GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bkdA in Frankia alni ACN14A

Align 3-methyl-2-oxobutanoate dehydrogenase subunit alpha; Branched-chain alpha-ketoacid dehydrogenase E1 component subunit alpha; BCKADH E1-alpha; EC 1.2.4.4 (characterized)
to candidate WP_041940013.1 FRAAL_RS00345 pyruvate dehydrogenase (acetyl-transferring) E1 component subunit alpha

Query= SwissProt::P9WIS3
         (367 letters)



>NCBI__GCF_000058485.1:WP_041940013.1
          Length = 424

 Score =  271 bits (694), Expect = 2e-77
 Identities = 154/333 (46%), Positives = 191/333 (57%), Gaps = 1/333 (0%)

Query: 35  YHRDLPEETLRWLYEMMVVTRELDTEFVNLQRQGELALYTPCRGQEAAQVGAAACLRKTD 94
           Y  DL ++ L  LY  MV+ R +D E  +LQRQGEL L+   RGQEAAQVG+   L   D
Sbjct: 61  YVADLTDDELFGLYRDMVLVRRMDEEATSLQRQGELGLWASLRGQEAAQVGSGRALGPDD 120

Query: 95  WLFPQYRELGVYLVRGIPPGHVGVAWRGTWHGGLQFTTKCCAPMSVPIGTQTLHAVGAAM 154
             FP YRE GV   RG+ P  V   +RG   GG    T   A  S+ +G+QTLHA G AM
Sbjct: 121 MAFPSYREHGVAWCRGVDPAAVLAIFRGVNLGGWDPATHGFALYSIVVGSQTLHATGYAM 180

Query: 155 AAQRLDEDSVTVAFLGDGATSEGDVHEALNFAAVFTTPCVFYVQNNQWAISMPVSRQTAA 214
                      +A+ GDGA+SEGDV+EA  +A+V+  P VF+ QNNQWAIS P  RQT  
Sbjct: 181 GMAWDRSAGAAIAYFGDGASSEGDVNEAFGWASVYRAPLVFFCQNNQWAISEPTRRQTRT 240

Query: 215 PSIAHKAIGYGMPGIRVDGNDVLACYAVMAEAAARARAGDGPTLIEAVTYRLGPHTTADD 274
             I H+A G+G P +RVDGNDVLAC AV   A A ARAG GP L+EAVTYR+G HTTADD
Sbjct: 241 -EIFHRAAGFGFPSVRVDGNDVLACLAVSRWALATARAGRGPVLVEAVTYRMGAHTTADD 299

Query: 275 PTRYRSQEEVDRWATLDPIPRYRTYLQDQGLWSQRLEEQVTARAKHVRSELRDAVFDAPD 334
           PTRYRS  E++ W+  DP+ R R +L   GL  +  +  +   A     ELR+      D
Sbjct: 300 PTRYRSPVELEAWSRRDPLDRMRAHLAACGLLGEERDRHLALEADAFAHELRNRCTAMLD 359

Query: 335 FDVDEVFTTVYAEITPGLQAQREQLRAELARTD 367
            D   +F  V       +  QR    A L  +D
Sbjct: 360 PDPTSLFDHVQVTENGLVAQQRSAFAATLDPSD 392


Lambda     K      H
   0.320    0.134    0.413 

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: 461
Number of extensions: 19
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: 367
Length of database: 424
Length adjustment: 31
Effective length of query: 336
Effective length of database: 393
Effective search space:   132048
Effective search space used:   132048
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 (21.8 bits)
S2: 50 (23.9 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