Aligments for a candidate for xad in Pseudomonas fluorescens FW300-N2E3

GapMind for catabolism of small carbon sources

Aligments for a candidate for xad in Pseudomonas fluorescens FW300-N2E3

Align xylonate dehydratase (EC 4.2.1.82) (characterized)
to candidate AO353_08345 AO353_08345 dihydroxy-acid dehydratase

Query= BRENDA::P39358
         (655 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_08345
          Length = 613

 Score =  199 bits (506), Expect = 3e-55
 Identities = 169/544 (31%), Positives = 257/544 (47%), Gaps = 63/544 (11%)

Query: 88  GHYEL-DIQMKAAAEVIKANH-ALPYAVYVSDPCDGRTQGTTGMFDSLPYRNDASMVMRR 145
           GH  L D+    A E+ +A   A  +     D  DG   G  GM  SLP R   +  +  
Sbjct: 49  GHVHLKDLGQLVAREIERAGGVAKEFNTIAVD--DGIAMGHDGMLYSLPSREIIADSVEY 106

Query: 146 LIRSLPDAKAVIGVASCDKGLPATMMALAAQHNIATVLVPGGA-----TLPAKDGEDNGK 200
           ++ +   A A++ +++CDK  P  +MA A + NI  + V GG      T  A  G D   
Sbjct: 107 MVNA-HCADAIVCISNCDKITPGMLMA-ALRLNIPVIFVSGGPMEAGKTKLASHGLDLVD 164

Query: 201 VQTIGARFANGELSLQDARRAGCKACASSGGGCQFLGTAGTSQVVAEGLGLAIPHSALAP 260
              I A  +  +  + +  R+ C  C    G C  + TA +   + E LGLA+P +    
Sbjct: 165 AMVIAADSSASDEKVAEYERSACPTC----GSCSGMFTANSMNCLTEALGLALPGNGSTL 220

Query: 261 SGEPVWREIARASARAALNLSQK-------GITTREILTDKAIENAMTVHAAFGGSTNLL 313
           +      ++   + R  + L ++        +  R I   KA ENAMT+  A GGSTN +
Sbjct: 221 ATHSDREQLFLQAGRTIVELCKRYYGENDESVLPRNIANFKAFENAMTLDIAMGGSTNTI 280

Query: 314 LHIPAIAHQAGCHIPTVDDWIRINKRVPRLVSVLPNGPVYHPTVNAFMAGGVPEVMLHLR 373
           LH+ A A +A      + D  R+++ VP+L  V PN   YH   +   AGG+  ++  L 
Sbjct: 281 LHLLAAAQEAEIDF-DLRDIDRLSRHVPQLCKVAPNIQKYH-MEDVHRAGGIFSILGSLA 338

Query: 374 SLGLLHEDVMTVTGSTLKENLDWWEHSER----------------------RQRFKQLLL 411
             GLLH D+ TV   T+ E +  W+ ++                        Q  +   L
Sbjct: 339 RGGLLHTDLPTVHSKTMAEGIAKWDITQTTDEAVHHFFKAGPAGIPTQTAFSQSTRWETL 398

Query: 412 DQEQINADEVIMSPQQAKARGLTSTITFPVGNIAPEGSVIKSTAIDPSMIDEQGIYYHKG 471
           D ++ N    I S + A ++     + +  GNIA +G V+K+  +D S      I+  +G
Sbjct: 399 DDDRENG--CIRSVEHAYSQEGGLAVLY--GNIALDGCVVKTAGVDES------IHVFEG 448

Query: 472 VAKVYLSEKSAIYDIKHDKIKAGDILVIIGVGP-SGTGMEETYQVTSALKHLSYGKHVSL 530
            AK++ S+ SA+  I  D++K GDI++I   GP  G GM+E    TS LK    GK  +L
Sbjct: 449 NAKIFESQDSAVRGILADEVKEGDIVIIRYEGPKGGPGMQEMLYPTSYLKSKGLGKACAL 508

Query: 531 ITDARFSGVSTGACIGHVGPEALAGGPIGKLRTGDLIEIKIDCRELHGEVNFLGTRSDEQ 590
           +TD RFSG ++G  IGH  PEA AGG IG +R GD + I I  R ++  V      SDE+
Sbjct: 509 LTDGRFSGGTSGLSIGHASPEAAAGGAIGLVRDGDKVLIDIPNRSINLLV------SDEE 562

Query: 591 LPSQ 594
           L ++
Sbjct: 563 LAAR 566


Lambda     K      H
   0.317    0.135    0.400 

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: 897
Number of extensions: 47
Number of successful extensions: 8
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 655
Length of database: 613
Length adjustment: 38
Effective length of query: 617
Effective length of database: 575
Effective search space:   354775
Effective search space used:   354775
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: 54 (25.4 bits)

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

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Protein sequences (fasta format)
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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, 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

GapMind for catabolism of small carbon sources