GapMind for catabolism of small carbon sources

 

Alignments for a candidate for vorB in Rhizorhabdus wittichii RW1

Align Ketoisovalerate oxidoreductase subunit VorB; VOR; 2-oxoisovalerate ferredoxin reductase subunit beta; 2-oxoisovalerate oxidoreductase beta chain; EC 1.2.7.7 (characterized)
to candidate WP_012049426.1 SWIT_RS16340 2-oxoacid:acceptor oxidoreductase subunit alpha

Query= SwissProt::P80908
         (352 letters)



>NCBI__GCF_000016765.1:WP_012049426.1
          Length = 615

 Score =  105 bits (263), Expect = 2e-27
 Identities = 100/373 (26%), Positives = 152/373 (40%), Gaps = 55/373 (14%)

Query: 6   VKGNTAVIIGAMYAGCDCYFGYPITPASEILHEASRYFPLV-----------GRKF--VQ 52
           V GNTA  +GA+Y G      YPITP++ +    + Y   +           G ++  VQ
Sbjct: 211 VDGNTAAGLGAVYGGATVCAWYPITPSTSLAEAFTAYCRKLRHDPETGPDGGGARYAIVQ 270

Query: 53  AESEEAAINMVYGAAAAGHRVMTASSGPGMSLKQEGISFLAGAELPAVIVDVMRAGPGLG 112
           AE E A+I MV GA   G R  T +SGPG+SL QE I     AE+P VI DV R GP  G
Sbjct: 271 AEDEIASIGMVTGAGWNGARAFTCTSGPGVSLMQEFIGLSYFAEIPGVIFDVQRGGPSTG 330

Query: 113 NIGPEQADYNQLVKG--GGHGNYRNIVLAPNSVQEMCDLTMDAFELADKYRNPVIILADA 170
              P +   + ++      HG+ ++++L P    E  +    AF+LAD+ +  + ++ D 
Sbjct: 331 M--PTRTQQSDILSAAYASHGDTKHVLLLPEGPNECFEFGALAFDLADRLQTMIFVMLDL 388

Query: 171 VLGQ---MAEPLRFPERAVEHRPDTSWA--------------VCGSRETMKNLVT----- 208
            +G    + EP R+ E  V  R     A              V G     + L       
Sbjct: 389 DMGMNEWLIEPFRWDEDRVLDRGKIMTAEMLEAGADFGRYKDVDGDGIPWRTLPATHPSK 448

Query: 209 -SIFLDFDELEEFNFYLQEKYAAVEENEVRYEEYMVEDAEIV--------------LVAY 253
            S F      + +  Y +E    V+  E    ++    + +               ++ Y
Sbjct: 449 GSYFTRGTSRDPYARYSEEGAVYVDNMERLLRKFETAKSLVPPPIVRRAARKTSYGVIYY 508

Query: 254 GISSRVAKSAVDTARADGIKVGLLRPITLFPFPSERIRELAEGGCTFISVEMSSGQMRED 313
           G +S     A+    ADG+ V  LR +  FPF  E    +A     F+  +    Q+R  
Sbjct: 509 GSTSPAMDEALAGLEADGVAVDALR-VRAFPFEGEIFEFIAAHDLVFVVEQNRDAQLRTL 567

Query: 314 IKMASGCRDVELV 326
           +    G     LV
Sbjct: 568 LINEGGVDPARLV 580


Lambda     K      H
   0.319    0.136    0.390 

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: 492
Number of extensions: 26
Number of successful extensions: 4
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: 352
Length of database: 615
Length adjustment: 33
Effective length of query: 319
Effective length of database: 582
Effective search space:   185658
Effective search space used:   185658
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: 51 (24.3 bits)

This GapMind analysis is from Apr 09 2024. 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