GapMind for catabolism of small carbon sources

 

Alignments for a candidate for catB in Dyella japonica UNC79MFTsu3.2

Align Muconate cycloisomerase 1; EC 5.5.1.1; Cis,cis-muconate lactonizing enzyme I; MLE; Muconate cycloisomerase I (uncharacterized)
to candidate N515DRAFT_2119 N515DRAFT_2119 o-succinylbenzoate synthase

Query= curated2:P95608
         (373 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2119
          Length = 365

 Score =  158 bits (400), Expect = 2e-43
 Identities = 111/361 (30%), Positives = 184/361 (50%), Gaps = 11/361 (3%)

Query: 4   LSIVSVETTILDVPLVRPHKFATTSMTAQPLLLVAVTTAGGVTGYGEGVVPGGPWWGGES 63
           + I  ++  +L VPL  P K A  ++     ++V V T  G  G+GE   P      G++
Sbjct: 1   MKITDIQFGMLRVPLKTPFKTALRTVERVDDIVVMVHTDTGHVGFGEA--PATAVITGDT 58

Query: 64  VETMQAIVERYIVPVLLGRGVDEITGIMPDIERVVANARFAKAAVDVALHDAWARSLGVP 123
             ++   +  YI P L+G  V ++  I   I+  +     AKAAV++A++D W +    P
Sbjct: 59  HGSIVDAIRHYIAPRLIGHEVADLNRITHLIQASMEKNTSAKAAVEIAVYDLWGQLYKAP 118

Query: 124 VHTLLGGAFRK-SVDVTWALGAAPAEEIIEEALDLVESKRHF-SFKLKMGALDPAVDTAR 181
           ++ LLGG     + D+T  +     ++++ +++  VE  R F S K+K+G  D  VD  R
Sbjct: 119 LYQLLGGGDPVITTDIT--ISVDYIDKMVADSISAVE--RGFESLKIKVGK-DIGVDIER 173

Query: 182 VVQIAQALQGKAGVRIDVNARWDRLTALKYVPRLVEGGV--ELIEQPTPGEQLEVLAELN 239
           V  I  A++ +A +R+D N  W    A+  +  L + GV  EL+EQP     LE +  + 
Sbjct: 174 VKAIYAAVEDRALLRLDANQGWTAKQAVYALQTLEDAGVKLELVEQPVKARDLEGMRYVT 233

Query: 240 RLVPVPVMADESVQTPHDALEVARRGAADVIALKTTKCGGLQKSREVVAIAKAAGIACHG 299
             V  PVMADESV  P + +E+ R  AAD+I +K  K GG+  +  +  IA   GI C  
Sbjct: 234 ERVHTPVMADESVFGPMEVIELIRLRAADIINIKLMKTGGISNAIRIADIAGLHGIDCMI 293

Query: 300 ATSIEGPIGTAASIHFACAEPGIDFGTELFGPLLFSEELLQEPIRYADGQVFLPEGPGLG 359
              +E  I  AA++H A A+  +    +L GP L   + +   + + + ++ + + PGLG
Sbjct: 294 GCMLESSISVAAAVHVAVAKADVITKVDLDGPSLCQYDPVDGGVNFNESEISITDAPGLG 353

Query: 360 V 360
           +
Sbjct: 354 I 354


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: 294
Number of extensions: 19
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: 373
Length of database: 365
Length adjustment: 30
Effective length of query: 343
Effective length of database: 335
Effective search space:   114905
Effective search space used:   114905
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.

Links

Downloads

Related tools

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