GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Marinobacter adhaerens HP15

Align 2-methylcitrate synthase (EC 2.3.3.5) (characterized)
to candidate GFF1554 HP15_1516 type II citrate synthase

Query= BRENDA::Q9I5E3
         (375 letters)



>FitnessBrowser__Marino:GFF1554
          Length = 424

 Score =  196 bits (499), Expect = 8e-55
 Identities = 122/381 (32%), Positives = 204/381 (53%), Gaps = 26/381 (6%)

Query: 11  GLRGQVAGQTALSTVGQEGAGLTYRGYDVRDLAAAAIFEEVAYLLLYGELPNKQQLDAYL 70
           G     A ++A++ +      L +RGY +  LA  + + EV YLLL+GELP+ ++   + 
Sbjct: 45  GFVSTAACESAITYIDGANGVLLHRGYPIEQLAEHSDYLEVCYLLLHGELPSAEENQKFH 104

Query: 71  KKLQGQRDLPQALKEVLERIPKDAHPMDVMRTGASVLGTL------EPELSFDQQRDV-A 123
             ++    L   ++   +   +DAHPM +M     V+G L      E +++  +QR++ A
Sbjct: 105 DTIKNHTMLHDQMRNFFQGFRRDAHPMAIM---CGVVGALSAFYHGEMDVASQEQREITA 161

Query: 124 DRLLAAFPAIMTYWYRFTHEGQRIDCNSDEPTIGGHFLALLHGK-----KPSELHVKVMN 178
            RL+A  P I  + Y++   GQ      ++ +   +FL ++ G      KP+ +  K M+
Sbjct: 162 HRLIAKMPTIAAWCYKYAI-GQPFIYPRNDLSYSENFLQMMFGVPCEEYKPNPILAKAMD 220

Query: 179 VSLILYAEHEFNASTFTARVCASTLSDLYSCVTGAIGSLRGPLHGGANEAAMELIERFSS 238
              IL+A+HE NAST T R+  ST ++ Y+C+   I +L GP HGGANEA ++++     
Sbjct: 221 KIFILHADHEQNASTSTVRLAGSTGANPYACIASGIAALWGPAHGGANEAVLDMLAEIGD 280

Query: 239 PQEATAELLKMLERKD--KIMGFGHAIYKDSDPRNEVIKGWSKQLADEVG--DKVLFAVS 294
                  + K  ++ D  ++MGFGH +YK+ DPR +V+   + ++  E+G  +  L  ++
Sbjct: 281 ESNIEKFIAKAKDKDDPFRLMGFGHRVYKNFDPRAKVMAETAHEVLTELGLENDPLLKIA 340

Query: 295 EAIDKTMWE-----QKKLFPNADFYHASAYHFMGIPTKLFTPIFVCSRTSGWTAHVFEQR 349
           + ++K   E     ++KL+PN DFY       +GIPT +FT IF  SRT GW +H  E  
Sbjct: 341 QRLEKIALEDEYFVKRKLYPNVDFYSGLILKAIGIPTSMFTVIFALSRTIGWFSHWNEMV 400

Query: 350 ANN-RIIRPSAEYTGVEQRAF 369
           + + RI RP   YTG + R +
Sbjct: 401 SGDYRIGRPRQLYTGSDSRDY 421


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: 379
Number of extensions: 23
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: 424
Length adjustment: 31
Effective length of query: 344
Effective length of database: 393
Effective search space:   135192
Effective search space used:   135192
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 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