GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gbuA in Echinicola vietnamensis KMM 6221, DSM 17526

Align Guanidinobutyrase; GBase; EC 3.5.3.7; D-arginase; EC 3.5.3.10 (uncharacterized)
to candidate Echvi_3131 Echvi_3131 Arginase/agmatinase/formimionoglutamate hydrolase, arginase family

Query= curated2:Q8KZT5
         (353 letters)



>FitnessBrowser__Cola:Echvi_3131
          Length = 356

 Score = 94.7 bits (234), Expect = 3e-24
 Identities = 94/323 (29%), Positives = 142/323 (43%), Gaps = 55/323 (17%)

Query: 41  ADVTVVGVPFDSGVSYRPGARFGANHVREASRLLRPYNP----AWDVSPF-----ENIQV 91
           A V +V VP++  VSY PG   G   + +AS  +  +      AW +        EN+  
Sbjct: 33  ASVVIVPVPWEVTVSYAPGTANGPQAILDASSQVDLFQDDITDAWTMGIHMLPIPENVYS 92

Query: 92  AD------AGD----------------MAVNPFNINEAIET----IQQNALDLTANGSKL 125
            +      AG+                    P  I++A ++    + + A D    G  +
Sbjct: 93  NNTKYRILAGNYIDWLERGSPKEERERFGAVPALIDKACQSMNDWVYETAKDQLNQGKLV 152

Query: 126 VTLGGDHTIALPLLRAAAERAGEPIAMLHFDAHLDTWDTYFGAEYTHGTPFRRAVEEGIL 185
             +GGDH+  L  ++A +ER      +L  DAH D  D Y G  Y+H +     +   I 
Sbjct: 153 ALVGGDHSTPLGHIKALSERYSS-FGILQIDAHADLRDQYEGFNYSHASISHNFLN--IP 209

Query: 186 DTEAISHVGTRGPLYGKKD-LDDDHRFGFGIVTSADVY-----YQGVLETVAKIRDRIGN 239
             E +  VG R     + D +D D R    I T  D +     Y+GV  T   I D++  
Sbjct: 210 QVEKLVQVGVRDYCEEESDRIDGDDR----ITTFFDHHIKEQLYEGV--TWRTICDQVIA 263

Query: 240 ---RPLYISVDIDVLDPAHAPGTGTPEAGGITSRELLEIIRGF--RGMNLVGADVVEVAP 294
              R +YI++DID LDP   P TGTP  GG    +LL +++     G  ++G D+VEVAP
Sbjct: 264 SLPREIYITIDIDGLDPKLCPHTGTPVPGGFDLNQLLYLMKLIVKSGRKIIGFDLVEVAP 323

Query: 295 AYDHAEITGVAGSHVAYELVTLM 317
             D +E  G  G+ + Y +  LM
Sbjct: 324 GEDDSEWDGNVGARLLYRMSNLM 346


Lambda     K      H
   0.318    0.137    0.402 

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: 339
Number of extensions: 22
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 353
Length of database: 356
Length adjustment: 29
Effective length of query: 324
Effective length of database: 327
Effective search space:   105948
Effective search space used:   105948
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 (21.7 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