GapMind for catabolism of small carbon sources

 

Alignments for a candidate for catB in Phaeobacter inhibens BS107

Align Muconate cycloisomerase 1; EC 5.5.1.1; Cis,cis-muconate lactonizing enzyme I; MLE; Muconate cycloisomerase I (uncharacterized)
to candidate GFF2998 PGA1_c30470 mandelate racemase / muconate lactonizing enzyme

Query= curated2:P95608
         (373 letters)



>FitnessBrowser__Phaeo:GFF2998
          Length = 321

 Score = 82.8 bits (203), Expect = 1e-20
 Identities = 95/307 (30%), Positives = 142/307 (46%), Gaps = 34/307 (11%)

Query: 44  GVTGYGEGVVPGGPWWGGESVETMQAIVERYIVPVLLGRGVDEITGIMPDIERVVANARF 103
           GVTG GE  VP   +  GE++E++ A +E   +P    R   E+  ++P        A  
Sbjct: 37  GVTGCGE-CVPYARY--GETLESVTAEIEG--LPETFNRA--ELQSLLP--------AGA 81

Query: 104 AKAAVDVALHDAWARSLGVPVHTLLGGAFRKSVDVTWALGAAPAEEIIEEALDLVESKRH 163
           A+ AVD AL D  A+  G  V  L G    K     + L     E +  +A    ++   
Sbjct: 82  ARNAVDCALWDLEAKQAGKRVWELAGLPEPKPEITAYTLSLDSPENMQAQA---AKNAHR 138

Query: 164 FSFKLKMGALDPAVDTARVVQIAQALQGKAGVRIDVNARWDRLTALKYVPRLVEGGVELI 223
              K+K+G  D   D AR+ +  +A   +A + +D N  W         P LV  GV+L+
Sbjct: 139 PLLKIKLGTAD---DMARL-EAVRAGAPEARIIVDANEGWSAEVYADLAPHLVRLGVDLV 194

Query: 224 EQPTPGEQLEVLAELNRLVPVPVMADESVQTPHDALEVAR-RGAADVIALKTTKCGGLQK 282
           EQP P  +   L  + R  PVPV ADES    HD   +A   G  DVI +K  K GGL +
Sbjct: 195 EQPLPAGEDAALLGMER--PVPVCADESC---HDRESLAALEGKYDVINIKLDKTGGLTE 249

Query: 283 SREVVAIAKAAGIACHGATSIEGPIGTAASIHFACAEPGIDFGTELFGPLLFSEELLQEP 342
           + ++   A A G        +   +G++ ++  A         T+L GPLL +E+  +EP
Sbjct: 250 ALKLRDAALAQGF----EVMVGCMVGSSLAMAPATLVAQGAVVTDLDGPLLLAED-REEP 304

Query: 343 IRY-ADG 348
           + + ADG
Sbjct: 305 LDFDADG 311


Lambda     K      H
   0.318    0.136    0.400 

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: 234
Number of extensions: 13
Number of successful extensions: 2
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: 373
Length of database: 321
Length adjustment: 29
Effective length of query: 344
Effective length of database: 292
Effective search space:   100448
Effective search space used:   100448
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 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