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_051184395.1 H567_RS0100390 3-methyl-2-oxobutanoate dehydrogenase subunit VorB

Query= SwissProt::P80908
         (352 letters)



>NCBI__GCF_000422285.1:WP_051184395.1
          Length = 339

 Score =  316 bits (810), Expect = 5e-91
 Identities = 163/336 (48%), Positives = 235/336 (69%), Gaps = 6/336 (1%)

Query: 14  IGAMYAGCDCYFGYPITPASEILHEASRYFPLVGRKFVQAESEEAAINMVYGAAAAGHRV 73
           +GA+ AGC  YFGYPITP ++I    S++ P VG  F+QAESE A+INM+ GA+A G R 
Sbjct: 1   MGAIEAGCRFYFGYPITPQNDIPEYMSKHLPAVGGTFIQAESEIASINMLLGASATGARA 60

Query: 74  MTASSGPGMSLKQEGISFLAGAELPAVIVDVMRAGPGLGNIGPEQADYNQLVKGGGHGNY 133
           MT+SS PG+SLKQEGIS+L G+++P VIV++ R+GPGLG I P Q DY Q  +GGGHG+Y
Sbjct: 61  MTSSSSPGISLKQEGISYLCGSQIPGVIVNMSRSGPGLGGISPSQGDYFQATRGGGHGDY 120

Query: 134 RNIVLAPNSVQEMCDLTMDAFELADKYRNPVIILADAVLGQMAEPLRF-PERAVEHRPDT 192
           R IVLAP+SVQE  DLTM AF+LADKYRNPV+IL DA+LGQ+ EPL+  P R     P+ 
Sbjct: 121 RTIVLAPSSVQEAYDLTMRAFDLADKYRNPVLILGDALLGQIKEPLKTRPYRGTP--PEK 178

Query: 193 SWAVCGSRETMKNLVTSIFLDFDELEEFNFYLQEKYAAVEENEVRYEEYMVEDAEIVLVA 252
            W + G+    + ++ S++L   EL + N++L  KY  + + E+R+E   ++DA++++VA
Sbjct: 179 DWILTGASGRPRRILKSLYLSEGELTDHNWFLYRKYQQM-KREIRFETQNLDDAKLLVVA 237

Query: 253 YGISSRVAKSAVDTARADGIKVGLLRPITLFPFPSERIRELAEGGCTFISVEMSSGQMRE 312
           +G  +R+ KSAV  AR  G+ +GLLRPITL+PFP   + +++     F++VE+S+GQM E
Sbjct: 238 FGSLARIVKSAVGMAREKGMLIGLLRPITLYPFPYAALEKISRKIRNFMAVELSTGQMVE 297

Query: 313 DIKMASGCR--DVELVNRMGGNLIELRDILRKIREI 346
           D+K+A G +   V+   R  G++    +I  +I ++
Sbjct: 298 DVKLAVGHKKNQVDFYGRPPGSIPSPDEIFHEIAKV 333


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: 351
Number of extensions: 12
Number of successful extensions: 3
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: 339
Length adjustment: 29
Effective length of query: 323
Effective length of database: 310
Effective search space:   100130
Effective search space used:   100130
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