GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kguD in Clostridium tyrobutyricum FAM22553

Align 2-ketogluconate 6-phosphate reductase (EC 1.1.1.43) (characterized)
to candidate WP_017751038.1 PN53_RS06710 D-glycerate dehydrogenase

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



>NCBI__GCF_000816635.1:WP_017751038.1
          Length = 323

 Score =  269 bits (687), Expect = 8e-77
 Identities = 148/315 (46%), Positives = 201/315 (63%), Gaps = 3/315 (0%)

Query: 3   KIVAWKSLPEDVLAYLQQHAQVV---QVDATQHDAFVAALKDADGGIGSSVKITPAMLEG 59
           K+   KS+PE+V  YL+Q+ +       +A         LKD +G + S  +I   +L  
Sbjct: 5   KVFIGKSIPEEVKNYLEQYCECKYWNSNNAISRQQLFKELKDVEGFLESGEEIDDELLLH 64

Query: 60  ATRLKALSTISVGFDQFDVADLTRRGIVLANTPDVLTESTADTVFSLILASARRVVELAE 119
           A  LK +S  SVG++ F +  +  +G++  NTP VL ++ AD VFSL++++ARR+ E+  
Sbjct: 65  APNLKIVSNSSVGYNNFHLQSMKSKGVIGTNTPFVLDDTVADLVFSLVISTARRIPEMDS 124

Query: 120 WVKAGHWQHSIGPALFGVDVQGKTLGIVGLGRIGGAVARRAALGFNMKVLYTNRSANPQA 179
           +VK G W+ S    L+GVDV   TLGI+G+GRIG  VA+RA LGF+M VLY NRS     
Sbjct: 125 YVKHGKWKSSDNENLYGVDVHHATLGIIGMGRIGQKVAKRARLGFSMDVLYHNRSRKFDT 184

Query: 180 EEAYGARRVELAELLATADFVCLQVPLTPETKHLIGAAELKSMKKSAILINASRGATVDE 239
           E   G + V L  LL  +D++ L +PLT ET HLI   E   MK +AI INASRG TV+E
Sbjct: 185 ESKLGVKYVSLDTLLIQSDYIVLMIPLTQETMHLIDYKEFDLMKDTAIFINASRGKTVNE 244

Query: 240 KALIEALQNGTIHGAGLDVFETEPLPSDSPLLKLANVVALPHIGSATHETRHAMARNAAE 299
           KALI+AL+N  I GAGLDV+  EP+  ++PLLK++NVV LPHIGSAT +TR +M   AAE
Sbjct: 245 KALIDALENKKILGAGLDVYAQEPVNKNNPLLKMSNVVTLPHIGSATEKTRFSMDMTAAE 304

Query: 300 NLVAALDGTLTSNIV 314
           NLV+ L G +   IV
Sbjct: 305 NLVSGLIGKIPKYIV 319


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: 220
Number of extensions: 9
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: 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.

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