Alignments for a candidate for xad in Dyella japonica UNC79MFTsu3.2

GapMind for catabolism of small carbon sources

Alignments for a candidate for xad in Dyella japonica UNC79MFTsu3.2

Align Xylonate dehydratase (EC 4.2.1.82) (characterized)
to candidate N515DRAFT_0569 N515DRAFT_0569 dihydroxy-acid dehydratase

Query= reanno::pseudo6_N2E2:Pf6N2E2_1668
         (594 letters)



>FitnessBrowser__Dyella79:N515DRAFT_0569
          Length = 568

 Score =  258 bits (659), Expect = 5e-73
 Identities = 180/557 (32%), Positives = 272/557 (48%), Gaps = 35/557 (6%)

Query: 45  RPIIGIAQTGSDLTPCNRHHLELAQRVKAGIRDAGGIPMEFPVHPIAEQSRRPTAALDRN 104
           +P++ +  T S+++PCN +  ELA++V  GIR AGG P+EF    + +     T  +  +
Sbjct: 31  KPLVAVVHTWSNVSPCNLNLRELAEQVAEGIRAAGGTPIEFNTIAVTDGIAMGTPGMRAS 90

Query: 105 LAYLGLVE-----ILHGYPLDGVVLTTGCDKTTPACLMAAATTDLPAIVLSGGPMLDGHH 159
           L    ++       + G+ LD +V+  GCDKT PA  MA A  D+PA+ L GG +  G H
Sbjct: 91  LISREVITDSIELAVDGHCLDAMVVLCGCDKTIPAAAMAMARLDIPAVALYGGTIAHGTH 150

Query: 160 KGELIGSGTVLWHARNLMAAGEIDYEGFMEMTTAASPSVGHCNTMGTALSMNALAEALGM 219
               I    V + A     AG+ID      +   A P  G C    TA +M  +   LG+
Sbjct: 151 DAHPITIQQV-FEAVGAHGAGKIDDAELAAVERDACPGAGACGGQFTANTMAMVLTTLGL 209

Query: 220 SLPGCASIPAPYRERGQMAYATGKRICDLVRQDIRPSQIMTRQAFENAIAVASALGASSN 279
           S  G   IPA +  +   A   G+ + D +R+   P  ++ R +  NA  + +A   S+N
Sbjct: 210 SPMGFNDIPATHPAKAAAARRCGELVMDCLREQRTPRALINRTSLRNAARMVAATAGSTN 269

Query: 280 CPPHLIAIARHMGVELSLEDWQRIGEDVPLLVNCMPAGKYLGEGFHRAGGVPSVMHELQK 339
              HL+AIAR  G   +LED++   +  P++ + +P G+Y       AGG   V  EL  
Sbjct: 270 AVLHLLAIAREAGAPWTLEDFEPASKHTPVIADLLPGGRYTAVEMFGAGGAARVAQELIA 329

Query: 340 AGRLHEDCATVSGKTI-GEIVSNSLTSNTDVIHPFDTPLKHRAGFIVLSGNFF-DSAIMK 397
           AG L +D  TV+G+++  E  +       DVI P   PLK R G+ +L GN   +  I+K
Sbjct: 330 AGML-DDVPTVTGRSLFEEAAAAPRAEQQDVILPVGQPLKPRGGYSILYGNLAPEGCILK 388

Query: 398 MSVVGEAFRKTYLSEPGAENSFEARAIVFEGPEDYHARIDDPALDIDERCILVIRGVGTV 457
           ++  G                FE  A VFE  E   A +      I +  ++VIR  G  
Sbjct: 389 LAGKG-------------ATHFEGTARVFESEEQAFAAVQQGR--IAKGDVIVIRNEGPA 433

Query: 458 GYPGSAEVVNMAPPAALIKQGI-DSLPCLGDGRQSGTSASPSILNMSPEAAVGGGLALLK 516
           G PG  E++ +   AALI +G+ D +  + DGR SG +    + +M+PEA  GG +ALL+
Sbjct: 434 GGPGMREMLGVT--AALIGRGLGDDVALITDGRFSGATHGFMVGHMAPEAVRGGPIALLR 491

Query: 517 TNDRLKVDLNTRTVNLLIDDAEMAQRRREWIPNIPPSQTPWQELYRQLVGQLSTGGCLEP 576
             DR+++D   R +     DA++A+RR+ W P  P   T     Y +LVG  S G    P
Sbjct: 492 DGDRIRIDAGLREI---ATDADLAERRQHWTPPAPKVTTGALAKYARLVGSASDGANTHP 548

Query: 577 AT-----LHLRVIARSG 588
            T      H++V A  G
Sbjct: 549 ETSVATPKHVQVTATEG 565


Lambda     K      H
   0.319    0.135    0.407 

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: 881
Number of extensions: 51
Number of successful extensions: 8
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: 594
Length of database: 568
Length adjustment: 36
Effective length of query: 558
Effective length of database: 532
Effective search space:   296856
Effective search space used:   296856
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 (21.7 bits)
S2: 53 (25.0 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
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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 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