GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pcaB in Dinoroseobacter shibae DFL-12

Align 3-Carboxy-cis,cis-muconate cycloisomerase (EC 5.5.1.2) (characterized)
to candidate 3610093 Dshi_3474 fumarate lyase (RefSeq)

Query= BRENDA::Q2HNZ1
         (353 letters)



>FitnessBrowser__Dino:3610093
          Length = 348

 Score =  260 bits (664), Expect = 4e-74
 Identities = 159/345 (46%), Positives = 203/345 (58%), Gaps = 8/345 (2%)

Query: 7   EHPFLSGLFGDSEIIELFSAKADIDAMIRFETALAQAEAEASIFADDEAEAIVSGLSEFA 66
           ++    GLF D EI  LFSA+        +E AL   EA+ ++    +A  I + +++F 
Sbjct: 6   QNRLFDGLFADPEIAALFSAETMFAHFRHYEMALT--EAQGAVGRVKDAARIAARIAKFE 63

Query: 67  ADMSALRHGVAKDGVVVPELIRQMRAAVAGQGADKVHFGATSQDVIDTSLMLRLKMAAEI 126
               A+   V +DGV VP  +  + AA+ G  A  VH  ATSQD++DTSL L L+  +E+
Sbjct: 64  IAPDAISDRVTQDGVPVPAYVAALEAAL-GVDAAAVHLDATSQDLMDTSLALSLRRLSEV 122

Query: 127 IATRLGHLIDTLGDLASRDGHKPLTGYTRMQAAIGITVADRAAGWIAPLERHLLRLETFA 186
           +A RL  +I  L  L +  G + L G TRMQAA+ I VA R   W  PL R   R     
Sbjct: 123 LAARLDRVIVALDGLQAAQGARTLMGRTRMQAALPIPVATRLEAWQTPLLRARDRFPEAR 182

Query: 187 QNGFALQFGGAAGTLEKLGDNAGAVRADLAKRLGLADR-PQWHNQRDGIPEFANLLSLVT 245
                LQFGG  G   +      A+   LAK L L    P WH+ RDG+  +   L+LVT
Sbjct: 183 AGVEQLQFGGPVG---QRSPQMAAIAERLAKALDLPPPGPVWHSTRDGVVGYGTWLALVT 239

Query: 246 GTLGKFGQDIALMAEIG-SEIRLSGGGGSSAMPHKQNPVNAETLVTLARFNAVQISALHQ 304
           G+LGK GQDIALM++ G  + RLSGGG SSAMPHKQNP+ AETLVTLARFNAVQI  LHQ
Sbjct: 240 GSLGKMGQDIALMSQQGLDDARLSGGGTSSAMPHKQNPIAAETLVTLARFNAVQIGGLHQ 299

Query: 305 SLVQEQERSGAGWMLEWLTLPQMVTATGTSLLVAERLAAQIDRLG 349
           ++V EQERSGA W LEW+ LPQ+  ATG +L  A  L   I+ LG
Sbjct: 300 AMVHEQERSGAAWALEWMILPQICEATGAALRHAAALLDSIETLG 344


Lambda     K      H
   0.318    0.133    0.376 

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: 347
Number of extensions: 17
Number of successful extensions: 5
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: 353
Length of database: 348
Length adjustment: 29
Effective length of query: 324
Effective length of database: 319
Effective search space:   103356
Effective search space used:   103356
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