GapMind for catabolism of small carbon sources

 

Aligments for a candidate for gbuA in Phaeobacter inhibens BS107

Align guanidinobutyrase subunit (EC 3.5.3.7) (characterized)
to candidate GFF1959 PGA1_c19920 agmatinase SpeB

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



>FitnessBrowser__Phaeo:GFF1959
          Length = 315

 Score =  416 bits (1069), Expect = e-121
 Identities = 195/311 (62%), Positives = 248/311 (79%)

Query: 10  HQPLGGNEMPRFGGIATMLRLPHLQSAKGLDAAFIGVPLDIGTSLRSGTRFGPRQIRAES 69
           +QP+ GN++ RF G  T +RLP   S  GLD A +GVP+DIGTS RSGTRFGP+QIRAES
Sbjct: 5   NQPISGNDLARFSGPNTFMRLPQATSLDGLDVAILGVPMDIGTSWRSGTRFGPKQIRAES 64

Query: 70  VMIRPYNMATGAAPFDSLSVADIGDVAINTFNLLDAVRIIEEAYDEIVEHNVIPMTLGGD 129
            MIRPYNM +GAAPFDSL++ DIGD+AINTF+L D++RII+E+Y  I+  +V P+ +GGD
Sbjct: 65  AMIRPYNMTSGAAPFDSLNIGDIGDLAINTFSLPDSLRIIQESYSAILASDVTPVAMGGD 124

Query: 130 HTITLPILRALHKKHGKIGLVHIDAHADVNDHMFGEKIAHGTTFRRAVEEGLLDCDRVVQ 189
           H+ITLPILRA+ +K+G + LVH+DAHADVND MFGE+  HGT FRRA EEGL+  D+  Q
Sbjct: 125 HSITLPILRAVAEKYGPVALVHVDAHADVNDDMFGERETHGTVFRRAYEEGLIVADKTYQ 184

Query: 190 IGLRAQGYTADDFNWSRRQGFRVVQAEECWHKSLEPLMAEVREKVGGGPVYLSFDIDGID 249
           IGLR  GY ADDF  ++R GF+   A E W++SL  + AE+R  +G  PVY+S+DID +D
Sbjct: 185 IGLRGTGYGADDFKEAQRWGFQHFPASELWNRSLHGMGAEIRRDIGNRPVYVSYDIDSLD 244

Query: 250 PAWAPGTGTPEIGGLTTIQAMEIIRGCHGLDLIGCDLVEVSPPYDTTGNTSLLGANLLFE 309
           PA+APGTGTPEIGGLTT QA+E+IR   GL+++GCD+VEVSPPYDT+GNT+L  ANLL+E
Sbjct: 245 PAYAPGTGTPEIGGLTTPQALELIRALRGLNIVGCDMVEVSPPYDTSGNTALTAANLLYE 304

Query: 310 MLCVLPGVVRR 320
           +LCVLPGV  +
Sbjct: 305 LLCVLPGVTTK 315


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: 402
Number of extensions: 13
Number of successful extensions: 1
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: 315
Length adjustment: 27
Effective length of query: 293
Effective length of database: 288
Effective search space:    84384
Effective search space used:    84384
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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