GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Lactobacillus silagei IWT126

Align 2-methylcitrate synthase (EC 2.3.3.5) (characterized)
to candidate WP_089136259.1 CES79_RS02950 methylcitrate synthase

Query= BRENDA::Q9I5E3
         (375 letters)



>NCBI__GCF_002217945.1:WP_089136259.1
          Length = 360

 Score =  240 bits (613), Expect = 4e-68
 Identities = 138/361 (38%), Positives = 208/361 (57%), Gaps = 11/361 (3%)

Query: 11  GLRGQVAGQTALSTVGQEGAGLTYRGYDVRDLAAAAIFEEVAYLLLYGELPNKQQLDAYL 70
           GL G V  QT +S+   + A LTY GY +++L  A  FEEV +LL +  LP+  +L  + 
Sbjct: 6   GLAGVVVDQTKVSST--KNAVLTYAGYPIKELKDAP-FEEVVFLLWHTRLPSADELSEFR 62

Query: 71  KKLQGQRDLPQALKEVLERIPKDA-HPMDVMRTGASVLGTLEPELSFDQQRDVADRLLAA 129
           K+L  +  LP+   +++ RI  +  HPM ++RT  S+LGT       D  R +A +LL A
Sbjct: 63  KRLVSEMVLPEKTVQLITRITYEPQHPMSILRTTVSLLGTTNDVKRDDPPRILA-KLLTA 121

Query: 130 FPAIMTYWYRFTHEGQRIDCNSDEPTIGGHFLALLHGKKPSELHVKVMNVSLILYAEHEF 189
             AI+        +GQ I        +  +F+ L  G++P+   V + N  ++L+A+HEF
Sbjct: 122 IAAIIRI-----RDGQPIKHAQKGWGVVENFIYLFSGQRPTPERVAMFNTVMVLHADHEF 176

Query: 190 NASTFTARVCASTLSDLYSCVTGAIGSLRGPLHGGANEAAMELIERFSSPQEATAELLK- 248
           NASTFTARV AST +D YSC+T A+ +L+GPLHGGANE   +++E      +   + +K 
Sbjct: 177 NASTFTARVVASTQADYYSCLTAAVCALKGPLHGGANERVFKMLETIRDTGQDPVQYVKD 236

Query: 249 MLERKDKIMGFGHAIYKDSDPRNEVIKGWSKQLADEVGDKVLFAVSEAIDKTMWEQKKLF 308
            +    KIMGFGH IYK+ DPR  +++  ++++A E  +   F + E I   M++   L 
Sbjct: 237 QMASGHKIMGFGHRIYKNGDPRAVILREVARKIAHETDNDSYFVLQEQIKDYMFKATHLH 296

Query: 309 PNADFYHASAYHFMGIPTKLFTPIFVCSRTSGWTAHVFEQRANNRIIRPSAEYTGVEQRA 368
           PN D+Y A  YH   +  + FT +F   RT+GW AH+ EQ+A   +IRPS+EY G   R 
Sbjct: 297 PNVDYYTALIYHCFDLDKQTFTMMFAACRTAGWLAHIVEQQAEGCLIRPSSEYVGETNRH 356

Query: 369 F 369
           +
Sbjct: 357 Y 357


Lambda     K      H
   0.319    0.134    0.396 

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: 332
Number of extensions: 20
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: 375
Length of database: 360
Length adjustment: 30
Effective length of query: 345
Effective length of database: 330
Effective search space:   113850
Effective search space used:   113850
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: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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