
Sbjct: 61  DSLGRFVTQTLENEGLDCRHVAVDPEHPTGFQFKSLTVDGSDPQVEYFRRSSAASHLSVG 120

Query: 121 DLDPALLRARHLHATGIPPALSDSARELSGHLMHTQRSAGHSVSFDPNLRPALWPSEALM 180
            + PALL ARH+HATGI PALS +ARE+S  LM   R+AG S+SFDPNLRP+LW SE+ M
Sbjct: 121 SIAPALLDARHVHATGIVPALSGTAREMSFELMSRMRAAGRSLSFDPNLRPSLWGSESTM 180

Query: 181 IREINRLAALAHWVLPGLAEGRLLTGRDDPADIAAFYLDQGAEAVVIKLGAHGAYYRTQL 240
           I  INRLAALAHWVLPGL EGRLLTG DDPADIAAFYLDQGAE VVIKLGA GAYYRT L
Sbjct: 181 ITAINRLAALAHWVLPGLGEGRLLTGFDDPADIAAFYLDQGAEIVVIKLGADGAYYRTAL 240

Query: 241 DAGFVEGVPVAQVVDTVGAGDGFAVGLISALLESRGILEAVQRANWIGSRAVQSRGDMEG 300
           D G + GVPVAQVVDTVGAGDGFAVGLISALLE R I EAVQRANWIGSRAVQSRGDMEG
Sbjct: 241 DQGVIPGVPVAQVVDTVGAGDGFAVGLISALLEGRAITEAVQRANWIGSRAVQSRGDMEG 300

Query: 301 LPLRHEL 307
           LP R EL
Sbjct: 301 LPTRIEL 307


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: 453
Number of extensions: 15
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: 326
Length adjustment: 28
Effective length of query: 292
Effective length of database: 298
Effective search space:    87016
Effective search space used:    87016
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 preprint 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