Alignments for a candidate for dgoD in Desulfovibrio vulgaris Hildenborough

GapMind for catabolism of small carbon sources

Alignments for a candidate for dgoD in Desulfovibrio vulgaris Hildenborough

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 208900 DVU3373 dihydroxy-acid dehydratase

Query= SwissProt::B5ZZ34
         (579 letters)



>MicrobesOnline__882:208900
          Length = 554

 Score =  315 bits (807), Expect = 3e-90
 Identities = 193/546 (35%), Positives = 302/546 (55%), Gaps = 20/546 (3%)

Query: 27  HRGWLKNQGYPHDLFDGRPVIGILNTWSDMTPCNGHLRELAEKVKAGVWEAGGFPLEVPV 86
           HR  L   G   +    RP++G++N  +++ P + HL ++AE VKAGV  AGG PLE P 
Sbjct: 15  HRSLLHALGLTREEL-ARPLVGVVNAANEVVPGHIHLDDIAEAVKAGVRAAGGTPLEFPA 73

Query: 87  FSASEN-TFRPTAMMY----RNLAALAVEEAIRGQPMDGCVLLVGCDKTTPSLLMGAASC 141
            +  +        M +    R L A ++E      P D  V +  CDK+ P +LM     
Sbjct: 74  IAVCDGLAMNHEGMRFSLPSRELIADSIEIMATAHPFDALVFIPNCDKSVPGMLMAMLRL 133

Query: 142 DLPSIVVTGGPMLNGYFRGERVGSGTHLWKFSEMVKAGEMTQAEFLEAEASMSRSSGTCN 201
           D+PS++V+GGPML G     R    T +++    V+ G+MT+AE  E         G+C 
Sbjct: 134 DVPSVMVSGGPMLAGATLAGRADLIT-VFEGVGRVQRGDMTEAELDELVEGACPGCGSCA 192

Query: 202 TMGTASTMASMAEALGMALSGNAAIPGVDSRRKVMAQLTGRRIVQMVKDDLKPSEIMTKQ 261
            M TA++M  +AE +G+AL GN   P V + R  +A+  G ++++M++ +++P +I+T++
Sbjct: 193 GMFTANSMNCLAETIGLALPGNGTTPAVTAARIRLAKHAGMKVMEMLERNIRPRDIVTEK 252

Query: 262 AFENAIRTNAAIGGSTNAVIHLLAIAGRVGIDLSLDDWDRCGRDVPTIVNLMPSGKYLME 321
           A  NA+  + A+G STN V+HL A+    G+DL+LD +D+  R  P +  L P+G + ++
Sbjct: 253 AVANAVAVDMALGCSTNTVLHLPAVFAEAGLDLTLDIFDKVSRKTPNLCKLSPAGHHHIQ 312

Query: 322 EFFYAGGLPVVLKRLGEAGLLHKDALTVSGETVWDEVKDVVN---WNEDVILPAEKALTS 378
           +   AGG+P V+  L   GL+ + A+TV+G TV + + D +     + DVI P +   + 
Sbjct: 313 DLHAAGGIPAVMAELDRIGLIDRSAMTVTGRTVGENL-DALGAKVRDADVIRPVDAPYSP 371

Query: 379 SGGIVVLRGNLAPKGAVLKPSAASPHLLVHKGRAVVFEDIDDYKAKINDDNLDIDENCIM 438
            GGI +L+G+LAP GAV+K SA +P ++V +  A VF+  +     I    +   +   +
Sbjct: 372 QGGIAILKGSLAPGGAVVKQSAVAPEMMVREAVARVFDSEEAACEAIMGGRIKAGD--AI 429

Query: 439 VMKNCGPKGYPGMAEVGNMGLPPKVLKKGI---LDMVRISDARMSGTAYGTVVLHTSPEA 495
           V++  GPKG PGM E+    L P     G+    D+  I+D R SG   G  + H SPEA
Sbjct: 430 VIRYEGPKGGPGMREM----LTPTSAIAGMGLGADVALITDGRFSGGTRGAAIGHVSPEA 485

Query: 496 AVGGPLAVVKNGDMIELDVPNRRLHLDISDEELARRLAEWQPNHDLPTSGYAFLHQQHVE 555
           A GGP+ +V+ GD I +D+P R L L + ++ELARR A + P     TS     + + V 
Sbjct: 486 AEGGPIGLVQEGDRIRIDIPARALDLLVDEDELARRRAAFVPVEKEITSPLLRRYARMVS 545

Query: 556 GADTGA 561
            A TGA
Sbjct: 546 SAATGA 551


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: 887
Number of extensions: 54
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: 554
Length adjustment: 36
Effective length of query: 543
Effective length of database: 518
Effective search space:   281274
Effective search space used:   281274
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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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