GapMind for catabolism of small carbon sources

 

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

Align putrescine-2-oxoglutarate transaminase (EC 2.6.1.82) (characterized)
to candidate 353284 BT3758 acetylornithine aminotransferase (NCBI ptt file)

Query= BRENDA::P42588
         (459 letters)



>FitnessBrowser__Btheta:353284
          Length = 373

 Score =  199 bits (507), Expect = 1e-55
 Identities = 127/373 (34%), Positives = 207/373 (55%), Gaps = 24/373 (6%)

Query: 78  DTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAKQPLHSQELLDPLRAMLAKTLAALT 137
           D  G E++D  GG  + ++GH +P  V  + NQ+A    +S  +++ L+  +A+ L  ++
Sbjct: 24  DENGTEYLDLYGGHAVISIGHAHPHYVEMISNQVATLGFYSNSVINKLQQQVAERLGKIS 83

Query: 138 PGKLKYSFFC-NSGTESVEAALKLAKAYQSPRGKFTFIATSGAFHGKSLGALSATAKSTF 196
            G   YS F  NSG E+ E ALKLA  Y    G+   I+ S AFHG++  A+ AT   T 
Sbjct: 84  -GYEDYSLFLINSGAEANENALKLASFYN---GRTKVISFSKAFHGRTSLAVEATNNPTI 139

Query: 197 RKPFMPLLPGFRHVPFGNIEAMRTALNECKKTGDDVAAVILEPIQGEGGVILPPPGYLTA 256
             P         ++P  +IEAM+  L +      DV AVI+E IQG GG+ +P   ++  
Sbjct: 140 IAPINNN-GHVTYLPLNDIEAMKQELAK-----GDVCAVIIEGIQGVGGIKIPTTEFMQE 193

Query: 257 VRKLCDEFGALMILDEVQTGMGRTGKMFACEHENVQPDILCLAKALGGGVMPIGATIATE 316
           +RK+C E G ++ILDE+Q+G GR+GK FA ++ ++QPDI+ +AK +G G    G  I+  
Sbjct: 194 LRKVCTETGTILILDEIQSGYGRSGKFFAHQYNHIQPDIITVAKGIGNGFPMAGVLIS-- 251

Query: 317 EVFSVLFDNPFLHTTTFGGNPLACAAALATINVLLEQNLPAQAEQKGDMLLDGFRQLARE 376
            +F  ++       TTFGGN LAC+AALA ++V+ + NL   A+  GD LL+  ++  + 
Sbjct: 252 PMFKPVYGQ---LGTTFGGNHLACSAALAVMDVIEQDNLVENAKAVGDYLLEELKKFPQ- 307

Query: 377 YPDLVQEARGKGMLMAIEFVDNEIGYNFASEMFRQRVLVAGTLNNAKTIRIEPPLTLTIE 436
               ++E RG+G+++ +EF   E      S +     +  G  +    +R+ PPL L++E
Sbjct: 308 ----IKEVRGRGLMIGLEF--EEPIKELRSRLIYDEHVFTGA-SGTNVLRLLPPLCLSME 360

Query: 437 QCELVIKAARKAL 449
           + +  +   ++ L
Sbjct: 361 EADEFLARFKRVL 373


Lambda     K      H
   0.320    0.135    0.393 

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: 348
Number of extensions: 14
Number of successful extensions: 4
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: 459
Length of database: 373
Length adjustment: 31
Effective length of query: 428
Effective length of database: 342
Effective search space:   146376
Effective search space used:   146376
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 (21.8 bits)
S2: 50 (23.9 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