GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuC in Acidovorax sp. GW101-3H11

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 Ac3H11_4530 Hydroxymethylglutaryl-CoA lyase (EC 4.1.3.4)

Query= CharProtDB::CH_122457
         (599 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_4530
          Length = 306

 Score =  184 bits (466), Expect = 6e-51
 Identities = 121/309 (39%), Positives = 166/309 (53%), Gaps = 15/309 (4%)

Query: 8   VRIVEVGPRDGLQNIPQSIDSTIKLDLIRRLRDAGLQTIELTSFVSPRAIPQLADAQVVV 67
           + I EVGPRDGLQ++  ++ +  KL  I  L  AGL+ IE+ SFV  R +PQ+AD   VV
Sbjct: 6   ILISEVGPRDGLQSVQATMPTADKLRWIDALVAAGLREIEVGSFVPARLLPQMADVAEVV 65

Query: 68  QNADIQKLLKNPKLRLPVLVPNLKGLERALHNGIKEVAVFISATEGFSRANINCTVDEGL 127
           ++A     L +P + +  L PNL+G E AL  G+ +V + +SA+   S AN+  T +  +
Sbjct: 66  RHA-----LTHPGITVMALAPNLRGAEAALAAGVHKVTLPVSASAAHSLANVRKTREAMV 120

Query: 128 ERARQVASR--AASAGLSVRGYVSCIFADPYDGPTRPSSVLRCTKALLDAGCYEVSLGDT 185
           E  R VA    A + G  V   +S  F     G      VL       +AG  EV L DT
Sbjct: 121 EEVRAVAQLRDAQAPGTLVEVGLSTAFGCTLQGAVPEDDVLWLAGLCAEAGADEVGLSDT 180

Query: 186 LGIGTPADVRWLITYLQDNGVPLEMLAGHFHDTYGGAVANVWEAYKCGLRMFDSSVAGLG 245
            G+  PA VR L T L+   +  +  A H H+T G  +AN   AY  G+R FD+S+ GLG
Sbjct: 181 TGMANPAQVRRLFTRLRAE-LGAKAGAAHMHNTRGLGLANCLAAYDVGVRTFDASLGGLG 239

Query: 246 GCPXALGAKGNVASEDLVYMFERSGIHTGVDLSKLVETGEWISRQLSIAISSRAGAALWA 305
           GCP A GA GNV +EDLV+MFE  GI TGVDL +L+     +   L        G  ++ 
Sbjct: 240 GCPYAPGASGNVVTEDLVFMFEAMGITTGVDLERLMAARAPLQAGL-------PGEPVYG 292

Query: 306 MRKQTAVPK 314
           M  +  +PK
Sbjct: 293 MTPEAGLPK 301


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: 406
Number of extensions: 20
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: 599
Length of database: 306
Length adjustment: 32
Effective length of query: 567
Effective length of database: 274
Effective search space:   155358
Effective search space used:   155358
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