GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Caulobacter crescentus NA1000

Align 2-methylbutanoyl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate CCNA_01875 CCNA_01875 acyl-CoA dehydrogenase, short-chain specific

Query= reanno::psRCH2:GFF2397
         (379 letters)



>FitnessBrowser__Caulo:CCNA_01875
          Length = 381

 Score =  291 bits (746), Expect = 2e-83
 Identities = 155/367 (42%), Positives = 220/367 (59%), Gaps = 1/367 (0%)

Query: 8   NAIAEMARQFAQERLKPFAEQWSREHRYPAEAIGEMAALGFFGMLVPEQWGGSDTGYLAY 67
           +A+ ++ ++F  ERL+P     S     P   I EM  LG FG+ +PE +GG        
Sbjct: 8   SALIDVIQRFVAERLRPIEGLVSETDEVPGSIIEEMKQLGLFGLSIPESYGGLGLSLEEE 67

Query: 68  AMALEEIAAGDGACSTIMSVHNSVGCVPILRFGNEQQKSDFLTPLARGEQIGAFALTEPQ 127
           A  +        A  +    +  +G   ++ FG+E QK+ +L  +A GE I AFALTE +
Sbjct: 68  ARVIVAFCHTAPAFRSTFGTNVGIGSQGLVMFGDEAQKARWLPSIASGETITAFALTEAE 127

Query: 128 AGSDASSLRTRARRDGDHYVLNGAKQFITSGKHAGTVIVFAVTDPDA-GKGGISAFIVPT 186
           AGSD++S++TRA RDGDHYVLNG K++IT+   A    V A TDP+  G  G+SAF+VP 
Sbjct: 128 AGSDSASVQTRAVRDGDHYVLNGVKRYITNAGRANLFTVMARTDPNTKGGAGVSAFLVPA 187

Query: 187 DSPGYQVVRVEDKLGQHASDTCQIAFEDLRVPVANRLGEEGEGYRIALANLEGGRIGIAA 246
           D PG  V + E K+GQ  +    + FED+RVPV NRLG EGEG+ +A+  L+ GR+ I+A
Sbjct: 188 DLPGLSVGKPEKKMGQQGAHIHDVVFEDVRVPVENRLGAEGEGFTVAMRVLDRGRVHISA 247

Query: 247 QAVGMARAAFEAARDYARDRETFGKPIIEHQAVAFRLADMATQIAVARQMVHHAAALREV 306
             VG+A         YA +R+ FG+PI   Q +   +AD  T+   A+ +V   A  R+ 
Sbjct: 248 VCVGVAERLIADCVAYASERKQFGQPIASFQLIQAMIADSKTEALAAKALVFDTARKRDA 307

Query: 307 GRPALVEASMAKLFASEMAEKVCSAAIQTLGGYGYLADFPVERIYRDVRVCQIYEGTSDI 366
           G    +EA+  KLFASEM  +V   A+Q  GG GY+AD+ +ER+YRDVR+ +IYEG S I
Sbjct: 308 GANVTLEAAATKLFASEMVGRVADRAVQVFGGAGYVADYGIERLYRDVRIFRIYEGASQI 367

Query: 367 QRLVISR 373
           Q+L+I+R
Sbjct: 368 QQLIIAR 374


Lambda     K      H
   0.320    0.135    0.391 

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: 369
Number of extensions: 15
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: 379
Length of database: 381
Length adjustment: 30
Effective length of query: 349
Effective length of database: 351
Effective search space:   122499
Effective search space used:   122499
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.

Links

Downloads

Related tools

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