Aligments for a candidate for D-LDH in Sphingomonas koreensis DSMZ 15582

GapMind for catabolism of small carbon sources

Aligments for a candidate for D-LDH in Sphingomonas koreensis DSMZ 15582

Align D-2-hydroxyglutarate--pyruvate transhydrogenase DLD2; D-2HG--pyruvate transhydrogenase DLD2; Actin-interacting protein 2; D-lactate dehydrogenase [cytochrome] 2, mitochondrial; D-lactate ferricytochrome C oxidoreductase; D-LCR; EC 1.1.99.40; EC 1.1.2.4 (characterized)
to candidate Ga0059261_1572 Ga0059261_1572 FAD/FMN-containing dehydrogenases

Query= SwissProt::P46681
         (530 letters)



>lcl|FitnessBrowser__Korea:Ga0059261_1572 Ga0059261_1572
           FAD/FMN-containing dehydrogenases
          Length = 480

 Score =  280 bits (717), Expect = 7e-80
 Identities = 154/458 (33%), Positives = 260/458 (56%), Gaps = 17/458 (3%)

Query: 82  SESEDLSFYNEDWMRKYKGQSKLVLRPKSVEKVSLILNYCNDEKIAVVPQGGNTGLVGGS 141
           ++++ ++ +  DW  +Y G +  +L+P S E V+ ++       +A+VPQGGNT +VGG+
Sbjct: 22  TDADVIAPWLNDWRGRYHGAAAAILQPDSTEAVAAMVTLAGQHGVALVPQGGNTSMVGGA 81

Query: 142 VPIFD--ELILSLANLNKIRDFDPVSGILKCDAGVILENANNYVMEQNYMFPLDLGAKGS 199
            P  D   LILSL  LN++R  D  + + + +AGVIL + ++  + Q   FPL LGAKGS
Sbjct: 82  TPPADGSALILSLRRLNRVRRIDAAANLAEVEAGVILADLHDAALAQGRRFPLTLGAKGS 141

Query: 200 CHVGGVVATNAGGLRLLRYGSLHGSVLGLEVVMPNGQIVNSMHSMRKDNTGYDLKQLFIG 259
             VGG+V+TNAGG ++LR+G++ G VLGLE V+ +G I   + +++KDN GYDL QL IG
Sbjct: 142 ATVGGLVSTNAGGTQVLRFGTMRGLVLGLEAVLADGSIHGGLAALKKDNRGYDLNQLLIG 201

Query: 260 SEGTIGIITGVSILTVPKPKAFNVSYLSVESFEDVQKVFVRARQELSEILSAFEFMDAKS 319
           +EGT+G++T  S+  V    A  V+++ + S     ++  R  +  ++ + +FE + A+S
Sbjct: 202 AEGTLGVVTAASLKLVAAVHARAVAWIGLASPHAGLELLQRL-EAATDTIESFEIIPARS 260

Query: 320 QVLAKSQLKDAAFPLEDEHPFYILIETSGSNKDHD--DSKLETFLENVMEEGIVTDGVVA 377
                  +     PL  +H +++LIE    + + +     +E  L   +E G+  D  +A
Sbjct: 261 LGAVLRHIPGTRAPLSGDHGWHVLIEAVAVSAEQEAPAQLIERLLGPALESGLAQDATIA 320

Query: 378 QDETELQNLWKWREMIPEASQANGGVYKYDVSLPLKDLYSLVEATNARLSEAELVGDSPK 437
            +E + +  WK RE I EA +A+G   ++D+S+P       V A    + +     ++  
Sbjct: 321 ANEAQAEAFWKLRESISEAERASGPALQHDISVP-------VAAMPDFMIDGAKAVETRF 373

Query: 438 PVVGAIGYGHVGDGNLHLNV-----AVREYNKNIEKTLEPFVYEFVSSKHGSVSAEHGLG 492
           P V A  +GH+GDGN+H +V     +  ++ K     + PFV++ V +  GS+SAEHG+G
Sbjct: 374 PGVSAGAFGHLGDGNVHFHVRAPAGSAADWAKTHSDIISPFVHDLVVAAGGSISAEHGIG 433

Query: 493 FQKKNYIGYSKSPEEVKMMKDLKVHYDPNGILNPYKYI 530
             K++ +    SP  +  +  +K  +DP  +LNP K +
Sbjct: 434 QMKRDELARLSSPARMHALAAIKRAFDPRNLLNPGKLV 471


Lambda     K      H
   0.316    0.135    0.385 

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: 493
Number of extensions: 19
Number of successful extensions: 6
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: 530
Length of database: 480
Length adjustment: 34
Effective length of query: 496
Effective length of database: 446
Effective search space:   221216
Effective search space used:   221216
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 (21.6 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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

GapMind for catabolism of small carbon sources