GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tpi in Phaeobacter inhibens BS107

Align triose-phosphate isomerase (EC 5.3.1.1) (characterized)
to candidate GFF1729 PGA1_c17530 phosphoglycerate kinase Pgk

Query= BRENDA::P36204
         (654 letters)



>FitnessBrowser__Phaeo:GFF1729
          Length = 396

 Score =  350 bits (897), Expect = e-101
 Identities = 186/387 (48%), Positives = 247/387 (63%), Gaps = 2/387 (0%)

Query: 9   VDLKGKRVIMRVDFNVPVKDGVVQDDTRIRAALPTIKYALEQGAKVILLSHLGRPKGEPS 68
           +DL GKRV++RVD NVPV+DG V DDTRI+   PTIK  L  G   ILL+H GRPKG+  
Sbjct: 9   MDLAGKRVLVRVDINVPVEDGRVTDDTRIQRVAPTIKDILAAGGTPILLAHFGRPKGKVV 68

Query: 69  PEFSLAPVAKRLSELLGKEVKFVPAVVGDEVKKAVEELKEGEVLLLENTRFHPGETKNDP 128
            E SL P+   L    G  V F     G   + AV+ L  G VLLLENTRFH GE KND 
Sbjct: 69  AEMSLRPLVPALEAAFGAPVTFAADCRGPAAEAAVQGLPAGGVLLLENTRFHAGEEKNDT 128

Query: 129 ELAKFWASLADIHVNDAFGTAHRAHASNVGIAQFIPSVAGFLMEKEIKFLSKVTYNPEKP 188
           +LA   A L DI+ NDAF  AHRAHAS   +A+ +P+ AG LM+ E+  L      P++P
Sbjct: 129 DLAAEMAKLGDIYCNDAFSAAHRAHASTEALARLLPACAGRLMQAELTALETALGQPQRP 188

Query: 189 YVVVLGGAKVSDKIGVITNLMEKADRILIGGAMMFTFLKALGKEVGSSRVEEDKIDLAKE 248
              V+GGAKVS K+ ++ NL+ K D ++IGG M  TFL A G +VG S  E D  D A+E
Sbjct: 189 VTAVVGGAKVSTKLELLGNLVGKVDNLVIGGGMANTFLAAQGIDVGKSLCEHDMADTARE 248

Query: 249 LLEKAKEKGVEIVLPVDAVIAQKIEPGVEKKVVRIDDGIPEGWMGLDIGPETIELFKQKL 308
           +L KA+++G +I+LPVD V+A++ + G + + V   D  P   M LD GP+T+      L
Sbjct: 249 ILSKAEDQGCKIILPVDVVVAREFKAGADNETVAA-DACPADAMILDAGPQTVAAVADTL 307

Query: 309 SDAKTVVWNGPMGVFEIDDFAEGTKQVALAIAALTEKGA-ITVVGGGDSAAAVNKFGLED 367
           S +KT++WNGPMG FEI  F   T   A   A+LT+ GA ++V GGGD+ AA+N+ G   
Sbjct: 308 STSKTLIWNGPMGAFEIAPFDAATNAAAQQAASLTKSGALVSVAGGGDTVAALNQAGAAA 367

Query: 368 KFSHVSTGGGASLEFLEGKELPGIASI 394
            F+++ST GGA LE++EGK LPG+A++
Sbjct: 368 DFTYISTAGGAFLEWMEGKTLPGVAAL 394


Lambda     K      H
   0.317    0.137    0.386 

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: 597
Number of extensions: 29
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: 654
Length of database: 396
Length adjustment: 34
Effective length of query: 620
Effective length of database: 362
Effective search space:   224440
Effective search space used:   224440
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 (21.6 bits)
S2: 52 (24.6 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