GapMind for catabolism of small carbon sources

 

Alignments for a candidate for D-LDH in Burkholderia phytofirmans PsJN

Align D-lactate dehydrogenase (EC 1.1.1.28) (characterized)
to candidate BPHYT_RS03835 BPHYT_RS03835 D-lactate dehydrogenase

Query= BRENDA::Q9I530
         (329 letters)



>FitnessBrowser__BFirm:BPHYT_RS03835
          Length = 332

 Score =  462 bits (1189), Expect = e-135
 Identities = 234/330 (70%), Positives = 268/330 (81%), Gaps = 1/330 (0%)

Query: 1   MRILFFSSQAYDSESFQASNHRHGFELHFQQAHLQADTAVLAQGFEVVCAFVNDDLSRPV 60
           MR++ FSS+ YD ++F  +N  H +ELH Q++HL ++TA+LAQG++VVC FVND++   V
Sbjct: 1   MRMILFSSRQYDRDTFTEANATHRYELHCQESHLDSETAILAQGYDVVCPFVNDNVDAAV 60

Query: 61  LERLAAGGTRLVALRSAGYNHVDLAAAEALGLPVVHVPAYSPHAVAEHAVGLILTLNRRL 120
           L RL AGGTR++ALRSAG+NHVDLAAAE LG+ V  VPAYSPHAVAEHAVGLIL LNRRL
Sbjct: 61  LARLHAGGTRMIALRSAGFNHVDLAAAERLGITVARVPAYSPHAVAEHAVGLILALNRRL 120

Query: 121 HRAYNRTREGDFSLHGLTGFDLHGKRVGVIGTGQIGETFARIMAGFGCELLAYDP-YPNP 179
            RA  RTREGDFSLHGL GFDLHGK VGVIGTG IG  F RIMAGFG ++LAYDP  P  
Sbjct: 121 PRAVARTREGDFSLHGLLGFDLHGKTVGVIGTGMIGRVFGRIMAGFGMQVLAYDPGKPAA 180

Query: 180 RIQALGGRYLALDALLAESDIVSLHCPLTADTRHLIDAQRLATMKPGAMLINTGRGALVN 239
            + ALG RY+ LDALLAESD+VSLHCPL  DT HLI+   LA MK GAMLINTGRG LV 
Sbjct: 181 DLLALGARYVPLDALLAESDVVSLHCPLVPDTYHLINGPALAKMKRGAMLINTGRGGLVE 240

Query: 240 AAALIEALKSGQLGYLGLDVYEEEADIFFEDRSDQPLQDDVLARLLSFPNVVVTAHQAFL 299
           + ALI ALK GQLG+LGLDVYEEE+ +FFED S+ PLQDDVLARLL FPNV+VTAHQAF 
Sbjct: 241 SNALIGALKDGQLGHLGLDVYEEESGLFFEDHSNLPLQDDVLARLLMFPNVIVTAHQAFF 300

Query: 300 TREALAAIADTTLDNIAAWQDGTPRNRVRA 329
           TREA+  IA TTLDN+AAWQ GTPRN VRA
Sbjct: 301 TREAMNEIAQTTLDNVAAWQAGTPRNVVRA 330


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: 443
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: 329
Length of database: 332
Length adjustment: 28
Effective length of query: 301
Effective length of database: 304
Effective search space:    91504
Effective search space used:    91504
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 17 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