GapMind for catabolism of small carbon sources

 

Alignments for a candidate for D-LDH in Stenotrophomonas chelatiphaga DSM 21508

Align D-lactate dehydrogenase (EC 1.1.1.28) (characterized)
to candidate WP_057509293.1 ABB28_RS14455 2-hydroxyacid dehydrogenase

Query= BRENDA::Q9I530
         (329 letters)



>NCBI__GCF_001431535.1:WP_057509293.1
          Length = 334

 Score =  357 bits (915), Expect = e-103
 Identities = 184/326 (56%), Positives = 227/326 (69%), Gaps = 5/326 (1%)

Query: 1   MRILFFSSQAYDSESFQASNHR----HGFELHFQQAHLQADTAVLAQGFEVVCAFVNDDL 56
           M++  FS++ YDS S   +N +    HG E  +  A L   TA LAQG + VC FVND L
Sbjct: 1   MKVAVFSARPYDSRSLDEANQQAGAAHGVEFLYYDATLDVHTAALAQGCDAVCVFVNDRL 60

Query: 57  SRPVLERLAAGGTRLVALRSAGYNHVDLAAAEALGLPVVHVPAYSPHAVAEHAVGLILTL 116
             PVL+ L   G R V LR AG+N+VDLAAAE LG  V  VPAYSP AVAEH + LI+TL
Sbjct: 61  DAPVLQALHGMGVRAVLLRCAGFNNVDLAAAERLGFFVARVPAYSPEAVAEHTLALIMTL 120

Query: 117 NRRLHRAYNRTREGDFSLHGLTGFDLHGKRVGVIGTGQIGETFARIMAGFGCELLAYDPY 176
           NR+ HRA+NR REG+F L GL G  LHGK  G++GTG+IG   ARI+ G GC +L +DPY
Sbjct: 121 NRQTHRAFNRVREGNFMLEGLLGRTLHGKTAGIVGTGKIGLATARILHGMGCTVLGHDPY 180

Query: 177 PNPRIQALGGRYLALDALLAESDIVSLHCPLTADTRHLIDAQRLATMKPGAMLINTGRGA 236
           P+P    L G +++L  LLA SDIVSLHCPLT  TRHLI+   LA MKPGAML+NT RG 
Sbjct: 181 PSPDFAGL-GEFVSLQDLLARSDIVSLHCPLTIQTRHLINDDSLALMKPGAMLVNTSRGG 239

Query: 237 LVNAAALIEALKSGQLGYLGLDVYEEEADIFFEDRSDQPLQDDVLARLLSFPNVVVTAHQ 296
           LV+  A+I ALKS QLG+L +DVYE+E+ +FF+DRS Q + DDV  RL++FPNV+VT HQ
Sbjct: 240 LVDTDAVIRALKSRQLGHLAIDVYEQESALFFQDRSGQIIDDDVFQRLMTFPNVLVTGHQ 299

Query: 297 AFLTREALAAIADTTLDNIAAWQDGT 322
            F T EAL  IA+TTL N+  +  GT
Sbjct: 300 GFFTTEALQEIAETTLGNLGHFAAGT 325


Lambda     K      H
   0.323    0.137    0.402 

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: 375
Number of extensions: 16
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: 329
Length of database: 334
Length adjustment: 28
Effective length of query: 301
Effective length of database: 306
Effective search space:    92106
Effective search space used:    92106
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.5 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (22.0 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