GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Pseudomonas benzenivorans DSM 8628

Align 2-methylbutanoyl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate WP_090448379.1 BLS63_RS24295 acyl-CoA dehydrogenase

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



>NCBI__GCF_900100495.1:WP_090448379.1
          Length = 375

 Score =  630 bits (1624), Expect = 0.0
 Identities = 313/375 (83%), Positives = 338/375 (90%)

Query: 1   MLPNEDQNAIAEMARQFAQERLKPFAEQWSREHRYPAEAIGEMAALGFFGMLVPEQWGGS 60
           MLPNED+  I +MARQFAQERLKPFA  W REHR+PAEAI EM  LGF GMLVPE+WGG+
Sbjct: 1   MLPNEDELLIRDMARQFAQERLKPFAADWDREHRFPAEAIAEMGQLGFMGMLVPEEWGGA 60

Query: 61  DTGYLAYAMALEEIAAGDGACSTIMSVHNSVGCVPILRFGNEQQKSDFLTPLARGEQIGA 120
            TG+LAYAMALEEIAAGDGACSTIMSVHNSVGC+PIL++G+E+QK  FL PLA G  +GA
Sbjct: 61  QTGHLAYAMALEEIAAGDGACSTIMSVHNSVGCMPILKYGSEEQKQRFLKPLAAGSMLGA 120

Query: 121 FALTEPQAGSDASSLRTRARRDGDHYVLNGAKQFITSGKHAGTVIVFAVTDPDAGKGGIS 180
           FALTEPQAGSDAS LR RARRDGDHYVL+G+KQFITSG HAG VIVFAVTDP AGK GIS
Sbjct: 121 FALTEPQAGSDASDLRARARRDGDHYVLSGSKQFITSGSHAGMVIVFAVTDPQAGKKGIS 180

Query: 181 AFIVPTDSPGYQVVRVEDKLGQHASDTCQIAFEDLRVPVANRLGEEGEGYRIALANLEGG 240
           AFIVPTD+PGY VVRVEDKLGQHASDTCQI  ++LR+P + RLGEEGEGYRIAL NLEGG
Sbjct: 181 AFIVPTDTPGYSVVRVEDKLGQHASDTCQIQLDELRLPASLRLGEEGEGYRIALGNLEGG 240

Query: 241 RIGIAAQAVGMARAAFEAARDYARDRETFGKPIIEHQAVAFRLADMATQIAVARQMVHHA 300
           RIGIAAQAVGMARAAFEAARDYA +R TFGKPIIEHQAVAFRLADMATQIAVARQMVHHA
Sbjct: 241 RIGIAAQAVGMARAAFEAARDYAHERVTFGKPIIEHQAVAFRLADMATQIAVARQMVHHA 300

Query: 301 AALREVGRPALVEASMAKLFASEMAEKVCSAAIQTLGGYGYLADFPVERIYRDVRVCQIY 360
           A+LRE G   L EASMAKLFASEMAE+VCSAAIQTLGGYGYL DFPVERIYRDVRVCQIY
Sbjct: 301 ASLREAGLACLSEASMAKLFASEMAERVCSAAIQTLGGYGYLKDFPVERIYRDVRVCQIY 360

Query: 361 EGTSDIQRLVISRNL 375
           EGTSD+QR+VI+RNL
Sbjct: 361 EGTSDVQRMVIARNL 375


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: 547
Number of extensions: 10
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: 379
Length of database: 375
Length adjustment: 30
Effective length of query: 349
Effective length of database: 345
Effective search space:   120405
Effective search space used:   120405
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