GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aguA in Phaeobacter inhibens BS107

Align agmatine deiminase (EC 3.5.3.12) (characterized)
to candidate GFF2608 PGA1_c26490 putative agmatine deiminase

Query= BRENDA::O86509
         (339 letters)



>FitnessBrowser__Phaeo:GFF2608
          Length = 356

 Score =  188 bits (477), Expect = 2e-52
 Identities = 118/338 (34%), Positives = 171/338 (50%), Gaps = 16/338 (4%)

Query: 3   FRMPPEWAPHERTWMAWPGPNATFTDAEELAGARAAWASVARAVRRFEPVTMVHGPGQAA 62
           F +PPE APH+R++M WP       D      A+ + A +A A+  FEPVT++      +
Sbjct: 30  FFVPPEEAPHQRSFMQWPVSRKVHPDPVFRDMAQQSIADIANAIAAFEPVTVLAAAADHS 89

Query: 63  TARELLGPDVDLVERELDDAWMRDIGPTFVTDGRGGLAAVDWVFNGWGAQDWARWEHDAE 122
            AR  L  DV+L +   +D W RD GP FV DG GG+A     FNGWG + + R   D++
Sbjct: 90  GARAKLSADVELWDIPTEDLWCRDSGPIFVIDGAGGMAISHIQFNGWGKKQFNR--RDSQ 147

Query: 123 IARHVADLAAAPVLSSPLVNEGGAIHVDGEGTVLLTDTVQLGSGRNPGWSREEVEAEIHA 182
           IA  VA+    P+L + L  E G +  DG G ++  ++  +   RNPG SR ++E  +  
Sbjct: 148 IAERVAERLGLPLLPTGLHGEAGGVEQDGHGLLMAHESSWVNKNRNPGLSRAQIEQRLLE 207

Query: 183 KLGTTTAIWLPHGLAGDYGRYGTQGHVDIVAAFARPGTVVVHSQRDPRHPDHERSQLYLE 242
             G    IW      G  G   T  H+D +A F  PG V+++    P  PD      ++ 
Sbjct: 208 AYGADRMIW----AEGVRGEDITDYHIDSLARFTGPGRVLMNL---PDAPD-SADPFHMA 259

Query: 243 IL--RGRTDARGRRLEVVEVPAPTVLKDEEGEWADYSYINHYVCNGGVVLCAFGD-PNDE 299
            L    R  A G  +EV  +P P + + +  ++   SY N+YVCNG V+   FGD   DE
Sbjct: 260 ALDTHDRLIAAGLGVEV--IPEPHIRRIKSFDFV-ASYANYYVCNGAVIAAEFGDRETDE 316

Query: 300 LAAGIFRRLFPERTVTLVDARTIFAGGGGIHCITQQQP 337
           +A     R +P R +  ++   +   GGGIHC TQQ P
Sbjct: 317 IARNALARHYPGREIVTLNVDPLGELGGGIHCATQQMP 354


Lambda     K      H
   0.319    0.137    0.443 

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: 403
Number of extensions: 27
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: 339
Length of database: 356
Length adjustment: 29
Effective length of query: 310
Effective length of database: 327
Effective search space:   101370
Effective search space used:   101370
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: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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