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_037571359.1 BS73_RS10585 alpha-hydroxy-acid oxidizing protein

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



>NCBI__GCF_000744815.1:WP_037571359.1
          Length = 420

 Score =  259 bits (661), Expect = 1e-73
 Identities = 148/369 (40%), Positives = 214/369 (57%), Gaps = 7/369 (1%)

Query: 7   IRDLKALARRRVPKLFFDYADSGAWTEGTYRANEEDFAGIKLRQRVLVDMSDRSLETTMI 66
           I DL+ +AR   P   F+Y D  A  E   R   + FA ++ R  +L D+S   L+T + 
Sbjct: 40  IADLRRIARHTTPTGPFEYVDGAADQEIGLRRARQAFADLEFRPGILRDVSHADLDTPVP 99

Query: 67  GQKVSMPVALAPTGLTGMQHADGEMLAAQAAEAFGVPFTLSTMSICSIEDVASVTTKPF- 125
           G   ++P  LAPTG T M H+ GE   A AA+  G+P+TLSTM   SI DVA+   +   
Sbjct: 100 GGSSALPFGLAPTGWTRMMHSAGERAVAAAAQRAGIPYTLSTMGTTSIGDVAAAAPEAVK 159

Query: 126 WFQLYVMREREFVLDLIDRAKAAKCSALVMTLDLQILGQRHKDLRNGLSAPPRLTPKHLW 185
           WFQLY+ ++RE  L L+  A+AA  SAL++T+D+ + G R +D+ NGL+ PP+LT +   
Sbjct: 160 WFQLYLWKDRERSLRLVSDARAAGYSALLVTVDVPVAGNRVRDVHNGLTIPPQLTLRTFL 219

Query: 186 MMATRPGWCMKMLGTNRRTFRNIVGHAKSVADLSSLQAWTNEQFDPQLSWKDVEWIKERW 245
             A RP W    L T    F      A       S   + ++ FD  +++ D+ W++E W
Sbjct: 220 DAAHRPRWWFDFLTTEPLRF------AADPTRSGSPGMFADDIFDSTVTFDDLVWLREAW 273

Query: 246 GGPLILKGILDPEDAKMAAKTGADAIIVSNHGGRQLDGAHSSISMLPRIVEAVGDQIEVH 305
            G LI+KG+    DA  A + GAD ++VSNHGGRQLD A   + +LP + +A+GD   V 
Sbjct: 274 PGTLIVKGVQTVADAVAAVEHGADGVVVSNHGGRQLDRAPVPLHLLPAVRKALGDGPTVM 333

Query: 306 LDGGIRSGQDVLKAIALGAKGTYIGRPFLYGLGALGKEGVTLALDIIRKEMDTTMALCGK 365
           LD GI  G D++ AIALGA    +GR +LYGL A G+ GVT A++I+  E++ T+ L G 
Sbjct: 334 LDTGITHGSDIVAAIALGADLALVGRAYLYGLMAGGEAGVTRAIEILADEVERTVRLLGA 393

Query: 366 RRITEVGRD 374
           R + ++  D
Sbjct: 394 RGVADLSPD 402


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: 416
Number of extensions: 23
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: 378
Length of database: 420
Length adjustment: 31
Effective length of query: 347
Effective length of database: 389
Effective search space:   134983
Effective search space used:   134983
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