GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lctO in Phaeobacter inhibens BS107

Align L-lactate oxidase (EC 1.1.3.2) (characterized)
to candidate GFF481 PGA1_c04920 l-lactate dehydrogenase IldD

Query= BRENDA::Q8Z0C8
         (365 letters)



>FitnessBrowser__Phaeo:GFF481
          Length = 388

 Score =  243 bits (621), Expect = 5e-69
 Identities = 145/370 (39%), Positives = 214/370 (57%), Gaps = 24/370 (6%)

Query: 9   NLFEYEQLAKTHLSQMAFDYYISGAGDEITLQENRAVFERIKLRPRMLVDVSQINLTTSV 68
           N+ + +++ +  + +M +DY  SG+  E T ++N   FE+I+LR R+ VD++  +  + +
Sbjct: 6   NINDLKRIYERRVPRMFYDYAESGSWTEQTFRDNTNDFEKIRLRQRVAVDMAGRSTASQM 65

Query: 69  LGQPLQLPLLIAPMAFQCLAHTEGELATAMAAASAGTGMVLSTLSTKSLEEVAEVGSKFS 128
           +GQ + +P+ +AP+    + H +GE+  A AA + G    LST+S  S+EEVAE  +K  
Sbjct: 66  IGQDVSMPVALAPVGLTGMQHADGEIKAARAAETFGVPFTLSTMSINSIEEVAEATTKPF 125

Query: 129 PSLQWFQLYIHKDRGLTRALVERAYAAGYKALCLTVDAPVLGQRERDRRNEFVLPPGLH- 187
               WFQLY  KD    R L++RA  A   AL +T+D  +LGQR +D +N    PP L  
Sbjct: 126 ----WFQLYTMKDDDYVRRLIQRAKDARCSALVITLDLQILGQRHKDLKNGLSAPPKLTP 181

Query: 188 --LANLTTI--------------SGLNIPHAPG---ESGLFTYFAQQLNPALTWDDLEWL 228
             +ANL T                G  + H  G    S L  + A+Q +P+L W  +  L
Sbjct: 182 KTIANLMTKWSWGLQMLSAKRRNFGNIVGHVEGISDASSLGAWTAEQFDPSLDWSKIAKL 241

Query: 229 QSLSPLPLVLKGILRGDDAARAVEYGAKAIVVSNHGGRQLDGAIASLDALPEIVAAVNGK 288
             L    ++LKGIL  +DA  A + GA AIVVSNHGGRQLDGA++S+  LP I+ AV  +
Sbjct: 242 IELWDGKVILKGILDVEDAKMAAKLGADAIVVSNHGGRQLDGALSSIQMLPAIMDAVGDQ 301

Query: 289 AEVLLDGGIRRGTDIIKALAIGAQAVLIGRPVLWGLAVGGQAGVSHVISLLQKELNVAMA 348
            EV LD GIR G D++KALA+GA+  +IGR  ++GL   GQ GV+  + +L KEL+  MA
Sbjct: 302 IEVHLDSGIRSGQDVLKALALGAKGTMIGRAFVYGLGAMGQHGVTRALEVLHKELDTTMA 361

Query: 349 LIGCSQLQDI 358
           L G   + D+
Sbjct: 362 LCGEKSVADL 371


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: 293
Number of extensions: 13
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: 365
Length of database: 388
Length adjustment: 30
Effective length of query: 335
Effective length of database: 358
Effective search space:   119930
Effective search space used:   119930
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: 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