GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Stenotrophomonas chelatiphaga DSM 21508

Align isobutyryl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate WP_057509244.1 ABB28_RS14005 acyl-CoA dehydrogenase

Query= reanno::psRCH2:GFF2392
         (383 letters)



>NCBI__GCF_001431535.1:WP_057509244.1
          Length = 387

 Score =  199 bits (507), Expect = 8e-56
 Identities = 125/373 (33%), Positives = 187/373 (50%), Gaps = 6/373 (1%)

Query: 6   LSEDQRMIRDMARDFARREIAPHAQAWEKAGWIDDTLVAQMGELGLLGMVVPEEWGGSYI 65
           LS+++R ++D    F  + + P              LV ++  LGLLG  +P  +GG  +
Sbjct: 15  LSDEERAVQDSVARFVDQRVLPVIGDCFDQARFPAELVPEIAALGLLGATLPPAYGGGGM 74

Query: 66  DYVAYALAVEEISAGDGATGALMSIHNSVGCGPVLNYGSQAQKDEWLTELASGRAIGCFA 125
           D VAY L  +E+  GD    + +S+ +S+   P+  YGS+AQ+  WL  +A G  IGCF 
Sbjct: 75  DAVAYGLICQELERGDSGLRSFVSVQSSLCMHPIFAYGSEAQRLRWLPAMARGERIGCFG 134

Query: 126 LTEPQAGSEAHNLRTRAELVDGHWVLNGSKQFCSNAKRSKLAIVFAVTDPELGKKGLSAF 185
           LTE   GS+  +++TRA      W L+GSK + +NA  + LAIV+A T+      G+  F
Sbjct: 135 LTEAHGGSDPSSMKTRAVREGDQWRLDGSKMWITNAPIADLAIVWAQTE-----DGVQGF 189

Query: 186 LVPTDTPGFAVERSEHKMGIRASDTCGVSLSDCRIPEANLLGERGKGLAIALSNLEGGRI 245
           ++     GF+V+    KM +RAS T  +     ++PEAN L     G+   L  L   R 
Sbjct: 190 ILERGMAGFSVQEIGRKMSLRASSTGALFFDQVQVPEANRLA-GVVGMKGPLGCLNQARF 248

Query: 246 GIGAQALGIARAAFEAALLYARERVQFGKPIAEHQSIANMLADMQTQLNAARLLILHAAR 305
           GI    +G A A     L YA +R  FG+P+A  QS    LADM  ++  A+LL L   R
Sbjct: 249 GISWGPIGAAIACLREVLAYAGQRELFGRPLAATQSAQIKLADMARRITGAQLLALQLGR 308

Query: 306 LKSAGLPCLSEASQAKLFASEMAEKVCSQAVQIHGGYGYLEDYPVERYYRDARITQIYEG 365
           LK AG     + S AK     MA  +  +   + G  G   ++   R+  +      YEG
Sbjct: 309 LKEAGRLQPQQVSLAKWNNCRMAIDIARECRDLLGAAGITTEHAAIRHALNLESVITYEG 368

Query: 366 SSEIQRLLIAREL 378
           +  + +L+I REL
Sbjct: 369 TETVHQLVIGREL 381


Lambda     K      H
   0.318    0.133    0.390 

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: 333
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: 383
Length of database: 387
Length adjustment: 30
Effective length of query: 353
Effective length of database: 357
Effective search space:   126021
Effective search space used:   126021
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 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