GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Pseudomonas putida KT2440

Align isobutyryl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate PP_3492 PP_3492 short-chain acyl-CoA dehydrogenase

Query= reanno::pseudo3_N2E3:AO353_25670
         (383 letters)



>FitnessBrowser__Putida:PP_3492
          Length = 383

 Score =  672 bits (1733), Expect = 0.0
 Identities = 333/381 (87%), Positives = 356/381 (93%)

Query: 1   MHDIELTEEQVMIRDMARDFARGEIAPHAQAWEKAGWIDDALVAKMGELGLLGMVVPEEW 60
           M D+EL+EEQ+MIRDMARDFARGEIAPHAQAWEKAGWIDD +V KMGELGLLGMVVPE++
Sbjct: 1   MQDLELSEEQIMIRDMARDFARGEIAPHAQAWEKAGWIDDGVVRKMGELGLLGMVVPEDF 60

Query: 61  GGTYVDYVAYALAVEEISAGDGATGALMSIHNSVGCGPVLNYGTEEQKQTWLADLASGQA 120
           GG+Y DYVAYALAVEEISAG GATGA+MSIHNSVGCGP+L YGT EQ+Q WL  LASG+ 
Sbjct: 61  GGSYTDYVAYALAVEEISAGCGATGAMMSIHNSVGCGPLLAYGTAEQQQQWLPRLASGEV 120

Query: 121 IGCFCLTEPQAGSEAHNLRTRAELRDGQWVINGAKQFVSNGRRAKLAIVFAVTDPDLGKK 180
           IGCFCLTEPQAGSEAHNLRTRAEL DGQWVINGAKQFVSN RRA LAIVFAVTDP+LGKK
Sbjct: 121 IGCFCLTEPQAGSEAHNLRTRAELVDGQWVINGAKQFVSNARRAGLAIVFAVTDPELGKK 180

Query: 181 GLSAFLVPTDTPGFIVDRSEHKMGIRASDTCAVTLNNCTIPEANLLGERGKGLAIALSNL 240
           GLSAFLVPTD PGF VDRSEHKMGIRASDTCAVT +NC IP AN+LGERGKGLAIALSNL
Sbjct: 181 GLSAFLVPTDNPGFKVDRSEHKMGIRASDTCAVTFDNCRIPAANILGERGKGLAIALSNL 240

Query: 241 EGGRIGIAAQALGIARAAFEAALAYARDRVQFDKPIIEHQSVANMLADMHTRLNAARLLI 300
           EGGRIGIAAQALGIARAAFEAAL Y+RDR+QF KPI EHQS+AN+LADM  ++NAARLLI
Sbjct: 241 EGGRIGIAAQALGIARAAFEAALVYSRDRIQFGKPINEHQSIANLLADMQVQVNAARLLI 300

Query: 301 LHAARLRSAGKPCLSEASQAKLFASEMAEKVCSSAIQIHGGYGYLEDYPVERYYRDARIT 360
           LHAARLRSAGKPCLSEASQAKLFASEMAE+VCS AIQ+HGGYGYLEDYPVERYYRDARIT
Sbjct: 301 LHAARLRSAGKPCLSEASQAKLFASEMAERVCSMAIQVHGGYGYLEDYPVERYYRDARIT 360

Query: 361 QIYEGSSEIQRMVIARELKNY 381
           QIYEGSSEIQRM+IARELKNY
Sbjct: 361 QIYEGSSEIQRMLIARELKNY 381


Lambda     K      H
   0.319    0.134    0.394 

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: 499
Number of extensions: 8
Number of successful extensions: 1
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: 383
Length of database: 383
Length adjustment: 30
Effective length of query: 353
Effective length of database: 353
Effective search space:   124609
Effective search space used:   124609
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