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 SMc01712 SMc01712 L-lactate dehydrogenase (cytochrome) protein

Query= BRENDA::Q8Z0C8
         (365 letters)



>FitnessBrowser__Smeli:SMc01712
          Length = 403

 Score =  256 bits (653), Expect = 1e-72
 Identities = 145/370 (39%), Positives = 214/370 (57%), Gaps = 24/370 (6%)

Query: 9   NLFEYEQLAKTHLSQMAFDYYISGAGDEITLQENRAVFERIKLRPRMLVDVSQINLTTSV 68
           N  ++ ++AK  L    F+Y    A DE+T + N A FE   L P +L  V  ++++ +V
Sbjct: 30  NFHDFRRMAKRRLPSPIFNYIDGAADDEVTYRRNTAAFEGCDLVPNVLRGVGDVDMSVTV 89

Query: 69  LGQPLQLPLLIAPMAFQCLAHTEGELATAMAAASAGTGMVLSTLSTKSLEEVAEVGSKFS 128
           +GQ L +P+  +P A Q L H +GE A A AAA  GT   +S+L T SLEE   +     
Sbjct: 90  MGQRLAMPVYCSPTALQRLFHHQGERAVAAAAAKFGTMFGVSSLGTVSLEEARRI----C 145

Query: 129 PSLQWFQLYIHKDRGLTRALVERAYAAGYKALCLTVDAPVLGQRERDRRNEFVLPPGLHL 188
              Q +Q Y HKDRGL R ++ RA  AG + + LTVD+   G RERD+R  F +P  L+L
Sbjct: 146 DGPQVYQFYFHKDRGLNREMMARAKQAGIEVMMLTVDSITGGNRERDKRTGFAIPFKLNL 205

Query: 189 ANLTTIS-----GLN-IPHAP--------------GESGLFTYFAQQLNPALTWDDLEWL 228
           A +T  +      +N + H P              G   +  YF + L+P+++WDD+  +
Sbjct: 206 AGITQFAIKPSWAVNYVRHEPFRLPQLENHVDMGRGAMSISRYFTEMLDPSMSWDDVAEM 265

Query: 229 QSLSPLPLVLKGILRGDDAARAVEYGAKAIVVSNHGGRQLDGAIASLDALPEIVAAVNGK 288
                    LKG++  +DA RAVE G   IV+SNHGGRQLDG+  + D L EIV AV  +
Sbjct: 266 VQHWGGQFCLKGVISVEDAKRAVEIGCTGIVLSNHGGRQLDGSRTAFDQLDEIVQAVGDR 325

Query: 289 AEVLLDGGIRRGTDIIKALAIGAQAVLIGRPVLWGLAVGGQAGVSHVISLLQKELNVAMA 348
            +V++DGG++RGT ++KAL++GA+AV +GR  L+ LA  GQAGV   + L++ E+   M 
Sbjct: 326 IDVMMDGGVQRGTHVLKALSLGAKAVGLGRYYLFPLAAAGQAGVERALELMRVEIERGMK 385

Query: 349 LIGCSQLQDI 358
           L+GCS + ++
Sbjct: 386 LMGCSSVDEL 395


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: 299
Number of extensions: 12
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: 403
Length adjustment: 30
Effective length of query: 335
Effective length of database: 373
Effective search space:   124955
Effective search space used:   124955
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.

Links

Downloads

Related tools

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