GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Thauera aminoaromatica S2

Align Isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate WP_004328657.1 C665_RS19360 acyl-CoA dehydrogenase

Query= reanno::Phaeo:GFF1011
         (386 letters)



>NCBI__GCF_000310185.1:WP_004328657.1
          Length = 378

 Score =  256 bits (653), Expect = 1e-72
 Identities = 139/377 (36%), Positives = 212/377 (56%), Gaps = 2/377 (0%)

Query: 6   MTFDLGEDVNALRDMVHRWAQERVRPMAQEIDQKNEFPAELWQEMGELGLLGITVPEEFG 65
           M F L  +   +RD+  R+A+  + P A + D    FP E+ Q   ELGLLGI +PE  G
Sbjct: 1   MDFQLNPEQREIRDLARRFAEREIAPRAAQADLDKAFPTEVHQRAQELGLLGINLPETVG 60

Query: 66  GAGMSYLAHTVAVEEIARASASVSLSYGAHSNLCVNQIKLNGNAEQKAKYLPRLVSGEHV 125
           G G+  L   +  E   R    +  +   ++ L    I + G   Q+++YL     G  +
Sbjct: 61  GGGLGCLELVLVTEAFCRGCLGIGTALCVNA-LATEPIVIAGTDAQRSRYLGAAARGA-L 118

Query: 126 GALAMSEAGAGSDVVSMSLRAEKRNDHYRLNGNKYWITNGPDADTLVVYAKTDPDAGSKG 185
            + AM+E GAGSDV  +  RAE+    YRL G+K WI+N   A+  VV+AKT PD G +G
Sbjct: 119 ASFAMTEPGAGSDVAGIRTRAERVEGGYRLTGSKIWISNANLAEFFVVFAKTAPDGGHRG 178

Query: 186 MTAFLIEKEFKGFSTSQHFDKLGMRGSNTAELVFEDVEVPFENVLGEEGKGVRVLMSGLD 245
           M+AF++ +   G +  +   KLG R S T E+  + V VP ++ LGEEG G  + M+  D
Sbjct: 179 MSAFIVPRASAGLTVGEPLGKLGQRCSPTCEVFLDQVFVPEDHRLGEEGGGFALAMAVFD 238

Query: 246 YERVVLAGIGTGIMAACMDEMMPYMKERKQFGQPIGNFQLMQGKIADMYTAMNTARAYVY 305
           + R ++A  G G++  C+DE + Y  +R   G+ + + Q +  K+A+M   +  AR   Y
Sbjct: 239 HSRPMVAAFGVGLIERCLDESLAYATQRSSMGKRLIDHQAVAHKLAEMRMRLEAARLLTY 298

Query: 306 EVAKACDKGTVTRQDAAACCLYASEVAMTQAHQAVQAFGGAGYLSDNPVGRIFRDAKLME 365
           + A   D+G     +A+    +A++ AM  A +AVQ FGG GY ++ PV ++FRDAK+++
Sbjct: 299 QSAWLLDQGRPNTIEASIAKAFAADAAMWAATEAVQIFGGMGYSTEYPVEKLFRDAKVLQ 358

Query: 366 IGAGTSEIRRMLIGREL 382
           I  GTSEI+R +I REL
Sbjct: 359 IYEGTSEIQRNIIAREL 375


Lambda     K      H
   0.318    0.132    0.382 

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: 386
Number of extensions: 20
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: 386
Length of database: 378
Length adjustment: 30
Effective length of query: 356
Effective length of database: 348
Effective search space:   123888
Effective search space used:   123888
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: 41 (21.7 bits)
S2: 50 (23.9 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