GapMind for catabolism of small carbon sources

 

Alignments for a candidate for odc in Sinorhizobium fredii NGR234

Align Lysine/ornithine decarboxylase; LDC; EC 4.1.1.17; EC 4.1.1.18 (uncharacterized)
to candidate WP_012709425.1 NGR_RS25770 ornithine/lysine decarboxylase

Query= curated2:O50657
         (393 letters)



>NCBI__GCF_000018545.1:WP_012709425.1
          Length = 377

 Score =  217 bits (552), Expect = 5e-61
 Identities = 134/362 (37%), Positives = 193/362 (53%), Gaps = 19/362 (5%)

Query: 16  KRIPTPFLVASLDKVEENYQFMRRHLPRAGVFYAMKANPTPEILSLLAGLGSHFDVASAG 75
           +R   P LV  LD V +N++  R  LP + ++YA+KANP PEIL LLAGLGS+FD AS  
Sbjct: 13  RRPEGPCLVVDLDIVRDNFKAFRHALPDSAIYYAVKANPAPEILRLLAGLGSNFDCASVA 72

Query: 76  EMEILHELGVDGSQMIYANPVKDARGLKAAADYNVRRFTFDDPSEIDKMAKAVPGADVLV 135
           E+E+  E G   S++ Y N +K  R +  A    +  F  D   E++K+A+A PGA V  
Sbjct: 73  EIEMALEAGATPSRISYGNTIKKERDIARAHALGINLFAVDSHEEVEKVARAAPGARVFC 132

Query: 136 RIAVRNNKALVDLNTKFGAPVEEALDLLKAAQDAGLHAMGICFHVGSQSLSTAAYEEALL 195
           R+      A   L+ KFG   + A+D+L  A   GL + G+ FHVGSQ     A++ AL 
Sbjct: 133 RVLTDGEGAEWPLSRKFGCVPQMAVDVLVYAHQLGLVSYGVSFHVGSQMTKLDAWDAALA 192

Query: 196 VARRLFDEAEEMGMHLTDLDIGGGFP------VPDAKGLNVDLAAMMEAINKQIDRLFPD 249
            A+R+F + ++ G+ L  +++GGGFP      VP A+       A+  A+ K      P+
Sbjct: 193 DAKRVFGQLDKQGIELKMVNMGGGFPTKYLRDVPSAEAYG---QAIFGALKKHFGNNIPE 249

Query: 250 TAVWTEPGRYMCGTAVNLVTSVIGTKTRGEQP---WYILDEGIYGCFSGIMYDHWTYPLH 306
           T +  EPGR M G A  +   V+    + +     W  LD G +G  +  M +   YP+ 
Sbjct: 250 TII--EPGRGMVGNAGVIKAEVVLVSKKSDNDSHRWVFLDIGKFGGLAETMDEAIRYPIR 307

Query: 307 CFGKGNK-KPSTFGGPSCDGIDVLYRDFMAP---ELKIGDKVLVTEMGSYTSV-SATRFN 361
                ++ +P    GP+CD  DVLY   M P    L IGD+VL+   G+YT+  SA  FN
Sbjct: 308 TARDADEMEPCVLAGPTCDSADVLYEKNMYPLPISLTIGDEVLIEGTGAYTTTYSAVAFN 367

Query: 362 GF 363
           GF
Sbjct: 368 GF 369


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: 393
Number of extensions: 28
Number of successful extensions: 3
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: 377
Length adjustment: 30
Effective length of query: 363
Effective length of database: 347
Effective search space:   125961
Effective search space used:   125961
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 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