Alignments for a candidate for edd in Flavobacterium glycines Gm-149

GapMind for catabolism of small carbon sources

Alignments for a candidate for edd in Flavobacterium glycines Gm-149

Align phosphogluconate dehydratase (characterized)
to candidate WP_066325983.1 BLR17_RS13755 dihydroxy-acid dehydratase

Query= CharProtDB::CH_024239
         (603 letters)



>NCBI__GCF_900100165.1:WP_066325983.1
          Length = 557

 Score =  214 bits (546), Expect = 6e-60
 Identities = 173/561 (30%), Positives = 266/561 (47%), Gaps = 45/561 (8%)

Query: 30  AKTSTVHRSQLACGNLAHGFAACQPEDKASLKSMLRNNIAIITSYNDMLSAHQPYEHYPE 89
           +KT T  ++Q A   + +G    + + K +        + I++   +  + +       +
Sbjct: 7   SKTITQDQTQPAAQAMLYGIGLTEEDLKKA-------QVGIVSMGYEGNTCNMHLNDLAK 59

Query: 90  IIRKALHEANAVGQVAGGVPAMCDGVTQGQDGMELSLLSREVIAMSAAVGLSHNMFDGAL 149
            +++ + +A+ VG +   +  + DG++ G DGM  SL+SR+VIA S    +    +D  +
Sbjct: 60  EVKQGVWDADLVGLIFNTI-GVSDGISNGTDGMRFSLVSRDVIADSIETVMGAQWYDSMI 118

Query: 150 FLGVCDKIVPGLTMAALSFGHLPAVFVPSGPMASGLPNKEKVRIRQLY-AEGKVDRMALL 208
            +  CDK +PG  MA +   + PA+ V  G + SG    E + I   + A GK     + 
Sbjct: 119 AIPGCDKNMPGAVMA-MGRVNRPAIMVYGGTIHSGKWKGESLNIVSAFEALGKKLNNRIT 177

Query: 209 ESEAA-----SYHAPGTCTFYGTANTNQMVVEFMGMQLPGSSFVHPDSPLRDALTAAAAR 263
             +       S    G C    TANT    +E +GM LP SS     SP +    A A +
Sbjct: 178 PEDFKGVIQNSCPGAGACGGMYTANTMASAIEALGMSLPYSSSNPALSPEKRQECAEAGK 237

Query: 264 QVTRMTGNGNEWMPIGKMIDEKVVVNGIVALLATGGSTNHTMHLVAMARAAGIQINWDDF 323
            +  +     +   I   +  K   N I  +   GGSTN  MHL+AMA +  ++I  DDF
Sbjct: 238 AIRVLLEKDIKPRDI---MTRKAFENAITIVAVLGGSTNAVMHLIAMAHSVDVEITLDDF 294

Query: 324 SDLSDVVPLMARLYPNGPADINHFQAAGGVPVLVRELLKAGLLHEDVNTVAGFGLSRYTL 383
             ++D  P++A L P+G   +      GGVP +++ LLK G LH D  TV G  L+   L
Sbjct: 295 QAINDKTPVLADLKPSGKYMMEDLHTVGGVPAVMKYLLKEGYLHGDCLTVTGKTLAE-NL 353

Query: 384 E--PWLNNGELDWREGAEKSLDSNVIASFEQPFSHHGGTKVLSGNLGRAVMKTSAVPVEN 441
           E  P L +G+              V+    +     G  +VL GNL            E 
Sbjct: 354 ESVPDLQDGQ-------------EVVHEIHKALKPTGNIQVLYGNLASEGCVAKISGKEG 400

Query: 442 QVIEAPAVVFESQHDVMPAFEAGLLDRDCVVVVRHQGPKAN-GMPELHKLMPPLGVLLDR 500
           +  E  AVVFES+ +V+P    G++    VVV+R+ GPK   GMPE+ K   P   ++  
Sbjct: 401 EFFEGTAVVFESEFEVIPGIAKGMVKPGNVVVIRYCGPKGGPGMPEMLK---PTSAIIGA 457

Query: 501 CF--KIALVTDGRLSGAS-GKVPSAIHVTPEAYDGGLLAKVRDGDIIRVNGQTGELTLLV 557
                +AL+TDGR SG S G V    HVTPEAYDGG +A V++GD+I ++     + L +
Sbjct: 458 GLGNSVALITDGRFSGGSHGFVVG--HVTPEAYDGGAIALVQNGDVITIDAVKNTIDLKI 515

Query: 558 DEAELAAREPH--IPDLSASR 576
            E E A R+ +   P L AS+
Sbjct: 516 SEEEFAKRKANWVQPPLKASK 536


Lambda     K      H
   0.318    0.134    0.392 

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: 801
Number of extensions: 49
Number of successful extensions: 6
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: 603
Length of database: 557
Length adjustment: 36
Effective length of query: 567
Effective length of database: 521
Effective search space:   295407
Effective search space used:   295407
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: 53 (25.0 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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 2024 update on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources