GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iolJ in Pseudomonas fluorescens FW300-N2E2

Align 5-dehydro-2-deoxygluconokinase (EC 2.7.1.92); possible 5-dehydro-2-deoxyphosphogluconate aldolase DUF2090 (EC 4.1.2.29) (characterized)
to candidate Pf6N2E2_629 2-ketogluconate kinase (EC 2.7.1.13)

Query= reanno::pseudo3_N2E3:AO353_21335
         (645 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_629
          Length = 324

 Score =  100 bits (248), Expect = 1e-25
 Identities = 101/337 (29%), Positives = 140/337 (41%), Gaps = 37/337 (10%)

Query: 11  QLDLICLGRLGVDLYAQQVGARLEDVSSFAKYLGGSSANIAFGTARLGLKSAMLSRVGDD 70
           + D++  G     L A Q G  L  V  F K + G+ +N+A G +RL  K A LSRVG D
Sbjct: 3   EFDVLSFGETMAMLVADQRGD-LASVDQFHKRIAGADSNVAIGLSRLDFKVAWLSRVGAD 61

Query: 71  HMGRFLVESLAREGCDVSGIKVDPERLTAMVLLGLKDRETFPLV-FYRENCADMALRAED 129
            +GRF+V++L  EG D   + VDP   T        D  + P V ++R   A   L  + 
Sbjct: 62  SLGRFVVQTLENEGLDCRHVAVDPTHPTGFQFKSRTDDGSDPQVEYFRRGSAASHLSIDS 121

Query: 130 ISEAFIASSKALLITGTHFSTDGVYKA-SIQALE-----YAEKHNVKRILDID--YRPVL 181
           I+ +        L+   H    G+  A S+ A E      +      R L  D   RP L
Sbjct: 122 IAPS--------LLEARHLHATGIVPALSVTAREMSFELMSRMRAAGRSLSFDPNMRPSL 173

Query: 182 WGLAGKADGETRFVADQQVSQHVQKILPRFDLIVGTEEEFLIAGGSEDLLSALRNVRRLT 241
           WG        T      +++     +LP      G  E  L+  G +D            
Sbjct: 174 WG-----SESTMITEINRLAALAHWVLP------GLGEGRLLT-GFDDPADIAAFYLDQG 221

Query: 242 AATLVVKLGPQGCTVIHGVIPVRLEDGAIYPGVRV-EVLNVLGAGDAFMSGFLSGWLEDA 300
           A  +V+KLG  G           L+ G I PGV V +V++ +GAGD F  G +S  LE  
Sbjct: 222 AELVVIKLGADG-----AYYRTALDQGVI-PGVPVAQVVDTVGAGDGFAVGLISALLEGQ 275

Query: 301 SDERCCQLANACGGLVVSRHACAPAMPTRAELDYLFN 337
           +     Q AN  G   V        +PTR EL   FN
Sbjct: 276 AITEAVQRANWIGSRAVQSRGDMEGLPTRIELLAEFN 312


Lambda     K      H
   0.321    0.138    0.412 

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: 437
Number of extensions: 19
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: 645
Length of database: 324
Length adjustment: 33
Effective length of query: 612
Effective length of database: 291
Effective search space:   178092
Effective search space used:   178092
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 bits)
S2: 51 (24.3 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