GapMind for catabolism of small carbon sources

 

Alignments for a candidate for D-LDH in Lactobacillus shenzhenensis LY-73

Align D-lactate dehydrogenase (EC 1.1.1.28) (characterized)
to candidate WP_022530758.1 L248_RS13205 lactate dehydrogenase

Query= BRENDA::C0LJH4
         (332 letters)



>NCBI__GCF_000469325.1:WP_022530758.1
          Length = 335

 Score =  188 bits (477), Expect = 2e-52
 Identities = 119/332 (35%), Positives = 182/332 (54%), Gaps = 7/332 (2%)

Query: 2   KIIAYAVRDDERPFFDTWMKENPDVEVKLVPELLTEDNVDLAKGFDGADVYQQKDYTAEV 61
           KI  + V D E PFF    +   D ++KL+PELLT DNV    G DG  +       A+ 
Sbjct: 4   KIACFGVHDYEVPFFKKLNQY--DYDLKLIPELLTHDNVGEIAGCDGVLLRGNCVADAQN 61

Query: 62  LNKLADEGVKNISLRNVGVDNLDVPTVKARGLNISNVPAYSPNAIAELSVTQLMQLLRQT 121
           L K+ D G+  +  R +G D++D+PT  + G+ ++ VP YS  ++AEL+++  + L R T
Sbjct: 62  LAKMHDYGITYVFTRTIGYDHIDLPTAASYGMKVARVPGYSAYSVAELALSLGLMLFRHT 121

Query: 122 PLFNKKLAKQDFRWAPD-IAKELNTMTVGVIGTGRIGRAAIDIFKGFGAKVIGYDVYRNA 180
                + A  D+R  P   ++E ++ T+G+IGTG IG     +++G GA V+GYDVY++ 
Sbjct: 122 ADATARTATGDYRVTPTFFSREAHSSTIGIIGTGHIGVTEAQLWRGMGATVLGYDVYQSD 181

Query: 181 ELEKEGMYVDTLDELYAQADVITLHVPALK-DNYHMLNADAFSKMKDGAYILNFARGTLI 239
             +    +VD L EL A+AD+I+LHVP     N  M+NA    +MK  A ++N ARG L+
Sbjct: 182 VAKAVVEFVD-LPELAARADIISLHVPYFPGQNDKMINAALIGQMKSSAVLVNTARGELV 240

Query: 240 DSEDLIKALDSGKVAGAALDTYEYETKIFNKDLEGQT-IDDKVFMNLFN-RDNVLITPHT 297
           D + ++ AL +G++ G A D    E++IF K L     +   V   L      VL TPH 
Sbjct: 241 DYDAVLAALQAGQLDGFASDVLLEESQIFGKKLPSNADLPLPVLQQLAALYPKVLFTPHM 300

Query: 298 AFYTETAVHNMVHVSMNSNKQFIETGKADTQV 329
              TE A+  M+ VS ++    + TG    +V
Sbjct: 301 GSLTEPALEGMISVSYDNFHTALTTGTVPNEV 332


Lambda     K      H
   0.317    0.135    0.383 

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: 288
Number of extensions: 18
Number of successful extensions: 5
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: 332
Length of database: 335
Length adjustment: 28
Effective length of query: 304
Effective length of database: 307
Effective search space:    93328
Effective search space used:    93328
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 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 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