GapMind for catabolism of small carbon sources

 

Alignments for a candidate for iolJ in Bacteroides thetaiotaomicron VPI-5482

Align 6-phospho-5-dehydro-2-deoxy-D-gluconate aldolase; DKGP aldolase; EC 4.1.2.29 (uncharacterized)
to candidate 351219 BT1691 fructose-bisphosphate aldolase (NCBI ptt file)

Query= curated2:Q5WKY5
         (293 letters)



>FitnessBrowser__Btheta:351219
          Length = 334

 Score =  177 bits (449), Expect = 3e-49
 Identities = 118/327 (36%), Positives = 165/327 (50%), Gaps = 42/327 (12%)

Query: 1   MGFVPMAPLLADAKKDSYAIGQFNINGLQWAKAILAGAESQQSPVIAAASDRLIDYLGGF 60
           +G V    + A A K  YAI  FN N ++  +AI+  A   +SPVI   S     Y    
Sbjct: 7   LGLVNTRDMFAKAIKGGYAIPAFNFNNMEQMQAIIKAAVETKSPVILQVSKGARQYANAT 66

Query: 61  QTVVAMMGAL--TDELGITVP-VVLHLDHGLSIERCKKAVDAGFSSVMFDGSHYPINENI 117
                  GA+    ELG   P +VLHLDHG + E CK  +D+GFSSVM DGSH P  EN+
Sbjct: 67  LLRYMAQGAVEYAKELGCAHPEIVLHLDHGDTFETCKSCIDSGFSSVMIDGSHLPYEENV 126

Query: 118 DMTKEVVAYAHAHNVSVEGEVGTVGGMEDGLMAE-IKYADVEECQRFVCETNVDALAAAL 176
            +TK+VV YAH  +V+VEGE+G + G+ED + ++   Y D EE   F   T  D+LA ++
Sbjct: 127 ALTKKVVEYAHQFDVTVEGELGVLAGVEDEVSSDHHTYTDPEEVIDFATRTGCDSLAISI 186

Query: 177 GSVHGKYKGEPK---------------LGFNEMAAISAS-TNVPLVLHGAS--------- 211
           G+ HG YK  P+               L F  + A+       P+VLHG+S         
Sbjct: 187 GTSHGAYKFTPEQCHIDPATGRMVPPPLAFEVLDAVMEKLPGFPIVLHGSSSVPEEEVET 246

Query: 212 ------------GIPDEQLQRAIKLGHAKININTECMIAWSDACRTTFAEQETAFEPRLL 259
                       GIP+E+L++A K    KINI+++  +A + A R TFAE+   F+PR  
Sbjct: 247 INKFGGALKAAIGIPEEELRKAAKSAVCKINIDSDSRLAMTAAIRKTFAEKPAEFDPRKY 306

Query: 260 LQEGLAMVQATVEKKI-KQFGAANKAA 285
           L      ++   + KI    G+ NK A
Sbjct: 307 LGPARDNMEKLYKHKILNVLGSDNKLA 333


Lambda     K      H
   0.317    0.132    0.378 

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: 251
Number of extensions: 16
Number of successful extensions: 5
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: 293
Length of database: 334
Length adjustment: 27
Effective length of query: 266
Effective length of database: 307
Effective search space:    81662
Effective search space used:    81662
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 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