GapMind for catabolism of small carbon sources

 

Alignments for a candidate for L-LDH in Burkholderia phytofirmans PsJN

Align L-lactate dehydrogenase; EC 1.1.1.27 (uncharacterized)
to candidate BPHYT_RS28460 BPHYT_RS28460 malate dehydrogenase

Query= curated2:Q07251
         (349 letters)



>FitnessBrowser__BFirm:BPHYT_RS28460
          Length = 363

 Score =  152 bits (384), Expect = 1e-41
 Identities = 106/336 (31%), Positives = 163/336 (48%), Gaps = 19/336 (5%)

Query: 2   KISLTSARQLARDILAAQQVPADIADDVAEHLVESDRCGYISHGLSILPNYRTALDGHSV 61
           ++    ARQ    IL A  +        A+ L++SD  G  SHG+S+L  Y        +
Sbjct: 3   RVGAAIARQQIEVILEAWGMSPGQVAASADILIDSDLKGIDSHGISMLMFYDQLYRAGQI 62

Query: 62  NPQGRAKCVLDQGTLMVFDGDGGFGQHVGKSVMQAAIERVRQHGHCIVTLRRSHHLGRMG 121
           + +  A+ V +  T  + DG+   G    +  M+ AIE+        V++  S H G  G
Sbjct: 63  DMKASARIVRETATTALIDGNAAMGHPTSRMAMELAIEKALACDMGAVSVFNSQHFGAAG 122

Query: 122 HYGEMAAAAGFVLLSFTNVINRAPVVAPFGGRVARLTTNPLCFAGPMPNGRPPLVVDIAT 181
           +Y EMAA  G  L++  +   R   V P  G    L TNP  FA P     PP+++D++T
Sbjct: 123 YYAEMAAERG--LIALVSCSTRLATVVPTFGAEPMLGTNPFAFATP-AGRHPPVILDMST 179

Query: 182 SAIAINKARVLAEKGEPAPEGSIIGADGNPTTDAS----TMFGEHPGALLP-------FG 230
           S +A NK +V A +G+P P G  + A+GNP TD++     +F    G L P        G
Sbjct: 180 SVVASNKVKVYALQGKPLPPGWALDANGNPLTDSAEAYRLLFERLGGGLAPLGGDGKTLG 239

Query: 231 GHKGYALGVVAELLAGVLSGGGTIQP--DNPRGGVATNNL--FAVLLNPALDLGLDWQSA 286
           GHKGY LG+ A++L   L GGG+  P  +  +     +N+  F + +NPA    ++   A
Sbjct: 240 GHKGYGLGLFAQILGSTL-GGGSFSPVRNRTQKSDEPDNIGHFFLAMNPAAFRPIEEYHA 298

Query: 287 EVEAFVRYLHDTPPAPGVDRVQYPGEYEAANRAQAS 322
           +++A +  L ++ PA     V  PG+ E   RA  S
Sbjct: 299 DLDAVIDALRESQPADPAQPVLIPGDPERLTRAARS 334


Lambda     K      H
   0.319    0.136    0.409 

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: 343
Number of extensions: 23
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: 349
Length of database: 363
Length adjustment: 29
Effective length of query: 320
Effective length of database: 334
Effective search space:   106880
Effective search space used:   106880
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 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