GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lctO in Pseudomonas simiae WCS417

Align L-lactate oxidase (EC 1.1.3.2) (characterized)
to candidate GFF3737 PS417_19130 lactate dehydrogenase

Query= BRENDA::Q8Z0C8
         (365 letters)



>FitnessBrowser__WCS417:GFF3737
          Length = 376

 Score =  237 bits (604), Expect = 4e-67
 Identities = 141/372 (37%), Positives = 198/372 (53%), Gaps = 24/372 (6%)

Query: 12  EYEQLAKTHLSQMAFDYYISGAGDEITLQENRAVFERIKLRPRMLVDVSQINLTTSVLGQ 71
           +Y   AK  L +  FDY   GA  E TL+ N +    I LR R+L +V  ++L T++ GQ
Sbjct: 8   DYRAAAKRKLPRFLFDYIDGGAYAEHTLRANSSDLAEISLRQRILRNVDNLSLKTTLFGQ 67

Query: 72  PLQLPLLIAPMAFQCLAHTEGELATAMAAASAGTGMVLSTLSTKSLEEVAEVGSKFSPSL 131
            L +P++++P+    +    GE+  A AAA+ G    LST+S   +EEVA      S   
Sbjct: 68  ELDMPVILSPVGLTGMYARRGEVQAAKAAANKGIPFCLSTVSVCPIEEVASQ----SAQA 123

Query: 132 QWFQLYIHKDRGLTRALVERAYAAGYKALCLTVDAPVLGQRERDRRNEFVLPPGLHLANL 191
            WFQLY+ KDRG  R  +ERA AAG   L  TVD P  G R RD  +    P       L
Sbjct: 124 IWFQLYVLKDRGFMRNALERAQAAGVTTLVFTVDMPTPGARYRDAHSGMSGPFAAQRRML 183

Query: 192 TTISG---------LNIPHAPGESGLFT-----------YFAQQLNPALTWDDLEWLQSL 231
             ++          +  PH  G    +            + A   + +++W DLEW++  
Sbjct: 184 QAVTKPQWAFDVGLMGRPHDLGNISKYLGKPTHLEDYIGWLANNFDASISWKDLEWIREF 243

Query: 232 SPLPLVLKGILRGDDAARAVEYGAKAIVVSNHGGRQLDGAIASLDALPEIVAAVNGKAEV 291
              P+++KGIL   DA  AV +GA  IVVSNHGGRQLDG +++  ALP I  AV     V
Sbjct: 244 WKGPMIIKGILDPQDAKDAVSFGADGIVVSNHGGRQLDGVLSTAKALPPIADAVGDDLTV 303

Query: 292 LLDGGIRRGTDIIKALAIGAQAVLIGRPVLWGLAVGGQAGVSHVISLLQKELNVAMALIG 351
           L+D GIR G D+++ LA+GA+A L+GR   + LA  GQ GV +++ +  KE+ VAM L G
Sbjct: 304 LVDSGIRSGLDVVRMLALGAKACLLGRATAYALAADGQHGVENLLDIFAKEMRVAMTLTG 363

Query: 352 CSQLQDIDTSFL 363
            + +  ID S L
Sbjct: 364 VTSIAQIDRSTL 375


Lambda     K      H
   0.320    0.136    0.391 

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: 299
Number of extensions: 13
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: 365
Length of database: 376
Length adjustment: 30
Effective length of query: 335
Effective length of database: 346
Effective search space:   115910
Effective search space used:   115910
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: 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