GapMind for catabolism of small carbon sources

 

Alignments for a candidate for vorB in Methanosarcina acetivorans C2A

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_048065602.1 MA_RS16080 2-oxoacid:acceptor oxidoreductase subunit alpha

Query= SwissProt::P80908
         (352 letters)



>NCBI__GCF_000007345.1:WP_048065602.1
          Length = 579

 Score =  117 bits (293), Expect = 8e-31
 Identities = 108/381 (28%), Positives = 170/381 (44%), Gaps = 48/381 (12%)

Query: 5   MVKGNTAVIIGAMYAGCDCYFGYPITPASEILHEASRYFPLVGRKFVQAESEEAAINMVY 64
           ++ G  A+ +GA+ +GC  Y  YP+TP++ IL+  +      G    QAE E +A+NM  
Sbjct: 201 LIDGVQAIGLGALMSGCKFYSAYPMTPSTGILNYLASKAEEHGLVVEQAEDEISAVNMAI 260

Query: 65  GAAAAGHRVMTASSGPGMSLKQEGISFLAGAELPAVIVDVMRAGPGLG-NIGPEQADYNQ 123
           GA+  G R MT SSG G +L  EG+S     E P VI ++ R GP  G     EQAD   
Sbjct: 261 GASFTGVRAMTGSSGGGFALMVEGLSLAGMTETPLVIAEIQRPGPATGLPTRTEQADL-L 319

Query: 124 LVKGGGHGNYRNIVLAPNSVQEMCDLTMDAFELADKYRNPVIILADAVLGQMA------- 176
            +   GHG +  ++  P + ++   LT  AFELA+KY+ PV I +D  LG          
Sbjct: 320 FILYAGHGEFPKVIFEPGTPKQAFYLTNRAFELAEKYQIPVFIQSDQYLGDSEWTFENFD 379

Query: 177 -EPLRFPE--------RAVEHRPDTSWAVCG------SRETMKNLVTSIFLDFDELEEFN 221
            E L + +          VE      ++  G        E  K+LV +   D DE +E  
Sbjct: 380 FEHLIYNDYRLRKKDLEGVEEYKRYKYSDTGISLLAVPGEAGKHLVVA---DSDEHDEEG 436

Query: 222 FYLQEKYAAVEENEVRYEE--------------YMVEDAEIVLVAYGISSRVAKSAVDTA 267
             +++    ++    R  +              Y     EIVLV +G +  V K  VD  
Sbjct: 437 HIIEDDETRIKMVRKRLLKKLPLIKKEIEAPLLYGDPSPEIVLVGHGSTYGVIKEVVDIL 496

Query: 268 RADGIKVGLLRPITLFPFPSERIR----ELAEGGCTFISVE-MSSGQMREDIKMASGCRD 322
             D  K+ ++    ++P P ER R    EL E     IS+E  ++GQ  + ++  +G   
Sbjct: 497 SRDR-KIAMMHFSQVYPLP-ERDRSDYIELLEKAKLTISIENNATGQFSKLVRAETGFDF 554

Query: 323 VELVNRMGGNLIELRDILRKI 343
              + +  G    + ++  ++
Sbjct: 555 THQILKYDGRPFSIENLKEEV 575


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: 429
Number of extensions: 20
Number of successful extensions: 2
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: 352
Length of database: 579
Length adjustment: 33
Effective length of query: 319
Effective length of database: 546
Effective search space:   174174
Effective search space used:   174174
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 Sep 24 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