GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Trichormus variabilis ATCC 29413

Align 2-methylcitrate synthase (EC 2.3.3.5) (characterized)
to candidate WP_011319469.1 AVA_RS13735 citrate synthase

Query= BRENDA::Q9I5E3
         (375 letters)



>NCBI__GCF_000204075.1:WP_011319469.1
          Length = 378

 Score =  269 bits (687), Expect = 1e-76
 Identities = 139/371 (37%), Positives = 219/371 (59%), Gaps = 7/371 (1%)

Query: 11  GLRGQVAGQTALSTVGQEGAGLTYRGYDVRDLAAAAIFEEVAYLLLYGELPNKQQLDAYL 70
           GL G  A Q+++S V  +   L YRG  + DLA  + F E AYLL++GELP K++L  + 
Sbjct: 9   GLEGIPAAQSSISYVDGQKGILEYRGIRIEDLAQKSTFLETAYLLIWGELPTKEELQVFE 68

Query: 71  KKLQGQRDLPQALKEVLERIPKDAHPMDVMRTGASVLGTLEPELSFDQQ---RDVADRLL 127
           ++++  R +   ++++++  P+  HPMD ++  A+ LG              RD   RL+
Sbjct: 69  EEVRLHRRIKYRIRDMMKCFPESGHPMDALQASAAALGLFYSRRDLHNPVYIRDAVVRLI 128

Query: 128 AAFPAIMTYWYRFTHEGQRIDCNSDEPTIGGHFLALLHGKKPSELHVKVMNVSLILYAEH 187
           A  P ++   ++   +G       D+     +FL +L+ K+P  L  K+ ++ LIL+ EH
Sbjct: 129 ATIPTMVAA-FQLMRKGNDPVKPRDDLDYSANFLYMLNEKEPDALAAKIFDICLILHVEH 187

Query: 188 EFNASTFTARVCASTLSDLYSCVTGAIGSLRGPLHGGANEAAMELIERFSSPQEATAELL 247
             NASTF+ARV ASTL+D Y+ V  A+G+L GPLHGGANE  ++++E   S +   + + 
Sbjct: 188 TMNASTFSARVTASTLTDPYAVVASAVGTLGGPLHGGANEEVIQMLEEIGSVENVRSYVE 247

Query: 248 KMLERKDKIMGFGHAIYKDSDPRNEVIKGWSKQLADEVGDKVLFAVSEAIDKTMWEQ--- 304
           + L+RKDK+MGFGH +YK  DPR  +++G ++QL  + G    + +++ +++ + E+   
Sbjct: 248 ERLQRKDKLMGFGHRVYKVKDPRATILQGLAEQLFAKFGADKYYDIAQEMERVVEEKLGH 307

Query: 305 KKLFPNADFYHASAYHFMGIPTKLFTPIFVCSRTSGWTAHVFEQRANNRIIRPSAEYTGV 364
           K ++PN DFY    Y  MGIPT LFTPIF  +R +GW AH  EQ   NRI RP+  Y G 
Sbjct: 308 KGIYPNVDFYSGLVYRKMGIPTDLFTPIFAIARVAGWLAHWKEQLEENRIFRPTQVYNGK 367

Query: 365 EQRAFVPLEQR 375
               + P++QR
Sbjct: 368 HSVTYTPIDQR 378


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: 363
Number of extensions: 15
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: 375
Length of database: 378
Length adjustment: 30
Effective length of query: 345
Effective length of database: 348
Effective search space:   120060
Effective search space used:   120060
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 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