GapMind for catabolism of small carbon sources

 

Alignments for a candidate for L-LDH in Streptacidiphilus oryzae TH49

Align L-lactate dehydrogenase (cytochrome) (EC 1.1.2.3) (characterized)
to candidate WP_161789654.1 BS73_RS07640 alpha-hydroxy-acid oxidizing protein

Query= reanno::Smeli:SM_b20850
         (378 letters)



>NCBI__GCF_000744815.1:WP_161789654.1
          Length = 369

 Score =  274 bits (701), Expect = 3e-78
 Identities = 146/364 (40%), Positives = 216/364 (59%), Gaps = 7/364 (1%)

Query: 14  ARRRVPKLFFDYADSGAWTEGTYRANEEDFAGIKLRQRVLVDMSDRSLETTMIGQKVSMP 73
           ARRR+P   + Y + GA  E T R N   F  ++       D+ +    TT++G    +P
Sbjct: 5   ARRRLPSAAWAYLEGGAEDEYTLRRNRAAFDELEFLPEAPGDVREIDTGTTVLGIHQPLP 64

Query: 74  VALAPTGLTGMQHADGEMLAAQAAEAFGVPFTLSTMSICSIEDVASVTTKPFWFQLYVMR 133
             L+P G   M H +GE+  A+AA   G+P+ +ST++  S+E+VA+ T  P WFQLY+  
Sbjct: 65  FVLSPVGAPRMVHHEGEVAVARAARHAGIPYGISTLANTSVEEVAAQTDTPLWFQLYLWS 124

Query: 134 EREFVLDLIDRAKAAKCSALVMTLDLQILGQRHKDLRNGLSAP-PRLTPKHLWMMATRPG 192
           +RE +   I+RA+ A   ALV+ +D  +  +R ++   GLS P P+LT       A  P 
Sbjct: 125 DREVIRGAIERARRAGFHALVLNIDTNVRSKREREKHAGLSLPRPQLTLPSFLDGALHPY 184

Query: 193 WCMKMLGTNRRTFRNIVGHAKSVADLSSLQAWTNEQFDPQLSWKDVEWIKERWGGPLILK 252
           W   +L +   TF NI    +   D+ +      + FD  + W D++WI+E+W GP+++K
Sbjct: 185 WSWHLLTSELITFPNIGPDDRRSLDVVA------DLFDGTVCWNDLKWIREQWEGPVVVK 238

Query: 253 GILDPEDAKMAAKTGADAIIVSNHGGRQLDGAHSSISMLPRIVEAVGDQIEVHLDGGIRS 312
           G+L PE+A  AA  GADAI+VSNHGGRQLD   ++I +LP IVEAVGD++EV +D G R 
Sbjct: 239 GVLRPEEAVRAAGAGADAIVVSNHGGRQLDHVPATIDVLPGIVEAVGDRVEVLVDSGFRR 298

Query: 313 GQDVLKAIALGAKGTYIGRPFLYGLGALGKEGVTLALDIIRKEMDTTMALCGKRRITEVG 372
           G D+  A+ALGA+   +GR  LYGL A G+ GV   +DI+  E+  TM LCG R ++E+ 
Sbjct: 299 GSDIAAALALGARAVLLGRAHLYGLAAAGEAGVRHCIDILAHELTVTMGLCGVRSVSELS 358

Query: 373 RDII 376
            D++
Sbjct: 359 PDLL 362


Lambda     K      H
   0.321    0.136    0.406 

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: 353
Number of extensions: 14
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: 378
Length of database: 369
Length adjustment: 30
Effective length of query: 348
Effective length of database: 339
Effective search space:   117972
Effective search space used:   117972
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 (21.9 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