GapMind for catabolism of small carbon sources

 

Alignments for a candidate for put1 in Azospirillum brasilense Sp245

Align proline dehydrogenase (EC 1.5.5.2) (characterized)
to candidate AZOBR_RS25515 AZOBR_RS25515 hypothetical protein

Query= BRENDA::Q5JFG7
         (386 letters)



>FitnessBrowser__azobra:AZOBR_RS25515
          Length = 379

 Score =  168 bits (426), Expect = 2e-46
 Identities = 116/383 (30%), Positives = 198/383 (51%), Gaps = 30/383 (7%)

Query: 10  SEITIIGGGIVGVTIAHELAKRGEEVTVI--EKRFIGSGSTFRCGTGIRQQFNDEANVQV 67
           ++I +IGGG  G++ A  L +   +++V+  ++       T RCG G R Q+    N+++
Sbjct: 3   ADIAVIGGGAYGLSAALWLRRLRPDLSVLLLDRSDFAGNETGRCGAGFRAQWGAAGNIRL 62

Query: 68  MKRSVELWKKYSEEYGFP----FQQTGYLFLLYDDEEVETFKRNIAIQNKFGVPTRLITP 123
            + S+  ++ ++EE+G+P    F+Q GYL L + +E+++  +RNIA+Q +FGV + L+T 
Sbjct: 63  CQESLPSYENFAEEFGYPEGIEFKQDGYLILAHGEEQLDQLRRNIALQARFGVDSALLTA 122

Query: 124 EEAKEIVPLLDISEVVAASWNPTDGKASPFHSTAKFALHAEEFGAKLVEYTEVKDFIIEN 183
           EE   + P L+ + VV  S+   DG  SPF     F   A   G  +     ++     N
Sbjct: 123 EEVARLAPGLNPAGVVGGSFCARDGSLSPFRVLDGFHRAALRSGVVIRHGVTIESIEPRN 182

Query: 184 GEIKGLKTSRGTIKTGIVVNATNAWAKLINAMAGIRTKIPIEPYKHQAVITQPIKKGSVK 243
           G  + L+    +I+ G VV AT+   ++   +  +   IP++PY +QA +T+P+    + 
Sbjct: 183 GAFR-LRAGGESIEAGRVVVATD--TRIPQLLGPLGIDIPVQPYPNQAFVTEPLPP-RLG 238

Query: 244 PMVISFRYGHAYLTQTSHGGII-------GGVGYEEGPTYDLNPTYEFLREVSYYFTKII 296
           P V+SF +   +L QT  G ++         +G +  PT DL P        + +   ++
Sbjct: 239 PCVVSFAH-EMFLNQTVRGSVVVVASDRRRALGADARPTADLFP------RAAAHAIDLL 291

Query: 297 PALRELLILRTWAGYYAKTPDSNPAIGKIEELSDYYIAAGFSGHGFMMAPAVAEMVADLI 356
           PAL    +LR+WAG Y+ TPD    +G+   L   ++A      GFM APA   ++A L+
Sbjct: 292 PALGTARLLRSWAGLYSITPDMLAVLGE-TALPGLFVALS-GAKGFMTAPAAGRLLAHLV 349

Query: 357 TKGKTDLPAWW--YDPYRFERGE 377
             G+  +P W+    P RF  GE
Sbjct: 350 -DGQA-VPDWFARLSPARFASGE 370


Lambda     K      H
   0.318    0.137    0.406 

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: 308
Number of extensions: 16
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: 386
Length of database: 379
Length adjustment: 30
Effective length of query: 356
Effective length of database: 349
Effective search space:   124244
Effective search space used:   124244
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: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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