GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Rhodopseudomonas palustris CGA009

Align 2-methylbutanoyl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate WP_011157692.1 TX73_RS10890 acyl-CoA dehydrogenase

Query= reanno::psRCH2:GFF2397
         (379 letters)



>NCBI__GCF_000195775.1:WP_011157692.1
          Length = 379

 Score =  266 bits (679), Expect = 9e-76
 Identities = 147/374 (39%), Positives = 216/374 (57%), Gaps = 4/374 (1%)

Query: 4   NEDQNAIAEMARQFAQERLKPFAEQWSREHRYPAEAIGEMAALGFFGMLVPEQWGGSDTG 63
           N D  A  ++ R+F Q  ++PFA +W     +P E   + AA+G  G+  PE++GG+   
Sbjct: 8   NADHIAFRDVIRRFVQNEIEPFATEWDEAGGFPRELYEKAAAIGLLGLGFPEEYGGTPCD 67

Query: 64  YLAYAMALEEIA-AGDGACSTIMSVHNSVGCVPILRFGNEQQKSDFLTPLARGEQIGAFA 122
              + +A +E+A A  G  S  ++ H S+G  PI R G+ + K+  L  +  G++I A A
Sbjct: 68  QFMWIVATQELARAAAGGVSASLNSH-SIGAPPIARAGSPELKARVLPEILSGKKISALA 126

Query: 123 LTEPQAGSDASSLRTRARRDGDHYVLNGAKQFITSGKHAGTVIVFAVTDPDAGKGGISAF 182
           +TEP  GSD ++LRTRA RDGDHYV+NG K FITSG  A   I  AV     G GG+S  
Sbjct: 127 ITEPSGGSDVANLRTRAVRDGDHYVVNGEKTFITSGMRAD-YITTAVRTGGEGPGGVSLL 185

Query: 183 IVPTDSPGYQVVRVEDKLGQHASDTCQIAFEDLRVPVANRLGEEGEGYRIALANLEGGRI 242
           ++P D+PG     ++ K+G  ASDT  + F++ RVP AN LG EG G+ I + N    R+
Sbjct: 186 LIPGDTPGLTRTPLK-KMGWWASDTATLHFDNCRVPAANLLGTEGAGFMIIMMNFNSERL 244

Query: 243 GIAAQAVGMARAAFEAARDYARDRETFGKPIIEHQAVAFRLADMATQIAVARQMVHHAAA 302
            +AA  +  ++   + A +YAR R TFGKP+++HQ +  +L DMA +IA ++ M+   A 
Sbjct: 245 TMAAGCIAASKVCLDEATEYARQRVTFGKPLVKHQVIRHKLVDMAQKIAASQAMLELLAW 304

Query: 303 LREVGRPALVEASMAKLFASEMAEKVCSAAIQTLGGYGYLADFPVERIYRDVRVCQIYEG 362
             + G   + E  M K  A++      S A+Q  GG GY+    VERIYRDV+V  I  G
Sbjct: 305 RVDQGESPIAEICMLKNQATQTMAFCASEAVQIFGGAGYMRGVKVERIYRDVKVNAIGGG 364

Query: 363 TSDIQRLVISRNLG 376
           T +I + + SR +G
Sbjct: 365 TEEIMKDLASRQMG 378


Lambda     K      H
   0.320    0.135    0.391 

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: 377
Number of extensions: 12
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: 379
Length of database: 379
Length adjustment: 30
Effective length of query: 349
Effective length of database: 349
Effective search space:   121801
Effective search space used:   121801
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 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