GapMind for catabolism of small carbon sources

 

Aligments for a candidate for cadA in Pseudomonas simiae WCS417

Align Lysine/ornithine decarboxylase; LDC; EC 4.1.1.17; EC 4.1.1.18 (uncharacterized)
to candidate GFF788 PS417_04005 ornithine decarboxylase

Query= curated2:O50657
         (393 letters)



>FitnessBrowser__WCS417:GFF788
          Length = 387

 Score =  180 bits (457), Expect = 5e-50
 Identities = 122/370 (32%), Positives = 190/370 (51%), Gaps = 12/370 (3%)

Query: 5   RLSEKEVKTLAKRIPTPFLVASLDKVEENYQFMRRHLPRAGVFYAMKANPTPEILSLLAG 64
           R +  ++K  A +  TPF+V     + + Y  +R     A V+YA+KANP  EI+ LL  
Sbjct: 11  RATFDKMKAFADKQETPFVVIDTAMISQAYDDLRAGFEFAKVYYAVKANPAVEIIDLLKE 70

Query: 65  LGSHFDVASAGEMEILHELGVDGSQMIYANPVKDARGLKAAADYNVRRFTFDDPSEIDKM 124
            GS FD+AS  E++ + + GV   ++ Y N +K ++ ++   +  VR F+ D  +++  +
Sbjct: 71  KGSSFDIASIYELDKVMDRGVSADRISYGNTIKKSKDIRYFYEKGVRLFSTDSEADLRNI 130

Query: 125 AKAVPGADVLVRIAVR-NNKALVDLNTKFGAPVEEALDLLKAAQDAGLHAMGICFHVGSQ 183
           AKA PG+ V VRI    +  A   L+ KFG   + A+DLL  A+D GL   GI FHVGSQ
Sbjct: 131 AKAAPGSKVYVRILTEGSTTADWPLSRKFGCQTDMAMDLLILARDLGLVPYGISFHVGSQ 190

Query: 184 SLSTAAYEEALLVARRLFDE-AEEMGMHLTDLDIGGGFPVPDAKGLNVDLAAMMEAINKQ 242
               + ++ A+   + +F+   EE G+HL  +++GGGFP       N  L    E I + 
Sbjct: 191 QRDISVWDAAIAKVKVIFERLKEEDGIHLKLINMGGGFPANYITRTN-SLETYAEEIIRF 249

Query: 243 IDRLFPD--TAVWTEPGRYMCGTAVNLVTSV--IGTKTR-GEQPWYILDEGIYGCFSGIM 297
           +   F D    +  EPGR +   A  LV+ V  +  K+R   + W   D G +      M
Sbjct: 250 LKEDFGDDLPEIILEPGRSLIANAGILVSEVVLVARKSRTAVERWVYTDVGKFSGLIETM 309

Query: 298 YDHWTYPLHCFGKGNKKPSTFGGPSCDGIDVLYRDF---MAPELKIGDKVLVTEMGSY-T 353
            +   +P+    KG  +     GP+CD  D++Y ++   +   L IGD++     G+Y T
Sbjct: 310 DEAIKFPIWTEKKGEMEEVVIAGPTCDSADIMYENYKYGLPLNLAIGDRLYWLSTGAYTT 369

Query: 354 SVSATRFNGF 363
           S SA  FNGF
Sbjct: 370 SYSAVEFNGF 379


Lambda     K      H
   0.320    0.137    0.407 

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: 398
Number of extensions: 19
Number of successful extensions: 4
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: 393
Length of database: 387
Length adjustment: 31
Effective length of query: 362
Effective length of database: 356
Effective search space:   128872
Effective search space used:   128872
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: 50 (23.9 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