GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Cupriavidus basilensis 4G11

Align isobutyryl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate RR42_RS11345 RR42_RS11345 acyl-CoA dehydrogenase

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



>FitnessBrowser__Cup4G11:RR42_RS11345
          Length = 378

 Score =  267 bits (683), Expect = 3e-76
 Identities = 141/372 (37%), Positives = 212/372 (56%), Gaps = 1/372 (0%)

Query: 7   TEEQVMIRDMARDFARGEIAPHAQAWEKAGWIDDALVAKMGELGLLGMVVPEEWGGTYVD 66
           TEE  M+R  AR F   E+APH + WE+ G++D  +  K G  G L   +PE++GG   D
Sbjct: 8   TEEHEMLRTAARRFMETEVAPHHERWEEQGYVDRDVWLKAGAAGFLCASMPEQYGGAGGD 67

Query: 67  YVAYALAVEEISAGDGATGALMSIHNSVGCGPVLNYGTEEQKQTWLADLASGQAIGCFCL 126
            + Y++ + E  A  G TG    +H+ +    + +YG+E  K  +L  +A+G+ IG   +
Sbjct: 68  KL-YSVVLMEEQARAGCTGLGFGLHSEIVAPYIEHYGSEYLKSAYLPKMAAGEMIGAIAM 126

Query: 127 TEPQAGSEAHNLRTRAELRDGQWVINGAKQFVSNGRRAKLAIVFAVTDPDLGKKGLSAFL 186
           TEP  GS+   ++  A      +++NG+K F++NG  A L IV A TDP  G KG+S F+
Sbjct: 127 TEPGTGSDLQGIKATAVRHGDHYLLNGSKTFITNGWHADLVIVVAKTDPQAGAKGISLFV 186

Query: 187 VPTDTPGFIVDRSEHKMGIRASDTCAVTLNNCTIPEANLLGERGKGLAIALSNLEGGRIG 246
           V T  PGF   +   K G++A DT  +  +N  +P ANLLG+ G+G    +  L   R+ 
Sbjct: 187 VDTSMPGFSKGKRLKKAGMKAQDTAELFFDNVRVPVANLLGDEGQGFGYLMRELSWERLQ 246

Query: 247 IAAQALGIARAAFEAALAYARDRVQFDKPIIEHQSVANMLADMHTRLNAARLLILHAARL 306
           IA  A+    A  E  LAY RDR  F +PI E Q+VA+ LAD+ T L   R+ +    +L
Sbjct: 247 IAITAVAAVEAGLEWTLAYTRDRKAFKRPISEFQTVAHALADIRTELEMGRVFVDRCLQL 306

Query: 307 RSAGKPCLSEASQAKLFASEMAEKVCSSAIQIHGGYGYLEDYPVERYYRDARITQIYEGS 366
              GK   + AS AK + +EM  +     +Q+HGGYGY+ +YP+ R + DAR+ +IY G+
Sbjct: 307 VLEGKLDAATASMAKYWTTEMQFRALDRCVQLHGGYGYMWEYPITRAWADARVQRIYGGA 366

Query: 367 SEIQRMVIAREL 378
           +EI + +I+R L
Sbjct: 367 NEIMKELISRNL 378


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: 320
Number of extensions: 19
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: 383
Length of database: 378
Length adjustment: 30
Effective length of query: 353
Effective length of database: 348
Effective search space:   122844
Effective search space used:   122844
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