GapMind for catabolism of small carbon sources

 

Alignments for a candidate for vorB in Desulfarculus baarsii DSM 2075

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_013259642.1 DEBA_RS14200 2-oxoglutarate ferredoxin oxidoreductase subunit alpha

Query= SwissProt::P80908
         (352 letters)



>NCBI__GCF_000143965.1:WP_013259642.1
          Length = 378

 Score =  203 bits (516), Expect = 7e-57
 Identities = 135/374 (36%), Positives = 201/374 (53%), Gaps = 36/374 (9%)

Query: 4   QMVKGNTAVIIGAMYAGCDCYFGYPITPASEILHEASRYFPLVGRKFVQAESEEAAINMV 63
           ++++GN A+  GA+ AGC  + GYPITPASEI     R  P  G  F+Q E E A++   
Sbjct: 7   ELLQGNEAIARGALAAGCRFFAGYPITPASEISEILGRRLPARGAAFIQMEDEIASLGAC 66

Query: 64  YGAAAAGHRVMTASSGPGMSLKQEGISFLAGAELPAVIVDVMRAGPGLG-NIGPEQADYN 122
            GA+ AG + MTA+SGPG SL QE + +    E P V+V+VMRAGP  G    P Q D  
Sbjct: 67  IGASLAGAKAMTATSGPGFSLMQENLGWACITETPLVLVNVMRAGPSTGMPTNPAQGDVQ 126

Query: 123 QLVKGGGHGNYRNIVLAPNSVQEMCDLTMDAFELADKYRNPVIILADAVLGQMAEPLRFP 182
           Q  + G HG++  IVL P SV +  +LT+ AF LA++ R PVI+LAD V+  + E +  P
Sbjct: 127 Q-ARWGTHGDHPAIVLCPASVAQCFELTVRAFNLAERLRTPVIVLADEVVAHLREKVSLP 185

Query: 183 E----RAVEHRPDT---SWAV------------CGSRETMKNLVTSIFLDF--------D 215
                  +E R  +    W V                +  +  VT +  D         D
Sbjct: 186 AEDELEIIERRKPSVPPDWYVPFKTDGGLIPHLADLGDGYRYHVTGLVHDERGFPTRRPD 245

Query: 216 ELEEFNFYLQEKYAAVEENEVRYEEYM---VEDAEIVLVAYGISSRVAKSAVDTARADGI 272
           E+E F    +  +  +  N    E+ +   ++DAE+VL+AYG ++R A++AV  ARA G+
Sbjct: 246 EVEPF---FRRLFGKIRRNFGELEQVLPMALDDAEVVLIAYGCTARAAQAAVRQARAAGM 302

Query: 273 KVGLLRPITLFPFPSERIRELAEGGCTFISVEMSSGQMREDIK-MASGCRDVELVNRMGG 331
           K+GLL+ + L+PFP   + +   G    +  E++ GQ+  ++K +A+G   V    RM G
Sbjct: 303 KLGLLQIVGLWPFPRRAVEKAVLGRRAVLVPELNMGQLSREVKRVAAGRARVVHHGRMDG 362

Query: 332 NLIELRDILRKIRE 345
            +I   +IL +IRE
Sbjct: 363 QVITPDEILNRIRE 376


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: 326
Number of extensions: 16
Number of successful extensions: 4
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: 378
Length adjustment: 30
Effective length of query: 322
Effective length of database: 348
Effective search space:   112056
Effective search space used:   112056
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