GapMind for catabolism of small carbon sources

 

Alignments for a candidate for L-LDH in Phaeobacter inhibens BS107

Align L-lactate dehydrogenase (cytochrome) (EC 1.1.2.3) (characterized)
to candidate GFF927 PGA1_c09430 l-lactate dehydrogenase IldD

Query= reanno::WCS417:GFF3737
         (376 letters)



>FitnessBrowser__Phaeo:GFF927
          Length = 401

 Score =  236 bits (602), Expect = 8e-67
 Identities = 139/370 (37%), Positives = 203/370 (54%), Gaps = 10/370 (2%)

Query: 7   SDYRAAAKRKLPRFLFDYIDGGAYAEHTLRANSSDLAEISLRQRILRNVDNLSLKTTLFG 66
           SD R  A+R+LPRF+++Y+D G   E T   N + L ++     IL       L     G
Sbjct: 14  SDLRQRARRRLPRFVWEYLDSGTGTEATKARNRAALDQLGFAPSILHGPQTPDLSRRFLG 73

Query: 67  QELDMPVILSPVGLTGMYARRGEVQAAKAAANKGIPFCLSTVSVCPIEEVASQSAQAIWF 126
            +  +P  ++PVG++G+     E   A+ AA +G+P+CLSTV+    E++      A WF
Sbjct: 74  IDRPLPFGVAPVGMSGLIWPDAERLLARCAAAQGLPYCLSTVASQSPEDLVDDLGAAPWF 133

Query: 127 QLYVLKDRGFMRNALERAQAAGVTTLVFTVDMPTPGARYRDAHSGMSGPFAAQRRML-QA 185
           QLY  KD    R+ L RA+AAG   LV TVD+P    R R   SG++ P     R+L Q 
Sbjct: 134 QLYPPKDPDIRRDLLARAKAAGFAGLVLTVDVPVASRRERQTRSGLTQPPRLTPRLLAQV 193

Query: 186 VTKPQWAFDVGLMGRPHDLGNISKYL---GKPTHLEDYIGWLANNFDASISWKDLEWIRE 242
             +P WA  +   G PH +  +  Y+   G       ++G+L      S  W  ++W+R+
Sbjct: 194 AMRPAWAVGMARRGLPH-MKTLDTYVSGAGASLSSTAHVGYLLR---TSPDWDYVQWLRD 249

Query: 243 FWKGPMIIKGILDPQDAKDAVSFGADGIVVSNHGGRQLDGVLSTAKALPPIADAVGDDLT 302
            W GP+IIKG++  +DA    + GAD + VSNH GRQ D   ST +ALP I  A    L 
Sbjct: 250 HWDGPLIIKGVMRAEDAAPLEAIGADALWVSNHAGRQFDAAPSTIEALPGIRAAT--RLP 307

Query: 303 VLVDSGIRSGLDVVRMLALGAKACLLGRATAYALAADGQHGVENLLDIFAKEMRVAMTLT 362
           ++ DSGI SGLD++R LALGA   +LGRA  +ALAA G  G ++L+DI  K++   M   
Sbjct: 308 LIFDSGIESGLDILRALALGADYVMLGRAFHFALAALGSRGPDHLVDILRKDLDANMGQL 367

Query: 363 GVTSIAQIDR 372
           G+ +++ + R
Sbjct: 368 GLETLSALPR 377


Lambda     K      H
   0.321    0.136    0.401 

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: 388
Number of extensions: 23
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: 376
Length of database: 401
Length adjustment: 30
Effective length of query: 346
Effective length of database: 371
Effective search space:   128366
Effective search space used:   128366
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 (21.9 bits)
S2: 50 (23.9 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