GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcB in Rhizobium johnstonii 3841

Align Citramalyl-CoA lyase, mitochondrial; (3S)-malyl-CoA thioesterase; Beta-methylmalate synthase; Citrate lyase subunit beta-like protein, mitochondrial; Citrate lyase beta-like; Malate synthase; EC 4.1.3.25; EC 3.1.2.30; EC 2.3.3.-; EC 2.3.3.9 (characterized)
to candidate WP_011654036.1 RL_RS24195 CoA ester lyase

Query= SwissProt::Q8R4N0
         (338 letters)



>NCBI__GCF_000009265.1:WP_011654036.1
          Length = 306

 Score =  144 bits (364), Expect = 2e-39
 Identities = 96/289 (33%), Positives = 143/289 (49%), Gaps = 14/289 (4%)

Query: 43  RRAVLYVPGNDEKKIRKIPSLKVDCAVLDCEDGVAENKKNEARLRIAKTLEDFDLGTTEK 102
           RR+VL VP  + + + K  ++  D  + D ED VA  KK EAR  +        L   E+
Sbjct: 13  RRSVLSVPAINPRALEKTHAVDCDAVIFDLEDSVAPEKKAEARENLRNFFSARPLQGKER 72

Query: 103 CVRINSVSS--GLAEVDLETFLQARVLPSSLMLPKVEGPEEIRWFSDKFSLHLKGRKLEQ 160
            +RINS+S+  GLA+++L T L     P +++LPKV+ P+++   SD  S         +
Sbjct: 73  IIRINSLSTDFGLADMELVTAL----CPDAVLLPKVDEPQDVMALSDLLS----EADAPE 124

Query: 161 PMNLIPFVETAMGLLNFKAVCEETLKTGPQVGLCLDAVVFGGEDFRASIGATSNKDTQDI 220
            + +   +ET  G+LN   + E     G   G  LD +V G  D R   G         +
Sbjct: 125 DLRIWAMIETPRGILNAAVIAE----AGRTPGSRLDCLVVGLNDLRKETGVLPQSGRSYL 180

Query: 221 LYARQKVVVTAKAFGLQAIDLVYIDFRDEDGLLRQSREAAAMGFTGKQVIHPNQIAVVQE 280
           +    +VV+   A+GL AID V+ DFR+E G   +  +  AMGF GK +IHP QI     
Sbjct: 181 VPWLMQVVLAVSAYGLDAIDSVFNDFRNEQGFDAECLQGRAMGFAGKMLIHPAQIEPANR 240

Query: 281 QFTPTPEKIQWAEELIAAFKEHQQLGKGAFTFRGSMIDMPLLKQAQNIV 329
            F P P  I  AE +I+AF +    G       G M++   L QA+++V
Sbjct: 241 HFGPDPAAIAEAEAIISAFADPASDGLNVINAGGRMVERLHLVQAESLV 289


Lambda     K      H
   0.319    0.135    0.385 

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: 244
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: 338
Length of database: 306
Length adjustment: 28
Effective length of query: 310
Effective length of database: 278
Effective search space:    86180
Effective search space used:    86180
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 (21.8 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Apr 09 2024. 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