GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mcl in Methylococcus capsulatus str. Bath

Align malyl-CoA lyase (EC 4.1.3.24) (characterized)
to candidate WP_010960993.1 MCA_RS08560 CoA ester lyase

Query= BRENDA::Q3J5L6
         (318 letters)



>NCBI__GCF_000008325.1:WP_010960993.1
          Length = 320

 Score =  325 bits (834), Expect = 7e-94
 Identities = 167/314 (53%), Positives = 220/314 (70%), Gaps = 8/314 (2%)

Query: 12  RPNRCQLFGPGSRPALFEKMAASAADVINLDLEDSVAPDDKAQARANIIEAINGLDWGRK 71
           R +R +L  PGS P + EK   + AD++ LDLED+VAPDDK QAR NI+ A+N  DW R 
Sbjct: 6   RLHRSELAVPGSNPRMLEKAPEAGADIVFLDLEDAVAPDDKEQARRNIVFALNTYDWSRC 65

Query: 72  YLSVRINGLDTPFWYRDVVDLLEQAGDRLDQIMIPKVGCAADVYAVDALVTAIERAKGRT 131
            +SVRINGLDT + YRD+V+++E  GD+LD I++PKVG A+DV  V  L++ IE  KG  
Sbjct: 66  AVSVRINGLDTHYAYRDLVEIVESCGDKLDTILVPKVGSASDVLFVATLLSQIEAYKG-F 124

Query: 132 KPLSFEVIIESAAGIAHVEEIAASSP-RLQAMSLGAADFAASMGMQTTGIGGTQENYYML 190
           KP++  V+IE+A G+A+VEEIA + P R++AM  G AD+AAS+  +TT IGG   +Y ML
Sbjct: 125 KPINIHVLIETAMGMANVEEIARTCPERMEAMVFGVADYAASVRARTTNIGGANPDYGML 184

Query: 191 HDGQK------HWSDPWHWAQAAIVAACRTHGILPVDGPFGDFSDDEGFRAQARRSATLG 244
            D  +      HW+D WH+  + +VAACR +G+ P+DGPFGDFSD EGFRA ARR+A LG
Sbjct: 185 TDPDESGTRAYHWADQWHFGISRMVAACRAYGLRPIDGPFGDFSDPEGFRAAARRAAALG 244

Query: 245 MVGKWAIHPKQVALANEVFTPSETAVTEAREILAAMDAAKARGEGATVYKGRLVDIASIK 304
             GKWAIHP Q+ L NE+FTP+E  VT A  IL AM+ A   G+GA    GRL+D ASI+
Sbjct: 245 CEGKWAIHPSQIPLCNEIFTPTEKEVTRAYRILEAMEQAAKEGKGAVSLDGRLIDAASIR 304

Query: 305 QAEVIVRQAEMISA 318
            AE +VRQ + I +
Sbjct: 305 MAENVVRQMKQIES 318


Lambda     K      H
   0.319    0.132    0.394 

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: 276
Number of extensions: 7
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: 318
Length of database: 320
Length adjustment: 28
Effective length of query: 290
Effective length of database: 292
Effective search space:    84680
Effective search space used:    84680
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