GapMind for catabolism of small carbon sources

 

Alignments for a candidate for patA in Shewanella loihica PV-4

Align putrescine-2-oxoglutarate transaminase (EC 2.6.1.82) (characterized)
to candidate 5210744 Shew_3172 4-aminobutyrate aminotransferase (RefSeq)

Query= BRENDA::P42588
         (459 letters)



>FitnessBrowser__PV4:5210744
          Length = 426

 Score =  203 bits (517), Expect = 8e-57
 Identities = 120/334 (35%), Positives = 188/334 (56%), Gaps = 20/334 (5%)

Query: 76  LVDTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAKQPLHSQELLDPLRAM--LAKTL 133
           L D +G+ +ID   G  + N GH +P VV+AV+ QL     H+  +++P  +   LA+ L
Sbjct: 34  LWDVEGKRYIDFGTGIAVCNTGHSHPKVVAAVKAQLDNFS-HTCVMVNPYESAVALAEQL 92

Query: 134 AALTPGKL-KYSFFCNSGTESVEAALKLAKAYQSPRGKFTFIATSGAFHGKSLGALSATA 192
             + PG   K + F  +G E+VE  +K+A+A+   RG    IA +G FHG++   ++ T 
Sbjct: 93  NRIAPGGSDKKAIFVTTGAEAVENCVKIARAHTGRRG---VIAFNGGFHGRTNLTMALTG 149

Query: 193 KST-FRKPFMPLLPGFRHVPFG------NIEAMRTALNECKKTGD---DVAAVILEPIQG 242
           K T ++  F P      H P+       +++    A+    K      DVAA+++EP+QG
Sbjct: 150 KITPYKHQFGPFAGDIFHAPYPVAFHGVSVKDSLKAIEHLFKVDIAPCDVAAIVVEPVQG 209

Query: 243 EGGVILPPPGYLTAVRKLCDEFGALMILDEVQTGMGRTGKMFACEHENVQPDILCLAKAL 302
           EGG    PP +L A+R LCD+ G ++++DE+QTG GRTGKMF+CEH  V+PD++ +AK +
Sbjct: 210 EGGFYAAPPEFLQALRALCDQHGIVLVMDEIQTGFGRTGKMFSCEHAGVEPDLMTMAKGI 269

Query: 303 GGGVMPIGATIATEEVFSVLFDNPFLHTTTFGGNPLACAAALATINVLLEQNLPAQAEQK 362
            GG  P+ A +   E+       P     T+GG+P+ C AALA + V+ E+ L  +A + 
Sbjct: 270 AGG-FPLAAVVGKSEIMDAPL--PGGLGGTYGGSPVGCVAALAVLEVMQEEQLVERAVKI 326

Query: 363 GDMLLDGFRQLAREYPDLVQEARGKGMLMAIEFV 396
           GD        L  +YP L+ E R +G ++A+E V
Sbjct: 327 GDSFNQALSALKEQYPQLIGEVRNQGAMIAMELV 360


Lambda     K      H
   0.320    0.135    0.393 

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: 474
Number of extensions: 25
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: 459
Length of database: 426
Length adjustment: 32
Effective length of query: 427
Effective length of database: 394
Effective search space:   168238
Effective search space used:   168238
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: 51 (24.3 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