GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PPDCbeta in Saccharomonospora cyanea NA-134

Align Putative branched-chain alpha keto acid dehydrogenase E1 subunit beta (characterized, see rationale)
to candidate WP_005456121.1 SACCYDRAFT_RS10830 alpha-ketoacid dehydrogenase subunit beta

Query= uniprot:G1UHX5
         (328 letters)



>NCBI__GCF_000244975.1:WP_005456121.1
          Length = 330

 Score =  235 bits (600), Expect = 1e-66
 Identities = 142/322 (44%), Positives = 185/322 (57%), Gaps = 6/322 (1%)

Query: 1   MSEITMAKALNTALRDALRDDPRTILFGEDIGALGGVFRITDGLAAEFGDERCFDTPLAE 60
           M  I+  +AL   LR+ LR D   +L GE+IG  GG ++IT GL  EFG++R  DTP+AE
Sbjct: 1   MPVISYREALRNTLREELRRDDDVLLIGEEIGVFGGSYKITSGLLEEFGEKRVRDTPIAE 60

Query: 61  SAILGTAVGMAMYGYRPVVEMQFDAFAYPAFEQLVSHVAKLRNRTRGAIGLPLTIRIPYG 120
              +G AVG AM G RP+VE+    F+  A +Q+V+H AK+     G   +P+ IR P G
Sbjct: 61  EGFVGAAVGAAMLGLRPIVEIMTINFSLLALDQIVNHAAKIYGMFGGQTSVPMVIRTPGG 120

Query: 121 GGIGGVEHHSDSSEIYYMATPGLTVVTPATAADAYSLLRRSIASPDPVVFLEPKRLYWRK 180
           GG      HS + E+YY   PGL VV P+T ADA +LL  ++   DPV+FLE   LY  K
Sbjct: 121 GGQQLGATHSQNIELYYAFVPGLKVVAPSTPADARALLLAAVRDDDPVLFLENLALYNTK 180

Query: 181 EALGLPVDTGP--LGSAVIRRHGTHATLIAYGPAVTTALEAAEAAA-EHGWDLEVIDLRT 237
               +P D GP  +G A + R GT  T++ Y      A+E A+    E G   EVIDLR+
Sbjct: 181 GE--VPDDLGPAEIGRAAVVREGTDITIVGYSRMAAVAVEVADRLRDESGVSAEVIDLRS 238

Query: 238 LMPLDDATVCASVRRTGRAVVVHEAHGFAGPGAEIAARITERCFYHLEAPVRRVTGFDVP 297
           L PLD  T+ AS RRTG  VV  +     G GAEIAA I++  F HL+APVRRV   +VP
Sbjct: 239 LRPLDRETLVASARRTGCVVVAEDDWLTYGVGAEIAASISDGAFDHLDAPVRRVAAAEVP 298

Query: 298 YP-PPLLERHYLPGVDRILDAV 318
            P    LE   LP  + +  AV
Sbjct: 299 LPYAKPLETAALPSAESLHTAV 320


Lambda     K      H
   0.322    0.138    0.418 

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: 306
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: 328
Length of database: 330
Length adjustment: 28
Effective length of query: 300
Effective length of database: 302
Effective search space:    90600
Effective search space used:    90600
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 (21.9 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