GapMind for catabolism of small carbon sources

 

Alignments for a candidate for vorB in Desulfotomaculum ruminis DSM 2154

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_013843010.1 DESRU_RS15405 3-methyl-2-oxobutanoate dehydrogenase subunit VorB

Query= SwissProt::P80908
         (352 letters)



>NCBI__GCF_000215085.1:WP_013843010.1
          Length = 355

 Score =  345 bits (885), Expect = 1e-99
 Identities = 182/349 (52%), Positives = 242/349 (69%), Gaps = 3/349 (0%)

Query: 1   MATQMVKGNTAVIIGAMYAGCDCYFGYPITPASEILHEASRYFPLVGRKFVQAESEEAAI 60
           M+  ++KGN A+  GA+ AGC  +FGYPITP SE+ H  ++  P VG  F+QAESE ++I
Sbjct: 1   MSKVLMKGNEAIGEGAIRAGCRHFFGYPITPQSELPHYLAKRMPEVGGVFLQAESETSSI 60

Query: 61  NMVYGAAAAGHRVMTASSGPGMSLKQEGISFLAGAELPAVIVDVMRAGPGLGNIGPEQAD 120
           NMVYGAA AG R MT+SS PG+SL QEGIS+L GAELP VIV+VMR GPGLGNI P Q+D
Sbjct: 61  NMVYGAAGAGFRTMTSSSSPGISLMQEGISYLVGAELPCVIVNVMRGGPGLGNIAPAQSD 120

Query: 121 YNQLVKGGGHGNYRNIVLAPNSVQEMCDLTMDAFELADKYRNPVIILADAVLGQMAEPLR 180
           Y Q VKGGGHG+YR IVLAP SVQE+ DL   +F LAD+YR PV+++ D +LGQM EP+ 
Sbjct: 121 YFQSVKGGGHGDYRLIVLAPASVQEIIDLMGLSFGLADQYRTPVMVVGDGILGQMMEPVE 180

Query: 181 FPER-AVEHRPDTSWAVCGSR-ETMKNLVTSIFLDFDELEEFNFYLQEKYAAVEENEVRY 238
             E   +   P   WA  G +  T  N++ S+++  +  E+ N  L  KY  + + E R+
Sbjct: 181 LDEEVTLPEIPAKPWAAGGLKGRTAPNIINSLYIVPEACEDLNKKLFAKYETITQRETRW 240

Query: 239 EEYMVEDAEIVLVAYGISSRVAKSAVDTARADGIKVGLLRPITLFPFPSERIRELAEGGC 298
           EEY +EDAEIVL  +G ++R+AKS VD ARA+GIK GL+RPITL+PFPSE   + AE   
Sbjct: 241 EEYRLEDAEIVLTGFGTAARIAKSVVDKARAEGIKAGLIRPITLWPFPSEVYAKAAEQAG 300

Query: 299 TFISVEMSSGQMREDIKMA-SGCRDVELVNRMGGNLIELRDILRKIREI 346
            F+ VEMS GQM ED+K+A +G + V    R GG +   +D+  +++++
Sbjct: 301 QFLCVEMSMGQMVEDVKLAVNGRKPVGFYGRSGGMVPLAKDVFAEVKKL 349


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: 378
Number of extensions: 16
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: 355
Length adjustment: 29
Effective length of query: 323
Effective length of database: 326
Effective search space:   105298
Effective search space used:   105298
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