GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bcd in Dyella japonica UNC79MFTsu3.2

Align butanoyl-CoA dehydrogenase (NAD+, ferredoxin) (subunit 3/3) (EC 1.3.1.109); short-chain acyl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate N515DRAFT_0941 N515DRAFT_0941 isovaleryl-CoA dehydrogenase

Query= BRENDA::Q18AQ1
         (378 letters)



>FitnessBrowser__Dyella79:N515DRAFT_0941
          Length = 385

 Score =  278 bits (712), Expect = 1e-79
 Identities = 144/373 (38%), Positives = 232/373 (62%), Gaps = 2/373 (0%)

Query: 6   KKYQMLKELYVSFAENEVKPLATELDEEERFPYETVEKMAKAGMMGIPYPKEYGGEGGDT 65
           ++  +L+E   +FAE E+ P AT++D +  FP +   K  + G++G+  P+ YGG G   
Sbjct: 8   EELDLLRESVHAFAEKEIAPRATQIDHDNVFPADLWRKFGEMGLLGMTIPEAYGGTGLGY 67

Query: 66  VGYIMAVEELSRVCGTTGVILSAHTSLGSWPIYQYGNEEQKQKFLRPLASGEKLGAFGLT 125
           + +++A+EE+SR  G+ G+   AH++L    ++  GNEEQ++K++  L SGE +GA  ++
Sbjct: 68  LAHMVAMEEISRASGSVGLSYGAHSNLCVQNLFHNGNEEQRRKYIPRLCSGEYVGALAMS 127

Query: 126 EPNAGTDASGQQTT-AVLDGDEYILNGSKIFITNAIAGDIYVV-MAMTDKSKGNKGISAF 183
           EP AG+D  G  +  A L GD ++ NG+K++ITN    D+ +V M    +  G++ ++AF
Sbjct: 128 EPGAGSDVVGSMSCKAELRGDVWVANGTKMWITNGPDADVLLVYMRTAPRPAGSRCMTAF 187

Query: 184 IVEKGTPGFSFGVKEKKMGIRGSATSELIFEDCRIPKENLLGKEGQGFKIAMSTLDGGRI 243
           I+EKG  GFS   K  K+G+RGS T EL+FEDC IP  N++G+  +G ++ MS LD  R+
Sbjct: 188 IIEKGMKGFSTAQKLDKLGMRGSNTCELVFEDCEIPAANIVGEVNEGVRVLMSGLDTERL 247

Query: 244 GIAAQALGLAQGALDETVKYVKERVQFGRPLSKFQNTQFQLADMEVKVQAARHLVYQAAI 303
            ++   LGL Q A+D  + YV+ER QF  P+  F   Q ++ADM   +Q++R   Y  A 
Sbjct: 248 VLSGGPLGLMQAAMDLVLPYVRERKQFNAPIGTFGMMQAKVADMYTALQSSRGFAYMVAR 307

Query: 304 NKDLGKPYGVEAAMAKLFAAETAMEVTTKAVQLHGGYGYTRDYPVERMMRDAKITEIYEG 363
             D G    ++ A   L A++ A++V  +A+Q  GG GY  ++P  R++RDAK+ EI  G
Sbjct: 308 EFDQGSKSRIDPAACLLNASQNAVKVALEAIQALGGNGYINEFPAGRLLRDAKLYEIGAG 367

Query: 364 TSEVQRMVISGKL 376
           T+E++RM+I  +L
Sbjct: 368 TNEIRRMLIGREL 380


Lambda     K      H
   0.315    0.133    0.373 

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: 360
Number of extensions: 16
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: 378
Length of database: 385
Length adjustment: 30
Effective length of query: 348
Effective length of database: 355
Effective search space:   123540
Effective search space used:   123540
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 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