GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Desulfacinum infernum DSM 9756

Align 2-methylcitrate synthase (EC 2.3.3.5) (characterized)
to candidate WP_073039145.1 BUB04_RS10620 citrate synthase

Query= BRENDA::Q9I5E3
         (375 letters)



>NCBI__GCF_900129305.1:WP_073039145.1
          Length = 397

 Score =  259 bits (661), Expect = 1e-73
 Identities = 148/381 (38%), Positives = 218/381 (57%), Gaps = 20/381 (5%)

Query: 1   MAEAKVLS-GAGLRGQVAGQTALSTVGQEGAGLTYRGYDVRDLAAAAIFEEVAYLLLYGE 59
           MAE  V +   GLRG     T +S +  E   L YRGY + DLA  + F E AYLLL+  
Sbjct: 1   MAEQTVRTKNIGLRGITVADTKISYIDGERGVLIYRGYKIEDLARNSTFPETAYLLLHEF 60

Query: 60  LPNKQQLDAYLKKLQGQRDLPQALKEVLERIPKDAHPMDVMRTGASVLGTLEPELSFDQQ 119
           LP  Q+L+++  K++  RDLP  + E ++  P++AHPMD ++    +L   +P+L+ D+ 
Sbjct: 61  LPTSQELESFEAKIREFRDLPAFVIEAMKTWPREAHPMDALQASIPLLAMADPDLA-DET 119

Query: 120 RD----VADRLLAAFPAIMTYWYRFTHEGQRIDCNSDEPTIGGHFLALLHGKKPSELHVK 175
           R+     A RL+A  PA++  W+R    G  +    D  T  G+FL  + GKKP E   +
Sbjct: 120 REGNVAKAIRLIARVPAVVAAWHRI-RRGLELPPPDDALTHAGNFLWQVFGKKPDEETAR 178

Query: 176 VMNVSLILYAEHEFNASTFTARVCASTLSDLYSCVTGAIGSLRGPLHGGANEAAMELIER 235
           VM+V LIL+A+H FNASTF  R   ST + +Y+ V   +G+L G LHGGAN   ME++++
Sbjct: 179 VMDVCLILHADHTFNASTFACREVVSTRAHMYAGVAAGVGALSGELHGGANARVMEMLQK 238

Query: 236 F--SSPQEATAELLKMLERKDKIMGFGHAIYKDSDPRNEVIKGWSKQLADEVGDKVLFAV 293
                  +  A + + L+RK++IMG GHA+YK  DPR  ++K  + QL ++ G K    +
Sbjct: 239 IDRDGVTDIAAWVRERLDRKERIMGMGHAVYKTLDPRARILKELAFQLGEKTGQKKWPEM 298

Query: 294 SEAIDKTMWEQKK------LFPNADFYHASAYHFMGIPTKLFTPIFVCSRTSGWTAHVFE 347
           +EAI++   E+ +      + PN DFY AS YH +G P  L T IF  SR +GW AH+ E
Sbjct: 299 TEAIERAAMEELQRRGKTGIQPNVDFYSASVYHILGFPGDLMTCIFAVSRIAGWCAHIIE 358

Query: 348 QR-----ANNRIIRPSAEYTG 363
           ++         + RP AEY G
Sbjct: 359 EKFGEAQGKPALYRPKAEYVG 379


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: 390
Number of extensions: 22
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: 397
Length adjustment: 30
Effective length of query: 345
Effective length of database: 367
Effective search space:   126615
Effective search space used:   126615
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