GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fucD in Acidovorax sp. GW101-3H11

Align L-fuconate dehydratase; L-rhamnonate dehydratase (EC 4.2.1.68; EC 4.2.1.90) (characterized)
to candidate Ac3H11_3953 D-galactarate dehydratase (EC 4.2.1.42)

Query= reanno::BFirm:BPHYT_RS34230
         (431 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_3953
          Length = 525

 Score =  159 bits (403), Expect = 1e-43
 Identities = 128/406 (31%), Positives = 188/406 (46%), Gaps = 47/406 (11%)

Query: 9   TLEGYLRGDGRKGIRNVVAVAYLVECAHHVAREIVTQFREPLDAFDDPSAEREPPVH-LI 67
           T EGY   DG  G RN++A+   V+C   V    V + ++ L           P V  +I
Sbjct: 116 TFEGYRNADGSVGTRNILAITTTVQCVAGVVANAVRRIKDEL-------LPLYPQVDDVI 168

Query: 68  GFPGCYPNGYAE---------KMLERLTTHPNVGA-VLFVSLGCESMNKHYLVDVVR--- 114
           G    Y  G A          + L  ++ +PN G  V+ VSLGCE +    L+       
Sbjct: 169 GLEHTYGCGVAIDAPDAIIPIRTLRNISLNPNFGGEVMVVSLGCEKLQPDRLLPAGSFPI 228

Query: 115 ------ASGRPVEVLTIQEKGGTRSTIQYGVDWIRGAREQLAAQQKVPMALSELVIGTIC 168
                 A G     L   E  G  S + + V   R   E+L A+++  +  SELV+G  C
Sbjct: 229 ADERDAALGPETVCLQADEHVGFMSMLDHIVQSARPHLERLNARRRETIRASELVLGVQC 288

Query: 169 GGSDGTSGITANPAVGRAFDHLIDAGATCIFEETGELVGCEFHMKTRAARPALGDEIVAC 228
           GGSD  SG+TANPAVG   D L+ AGAT +F E  E+      + +RAA P + + IV  
Sbjct: 289 GGSDAFSGVTANPAVGFCADLLVRAGATVMFSENTEVRDAVEQLTSRAATPEVAESIVRE 348

Query: 229 VAKAARYYS---ILGHGSFAVGNADGGLTTQEEKSLGAYAKSGASPIVGIIKPGDI---P 282
           +    RY     +    +   GN  GGL+   EK++G+  KSG +PI  ++ PG+     
Sbjct: 349 LGWYDRYLDRGRVDRAANTTPGNKAGGLSNIAEKAMGSIIKSGTAPISHVLAPGEKLRRD 408

Query: 283 PTGGLYLLDVVPDGEPRFGFPNISDNAEIGEL-IACGAHVILFTTGRGSVVGSAISPVIK 341
             G +Y      D                G L +A G ++ +FTTGRG+  G A  PV+K
Sbjct: 409 QRGLVYAATPASD-------------FICGTLQLAAGMNLHVFTTGRGTPYGLAECPVVK 455

Query: 342 VCANPATYRNLSGDMDVDAGRILEGRGTLDEVGREVFEQTVAVSRG 387
           V       R     MD++AG+I +G  +++E+G E+F   + V+ G
Sbjct: 456 VATRTDLARRWHDLMDINAGKIADGEASIEELGWEMFHLLLDVASG 501


Lambda     K      H
   0.318    0.137    0.408 

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: 627
Number of extensions: 37
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 431
Length of database: 525
Length adjustment: 33
Effective length of query: 398
Effective length of database: 492
Effective search space:   195816
Effective search space used:   195816
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: 51 (24.3 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:

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