GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaK in Halomonas desiderata SP1

Align phenylacetate-CoA ligase (EC 6.2.1.30) (characterized)
to candidate WP_086509765.1 BZY95_RS09865 long-chain fatty acid--CoA ligase

Query= BRENDA::A7KUK6
         (562 letters)



>NCBI__GCF_002151265.1:WP_086509765.1
          Length = 533

 Score =  176 bits (445), Expect = 3e-48
 Identities = 126/373 (33%), Positives = 197/373 (52%), Gaps = 30/373 (8%)

Query: 181 AKDVAFLVYSSGTTGVPKGVMISHRNIVANIRQQFIAEGEMLSWNGGPDG--KGDRVLAF 238
           A+ VA ++Y+SGTTG PKGVM++HR I+      +IA     S +GG     +G+RV   
Sbjct: 177 AEQVAAMIYTSGTTGTPKGVMLTHRGIL------YIA-----SLSGGMRHLREGERVYGV 225

Query: 239 LPFYHIYGLTCLITQALYKGYHLIVMSKFDIEKWCAHVQNYRCSFSYIVPPVVLLLGKHP 298
           LP  H++GL+ +   +LY G  L  + +FD     A +   R +    VP +     +  
Sbjct: 226 LPMSHVFGLSSVCMGSLYNGACLYSVPRFDAAAMLAALGQERITVLQGVPAMFARTLEFL 285

Query: 299 VVDKYDLSS--LRMMNSGAAPLTQELVEAVYSRIKVGIKQGYGLSETSPTTHSQRWEDWR 356
             +   L++  LR +++G +PL  +L   V +   + +  GYGL+E SPT    R ED R
Sbjct: 286 RREGRALAAPALRYISAGGSPLDADLKRRVQALFGLTLHNGYGLTEASPTISQTRIED-R 344

Query: 357 EAMGSVGRLMPNMQAKYMTMPEDGS-EPKEVGEGEVGELYLKGPNVFLGYHENPEATKGC 415
               +VGR++P ++ +   + E G  EP+  G    GEL+++GPNV  GY   P AT+ C
Sbjct: 345 FDSNTVGRVLPLLEYRLEPLGEGGEDEPEHAG---AGELWVRGPNVMKGYFRQPSATRAC 401

Query: 416 LSEDGWFQTGDVGYQDAKGNFYITDRVKELIKYKGFQVPPAELEGYLVDNDAIDDVAVIG 475
           LSEDGW  TGD+   D     YI  R KELI   GF + P ++E  + ++  +   AV+G
Sbjct: 402 LSEDGWLNTGDIARFDEDDQLYIVGRSKELIIRSGFNIYPPDVEAVINEHPDVTLSAVVG 461

Query: 476 IESETHGSEVPMACVVRSAKSKSSGTSEKDEAARIIKWLDSKVASHKRLRGGVHFVDEIP 535
            + E  G+E  +A V         G    +EA R  ++L +++A +KR    +  ++ +P
Sbjct: 462 RQVE--GNEEVVAFV-----QCEPGAMLSEEALR--EFLAARLAPYKR-PARLILMESLP 511

Query: 536 KNPSGKILRRILK 548
              SGKIL+  L+
Sbjct: 512 ATASGKILKGCLR 524


Lambda     K      H
   0.317    0.136    0.410 

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: 636
Number of extensions: 32
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: 562
Length of database: 533
Length adjustment: 36
Effective length of query: 526
Effective length of database: 497
Effective search space:   261422
Effective search space used:   261422
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: 53 (25.0 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