GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Steroidobacter denitrificans DSM 18526

Align 2-methylbutanoyl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate WP_066918738.1 ACG33_RS03535 acyl-CoA dehydrogenase

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



>NCBI__GCF_001579945.1:WP_066918738.1
          Length = 383

 Score =  281 bits (720), Expect = 2e-80
 Identities = 165/375 (44%), Positives = 224/375 (59%), Gaps = 5/375 (1%)

Query: 6   DQNAIA---EMARQFAQERLKPFAEQWSREHRYPAEAIGEMAALGFFGMLVPEQWGGSDT 62
           DQ+A+    E   +F +ERL             PA+ + EM A+G FG+ +PE++GG   
Sbjct: 4   DQDALRSLLETVSRFVRERLVQAERIVDETDEIPADIVAEMKAMGLFGLTIPEEYGGLGL 63

Query: 63  GYLAYAMALEEIAAGDGACSTIMSVHNSVGCVPILRFGNEQQKSDFLTPLARGEQIGAFA 122
                 +A+  +     A  ++      +G   IL  G  +QK+ +L  LA GE I +FA
Sbjct: 64  TMEEEVLAMFVMGQTSPAFRSLFGTTVGIGSQGILMDGTPEQKARYLPRLATGELIASFA 123

Query: 123 LTEPQAGSDASSLRTRARRDGDHYVLNGAKQFITSGKHAGTVIVFAVTDPDA-GKGGISA 181
           LTEP+AGSDA+SLRT A   GD YVLNG K+FIT+   AG   V A TDP + G GG+SA
Sbjct: 124 LTEPEAGSDAASLRTSATLSGDSYVLNGTKRFITNAPLAGMFTVMARTDPGSKGAGGVSA 183

Query: 182 FIVPTDSPGYQVVRVEDKLGQHASDTCQIAFEDLRVPVANRLG-EEGEGYRIALANLEGG 240
           FIV   +PG ++ + + K+GQ  + TC + FED RVP AN +G   G G++ A+  LE G
Sbjct: 184 FIVEAGTPGLRLGKRDRKMGQRGAWTCDVIFEDCRVPAANIIGGRPGLGFKTAMKVLEKG 243

Query: 241 RIGIAAQAVGMARAAFEAARDYARDRETFGKPIIEHQAVAFRLADMATQIAVARQMVHHA 300
           RI IAA  VG+A      A  YAR+R+ FG+ I E Q V   LAD   ++  AR M   A
Sbjct: 244 RIHIAAICVGVAERMLGDALRYARERKQFGQAIGEFQLVQAMLADSKAELYAARCMTLDA 303

Query: 301 AALREVGRPALVEASMAKLFASEMAEKVCSAAIQTLGGYGYLADFPVERIYRDVRVCQIY 360
           A  R+ G     EAS AKLFASEM  +V   A+Q LGG GY+A++ +ER YRDVR+ +I+
Sbjct: 304 AQRRDRGENVSTEASCAKLFASEMCGRVADRAVQILGGAGYMAEYGIERFYRDVRLFRIF 363

Query: 361 EGTSDIQRLVISRNL 375
           EGT+ IQ+LVI+RN+
Sbjct: 364 EGTTQIQQLVIARNM 378


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: 355
Number of extensions: 16
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: 383
Length adjustment: 30
Effective length of query: 349
Effective length of database: 353
Effective search space:   123197
Effective search space used:   123197
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 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