GapMind for catabolism of small carbon sources

 

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

Align short-chain acyl-CoA dehydrogenase monomer (EC 1.3.8.1) (characterized)
to candidate CA265_RS09630 CA265_RS09630 acyl-CoA dehydrogenase

Query= metacyc::MONOMER-17424
         (375 letters)



>FitnessBrowser__Pedo557:CA265_RS09630
          Length = 396

 Score =  213 bits (542), Expect = 7e-60
 Identities = 125/369 (33%), Positives = 196/369 (53%), Gaps = 5/369 (1%)

Query: 2   LVNDEQQQIADAVRAFAQERLKPFAEQWDKDHRFPKEAIDEMAELGLFGMLVPEQWGGSD 61
           L+ DE + I    R + ++ + P  E + +   FPK  I  +A++G FG  +P ++GG+ 
Sbjct: 21  LLTDEHKLIRATARDWVKKEVSPIIEDYAQKAEFPKHLIKGLADIGAFGPTIPVEYGGAG 80

Query: 62  TGYVAYAMALEEIAAGDGACSTIMSVHNSVGCVPILRFGNEQQKEQFLTPLATGAMLGAF 121
             Y AY + ++EI  GD    +  SV  S+   PI  +G+E+Q++++L  LA+G M+G F
Sbjct: 81  LDYTAYGILMQEIERGDSGIRSTASVQGSLVMYPIYAYGSEEQRKKYLPKLASGEMMGCF 140

Query: 122 ALTEPQAGSDASSLKTRARLEGDHYVLNGSKQFITSGQNAGVVIVFAVTDPEAGKRGISA 181
            LTEP  GS+   + T  +  G HY+LNG+K +I++   A + +V+A    E+GK  I  
Sbjct: 141 GLTEPDHGSNPGGMVTNIKDAGSHYILNGAKMWISNAPFADIAVVWA--KDESGK--IRG 196

Query: 182 FIVPTDSPGYQVARVEDKLGQHASDTCQIVFDNVQVPVANRLGAEGEGYKIALANLEGGR 241
            IV     G+       K    AS T ++VFDNV+VP  N +  E  G K  L  L   R
Sbjct: 197 LIVERGMEGFSTPETHHKWSLRASATGELVFDNVKVPKEN-IFPEISGLKGPLGCLNQAR 255

Query: 242 IGIASQAVGMARAAFEVARDYANERQSFGKPLIEHQAVAFRLADMATKISVARQMVLHAA 301
            GIA  A+G A   ++ A  Y+ ER  FGKP+   Q    +LA+M T+I+  + +V    
Sbjct: 256 YGIAWGALGAAMDCYDTALRYSKERVQFGKPIGGFQLQQKKLAEMVTEITKGQLLVWRLG 315

Query: 302 ALRDAGRPALVEASMAKLFASEMAEKVCSDALQTLGGYGYLSDFPLERIYRDVRVCQIYE 361
            L+   R +  + SMAK  + E+A  +  +A Q LGG G   ++ + R   ++     YE
Sbjct: 316 VLKSENRASAEQISMAKRNSVEIALDIARNARQMLGGMGITGEYSIMRHMMNLESVVTYE 375

Query: 362 GTSDIQRMV 370
           GT DI  ++
Sbjct: 376 GTHDIHLLI 384


Lambda     K      H
   0.319    0.134    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: 335
Number of extensions: 14
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: 375
Length of database: 396
Length adjustment: 30
Effective length of query: 345
Effective length of database: 366
Effective search space:   126270
Effective search space used:   126270
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