GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kguD in Azohydromonas australica DSM 1124

Align 2-ketogluconate 6-phosphate reductase (EC 1.1.1.43) (characterized)
to candidate WP_029000246.1 H537_RS0126340 D-glycerate dehydrogenase

Query= reanno::BFirm:BPHYT_RS11290
         (321 letters)



>NCBI__GCF_000430725.1:WP_029000246.1
          Length = 323

 Score =  277 bits (708), Expect = 3e-79
 Identities = 155/309 (50%), Positives = 198/309 (64%), Gaps = 3/309 (0%)

Query: 2   KKIVAWKSLPEDVLAYLQQHAQVVQVD---ATQHDAFVAALKDADGGIGSSVKITPAMLE 58
           K +V +++LP D+LA + +   VV  D     +   F+ AL  A G IGSS  +    L+
Sbjct: 4   KNVVVFRALPPDLLARITERHDVVVADPRRTEERQRFLDALPQAQGLIGSSFALDAQTLD 63

Query: 59  GATRLKALSTISVGFDQFDVADLTRRGIVLANTPDVLTESTADTVFSLILASARRVVELA 118
            A  L+ +S+ISVG D +++  L RRGI L NTP VLTE+TADT+F+LIL ++RR+VEL+
Sbjct: 64  RAPALEVISSISVGVDNYELPYLERRGITLCNTPGVLTETTADTLFALILCASRRLVELS 123

Query: 119 EWVKAGHWQHSIGPALFGVDVQGKTLGIVGLGRIGGAVARRAALGFNMKVLYTNRSANPQ 178
             V+ G W  +IG  LFG DV GKTLGI+G GRIG A+ARRAALGF M VLY +      
Sbjct: 124 NLVREGRWTRNIGEDLFGWDVHGKTLGILGFGRIGQALARRAALGFGMPVLYHDPFEVRV 183

Query: 179 AEEAYGARRVELAELLATADFVCLQVPLTPETKHLIGAAELKSMKKSAILINASRGATVD 238
            E +    R+ + E+L  AD V L +PL+  T+ L+GA E   MK  AI +N +RG  V 
Sbjct: 184 PELSGLVTRLPMDEVLQRADIVALTLPLSEATRGLMGAREFALMKSGAIFVNGARGGLVQ 243

Query: 239 EKALIEALQNGTIHGAGLDVFETEPLPSDSPLLKLANVVALPHIGSATHETRHAMARNAA 298
           E AL++AL NG +  A LDVF TEPLP  SPL     V  LPHIGSATHETR AMA  A 
Sbjct: 244 EDALLQALDNGPLRAAALDVFATEPLPQASPLRTHPRVTPLPHIGSATHETRRAMAELAT 303

Query: 299 ENLVAALDG 307
           ENL+A LDG
Sbjct: 304 ENLLAVLDG 312


Lambda     K      H
   0.317    0.131    0.366 

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: 263
Number of extensions: 12
Number of successful extensions: 3
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: 321
Length of database: 323
Length adjustment: 28
Effective length of query: 293
Effective length of database: 295
Effective search space:    86435
Effective search space used:    86435
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 (21.7 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Apr 09 2024. 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