GapMind for catabolism of small carbon sources

 

Alignments for a candidate for vorB in Desulfatiglans anilini DSM 4660

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_028322983.1 H567_RS0121655 2-oxoglutarate ferredoxin oxidoreductase subunit alpha

Query= SwissProt::P80908
         (352 letters)



>NCBI__GCF_000422285.1:WP_028322983.1
          Length = 387

 Score =  214 bits (544), Expect = 4e-60
 Identities = 143/370 (38%), Positives = 201/370 (54%), Gaps = 32/370 (8%)

Query: 8   GNTAVIIGAMYAGCDCYFGYPITPASEILHEASRYFPLVGRKFVQAESEEAAINMVYGAA 67
           G+ A   GA+ AGC  + GYPITPA+EI    S   P VG  F+Q E E AA+  V GA+
Sbjct: 14  GDVACAEGALAAGCLFFGGYPITPATEIAEHMSERLPEVGGTFIQMEDEIAAMASVVGAS 73

Query: 68  AAGHRVMTASSGPGMSLKQEGISFLAGAELPAVIVDVMRAGP--GLGNIGPEQADYNQLV 125
            AG + MTA+SGPG SL  E I      E P V+V+V RAGP  GL  +G  QAD  Q  
Sbjct: 74  CAGVKSMTATSGPGFSLMMENIGLAVCTETPCVVVNVQRAGPSTGLPTLG-AQADMMQ-A 131

Query: 126 KGGGHGNYRNIVLAPNSVQEMCDLTMDAFELADKYRNPVIILADAVLGQMAEPLRFPE-- 183
           + G HG+Y  I LAP+S QE+   T+ AF LA++YR PV+++ D  +G ++E +  PE  
Sbjct: 132 RWGSHGHYEIIALAPSSPQEIFYQTITAFNLAERYRIPVLVMTDEFVGHLSERVVIPEPK 191

Query: 184 ------------RAVEHRP-----DTSWAVCGSRETMKNLVTSIFLD--------FDELE 218
                       R    +P     D    +  + E  +  VT +  D         +   
Sbjct: 192 DIRLVSRLAPKGRKDRFKPFRAGSDGIAPMAAAGEGYRIHVTGLTHDERGYPTMTVEAQT 251

Query: 219 EFNFYLQEKYAAVEENEVRYEEYMVEDAEIVLVAYGISSRVAKSAVDTARADGIKVGLLR 278
           E    L  K    EE  +  + Y ++DAEIV+V+YG+S+R A +AVD AR  GIK GL R
Sbjct: 252 EMMERLVGKIRGHEEEIILTDGYRLDDAEIVVVSYGVSARTAYAAVDEARRSGIKAGLFR 311

Query: 279 PITLFPFPSERIRELAEGGCTFISVEMSSGQMREDI-KMASGCRDVELVNRMGGNLIELR 337
            IT++PFP  RIR+LAE    F++VE++ GQ+  ++ + A+G     LV   GG +I   
Sbjct: 312 LITVWPFPERRIRQLAERVKAFVTVEINLGQIHLEVERCAAGKAPALLVGHPGGAIIPPE 371

Query: 338 DILRKIREIA 347
            ++  ++ IA
Sbjct: 372 HVIEAMQSIA 381


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: 324
Number of extensions: 11
Number of successful extensions: 3
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: 387
Length adjustment: 30
Effective length of query: 322
Effective length of database: 357
Effective search space:   114954
Effective search space used:   114954
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: 49 (23.5 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