GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lctC in Alkalitalea saponilacus SC/BZ-SP2

Align lactate dehydrogenase (NAD+, ferredoxin) (subunit 2/3) (EC 1.3.1.110) (characterized)
to candidate WP_079559050.1 CDL62_RS14385 electron transfer flavoprotein subunit alpha/FixB family protein

Query= BRENDA::H6LBB1
         (418 letters)



>NCBI__GCF_002201795.1:WP_079559050.1
          Length = 339

 Score =  205 bits (522), Expect = 1e-57
 Identities = 116/320 (36%), Positives = 188/320 (58%), Gaps = 12/320 (3%)

Query: 82  EGQIHPVTFELIGKARELAAVIGHPVYALLMGTNITEKADELLKYGVDKVFVYDKPELKH 141
           EG++  V+ EL+ K R LA  +   + A+++G  I+    E++ YG D V + D P+L  
Sbjct: 12  EGKVADVSLELLTKGRTLANTLKCKLEAVVLGHKISGIEKEIIPYGADVVHIGDDPKLSP 71

Query: 142 FVIEPYANVLEDFIEKVKPSSILVGATNVGRSLAPRVAARYRTGLTADCTILEMKENTD- 200
           +   P++ V+     + KP   L+GA+ +GR L PRV++   +GLTADCT LE+ ++ D 
Sbjct: 72  YTTLPHSAVINGLFAETKPQIGLLGASTMGRDLGPRVSSALVSGLTADCTALEIGDHEDK 131

Query: 201 ---------LVQIRPAFGGNIMAQIVTENTRPQFCTVRYKVFTAPERVNEPWGDVEMMDI 251
                    L QIRPAFGGNI+A I+  + RPQ  TVR  V           G+V+ +D+
Sbjct: 132 KAGKNYKDLLYQIRPAFGGNIVATIINPDCRPQMATVREGVMKKEIYSPNHKGEVKTIDV 191

Query: 252 EKAKLVS--AIEVMEVIKKEKGIDLSEAETIVAVGRGVKCEKDLDMIHEFAEKIGATVAC 309
            K        ++V+E   ++  +++  +  IV+ G G+  +++ +++++ AE IG  V  
Sbjct: 192 SKYIKPEDLVVKVIERHMEKSRVNIKNSSIIVSGGYGMGSKENFNVLYDLAEAIGGEVGA 251

Query: 310 TRPGIEAGWFDARLQIGLSGRTVKPKLIIALGISGAVQFAAGMQNSEYIIAINSDPKAPI 369
           +R  ++AG+ D   Q+G +G TV+PKL IA GISG +Q  AGM++S  +IAIN+D  API
Sbjct: 252 SRAAVDAGYADHDRQVGQTGITVRPKLYIACGISGQIQHTAGMEDSAMVIAINNDANAPI 311

Query: 370 FNIAHCGMVGDLYEILPELL 389
             IA   + GD+ EI+P+++
Sbjct: 312 NKIADYVITGDVMEIIPKMI 331


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: 399
Number of extensions: 21
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: 339
Length adjustment: 30
Effective length of query: 388
Effective length of database: 309
Effective search space:   119892
Effective search space used:   119892
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 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