GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lctC in Sinorhizobium meliloti 1021

Align lactate dehydrogenase (NAD+, ferredoxin) (subunit 2/3) (EC 1.3.1.110) (characterized)
to candidate SMa0819 SMa0819 FixB electron transfer flavoprotein alpha chain

Query= BRENDA::H6LBB1
         (418 letters)



>FitnessBrowser__Smeli:SMa0819
          Length = 353

 Score =  231 bits (588), Expect = 3e-65
 Identities = 122/324 (37%), Positives = 183/324 (56%), Gaps = 6/324 (1%)

Query: 71  YRGITVYVDHIEGQIHPVTFELIGKARELAAVIGHPVYALLMGT----NITEKADELLKY 126
           YR + V+++   GQ+HPV+ EL+G+ R+LA  +G  +  +++G            +   Y
Sbjct: 12  YRNVWVFIELEHGQVHPVSIELLGEGRKLADKLGVHLAGVVIGPPGGQGTANAIADAFAY 71

Query: 127 GVDKVFVYDKPELKHFVIEPYANVLEDFIEKVKPSSILVGATNVGRSLAPRVAARYRTGL 186
           G D  ++ + P L H+  EP+   L D +   KP  +L+GAT +GR LA  VA   +TGL
Sbjct: 72  GADLSYLVESPLLAHYRNEPFTKALTDLVLANKPEILLLGATTLGRDLAGSVATTLKTGL 131

Query: 187 TADCTILEMKENTDLVQIRPAFGGNIMAQIVTENTRPQFCTVRYKVFTAPERVNEPWGDV 246
           TADCT L +  +  L   RP FGG+++  I T   RPQ  TVR  V   P+RVN P G +
Sbjct: 132 TADCTELNVDSDGSLAATRPTFGGSLLCTIYTLKCRPQMATVRPSVMATPQRVNRPTGSI 191

Query: 247 EMMDIEKAKLVSAIEVMEVIKKEKGI--DLSEAETIVAVGRGVKCEKDLDMIHEFAEKIG 304
              D++  +   A +V+           +L+ A+ +VA G G+   ++L ++ + A  +G
Sbjct: 192 IRHDLKMLEEEIATKVLAFFSDCDSTIANLAYADVVVAGGLGLGAVQNLQLLKDLARTLG 251

Query: 305 ATVACTRPGIEAGWFDARLQIGLSGRTVKPKLIIALGISGAVQFAAGMQNSEYIIAINSD 364
               C+RP ++ GW     QIG +G T++PKL IA GISGAVQ   G++ S+ I+AIN+D
Sbjct: 252 GDFGCSRPLVQKGWMPFDRQIGQTGNTIRPKLYIAAGISGAVQHRVGVEGSDLIVAINTD 311

Query: 365 PKAPIFNIAHCGMVGDLYEILPEL 388
           P APIF+ AH G+V D    LP L
Sbjct: 312 PNAPIFDFAHLGVVADAISFLPAL 335


Lambda     K      H
   0.319    0.137    0.395 

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: 362
Number of extensions: 13
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: 418
Length of database: 353
Length adjustment: 30
Effective length of query: 388
Effective length of database: 323
Effective search space:   125324
Effective search space used:   125324
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 (21.7 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