GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lctO in Sinorhizobium meliloti 1021

Align L-lactate oxidase (EC 1.1.3.2) (characterized)
to candidate SM_b20850 SM_b20850 L-lactate dehydrogenase

Query= BRENDA::Q8Z0C8
         (365 letters)



>FitnessBrowser__Smeli:SM_b20850
          Length = 378

 Score =  257 bits (656), Expect = 4e-73
 Identities = 150/371 (40%), Positives = 222/371 (59%), Gaps = 24/371 (6%)

Query: 8   INLFEYEQLAKTHLSQMAFDYYISGAGDEITLQENRAVFERIKLRPRMLVDVSQINLTTS 67
           + + + + LA+  + ++ FDY  SGA  E T + N   F  IKLR R+LVD+S  +L T+
Sbjct: 5   LEIRDLKALARRRVPKLFFDYADSGAWTEGTYRANEEDFAGIKLRQRVLVDMSDRSLETT 64

Query: 68  VLGQPLQLPLLIAPMAFQCLAHTEGELATAMAAASAGTGMVLSTLSTKSLEEVAEVGSKF 127
           ++GQ + +P+ +AP     + H +GE+  A AA + G    LST+S  S+E+VA V +K 
Sbjct: 65  MIGQKVSMPVALAPTGLTGMQHADGEMLAAQAAEAFGVPFTLSTMSICSIEDVASVTTKP 124

Query: 128 SPSLQWFQLYIHKDRGLTRALVERAYAAGYKALCLTVDAPVLGQRERDRRNEFVLPPGL- 186
                WFQLY+ ++R     L++RA AA   AL +T+D  +LGQR +D RN    PP L 
Sbjct: 125 F----WFQLYVMREREFVLDLIDRAKAAKCSALVMTLDLQILGQRHKDLRNGLSAPPRLT 180

Query: 187 --HLANLTT-------ISGLN-------IPHAPGESGLFTYFA---QQLNPALTWDDLEW 227
             HL  + T       + G N       + HA   + L +  A   +Q +P L+W D+EW
Sbjct: 181 PKHLWMMATRPGWCMKMLGTNRRTFRNIVGHAKSVADLSSLQAWTNEQFDPQLSWKDVEW 240

Query: 228 LQSLSPLPLVLKGILRGDDAARAVEYGAKAIVVSNHGGRQLDGAIASLDALPEIVAAVNG 287
           ++     PL+LKGIL  +DA  A + GA AI+VSNHGGRQLDGA +S+  LP IV AV  
Sbjct: 241 IKERWGGPLILKGILDPEDAKMAAKTGADAIIVSNHGGRQLDGAHSSISMLPRIVEAVGD 300

Query: 288 KAEVLLDGGIRRGTDIIKALAIGAQAVLIGRPVLWGLAVGGQAGVSHVISLLQKELNVAM 347
           + EV LDGGIR G D++KA+A+GA+   IGRP L+GL   G+ GV+  + +++KE++  M
Sbjct: 301 QIEVHLDGGIRSGQDVLKAIALGAKGTYIGRPFLYGLGALGKEGVTLALDIIRKEMDTTM 360

Query: 348 ALIGCSQLQDI 358
           AL G  ++ ++
Sbjct: 361 ALCGKRRITEV 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: 300
Number of extensions: 9
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: 378
Length adjustment: 30
Effective length of query: 335
Effective length of database: 348
Effective search space:   116580
Effective search space used:   116580
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