GapMind for catabolism of small carbon sources

 

Alignments for a candidate for vorB in Calditerrivibrio nitroreducens DSM 19672

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_013450413.1 CALNI_RS01395 3-methyl-2-oxobutanoate dehydrogenase subunit VorB

Query= SwissProt::P80908
         (352 letters)



>NCBI__GCF_000183405.1:WP_013450413.1
          Length = 349

 Score =  301 bits (771), Expect = 2e-86
 Identities = 159/345 (46%), Positives = 226/345 (65%), Gaps = 2/345 (0%)

Query: 5   MVKGNTAVIIGAMYAGCDCYFGYPITPASEILHEASRYFPLVGRKFVQAESEEAAINMVY 64
           ++KGN A+   A+ AG   YFGYPITP +E+    S+    +GR FVQAESE AAINMVY
Sbjct: 6   LMKGNEAIAEAAVRAGVKGYFGYPITPQNEVTAYMSKRMVELGRAFVQAESEVAAINMVY 65

Query: 65  GAAAAGHRVMTASSGPGMSLKQEGISFLAGAELPAVIVDVMRAGPGLGNIGPEQADYNQL 124
           GAA+ G   MT SS PG++L QEGIS++ GAE+PAVIV++ R GPGLGNIGP Q DYNQ 
Sbjct: 66  GAASTGELAMTTSSSPGIALMQEGISYMCGAEVPAVIVNISRGGPGLGNIGPSQGDYNQS 125

Query: 125 VKGGGHGNYRNIVLAPNSVQEMCDLTMDAFELADKYRNPVIILADAVLGQMAEPLRFPER 184
            +GGG+G+Y  IV  P+++QE  D+T  AF++A++YRNPV+IL D  LGQMAE +  P  
Sbjct: 126 TRGGGNGDYFLIVYTPSTLQEAVDITYKAFDVANRYRNPVLILGDGALGQMAETVVLPPF 185

Query: 185 AVEHRPDTSWAVCGSRETMKNLVTSIFLDFDELEEFNFYLQEKYAAVEENEVRYEEYMVE 244
                 D  W + G +      V S+ L    L+  NF+L+EK+  V+ NEV Y E + +
Sbjct: 186 KELESKDKGWELNGCKGREPRSVKSLRLAEGMLKLHNFHLKEKFEQVKRNEVEY-ELIGD 244

Query: 245 DAEIVLVAYGISSRVAKSAVDTARADGIKVGLLRPITLFPFPSERIRELAEGGCTFISVE 304
           D +I++VA+G ++RV+KSA+  A   G+KVG+ RPI ++P+P  ++ E A+     + VE
Sbjct: 245 DYDILIVAFGTAARVSKSAIKEAAKHGVKVGMFRPILIWPYPYAQLTEAAKKAKKVLVVE 304

Query: 305 MSSGQMREDIKMA-SGCRDVELVNRMGGNLIELRDILRKIREIAG 348
           M++GQM  D+ +A      +E + + GG +++  +IL KI  I G
Sbjct: 305 MNNGQMLFDVMLAVKDDNKIEFLGKPGGEVVDPDEILEKILSIKG 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: 295
Number of extensions: 12
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: 349
Length adjustment: 29
Effective length of query: 323
Effective length of database: 320
Effective search space:   103360
Effective search space used:   103360
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