GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galactonolactonase in Jannaschia aquimarina GSW-M26

Align 1,4-lactonase (EC 3.1.1.25) (characterized)
to candidate WP_043918795.1 jaqu_RS09765 isochorismatase family protein

Query= BRENDA::B2LYJ5
         (401 letters)



>NCBI__GCF_000877395.1:WP_043918795.1
          Length = 517

 Score = 81.6 bits (200), Expect = 5e-20
 Identities = 91/342 (26%), Positives = 139/342 (40%), Gaps = 65/342 (19%)

Query: 72  YDEEFYDVIGKDPSLTLIATSDTDPIFHEAVVWYPPTEEVFFVQNAGAPAAGTGLNKSSI 131
           +D  F D+I +   +  +A+  T   F E  +W+P    + F                  
Sbjct: 6   FDPAFRDLIDEHAPVLQVASGCT---FTEGPIWHPVDRYLLF------------------ 44

Query: 132 IQKISLKEADEVRKGKKDEVKVTVVDSNPQVINPNGGTYYKGNIIFAGEGQGDDVPSALY 191
               S   AD  R+     V+  +  SN      NG TY     +   E     V     
Sbjct: 45  ----SDMPADVRRRLDAGGVREVLSPSN----KGNGMTYDASLNLLVCEHSTSSVAR--- 93

Query: 192 LMNPLPPYNTTTLLNNYF-GRQFNSLNDVGINPRNGDLYFTDTLYGYLQDF---RPVPGL 247
                 P  T  +L ++F GR+ NS ND+ +   +G ++FTD  YG +  F   RP    
Sbjct: 94  ----FRPDGTRDVLASHFEGRELNSPNDLCVKS-DGSIWFTDPWYGRMPGFGVERPRELG 148

Query: 248 RNQVYRYN-----FDTGAVTVVADDFTLPNGIGFGPDGKKVYVTDTGIALGFYGRNLSSP 302
              VYR        D  A+ V    FT+PNG+ F PD   +YV DT              
Sbjct: 149 FQGVYRLAPDHRPGDEPALMVDRYTFTMPNGLCFSPDESLLYVNDT------------EQ 196

Query: 303 ASVYSFDVNQDGTLQNRKTFAY-----VASFIPDGVHTDSKGRVYAGCGDGVHVWNPSGK 357
           A++  F+V  D  L+N + FA      +   +PDG+  D+ G V+     G+ V++P+GK
Sbjct: 197 ANIRVFEVQGD-RLENGRIFAAGIKDSLRPGVPDGMKCDASGNVWVTAPGGLWVYSPTGK 255

Query: 358 LIGKIYTGTVAANFQFAGKG-RMIITGQTKLFYVTLGASGPK 398
           L+G++    +AAN  + G   R +    T   Y      GP+
Sbjct: 256 LLGEVAIPELAANLHWGGPDWRTLYVCATTSVYALTTKVGPR 297


Lambda     K      H
   0.317    0.138    0.415 

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: 514
Number of extensions: 31
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: 401
Length of database: 517
Length adjustment: 33
Effective length of query: 368
Effective length of database: 484
Effective search space:   178112
Effective search space used:   178112
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 (21.6 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Sep 24 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