GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aguA in Pedobacter sp. GW460-11-11-14-LB5

Align Putative agmatine deiminase; EC 3.5.3.12; Agmatine iminohydrolase (uncharacterized)
to candidate CA265_RS15455 CA265_RS15455 agmatine deiminase

Query= curated2:C1C6Q3
         (361 letters)



>FitnessBrowser__Pedo557:CA265_RS15455
          Length = 358

 Score =  246 bits (627), Expect = 9e-70
 Identities = 141/365 (38%), Positives = 203/365 (55%), Gaps = 34/365 (9%)

Query: 4   SPKKLGYHMPAEYEPHHGTLMIWPTRPGSWPFQGKAAKRAFTQIIETIAEGERVYLLVEQ 63
           SPK+ GY  PAE+  H  T + WP +  SWP + +     + Q I+ +AEGE+V + V+ 
Sbjct: 18  SPKQQGYAFPAEWAKHEATWLSWPHKEASWPDKIETIYEPYCQFIKAVAEGEKVRINVKD 77

Query: 64  --------AYLSEAQSYLGDKVVYLDIPTNDAWARDTGPTILVNDKGKKLAVDWAFNAWG 115
                   + L++  + L     Y +  TNDAW RD GP  L+    +K  VDW +NAWG
Sbjct: 78  EEMKAFAVSELTKVDADLSQIEFYFN-ETNDAWCRDHGPAFLLKGN-EKAVVDWGYNAWG 135

Query: 116 GTYDGLYQDYEEDDQVASRFAEALERPVYDAKPFVLEGGAIHSDGQGTILVTESCLLSPG 175
           G Y      ++ DD V ++ A   + P++     V+EGG++  +G GT+L T +CLL+  
Sbjct: 136 GKYP----PFDLDDVVPTKIANHFKLPLF-TPDIVMEGGSVEFNGAGTVLTTTACLLNEN 190

Query: 176 RNPNLTKEEIENTLLESLGAEKVIWLPYGIYQDETNEHVDNVAAFVGPAELVLAWTDDEN 235
           RNP+LTK +IE  LLE  G E+V+WL  GI  D+T+ H+D++  FV    ++     +  
Sbjct: 191 RNPHLTKAQIEQYLLEYYGQEQVLWLGDGIVGDDTDGHIDDITRFVNEDTVLTVVESNPL 250

Query: 236 DPQYAMSKADLELLEQETDAKGCHFTIHKLPIPAVRQVVTEEDLPGYIYEEGEEKRYAGE 295
           D  Y + + +L  L+      G    I +LP+P+    V  ED                 
Sbjct: 251 DENYLLLQENLAALKAMKLKDGRALNIVELPMPSP---VIHEDT---------------- 291

Query: 296 RLAASYVNFYIANKAVLVPQFEDVNDQVALDILSKCFPDRKVVGIPARDILLGGGNIHCI 355
           RL ASY NFYIAN AV+VP F+DVNDQ AL I+  CFPDRKV+GI + DI+ G G+ HC+
Sbjct: 292 RLPASYANFYIANAAVIVPVFDDVNDQKALAIIQGCFPDRKVIGINSVDIIWGLGSFHCL 351

Query: 356 TQQIP 360
           +QQ P
Sbjct: 352 SQQEP 356


Lambda     K      H
   0.316    0.136    0.413 

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: 409
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: 361
Length of database: 358
Length adjustment: 29
Effective length of query: 332
Effective length of database: 329
Effective search space:   109228
Effective search space used:   109228
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 49 (23.5 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