GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Azospirillum brasilense Sp245

Align 2-methylcitrate synthase (EC 2.3.3.5) (characterized)
to candidate AZOBR_RS25925 AZOBR_RS25925 type II citrate synthase

Query= BRENDA::Q8NSL1
         (383 letters)



>FitnessBrowser__azobra:AZOBR_RS25925
          Length = 427

 Score =  187 bits (476), Expect = 4e-52
 Identities = 129/379 (34%), Positives = 187/379 (49%), Gaps = 20/379 (5%)

Query: 21  TAVSKVMPETNSLTYRGYAVEDLVENCSFEEVFYLLWHGELPTAQQLAEFNERGRSYRSL 80
           +A++ +  +   L +RGYA++DL ENC + EV +LL  GELP  QQ  EF ER  +Y ++
Sbjct: 52  SAITYIDGDEGILLHRGYAIQDLAENCDYLEVCHLLLRGELPNPQQKEEF-ERTITYHTM 110

Query: 81  DAGLISLIHS-LPKEAHPMDVMRTAVSYMGTKDSEYFTT----DSEHIRKVGHTLLAQLP 135
               +S  +S   ++AHPM VM       G   + Y  +    D        H L+A++P
Sbjct: 111 VHEQLSRFYSGFRRDAHPMAVM---CGVTGALSAFYHDSTDILDPRQRMIAAHRLIAKMP 167

Query: 136 MVLAMDIRRRKGLDIIAPDSSKSVAENLLSMVFGTGPESPASNPADVRDFEKSLILYAEH 195
            + AM  +   G   + P +  S AEN L M FGT  E+   +P   R  +K  IL+A+H
Sbjct: 168 TMAAMAYKYSVGQPFMYPRNDLSYAENFLYMTFGTPCETWKVDPVLARAMDKIFILHADH 227

Query: 196 SFNASTFTARVITSTKSDVYSAITGAIGALKGPLHGGANEFVMHTMLAIDDPNKAAAWIN 255
             NAST T R+  S+ ++ ++ I   I AL GP HGGANE V+  +  I    +   +I 
Sbjct: 228 EQNASTSTVRLAGSSHANPFACIASGIAALWGPAHGGANEAVLLMLEEIGSVERIPKFIK 287

Query: 256 NALDNKNV--VMGFGHRVYKRGDSRVPSMEKSFRE----LAARHDGEKWVAMYEN---MR 306
            A D  +   +MGFGHRVYK  D R   M ++  E    L  + +    +AM      + 
Sbjct: 288 RAKDKNDPFRLMGFGHRVYKNYDPRAKIMRQTCYEVLDVLGIKDEPHLAIAMELEKIALE 347

Query: 307 DAMDARTGIKPNLDFPAGPAYHLLGFPVDFFTPLFVIARVAGWTAHIVEQYEN--NSLIR 364
           D       + PN+DF +G     +GFP   FT LF +AR  GW +   E  E+    + R
Sbjct: 348 DPYFVEKKLYPNVDFYSGIILKAMGFPTSMFTVLFALARTVGWISQWQEMIEDPQQKIGR 407

Query: 365 PLSEYNGEEQREVAPIEKR 383
           P   Y G   R   P+ KR
Sbjct: 408 PRQLYTGNPGRAFVPLNKR 426


Lambda     K      H
   0.318    0.133    0.388 

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: 394
Number of extensions: 16
Number of successful extensions: 4
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: 383
Length of database: 427
Length adjustment: 31
Effective length of query: 352
Effective length of database: 396
Effective search space:   139392
Effective search space used:   139392
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 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