GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gbuA in Cupriavidus basilensis 4G11

Align guanidinobutyrase subunit (EC 3.5.3.7) (characterized)
to candidate RR42_RS02455 RR42_RS02455 agmatinase

Query= metacyc::MONOMER-11557
         (320 letters)



>FitnessBrowser__Cup4G11:RR42_RS02455
          Length = 328

 Score =  470 bits (1210), Expect = e-137
 Identities = 225/318 (70%), Positives = 261/318 (82%)

Query: 3   PTVDKTLHQPLGGNEMPRFGGIATMLRLPHLQSAKGLDAAFIGVPLDIGTSLRSGTRFGP 62
           P  +  L QP+ GN MPRFGGIATM+RLP   S  GLDA F+GVP D+GTS R+G R GP
Sbjct: 9   PADEAGLFQPMSGNAMPRFGGIATMMRLPAAASTAGLDACFVGVPFDLGTSNRNGARLGP 68

Query: 63  RQIRAESVMIRPYNMATGAAPFDSLSVADIGDVAINTFNLLDAVRIIEEAYDEIVEHNVI 122
           RQIRAESV++RPYNMAT AAPFDSL VADIGDVA N +NL DA+  IE AY +I+     
Sbjct: 69  RQIRAESVLLRPYNMATRAAPFDSLRVADIGDVATNPYNLHDAIARIEAAYRDIIATGCR 128

Query: 123 PMTLGGDHTITLPILRALHKKHGKIGLVHIDAHADVNDHMFGEKIAHGTTFRRAVEEGLL 182
           P+ LGGDHT+TLPILRA+H +HG++GL+H+DAHADVND MFGEKIAHGT FRRAVEEGLL
Sbjct: 129 PIGLGGDHTVTLPILRAMHARHGRLGLIHVDAHADVNDTMFGEKIAHGTPFRRAVEEGLL 188

Query: 183 DCDRVVQIGLRAQGYTADDFNWSRRQGFRVVQAEECWHKSLEPLMAEVREKVGGGPVYLS 242
           DC RVVQIGLR  GY A+DF+W R+QGFRV+ AE CW++SL PLM E+  ++ GGPVY+S
Sbjct: 189 DCGRVVQIGLRGTGYAAEDFDWCRQQGFRVITAEACWYRSLAPLMEEIGMRLQGGPVYIS 248

Query: 243 FDIDGIDPAWAPGTGTPEIGGLTTIQAMEIIRGCHGLDLIGCDLVEVSPPYDTTGNTSLL 302
           FDIDGIDPA+APGTGTPEIGGLT  QA+EIIRG  GLD++G DLVEVSPPYD  G T+LL
Sbjct: 249 FDIDGIDPAYAPGTGTPEIGGLTVPQALEIIRGARGLDIVGADLVEVSPPYDPFGTTALL 308

Query: 303 GANLLFEMLCVLPGVVRR 320
           GANL FE+LCVLPGVV R
Sbjct: 309 GANLAFELLCVLPGVVYR 326


Lambda     K      H
   0.322    0.141    0.431 

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: 467
Number of extensions: 26
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: 320
Length of database: 328
Length adjustment: 28
Effective length of query: 292
Effective length of database: 300
Effective search space:    87600
Effective search space used:    87600
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 (21.9 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