GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdH in Shewanella oneidensis MR-1

Align glutaryl-CoA dehydrogenase (ETF) (EC 1.3.8.6) (characterized)
to candidate 201539 SO2395 acyl-CoA dehydrogenase family protein (NCBI ptt file)

Query= BRENDA::Q3JP94
         (395 letters)



>FitnessBrowser__MR1:201539
          Length = 585

 Score =  107 bits (266), Expect = 1e-27
 Identities = 102/380 (26%), Positives = 174/380 (45%), Gaps = 50/380 (13%)

Query: 53  AIFREMGEIGLLGPTIPEQYGGPGLDYVSYGLIAREVERVDSGYRSMMSVQSSLVMVPIF 112
           A++ +  + G +G     ++GG G+  +  G++  E+        ++    ++   + I 
Sbjct: 82  AVYDQYSQGGWVGLCGEPEFGGMGMPKM-LGVLVDEMAYSACNAFTLYGSLTAGAALCIN 140

Query: 113 EFGSDAQKEKYLPKLATGEWIGCFGLTEPNHGSDPGSMVTRA-RKVPGGYSLSGSKMWIT 171
             GS+  K+ YLPKL +GEW G   +TEP  GSD  ++ TRA  +  G Y++SGSK++IT
Sbjct: 141 AHGSEVLKQAYLPKLYSGEWAGAMDMTEPQAGSDLRNIRTRAVPQEDGSYAISGSKIFIT 200

Query: 172 --NSPIAD--VFVVWAKLDEDGRDEIRGFILEK----------GCKGLSAPAIHGKVGLR 217
             +  + +  + +V AKL E     I  F++ K          G  G+S  +I  K+GL+
Sbjct: 201 GGDHDLTENVIHLVLAKLPES--KGISLFLVPKITVNKDGCLGGTNGVSVGSIEHKMGLK 258

Query: 218 ASITGEIVLDEA---FVPEENILPHVKGLRGPFTCLNSARYGIAWGALGAAESCWHIARQ 274
            S T  +  DEA    + E N     +GL   FT +N  R  I    LG+A++ + +A  
Sbjct: 259 GSATCVMNFDEAKGYLIGEPN-----RGLVCMFTMMNYERLAIGIQGLGSAQAAYQMATD 313

Query: 275 YVLDRKQ-----------FGRPLAANQLIQKKLADMQTEITLGLQGVLRLGRMKDEGTAA 323
           Y  +R Q              P+  +  +++ L  ++     G    +  G+  D    A
Sbjct: 314 YAKERSQGVAAGGSPTGSDSDPIIVHGDVRRMLLTIRAMTEAGRALSVFTGKQLDLAKYA 373

Query: 324 VE------------ITSIMKRNSCGKALDIARLARDMLGGNGISDEFGVARHLVNLEVVN 371
            +            +T + K     + LD   +A+ + GG+G   E GV + + +  +  
Sbjct: 374 QDDVKAKAARYVGLLTPVAKAFLTDRGLDATIMAQQVFGGHGYIRETGVEQLVRDTRIAQ 433

Query: 372 TYEGTHDIHAL-ILGRAQTG 390
            YEGT+ I A+  LGR  TG
Sbjct: 434 IYEGTNGIQAIDFLGRKVTG 453


Lambda     K      H
   0.320    0.138    0.414 

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: 34
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 395
Length of database: 585
Length adjustment: 34
Effective length of query: 361
Effective length of database: 551
Effective search space:   198911
Effective search space used:   198911
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: 51 (24.3 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