GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gbuA in Herbaspirillum seropedicae SmR1

Align guanidinobutyrase subunit (EC 3.5.3.7) (characterized)
to candidate HSERO_RS08555 HSERO_RS08555 agmatinase

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



>FitnessBrowser__HerbieS:HSERO_RS08555
          Length = 317

 Score =  473 bits (1218), Expect = e-138
 Identities = 226/316 (71%), Positives = 263/316 (83%)

Query: 5   VDKTLHQPLGGNEMPRFGGIATMLRLPHLQSAKGLDAAFIGVPLDIGTSLRSGTRFGPRQ 64
           ++  L+QPLGGN MPRFGGIATM+RLPH++   GLD  F+GVPLDIGTS RSGTRFGPRQ
Sbjct: 1   MEHALYQPLGGNVMPRFGGIATMMRLPHVEDPAGLDVGFVGVPLDIGTSNRSGTRFGPRQ 60

Query: 65  IRAESVMIRPYNMATGAAPFDSLSVADIGDVAINTFNLLDAVRIIEEAYDEIVEHNVIPM 124
           IR ESV++RPYNMAT AAPFDSL VAD+GDVA+N ++LLD+VR+IEEAYD I       +
Sbjct: 61  IRTESVLLRPYNMATRAAPFDSLKVADLGDVALNPYSLLDSVRMIEEAYDRIYATGCKTI 120

Query: 125 TLGGDHTITLPILRALHKKHGKIGLVHIDAHADVNDHMFGEKIAHGTTFRRAVEEGLLDC 184
           +LGGDHT+TLPILRAL +  G +GL+H+DAHADVND M GEKIAHGT FRRA EEGLLD 
Sbjct: 121 SLGGDHTLTLPILRALARYRGPVGLIHVDAHADVNDTMNGEKIAHGTPFRRAFEEGLLDP 180

Query: 185 DRVVQIGLRAQGYTADDFNWSRRQGFRVVQAEECWHKSLEPLMAEVREKVGGGPVYLSFD 244
            RVVQIGLR  GY ADDF+W R QGFRVVQAEECWH+SL PLM EVR ++G GPVYL+FD
Sbjct: 181 QRVVQIGLRGTGYHADDFDWCRAQGFRVVQAEECWHRSLAPLMEEVRAQMGDGPVYLTFD 240

Query: 245 IDGIDPAWAPGTGTPEIGGLTTIQAMEIIRGCHGLDLIGCDLVEVSPPYDTTGNTSLLGA 304
           IDG+DPA+APGTGTPEIGGLT  Q +EIIRGC GLD++  D+VEVSPPYD  G T+L+ A
Sbjct: 241 IDGLDPAFAPGTGTPEIGGLTVQQGLEIIRGCKGLDIVSADVVEVSPPYDQAGTTALVAA 300

Query: 305 NLLFEMLCVLPGVVRR 320
           NL +EMLC+LPGV  R
Sbjct: 301 NLAYEMLCILPGVTYR 316


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: 442
Number of extensions: 19
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: 320
Length of database: 317
Length adjustment: 27
Effective length of query: 293
Effective length of database: 290
Effective search space:    84970
Effective search space used:    84970
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