GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuC in Acidovorax caeni R-24608

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 WP_054255928.1 BN2503_RS06965 hydroxymethylglutaryl-CoA lyase

Query= CharProtDB::CH_122457
         (599 letters)



>NCBI__GCF_001298675.1:WP_054255928.1
          Length = 315

 Score =  253 bits (646), Expect = 8e-72
 Identities = 138/311 (44%), Positives = 189/311 (60%), Gaps = 6/311 (1%)

Query: 3   NSTKTVRIVEVGPRDGLQNIPQSIDSTIKLDLIRRLRDAGLQTIELTSFVSPRAIPQLAD 62
           N    VRI++VGPRDGLQN  Q++ S +K+ L++RL+DAGL+ IE+TS+VSP+ +PQ+AD
Sbjct: 2   NIPTRVRIIDVGPRDGLQNEKQAVPSEVKIGLVQRLQDAGLREIEVTSYVSPKWVPQMAD 61

Query: 63  AQVVVQNADIQKLLKNPKLRLPVLVPNLKGLERALHNGIKEVAVFISATEGFSRANINCT 122
              V+       + +   +R  VL PNLKG E A+ +   E+ VF +A+E FS+ NINC+
Sbjct: 62  NHAVMSG-----IARQAGVRYSVLTPNLKGWEAAVADRPDEIVVFGAASEAFSQKNINCS 116

Query: 123 VDEGLERARQVASRAASAGLSVRGYVSCIFADPYDGPTRPSSVLRCTKALLDAGCYEVSL 182
           + E +ER   V   A +AG++VRG +SC    PY+G   P  V      +   G   V +
Sbjct: 117 IAESIERFAPVVEAARAAGVAVRGAMSCTVGCPYEGEIAPERVAYLAGLMKGIGVQRVDV 176

Query: 183 GDTLGIGTPADVRWLITYLQDNGVPLEMLAGHFHDTYGGAVANVWEAYKCGLRMFDSSVA 242
            DT+G+GTP  V+  I     +   L+ ++GHFHDTYG A++N   A + G+  F SSVA
Sbjct: 177 ADTIGVGTPLKVQRAIAATLQH-YELDAVSGHFHDTYGQALSNTLAALELGVWNFQSSVA 235

Query: 243 GLGGCPXALGAKGNVASEDLVYMFERSGIHTGVDLSKLVETGEWISRQLSIAISSRAGAA 302
           GLGGCP A GA GNVA+EDLVY+    GI TG+DL KLV+ G +IS  L     SR   A
Sbjct: 236 GLGGCPYAKGATGNVATEDLVYLLHGMGIETGIDLDKLVDAGAYISDFLGRKSGSRVAVA 295

Query: 303 LWAMRKQTAVP 313
           L   R     P
Sbjct: 296 LLNKRAGQGTP 306


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: 426
Number of extensions: 14
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: 315
Length adjustment: 32
Effective length of query: 567
Effective length of database: 283
Effective search space:   160461
Effective search space used:   160461
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 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