GapMind for catabolism of small carbon sources

 

Alignments for a candidate for D-LDH in Sphingobium czechense LL01

Align D-lactate dehydrogenase (EC 1.1.1.28) (characterized)
to candidate WP_066607980.1 V473_RS17445 D-glycerate dehydrogenase

Query= BRENDA::Q9I530
         (329 letters)



>NCBI__GCF_001046645.1:WP_066607980.1
          Length = 319

 Score =  141 bits (356), Expect = 2e-38
 Identities = 102/307 (33%), Positives = 150/307 (48%), Gaps = 26/307 (8%)

Query: 25  FELHFQQAHLQADTAVLAQGF---EVVCAFVNDDLSRPVLERLAAGG-TRLVALRSAGYN 80
           + + F +     D A LAQ     + +C  V D ++R VL  L  G   R+VA   AGY+
Sbjct: 25  YHVTFNEDDRPMDAAALAQAMRDHDALCPTVTDRVTREVL--LTQGRRARIVANYGAGYD 82

Query: 81  HVDLAAAEALGLPVVHVPAYSPHAVAEHAVGLILTLNRRLHRAYNRTREGDFS----LHG 136
           H+DL AA   GL V + P     A A+ A+ L+L   RR        R GD+S     H 
Sbjct: 83  HIDLDAARGAGLAVTNTPDVLTDATADIAMTLMLMAMRRAGEGERELRAGDWSGWRPTH- 141

Query: 137 LTGFDLHGKRVGVIGTGQIGETFARIMAGFGCELLAYDPYPNPRIQALGGRYLALDALLA 196
           + G  L GK + ++G G+I    A+    FG  +  +   P   +  +   +  L AL  
Sbjct: 142 MIGQSLDGKLLALVGFGRIARAVAKRAQAFGMRVAYHSRRPAADMP-INAYFADLGALAQ 200

Query: 197 ESDIVSLHCPLTADTRHLIDAQRLATMKPGAMLINTGRGALVNAAALIEALKSGQLGYLG 256
           ++D++SLH P   +TRH++DA  LA M    +L+NTGRG+LV+ AAL +AL + ++   G
Sbjct: 201 QADVLSLHAPGGVETRHMVDAALLARMPAHGVLVNTGRGSLVDEAALAQALAARRIAAAG 260

Query: 257 LDVYEEEADIFFEDRSDQPLQDDVLARLLSFPNVVVTAHQAFLTREALAAIADTTLDNIA 316
           LDVYE E  +                 L++ PNVV+  H    T EA  A+     DN+ 
Sbjct: 261 LDVYEGEPQVH--------------PSLIALPNVVLLPHLGSATIEARTAMGMKVADNLD 306

Query: 317 AWQDGTP 323
            +  G P
Sbjct: 307 RFFAGEP 313


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: 278
Number of extensions: 17
Number of successful extensions: 4
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: 319
Length adjustment: 28
Effective length of query: 301
Effective length of database: 291
Effective search space:    87591
Effective search space used:    87591
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: 48 (23.1 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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