GapMind for catabolism of small carbon sources

 

Alignments for a candidate for hcl in Pseudomonas fluorescens GW456-L13

Align Benzoate--CoA ligase; Benzoyl-CoA synthetase; EC 6.2.1.25 (characterized)
to candidate PfGW456L13_1963 Acetyl-coenzyme A synthetase (EC 6.2.1.1)

Query= SwissProt::Q8GQN9
         (527 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1963
          Length = 651

 Score =  123 bits (308), Expect = 2e-32
 Identities = 112/365 (30%), Positives = 167/365 (45%), Gaps = 22/365 (6%)

Query: 179 DDHCFWLYSSGSTGAPKGTVHIHSDLIHTAELYARPILGIREGDVVFSAAKLFFAYGLGN 238
           ++  F LY+SGSTG PKG  H     +  A +    +   R G++ +  A + +  G   
Sbjct: 256 EEALFILYTSGSTGKPKGVQHTTGGYLLYAAMTHERVFDYRPGEIYWCTADVGWVTGHSY 315

Query: 239 GLIFPLAVGATAVL---MAERPTPAAVFERLRRHQPDIFYGVPTLYASMLANPDCPKEGE 295
            +  PLA GAT +L   +   P    V + + +H+ +I Y  PT   +M+A+     EG 
Sbjct: 316 IVYGPLANGATTLLFEGVPNYPDITRVAKIVDKHKVNILYTAPTAIRAMMASGTAAVEGA 375

Query: 296 --LRLRACTSAGEALPEDVGRRWQARFGVD---ILDGIGSTEMLHIFLSNRAGD--VHYG 348
               LR   S GE +  +    +    G     I+D    TE     +S   G   +  G
Sbjct: 376 DGSSLRLLGSVGEPINPEAWDWYYKNVGKSRCPIVDTWWQTETGGNMMSPLPGAHALKPG 435

Query: 349 TSGKPVPGYRLRLIDEDGAEITTAGVAGELQI--SGPSSAVMYWNNPEKTAATFMGEWTR 406
           ++ +P  G    L+D  G  I      G L I  S P  A   + + ++   T+   +  
Sbjct: 436 SAARPFFGVVPALVDNLG-NIVEGEAEGNLVILDSWPGQARTLFGDHDRFVDTYFKTFRG 494

Query: 407 ---SGDKYLVNDEGYYVYAGRSDDMLKVSGIYVSPIEVESALIAHEAVLEAAVVGWEDED 463
              +GD    + +GYY   GR DD+L VSG  +   E+ESA++AH  V EAAVVG     
Sbjct: 495 MYFTGDGARRDADGYYWITGRVDDVLNVSGHRMGTAEIESAMVAHPKVAEAAVVG---VP 551

Query: 464 HLIKPK---AFIVLKPGYGAGEALRTDLKAHVKNLLAPYKYPRWIEFVDDLPKTATGKIQ 520
           H IK +    ++ LK G    E LR +LK  V+  + P   P  I++   LPKT +GKI 
Sbjct: 552 HDIKGQGIYVYVTLKNGEEPNEQLRLELKNWVRKEIGPIASPDVIQWAPGLPKTRSGKIM 611

Query: 521 RFKLR 525
           R  LR
Sbjct: 612 RRILR 616


Lambda     K      H
   0.319    0.138    0.412 

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: 922
Number of extensions: 57
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: 527
Length of database: 651
Length adjustment: 37
Effective length of query: 490
Effective length of database: 614
Effective search space:   300860
Effective search space used:   300860
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: 53 (25.0 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