GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Caulobacter crescentus NA1000

Align isovaleryl-CoA dehydrogenase (EC 1.3.8.4) (characterized)
to candidate CCNA_01412 CCNA_01412 acyl-CoA dehydrogenase, short-chain specific

Query= BRENDA::B5UB85
         (416 letters)



>FitnessBrowser__Caulo:CCNA_01412
          Length = 381

 Score =  248 bits (633), Expect = 2e-70
 Identities = 143/380 (37%), Positives = 221/380 (58%), Gaps = 7/380 (1%)

Query: 33  FGLSEEQQQLRKMVFDFAQKELAPKAAEIDKENNFKELRPFWKKLGDLGLLGITASSDYG 92
           F L+E+Q  ++     FA+ +LAP +A+ D+  +F       ++  +LG  GI  + D G
Sbjct: 5   FALNEDQVAIQDAARAFAEGQLAPHSADWDENKHFPV--DVLRQAAELGFAGIYVNEDVG 62

Query: 93  GTGGKYSDHCVIMEELSRASGGIALSYGAHSNLCVNQINRNGTEEQKSKYLPKLCSGEHI 152
           G+G    D  +I E LS     +A     H N+    I+R G+++ + +YLP+L + E I
Sbjct: 63  GSGLSRLDASIIFEALSYGDVPVAAYLTIH-NMASWMIDRFGSDDLRQRYLPRLTTMELI 121

Query: 153 GALAMSEPGSGSDVVSMKLRAEKKGDYYVLNGNKFWITNGPDADVLVVYAKTNWSTSKQQ 212
            +  ++EPGSGSD  +M+  A+  GD+YVLNG K +I+ G  +D+ VV A+T    +K  
Sbjct: 122 ASYCLTEPGSGSDAAAMRTTAKLDGDHYVLNGGKAFISGGGVSDIYVVMARTGGEGAK-- 179

Query: 213 HGISAFLIEKDYPGFSTAQKLDKLGMRGSNTGELVFEDCKVPAANLLGQENKGVYVLMSG 272
            G+SAF++EK   G S      K+G     T ++ F++C+VP AN +GQE +G    M G
Sbjct: 180 -GVSAFVVEKGMEGLSFGANERKMGWNAQPTAQVNFDNCRVPVANRIGQEGEGFRFAMMG 238

Query: 273 LDLERLVLAAGPVGLMQAAIDTAFLYAHTRKQFGKNIGEFQLIQGKMADMYTTLSACRSY 332
           LD  RL +A+  +G  Q A+DTA  Y  TR QFG+ + +FQ +Q K+ADM T L A R  
Sbjct: 239 LDGGRLNIASCSLGGAQFALDTAKAYLETRNQFGRPLKDFQALQFKLADMATELEAARLM 298

Query: 333 LYNVAKACDNGHVN-SKDCAGVILYCAEKATQVALDAIQILGGNGYINDYPTGRILRDAK 391
           +   A A D+ H   +K CA    +  +   QVA DA+Q+ GG GY+ DYP  R++RD +
Sbjct: 299 VRRAAHALDSKHPEATKLCAMAKRFATDAGFQVANDALQLHGGYGYLQDYPLERLVRDLR 358

Query: 392 LYEIGAGTSEVRRMLIGRAL 411
           +++I  GT+E+ R++I R +
Sbjct: 359 VHQILEGTNEIMRVIIAREM 378


Lambda     K      H
   0.318    0.135    0.399 

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: 386
Number of extensions: 26
Number of successful extensions: 5
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: 416
Length of database: 381
Length adjustment: 31
Effective length of query: 385
Effective length of database: 350
Effective search space:   134750
Effective search space used:   134750
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 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