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 GFF755 PGA1_c07690 (S)-mandelate dehydrogenase MdlB

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



>FitnessBrowser__Phaeo:GFF755
          Length = 363

 Score =  229 bits (585), Expect = 7e-65
 Identities = 141/372 (37%), Positives = 200/372 (53%), Gaps = 21/372 (5%)

Query: 3   ISSASDYRAAAKRKLPRFLFDYIDGGAYAEHTLRANSSDLAEISLRQRILRNVDNLSLKT 62
           I SA D R  A+R+LP  +FDYIDG A  E     N + L  I+LR RILR+V   SL T
Sbjct: 6   IHSAEDARRLARRRLPWMVFDYIDGAAGQETGAARNRAALDAITLRPRILRDVSQRSLAT 65

Query: 63  TLFGQELDMPVILSPVGLTGMYARRGEVQAAKAAANKGIPFCLSTVSVCPIEEVASQSAQ 122
           ++FG E D P  ++P+G+  + A   ++  A+ AA+  +P  +STV+  P+E +   +  
Sbjct: 66  SIFGAETDRPFGIAPMGMCNLAAPGADLMLARLAAHHRVPHGVSTVASTPLEILLEAAEG 125

Query: 123 AIWFQLYVLKDRGFMRNALERAQAAGVTTLVFTVDMPTPGARYRDAHSGMSGPF-AAQRR 181
             WFQLY   D        ERA+AAG  TLV TVD+P  G R R+   G   PF    R+
Sbjct: 126 YAWFQLYFSGDGTGTFKLAERARAAGYQTLVLTVDVPEVGRRPRELRHGFKMPFRIGPRQ 185

Query: 182 MLQAVTKPQWAFDVGLMGRPHDLGNISKYLGKPTHLEDYIGWLANNFD-----ASISWKD 236
            +     P+W+    L G+P  + N          +E Y      +FD     A  +W  
Sbjct: 186 FIDFALHPRWSLATLLKGKP-VMANF--------EMEGY------DFDRTESRARATWDT 230

Query: 237 LEWIREFWKGPMIIKGILDPQDAKDAVSFGADGIVVSNHGGRQLDGVLSTAKALPPIADA 296
           L  +R+ W G +++KG+LD +DA+  VS GAD I +S+HG RQL+   +  + L  I   
Sbjct: 231 LARLRDLWPGKLVVKGVLDVEDARALVSAGADAIQISSHGARQLEAAPAPIEMLAKIRAD 290

Query: 297 VGDDLTVLVDSGIRSGLDVVRMLALGAKACLLGRATAYALAADGQHGVENLLDIFAKEMR 356
            G    V  DSGIRSG DV++ +  GA    LGR   YA+AA G+ G+E L D  ++E+ 
Sbjct: 291 FGPTFPVFYDSGIRSGEDVLKAITTGADFVFLGRILQYAIAARGEAGLEQLWDALSEELS 350

Query: 357 VAMTLTGVTSIA 368
           +AM  TG  S+A
Sbjct: 351 IAMAQTGRVSLA 362


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: 295
Number of extensions: 9
Number of successful extensions: 2
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: 363
Length adjustment: 30
Effective length of query: 346
Effective length of database: 333
Effective search space:   115218
Effective search space used:   115218
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: 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