GapMind for catabolism of small carbon sources

 

Alignments for a candidate for L-LDH in Pedobacter sp. GW460-11-11-14-LB5

Align L-lactate dehydrogenase (cytochrome) (EC 1.1.2.3) (characterized)
to candidate CA265_RS08335 CA265_RS08335 alpha-hydroxy-acid oxidizing enzyme

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



>FitnessBrowser__Pedo557:CA265_RS08335
          Length = 389

 Score =  241 bits (614), Expect = 3e-68
 Identities = 131/370 (35%), Positives = 208/370 (56%), Gaps = 2/370 (0%)

Query: 3   QILEIRDLKALARRRVPKLFFDYADSGAWTEGTYRANEEDFAGIKLRQRVLVDMSDRSLE 62
           Q   + DL+  A+ R+PK  FDY + G         NE DF  I L+   L    D  + 
Sbjct: 12  QFPSVADLRKKAKSRIPKFAFDYLEGGCNEGLNLSRNESDFDNIYLKPNYLRVGGDIDMS 71

Query: 63  TTMIGQKVSMPVALAPTGLTGMQHADGEMLAAQAAEAFGVPFTLSTMSICSIEDVASVTT 122
             + G++ S P  ++P GL G+   +   + A+AA    +P+TLST+S  SIE +A V+ 
Sbjct: 72  VELFGRRYSAPFGISPIGLQGLMWPNAPEILARAAAKADIPYTLSTVSTSSIERIAEVSE 131

Query: 123 KPFWFQLYVMREREFVLDLIDRAKAAKCSALVMTLDLQILGQRHKDLRNGLSAPPRLTPK 182
              WFQLY   E     D+++R KA +C  LV+ +D+   G R+K++++GLS PP+++  
Sbjct: 132 GKAWFQLYHPTEDRLRDDILNRLKAVECPVLVVLVDVPAFGLRYKEIKSGLSIPPKMSIN 191

Query: 183 HLWMMATRPGWCMKMLGTNRRTFRNIVGHAKSVADLSSLQAWTNEQFDPQLSWKDVEWIK 242
           ++     RP W +K L     +F  +  + +   D+S L  + N  F  ++  + V  I+
Sbjct: 192 NILQAFARPLWGIKTLQHGIPSFATLKPYMEKGMDMSQLGQFMNRTFTGKVDIEKVSAIR 251

Query: 243 ERWGGPLILKGILDPEDAKMAAKTGADAIIVSNHGGRQLDGAHSSISMLPRIVE--AVGD 300
           + W GPLILKGI   ED + A + GAD +IVSNHGGRQ+D   SSI+ L ++        
Sbjct: 252 DLWKGPLILKGITTDEDMQAAIQIGADGVIVSNHGGRQIDAGESSINSLIKMTNNPIYKS 311

Query: 301 QIEVHLDGGIRSGQDVLKAIALGAKGTYIGRPFLYGLGALGKEGVTLALDIIRKEMDTTM 360
           ++++ LDGGIRSG D+ +A A+G++  ++GRPF+YG+GALG EG    +++ +  +   M
Sbjct: 312 KLKIMLDGGIRSGVDLARAHAVGSEFNFMGRPFMYGVGALGNEGGDHTINMFKTHLYQIM 371

Query: 361 ALCGKRRITE 370
                 +IT+
Sbjct: 372 QQLTIEKITQ 381


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: 329
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: 389
Length adjustment: 30
Effective length of query: 348
Effective length of database: 359
Effective search space:   124932
Effective search space used:   124932
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 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