GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lctC in Mesorhizobium ciceri WSM1271

Align lactate dehydrogenase (NAD+, ferredoxin) (subunit 2/3) (EC 1.3.1.110) (characterized)
to candidate YP_004140783.1 Mesci_1575 electron transfer flavoprotein subunit alpha

Query= BRENDA::H6LBB1
         (418 letters)



>NCBI__GCF_000185905.1:YP_004140783.1
          Length = 309

 Score =  135 bits (341), Expect = 1e-36
 Identities = 99/305 (32%), Positives = 159/305 (52%), Gaps = 30/305 (9%)

Query: 95  KARELAAVIGHPVYALLMGTNITEKADELLKY-GVDKVFVYDKPELKHFVIEPYANVLED 153
           KA   A  IG  V+ L+ G      AD   K  GV KV + +  EL   + EP A ++  
Sbjct: 20  KALSAALQIGSDVHVLVAGKGAKPAADAAAKLKGVSKVLLAEADELAERLAEPTAALIVS 79

Query: 154 FIEKVKPSSILVGATNVGRSLAPRVAARYRTGLTADCTILEMKENTDLVQI-------RP 206
                   +I+  AT+ G+++APRVAA           +L++ + ++++++       RP
Sbjct: 80  LAGAY--DTIIAPATSSGKNVAPRVAA-----------LLDVAQVSEIIEVVSPDTFKRP 126

Query: 207 AFGGNIMAQIVTENTRPQFCTVRYKVFTAPERVNEPWGDVEMMDIEKAKLVSAIE--VME 264
            + GN + Q V  +   +  TVR   F A      P G    ++  K      +   +  
Sbjct: 127 IYAGNAI-QTVQSSDAKKVITVRTASFQAA-----PEGGSAAVETVKVAANPGLSTFIEN 180

Query: 265 VIKKEKGIDLSEAETIVAVGRGV-KCEKDLDMIHEFAEKIGATVACTRPGIEAGWFDARL 323
            + +    +L+ A+ I++ GR +   EK  ++I   A+K+GA V  +R  ++AG+     
Sbjct: 181 KLSETDRPELTSAKIIISGGRALGSSEKFQEVILPVADKLGAAVGASRAAVDAGYAPNDW 240

Query: 324 QIGLSGRTVKPKLIIALGISGAVQFAAGMQNSEYIIAINSDPKAPIFNIAHCGMVGDLYE 383
           Q+G +G+ V P L IA+GISGA+Q  AGM++S+ I+AIN D +APIF +A  G+VGDL+ 
Sbjct: 241 QVGQTGKVVAPDLYIAVGISGAIQHLAGMKDSKVIVAINKDEEAPIFQVADYGLVGDLFV 300

Query: 384 ILPEL 388
           ILPEL
Sbjct: 301 ILPEL 305


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: 297
Number of extensions: 20
Number of successful extensions: 2
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: 309
Length adjustment: 29
Effective length of query: 389
Effective length of database: 280
Effective search space:   108920
Effective search space used:   108920
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: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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