GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Pedobacter sp. GW460-11-11-14-LB5

Align glutaryl-CoA dehydrogenase (ETF) (EC 1.3.8.6) (characterized)
to candidate CA265_RS14465 CA265_RS14465 acyl-CoA dehydrogenase

Query= BRENDA::Q92947
         (438 letters)



>FitnessBrowser__Pedo557:CA265_RS14465
          Length = 453

 Score =  247 bits (630), Expect = 6e-70
 Identities = 141/379 (37%), Positives = 212/379 (55%), Gaps = 2/379 (0%)

Query: 57  EEQLTTDEILIRDTFRTYCQERLMPRILLANRNEVFHREIISEMGELGVLGPTIKGYGCA 116
           +E L  ++  ++   R + ++ + P +        F  EII ++ EL + G T KGYGC 
Sbjct: 75  DEALKDEDRELQLKVRAFLEKEVKPIVNHYWNKAEFPFEIIPKLAELNICGLTYKGYGCP 134

Query: 117 GVSSVAYGLLARELERVDSGYRSAMSVQSSLVMHPIYAYGSEEQRQKYLPQLAKGELLGC 176
           G S++  G+LA E+ R+D+   +   VQS L M  IY  GSEEQ+Q++LP + + +++G 
Sbjct: 135 GKSNLMEGILAMEMARIDTSISTFFGVQSGLAMGSIYLCGSEEQKQQWLPLMQQFKIIGA 194

Query: 177 FGLTEPNSGSDPSSMETRAHYNSSNKSYTLNGTKTWITNSPMADLFVVWARCED-GCIRG 235
           FGLTEP  GS  +   T        K + LNG K WI N+  AD+ ++WAR E+ G ++G
Sbjct: 195 FGLTEPEVGSAAAGGLTTTCKKVDGK-WVLNGQKKWIGNATFADILIIWARDEESGEVKG 253

Query: 236 FLLEKGMRGLSAPRIQGKFSLRASATGMIIMDGVEVPEENVLPGASSLGGPFGCLNNARY 295
           F+++K   G +  ++Q K +LR    G+I +   EV E + L  A+S       L   R 
Sbjct: 254 FIVKKDNPGFAVEKMQDKMALRIVQNGIITLTNCEVEEADRLQNANSFKDTAKVLQMTRA 313

Query: 296 GIAWGVLGASEFCLHTARQYALDRMQFGVPLARNQLIQKKLADMLTEITLGLHACLQLGR 355
           G+AW  +G +      A  Y   R QFG P+A  QLIQ  L +ML+ +T     C +L +
Sbjct: 314 GVAWQAVGCARGAYENALDYTRTRKQFGKPIASFQLIQNHLVEMLSNLTAMQTLCFRLSQ 373

Query: 356 LKDQDKAAPEMVSLLKRNNCGKALDIARQARDMLGGNGISDEYHVIRHAMNLEAVNTYEG 415
           L+DQ     E  SL K     +  D+  +AR+++GGNGI  EY+V R   + EA+ +YEG
Sbjct: 374 LQDQGLLKDEHASLAKVFCSLRTRDVVSRAREVMGGNGILLEYNVARFVADAEAIYSYEG 433

Query: 416 THDIHALILGRAITGIQAF 434
           T +I+ LI+GRAITG  AF
Sbjct: 434 TKEINTLIVGRAITGFSAF 452


Lambda     K      H
   0.319    0.135    0.400 

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: 423
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: 438
Length of database: 453
Length adjustment: 32
Effective length of query: 406
Effective length of database: 421
Effective search space:   170926
Effective search space used:   170926
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: 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:

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