Aligments for a candidate for bkdC in Bacteroides thetaiotaomicron VPI-5482

GapMind for catabolism of small carbon sources

Aligments for a candidate for bkdC in Bacteroides thetaiotaomicron VPI-5482

Align Lipoamide acyltransferase component of branched-chain alpha-keto acid dehydrogenase complex; EC 2.3.1.168; Branched-chain alpha-keto acid dehydrogenase complex component E2; BCKAD-E2; BCKADE2; Dihydrolipoamide acetyltransferase component of branched-chain alpha-keto acid dehydrogenase complex; Dihydrolipoamide branched chain transacylase; Dihydrolipoyllysine-residue (2-methylpropanoyl)transferase (uncharacterized)
to candidate 349839 BT0311 lipoamide acyltransferase component of branched-chain alpha-keto acid dehydrogenase complex (NCBI ptt file)

Query= curated2:P37942
         (424 letters)



>lcl|FitnessBrowser__Btheta:349839 BT0311 lipoamide acyltransferase
           component of branched-chain alpha-keto acid
           dehydrogenase complex (NCBI ptt file)
          Length = 456

 Score =  263 bits (672), Expect = 8e-75
 Identities = 167/449 (37%), Positives = 245/449 (54%), Gaps = 37/449 (8%)

Query: 5   QMTMPQLGESVTEGTISKWLVAPGDKVNKYDPIAEVMTDKVNAEVPSSFTGTITELVGEE 64
           ++ MP+LGES+TEGTI  W V  GD + + D + EV T KV+AE+PS   G + E++ +E
Sbjct: 5   EIKMPKLGESITEGTIVSWSVKVGDVIQEDDVLFEVNTAKVSAEIPSPVAGKVVEILFKE 64

Query: 65  GQTLQVGEMICKIETEGANPAEQK----QEQPAASEAAENPVAKSAGAADQPNKKRYSPA 120
           G T+ VG ++  ++  G   ++++    +E P + E A +   K +    +  ++ YSP 
Sbjct: 65  GDTVAVGTVVAVVDMGGEEASDEETASGKETPESKENASSDAEKVSSQVAKAEERWYSPV 124

Query: 121 VLRLAGEHGI---DLDQVTGTGAGGRITRKDIQRLIETG--GVQEQNPEELKTA----AP 171
           V++LA    I   +LD + GTG  GR+++KDI+  IE    G+ E +   + T     A 
Sbjct: 125 VIQLARGANIPKEELDSIQGTGYEGRLSKKDIKDYIEKKKRGISEVSKAAIPTGDALTAS 184

Query: 172 APKSA--------SKPEPKEETSYPASAAGDKEIPVTG------------VRKAIASNMK 211
            P S         S      +T   A +A  K+ P               VR+ IA +M 
Sbjct: 185 MPSSTGGAGSMTTSPVAASVQTPVAAPSAPSKQAPAAANIPGVEVKEMDRVRRIIADHMV 244

Query: 212 RSKTEIPHAWTMMEVDVTNMVAYRNSIKDSFKKTEGFNLTFFAFFVKAVAQALKEFPQMN 271
            SK   PH   ++EVDVT +V +R   KD+F + EG  LT+     +AVA+AL  +PQ+N
Sbjct: 245 MSKKVSPHVTNVVEVDVTKLVRWREKNKDAFFRREGVKLTYMPVITEAVAKALAAYPQVN 304

Query: 272 SMWAGDKIIQKKDINISIAVATED-SLFVPVIKNADEKTIKGIAKDITGLAKKVRDGKLT 330
               G  I+ KK INI IAV+  D +L VPV+ +AD   + G+A  I  LA K RD KL 
Sbjct: 305 VSVDGYNILFKKHINIGIAVSLNDGNLIVPVVHDADHLNLNGLAVAIDSLALKARDNKLM 364

Query: 331 ADDMQGGTFTVNNTGSFGSVQSMGIINYPQAAILQVESIVKRPVVM---DNGMIAVRDMV 387
            DD+ GGTFT+ N G+F S+    +IN PQ AIL V  I K+P V+   +   IA+R  +
Sbjct: 365 PDDIDGGTFTITNFGTFKSLFGTPVINQPQVAILGVGYIEKKPAVIETPEGDTIAIRHKM 424

Query: 388 NLCLSLDHRVLDGLVCGRFLGRVKQILES 416
            L LS DHRV+DG++ G FL  +   LE+
Sbjct: 425 YLSLSYDHRVVDGMLGGNFLHFIADYLEN 453


Lambda     K      H
   0.312    0.129    0.359 

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: 493
Number of extensions: 31
Number of successful extensions: 6
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: 424
Length of database: 456
Length adjustment: 32
Effective length of query: 392
Effective length of database: 424
Effective search space:   166208
Effective search space used:   166208
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Sep 17 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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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

GapMind for catabolism of small carbon sources