GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuC in Paraburkholderia bryophila 376MFSha3.1

Align 3-hydroxy-3-methylglutaryl-coenzyme A lyase/3-methylglutaconyl-coenzyme A hydratase; EC 4.1.3.4; EC 4.2.1.18 (characterized)
to candidate H281DRAFT_02101 H281DRAFT_02101 hydroxymethylglutaryl-CoA lyase

Query= CharProtDB::CH_122457
         (599 letters)



>FitnessBrowser__Burk376:H281DRAFT_02101
          Length = 308

 Score =  249 bits (636), Expect = 1e-70
 Identities = 133/306 (43%), Positives = 187/306 (61%), Gaps = 6/306 (1%)

Query: 6   KTVRIVEVGPRDGLQNIPQSIDSTIKLDLIRRLRDAGLQTIELTSFVSPRAIPQLADAQV 65
           K V+IVEVGPRDGLQN  + + +  K++LI RL  AG + +E  SFVSP+ +PQ+AD   
Sbjct: 5   KQVKIVEVGPRDGLQNEKEFVPTATKIELINRLSAAGFRNVEAASFVSPKWVPQMADGAE 64

Query: 66  VVQNADIQKLLKNPKLRLPVLVPNLKGLERALHNGIKEVAVFISATEGFSRANINCTVDE 125
           V+   +     + P     VL PNL+G E AL     E+ +F +A+E FS+ NINC++ E
Sbjct: 65  VMSGIE-----RRPGTIYSVLTPNLRGFEGALAARADEIVIFGAASEAFSQKNINCSIAE 119

Query: 126 GLERARQVASRAASAGLSVRGYVSCIFADPYDGPTRPSSVLRCTKALLDAGCYEVSLGDT 185
            +ER   VA  A   GL +RG VSC    PY G    +SV+   +     GC E+ + DT
Sbjct: 120 SIERFAPVAQAAKEHGLRIRGSVSCALGCPYQGEVPVASVVDVVQRFAALGCDEIDIADT 179

Query: 186 LGIGTPADVRWLITYLQDNGVPLEMLAGHFHDTYGGAVANVWEAYKCGLRMFDSSVAGLG 245
           +G+GTP   R +   +     P E L+GHFHDTYG A+AN++ A + G+ ++ +SVAGLG
Sbjct: 180 IGVGTPKRTREVFEAVTQV-FPRERLSGHFHDTYGQALANIYAALQEGIEIYHASVAGLG 238

Query: 246 GCPXALGAKGNVASEDLVYMFERSGIHTGVDLSKLVETGEWISRQLSIAISSRAGAALWA 305
           GCP A GA GNVA+ED++Y+    GI TG+DL+++V  G++IS  +     SRAG AL A
Sbjct: 239 GCPYAKGATGNVATEDVLYLMNGLGIETGIDLAQVVAIGDFISTSIGRPNVSRAGKALLA 298

Query: 306 MRKQTA 311
             +  A
Sbjct: 299 KARSEA 304


Lambda     K      H
   0.318    0.134    0.389 

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: 412
Number of extensions: 13
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: 599
Length of database: 308
Length adjustment: 32
Effective length of query: 567
Effective length of database: 276
Effective search space:   156492
Effective search space used:   156492
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: 51 (24.3 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