GapMind for catabolism of small carbon sources

 

Alignments for a candidate for D-LDH in Pseudomonas fluorescens FW300-N2E2

Align D-lactate dehydrogenase (EC 1.1.1.28) (characterized)
to candidate Pf6N2E2_5719 D-lactate dehydrogenase (EC 1.1.1.28)

Query= BRENDA::Q9I530
         (329 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_5719
          Length = 329

 Score =  491 bits (1264), Expect = e-143
 Identities = 246/327 (75%), Positives = 276/327 (84%)

Query: 1   MRILFFSSQAYDSESFQASNHRHGFELHFQQAHLQADTAVLAQGFEVVCAFVNDDLSRPV 60
           MR++FFSSQ YD +SF  +    G +L FQ A L  DT  LA+  EVVCAF+NDDLS PV
Sbjct: 1   MRVIFFSSQTYDRDSFTKAPTPAGLQLQFQPARLNLDTVALAERHEVVCAFINDDLSAPV 60

Query: 61  LERLAAGGTRLVALRSAGYNHVDLAAAEALGLPVVHVPAYSPHAVAEHAVGLILTLNRRL 120
           LE+LA GGTRL+ALRSAGYNHVDL AA+ LGL +V VPAYSPHAVAEHAV LI+ LNR L
Sbjct: 61  LEQLAEGGTRLIALRSAGYNHVDLLAAQRLGLSIVRVPAYSPHAVAEHAVALIMALNRCL 120

Query: 121 HRAYNRTREGDFSLHGLTGFDLHGKRVGVIGTGQIGETFARIMAGFGCELLAYDPYPNPR 180
           HRAYNRTR+G+FSLHGLTGFDL GK VGVIGTGQIG TFARIMAGFGC+LLAYDPYPNP+
Sbjct: 121 HRAYNRTRDGNFSLHGLTGFDLVGKTVGVIGTGQIGATFARIMAGFGCQLLAYDPYPNPQ 180

Query: 181 IQALGGRYLALDALLAESDIVSLHCPLTADTRHLIDAQRLATMKPGAMLINTGRGALVNA 240
           ++ALG RYL L  LLA++ I+SLHCPL   +RHLI+AQ LA M+ GAMLINTGRG LV+ 
Sbjct: 181 VEALGARYLPLAELLAQAQIISLHCPLNEQSRHLINAQSLAAMQRGAMLINTGRGGLVDT 240

Query: 241 AALIEALKSGQLGYLGLDVYEEEADIFFEDRSDQPLQDDVLARLLSFPNVVVTAHQAFLT 300
            ALIEALKSGQLGYLGLDVYEEEA +FF+DRSD PLQDDVLARLL+FPNV+VTAHQAFLT
Sbjct: 241 PALIEALKSGQLGYLGLDVYEEEAQLFFKDRSDLPLQDDVLARLLTFPNVIVTAHQAFLT 300

Query: 301 REALAAIADTTLDNIAAWQDGTPRNRV 327
            EALAAIA TTLDNIAAW  GTP+N V
Sbjct: 301 HEALAAIAMTTLDNIAAWAAGTPQNLV 327


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: 424
Number of extensions: 8
Number of successful extensions: 1
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: 329
Length adjustment: 28
Effective length of query: 301
Effective length of database: 301
Effective search space:    90601
Effective search space used:    90601
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.

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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