GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Pseudomonas fluorescens FW300-N2C3

Align glutaryl-CoA dehydrogenase (ETF) (EC 1.3.8.6) (characterized)
to candidate AO356_26365 AO356_26365 acyl-CoA dehydrogenase

Query= BRENDA::Q60759
         (438 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_26365
          Length = 383

 Score =  163 bits (413), Expect = 8e-45
 Identities = 113/376 (30%), Positives = 175/376 (46%), Gaps = 8/376 (2%)

Query: 59  QLTADEKLIRDTFRNYCQERLMSRILLANRNEVFHRDIVYEMGELGVLGPTI-KGYGCAG 117
           +LT ++ +IRD  R++ +  +        +       +V  MGELG+LG  + + +G   
Sbjct: 5   ELTEEQVMIRDMARDFARGEIAPHAQAWEKAGWIDDGLVANMGELGLLGMVVPEEWGGTY 64

Query: 118 VSSVAYGLLTRELERVDSGYRSMMSVQSSLVMHPIYTYGSEEQRQKYLPGLAKGELLGCF 177
           V  VAY L   E+   D    ++MS+ +S+   P+  +G++EQ+Q +L  LA G+ +GCF
Sbjct: 65  VDYVAYALAVEEISAGDGATGALMSIHNSVGCGPVLNFGTDEQKQTWLAELASGQAIGCF 124

Query: 178 GLTEPNHGSDPGGMETRARHNPSNQSYTLSGTKTWITNSPVADLFIVWARCEDNC----I 233
            LTEP  GS+   + TRA     +  + ++G K +++N   A L IV+A  +       I
Sbjct: 125 CLTEPQAGSEAHNLRTRAELR--DGQWVINGAKQFVSNGKRAKLAIVFAVTDPELGKKGI 182

Query: 234 RGFILEKGMRGLSAPRIEGKFSLRASATGMIIMDSVEVPEENVL-PNVSSLAGPFGCLNT 292
             F++     G    R E K  +RAS T  + + +  VPE N+L      LA     L  
Sbjct: 183 SAFLVPTDTPGFIVDRTEHKMGIRASDTCAVTLSNCTVPEANLLGARGKGLAIALSNLEG 242

Query: 293 ARYGITWGVLGAAEFCLHTARQYALDRIQFGVPLARNQLVQKKLADMLTEITLGLHACLQ 352
            R GI    LG A      A  YA DR+QF  P+  +Q +   LADM T I       L 
Sbjct: 243 GRIGIAAQALGIARAAFEAALAYARDRVQFDKPIIEHQSIANLLADMHTRINATRLLILH 302

Query: 353 LGRLKDQDKATPEMVSMLKRNNCGKALDIARQARDILGGNGISDEYHVIRHAMNLEAVNT 412
             RL+   K      S  K      A  +   A  I GG G  ++Y V R+  +      
Sbjct: 303 AARLRSAGKPCLSEASQAKLFASEMAEKVCSSAIQIHGGYGYLEDYPVERYYRDARITQI 362

Query: 413 YEGTHDIHALILGRAI 428
           YEG+ +I  +++ R +
Sbjct: 363 YEGSSEIQRMVIAREL 378


Lambda     K      H
   0.320    0.136    0.408 

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: 349
Number of extensions: 21
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: 438
Length of database: 383
Length adjustment: 31
Effective length of query: 407
Effective length of database: 352
Effective search space:   143264
Effective search space used:   143264
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