GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ch1CoA in Dyadobacter tibetensis Y620-1

Align Cyclohex-1-ene-1-carbonyl-CoA dehydrogenase; Ch1CoA; EC 1.3.8.10 (characterized)
to candidate WP_025764020.1 X939_RS0114560 acyl-CoA dehydrogenase

Query= SwissProt::Q2LQN9
         (414 letters)



>NCBI__GCF_000566685.1:WP_025764020.1
          Length = 379

 Score =  281 bits (718), Expect = 3e-80
 Identities = 160/378 (42%), Positives = 225/378 (59%), Gaps = 5/378 (1%)

Query: 36  ELTEEQKLLMEMVRNLAVREIAPRAIEIDENHSFPVHARDLFADLGLLSPLVPVEYGGTG 95
           ELTEE K + +  R+ A   + P  IE D    F         ++GL+  +V  +YGG G
Sbjct: 4   ELTEEHKAIQQATRDFARTTLLPGIIERDNAQKFDPSLVRQMGEMGLMGMMVEEQYGGGG 63

Query: 96  MDITTFAMVLEEIGKVCASTALMLLAQADGML-SIILDGSPALKEKYLPRFGEKSTLMTA 154
           +D  ++ + +EEI K+ AS  +++      +   I   GS   K+KYLP       +  A
Sbjct: 64  LDTLSYVLAMEEICKIDASAGVIMSVNNSLVCWGIQQYGSEEQKQKYLPDLASAQKI-GA 122

Query: 155 FAATEPGAGSDLLAMKTRAVKKGDKYVINGQKCFITNGSVADILTVWAYTDPSKGAKGMS 214
           F  +EP AGSD  +  T AV +GD Y++NG K +ITNG++++I  V A T P K  KG++
Sbjct: 123 FCLSEPEAGSDATSQHTTAVDQGDYYILNGTKNWITNGNLSEICLVMAQTHPEKRHKGIN 182

Query: 215 TFVVERGTPGLIYGHNEKKMGMRGCPNSELFFEDLEVPAENLVGEEGKGFAYLMGALSIN 274
            F+VE+G  G   G  E KMG+R      L F D+ VP  N +G +G GF + M  L+  
Sbjct: 183 VFLVEKGIAGFTVGRKEDKMGIRASDTHSLMFADVMVPKGNRIGPDGFGFKFAMDTLNGG 242

Query: 275 RVFCASQAVGIAQGALERAMQHTREREQFGKPIAHLTPIQFMIADMATEVEAARLLVRKA 334
           R+  A+QA+GIA GA E ++ + ++R  FGKPI+    IQF +A+MAT +EAARLLV KA
Sbjct: 243 RIGIAAQALGIAAGAYELSLAYAKQRRTFGKPISEHQAIQFKLAEMATRIEAARLLVYKA 302

Query: 335 TTLLD-AKDKRGPLIGGMAKTFASDTAMKVTTDAVQVMGGSGYMQEYQVERMMREAKLTQ 393
               D  KD  G     MAK +ASD AM VTT+AVQ+ GG GY++EY VER MR+AK+TQ
Sbjct: 303 AYTKDVGKDYIGE--AAMAKLYASDVAMWVTTEAVQIHGGYGYVKEYHVERHMRDAKITQ 360

Query: 394 IYTGTNQITRMVTGRSLL 411
           IY GT++I ++V  R +L
Sbjct: 361 IYEGTSEIQKLVIAREIL 378


Lambda     K      H
   0.318    0.133    0.375 

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: 357
Number of extensions: 20
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: 414
Length of database: 379
Length adjustment: 31
Effective length of query: 383
Effective length of database: 348
Effective search space:   133284
Effective search space used:   133284
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.

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