GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xad in Dinoroseobacter shibae DFL-12

Align Xylonate dehydratase (EC 4.2.1.82) (characterized)
to candidate 3607836 Dshi_1244 Dihydroxy-acid dehydratase (RefSeq)

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



>FitnessBrowser__Dino:3607836
          Length = 569

 Score =  423 bits (1088), Expect = e-123
 Identities = 242/533 (45%), Positives = 323/533 (60%), Gaps = 16/533 (3%)

Query: 44  GRPIIGIAQTGSDLTPCNRHHLELAQRVKAGIRDAGGIPMEFPVHPIAEQSRRPTAALDR 103
           GRP+IGI  T S+LTPCN     LA+ VK G+ +AGG P+EFPV  + E   +PTA L R
Sbjct: 37  GRPVIGICNTWSELTPCNHGLRTLAEGVKRGVWEAGGFPVEFPVMSLGETQMKPTAMLFR 96

Query: 104 NLAYLGLVEILHGYPLDGVVLTTGCDKTTPACLMAAATTDLPAIVLSGGPMLDGHHKGEL 163
           NL  + + E +  Y +DGVVL  GCDKTTP  LM AA+ DLP+IV+S GPML+G ++G+ 
Sbjct: 97  NLLAMDVEESIRAYGMDGVVLLGGCDKTTPGQLMGAASVDLPSIVVSAGPMLNGKYRGQD 156

Query: 164 IGSGTVLWHARNLMAAGEIDYEGFMEMTTAASPSVGHCNTMGTALSMNALAEALGMSLPG 223
           IGSGT +W     + AGE+    FM      S S G C TMGTA +M +L EA+GMSLP 
Sbjct: 157 IGSGTDVWKFSEAVRAGEMTLADFMNAEAGMSRSAGVCMTMGTASTMASLVEAMGMSLPL 216

Query: 224 CASIPAPYRERGQMAYATGKRICDLVRQDIRPSQIMTRQAFENAIAVASALGASSNCPPH 283
            A++PA    R  +A+ TGKRI ++V +D+RPS I+T+ AFENAI   +A+G S+N   H
Sbjct: 217 NAALPAVDARRMALAHLTGKRIVEMVEEDLRPSAILTKPAFENAILANAAVGGSTNAVMH 276

Query: 284 LIAIARHMGVELSLEDWQRIGEDVPLLVNCMPAGKYLGEGFHRAGGVPSVMHELQKAGRL 343
           L+A+A   GV+L+L+D++ IG ++PLLVNCMP+GKYL E F  AGG+P V+ EL+   R 
Sbjct: 277 LLALAGRAGVDLTLKDFE-IGGEIPLLVNCMPSGKYLMEDFAYAGGMPVVLSELRDHLR- 334

Query: 344 HEDCATVSGKTIGEIVSNSLTSNTDVIHPFDTPLKHRAGFIVLSGNFF-DSAIMKMSVVG 402
                TV GK I      +   N DVIH +D P+K  AG  VL G+   D AI+K S   
Sbjct: 335 --PATTVLGKDIAAYTEGAECFNRDVIHAYDAPVKPAAGLRVLRGSLAPDGAIVKPSAAT 392

Query: 403 EAFRKTYLSEPGAENSFEARAIVFEGPEDYHARIDDPALDIDERCILVIRGVGTVGYPGS 462
           +A  +            E  A VFE  ED  A ID   L I    ILV++G G  GYPG 
Sbjct: 393 DALLE-----------HEGPAFVFENIEDMKANIDRDDLPITPDTILVLKGCGPKGYPGM 441

Query: 463 AEVVNMAPPAALIKQGIDSLPCLGDGRQSGTSASPSILNMSPEAAVGGGLALLKTNDRLK 522
            EV NM  PA L+++G+  +  + D R SGT+    IL+++PEA  GG LAL+KT DR++
Sbjct: 442 PEVGNMPIPAKLVREGVRDMIRVSDARMSGTAYGTVILHVAPEAQAGGPLALVKTGDRIR 501

Query: 523 VDLNTRTVNLLIDDAEMAQRRREWIPNIPPSQTPWQELYRQLVGQLSTGGCLE 575
           V      ++LL+D  E+A RR  W P+ P     + +LY   V Q   G  L+
Sbjct: 502 VSAREGVLDLLVDATELAARRAAWQPDPPHYTRGYAKLYIDHVLQADRGADLD 554


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: 925
Number of extensions: 61
Number of successful extensions: 4
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: 569
Length adjustment: 36
Effective length of query: 558
Effective length of database: 533
Effective search space:   297414
Effective search space used:   297414
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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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