GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lctO in Acidovorax sp. GW101-3H11

Align L-lactate oxidase (EC 1.1.3.2) (characterized)
to candidate Ac3H11_2838 L-lactate dehydrogenase (EC 1.1.2.3)

Query= BRENDA::Q8Z0C8
         (365 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_2838
          Length = 381

 Score =  331 bits (849), Expect = 2e-95
 Identities = 183/357 (51%), Positives = 240/357 (67%), Gaps = 5/357 (1%)

Query: 9   NLFEYEQLAKTHLSQMAFDYYISGAGDEITLQENRAVFERIKLRPRMLVDVSQINLTTSV 68
           NL ++E  A+  L   A+ Y+  GAGDEITL+ NR+ ++ + L PR+L  ++  +    +
Sbjct: 16  NLADHELQARQQLDDNAWAYFSGGAGDEITLRANRSAWDALPLWPRVLRPLAGGHTRVQL 75

Query: 69  LGQPLQLPLLIAPMAFQCLAHTEGELATAMAAASAGTGMVLSTLSTKSLEEVAE-VGSKF 127
           LG+ L  P+L+AP+AFQ LAH +GELA A AAA+ G G+VLST ++ SLE +AE V    
Sbjct: 76  LGRTLAHPILLAPVAFQRLAHADGELAMAYAAAALGAGVVLSTQASVSLEAIAEAVQPDP 135

Query: 128 SPSLQWFQLYIHKDRGLTRALVERAYAAGYKALCLTVDAPVLGQRERDRRNEFVLPPGLH 187
                WFQLY+  DRG T+ALV+RA AAGY+AL LTVDAP  G R+R+RR  F LPPG+ 
Sbjct: 136 GRGPLWFQLYLQHDRGFTQALVQRAEAAGYEALVLTVDAPTSGVRDRERRAGFRLPPGVG 195

Query: 188 LANLTTISGLNIPHA-PGESGLFTYFAQQLNPALTWDDLEWLQSLSPLPLVLKGILRGDD 246
             NL  +     P   PG+S LF     Q   A TWDD+ WLQS++ LP++LKG+L   D
Sbjct: 196 PVNLAGLPPPPPPDLRPGQSALFDGLLHQ---APTWDDVAWLQSITRLPVLLKGVLHPAD 252

Query: 247 AARAVEYGAKAIVVSNHGGRQLDGAIASLDALPEIVAAVNGKAEVLLDGGIRRGTDIIKA 306
           A +AV  GA  ++VSNHGGR LD A A+  ALP +V AV G   VL+DGGIRRGTD++KA
Sbjct: 253 ARQAVAAGAAGLIVSNHGGRTLDTAPATATALPRVVQAVGGAVPVLVDGGIRRGTDVLKA 312

Query: 307 LAIGAQAVLIGRPVLWGLAVGGQAGVSHVISLLQKELNVAMALIGCSQLQDIDTSFL 363
           +A+GA AVL+GRP +WGLA  G  GV+HV+ LL+ EL VAMAL GC+ L D   + L
Sbjct: 313 MALGASAVLVGRPAVWGLANAGATGVAHVLRLLRDELEVAMALTGCATLADATPALL 369


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: 387
Number of extensions: 22
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: 381
Length adjustment: 30
Effective length of query: 335
Effective length of database: 351
Effective search space:   117585
Effective search space used:   117585
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