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

GapMind for catabolism of small carbon sources

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

Align L-arabinonate dehydratase; ArDHT; D-fuconate dehydratase; Galactonate dehydratase; L-arabonate dehydratase; EC 4.2.1.25; EC 4.2.1.67; EC 4.2.1.6 (characterized)
to candidate Ac3H11_954 Dihydroxy-acid dehydratase (EC 4.2.1.9)

Query= SwissProt::B5ZZ34
         (579 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_954
          Length = 567

 Score =  306 bits (783), Expect = 2e-87
 Identities = 189/530 (35%), Positives = 296/530 (55%), Gaps = 16/530 (3%)

Query: 44  RPVIGILNTWSDMTPCNGHLRELAEKVKAGVWEAGGFPLEVPVFSASENTFRPT-----A 98
           +P++G+ N  S +TPCN  L++LA+   AG+ EAGG        + S+     T     +
Sbjct: 43  KPMVGVANGHSTITPCNSGLQKLADAAIAGIEEAGGNAQVFGTPTISDGMAMGTEGMKYS 102

Query: 99  MMYRNLAALAVEEAIRGQPMDGCVLLVGCDKTTPSLLMGAASCDLPSIVVTGGPMLNGYF 158
           ++ R + +  +E  + GQ MDG +++ GCDK  P  LMG    ++P+I V GG +L G++
Sbjct: 103 LVSREVISDCIETCVGGQWMDGVLVVGGCDKNMPGGLMGMLRANVPAIYVYGGTILPGHY 162

Query: 159 RGERVGSGTHLWKFSEMVKAGEMTQAEFLEAEASMSRSSGTCNTMGTASTMASMAEALGM 218
           +G+ +   +      E   AG+++  +  E E      +G+C  M TA+TM+S  EALG+
Sbjct: 163 QGKDLNIVSVFEAVGENA-AGKLSDFDLKEIEKRAIPGTGSCGGMYTANTMSSAFEALGI 221

Query: 219 ALSGNAAIPGVDSRRKVMAQLTGRRIVQMVKDDLKPSEIMTKQAFENAIRTNAAIGGSTN 278
           +L  ++ +      +   A+ + + +++ +K D+KP +I+TK++ ENA+    A GGSTN
Sbjct: 222 SLPYSSTMANPHDEKMNSAKESAKVLIEAIKKDIKPRDIVTKKSIENAVAVIMATGGSTN 281

Query: 279 AVIHLLAIAGRVGIDLSLDDWDRCGRDVPTIVNLMPSGKYLMEEFFYAGGLPVVLKRLGE 338
           AV+H LAIA   G++ S+DD++R     P + +L PSGKYL  +   AGG+P V+K L  
Sbjct: 282 AVLHFLAIAHAAGVEWSIDDFERVRVKTPVLCDLKPSGKYLAVDLHRAGGIPQVMKVLLN 341

Query: 339 AGLLHKDALTVSGETVWDEVKDVVNW---NEDVILPAEKALTSSGGIVVLRGNLAPKGAV 395
           AGLLH D LT+ G+TV + +KDV +    ++DVI P    + + G + +L+GNL+P+GAV
Sbjct: 342 AGLLHGDCLTIEGKTVAEVLKDVPDQPRADQDVIRPINNPMYAQGHLAILKGNLSPEGAV 401

Query: 396 LKPSAASPHLLVHKGRAVVFEDIDDYKAKINDDNLDIDENCIMVMKNCGPKGYPGMAEVG 455
            K +     ++   G A VFED       I    +   +  +MV++  GPKG PGM E+ 
Sbjct: 402 AKITGLKNPVIT--GPARVFEDEQSALEAILAGKIKAGD--VMVLRYLGPKGGPGMPEM- 456

Query: 456 NMGLPPKVLKKGILDMV-RISDARMSGTAYGTVVLHTSPEAAVGGPLAVVKNGDMIELDV 514
            +     ++  G+ + V  I+D R SG  +G VV H +PEAA GG +A V  GD I +D 
Sbjct: 457 -LAPTGALIGAGLGESVGLITDGRFSGGTWGMVVGHVAPEAAAGGTIAFVHEGDSITIDA 515

Query: 515 PNRRLHLDISDEELARRLAEWQPNHDLPTSGYAFLHQQHVEGADTGADLD 564
               L L++S+EE+ARR A W       T G       +   A  GA LD
Sbjct: 516 RQLLLELNVSEEEIARRRAAWTAPAPRYTRGVQAKFAFNASSASKGAVLD 565


Lambda     K      H
   0.318    0.135    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: 938
Number of extensions: 62
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: 579
Length of database: 567
Length adjustment: 36
Effective length of query: 543
Effective length of database: 531
Effective search space:   288333
Effective search space used:   288333
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 17 2021. The underlying query database was built on Sep 17 2021.

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Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

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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