GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Marinobacter adhaerens HP15

Align 2-methylbutanoyl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate GFF56 HP15_56 acyl-CoA dehydrogenase domain protein

Query= reanno::MR1:200844
         (385 letters)



>FitnessBrowser__Marino:GFF56
          Length = 374

 Score =  223 bits (569), Expect = 5e-63
 Identities = 126/373 (33%), Positives = 205/373 (54%), Gaps = 4/373 (1%)

Query: 5   FNEDQRQFAELARQFATDELAPFAAKWDEEHHFPKDVIQKAGELGFCSLYSPESEGGMGL 64
           F ED   F E AR+F   E+ P   +W++    PK++ +KAGE+G      PE  GG G 
Sbjct: 5   FREDHNMFREQARRFIEREICPHLEEWEKSGIVPKEIWRKAGEMGLLCSTVPEEYGGAGG 64

Query: 65  SRLDASIIFEELSKGCTATTAMLTIHNMATWMVTTWGTETLRQAWSEPLTTGQMLASYCL 124
               ++++ EEL++         T   +    +  +GTE  +Q W   + +G+++    +
Sbjct: 65  DFGHSAVMIEELARVNATAIGFTTHSEIVAPYIVAYGTEEQKQKWLPRMVSGEIIGVIAM 124

Query: 125 TEPGAGSDAASLQTKAVPDGDEYVVSGSKMFISGAGSTELLVVMCRTGQAGPKGISAIAI 184
           +EPG GSD  S++T+   DGD+Y++SG K FI+  G+ +L+V   +   A  K ++ + +
Sbjct: 125 SEPGIGSDLRSMRTQLRRDGDQYIISGQKTFITNGGNADLVVTATKVDPAS-KDLTLVCV 183

Query: 185 PADSEGIIYGKAEDKMGWNAQPTRLVTFDNVRVPVANLLGEEGQGFTFAMKGLDGGRINI 244
             D +G   G+  DK+G   Q T  + FD+VRVPV+N LGEE +GF +    L   R+ I
Sbjct: 184 ETDRDGFAKGRLLDKIGLKGQDTAELFFDDVRVPVSNRLGEENEGFGYLTHQLAWERLII 243

Query: 245 ATCSVGTAQAALERASQYMNERQQFGKPLAAFQALQFKLADMATELVAARQMVRLAAFKL 304
           A  +  +  + L+    Y  ER+ FGK +  FQ  +FKLA++  +    R  V     ++
Sbjct: 244 AIRAAESIDSFLDMTIGYTKERKVFGKTVFDFQNTRFKLAEIKAQATMLRVFVDNCLERV 303

Query: 305 DSGD-PEGTAYCAMAKRFATDVGFQVCDAALQIHGGYGYIREYPLERHFRDVRVHQILEG 363
            + D P   A  AMAK   +++  ++ D  LQ+HGGYG++ EY + + + D RV +I  G
Sbjct: 304 MNNDLPADVA--AMAKLMGSELQGKLLDEMLQLHGGYGFMSEYRIGQAWIDARVARIYGG 361

Query: 364 TNEIMRLIIARRL 376
           T+EIM+ II+R+L
Sbjct: 362 TSEIMKEIISRKL 374


Lambda     K      H
   0.319    0.134    0.396 

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: 346
Number of extensions: 11
Number of successful extensions: 3
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: 385
Length of database: 374
Length adjustment: 30
Effective length of query: 355
Effective length of database: 344
Effective search space:   122120
Effective search space used:   122120
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 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:

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