GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ch1CoA in Caulobacter crescentus NA1000

Align cyclohex-1-ene-1-carbonyl-CoA dehydrogenase (EC 1.3.8.10) (characterized)
to candidate CCNA_02254 CCNA_02254 isovaleryl-CoA dehydrogenase

Query= BRENDA::Q39QF5
         (380 letters)



>FitnessBrowser__Caulo:CCNA_02254
          Length = 386

 Score =  242 bits (617), Expect = 1e-68
 Identities = 151/374 (40%), Positives = 216/374 (57%), Gaps = 11/374 (2%)

Query: 11  TLDMVRDVATR----EIAPRALELDEKSLFPEYARDLFAKLGLLNPLLPAAYGGTEMGVL 66
           T D +R+   R    +IAP A ++DE + FP         LGL    +   +GG  +G L
Sbjct: 16  TADAIRETTARFAADKIAPIAAKIDETNSFPRELWVPMGDLGLHGITVEEEFGGLGLGYL 75

Query: 67  TLALILEELGRVCASTALLLIAQTDGML-PIIHGGSPELKERYLRRF-AGESTLLTALAA 124
              + +EE+ R  AS  L   A ++  +  I    +PE K RYL +  +GE   + +LA 
Sbjct: 76  EHVVAMEEVSRASASVGLSYGAHSNLCVNQIRRWATPEQKARYLPKLISGEH--VGSLAM 133

Query: 125 TEPAAGSDLLAMKTRAVRQGDKYVINGQKCFITNGSVADVIVVYAYTDPEKGSKGISAFV 184
           +E  AGSD+++MK RA + GD+Y++NG K +ITN   AD +VVYA T   +GS+GI+AF+
Sbjct: 134 SEAGAGSDVVSMKLRAEQVGDRYILNGTKFWITNAPHADTLVVYAKTG--EGSRGITAFI 191

Query: 185 VEKGTPGLVYGRNESKMGMRGSINSELFFENMEVPAENIIGAEGTGFANLMQTLSTNRVF 244
           VEKG  G    +   KMGMRGS  +EL FE+ E+P EN++G  G G   LM  L   R  
Sbjct: 192 VEKGMKGFSVSKKLDKMGMRGSDTAELVFEDCEIPEENVMGPVGGGVGVLMSGLDYERAV 251

Query: 245 CAAQAVGIAQGALDIAVRHTQDRVQFGKPIAHLAPVQFMVADMATAVEASRLLTRKAAEL 304
            AA  +GI Q  LD+ + + +DR QFG+PI     +Q  +ADM  A+ ++R      A+ 
Sbjct: 252 LAAGPLGIMQACLDVVLPYVRDRKQFGQPIGSFQLMQGKIADMYVALNSARAYVYAVAKA 311

Query: 305 LDDGDKKAVLYGSMAKTMASDTAMRVTTDAVQVLGGSGYMKENGVERMMRDAKLTQIYTG 364
            D G K      + A  MAS+ A++V+ +A+Q LGG+GY KE  VER++RDAKL  I  G
Sbjct: 312 CDAG-KTTRFDAAGAILMASENAVKVSLEAIQALGGAGYTKEWPVERLLRDAKLYDIGAG 370

Query: 365 TNQITRMVTGRALL 378
           TN+I R + GR L+
Sbjct: 371 TNEIRRFLIGRELI 384


Lambda     K      H
   0.319    0.134    0.371 

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: 307
Number of extensions: 13
Number of successful extensions: 4
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: 380
Length of database: 386
Length adjustment: 30
Effective length of query: 350
Effective length of database: 356
Effective search space:   124600
Effective search space used:   124600
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 (21.7 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