GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Thiomicrospira microaerophila ASL8-2

Align 2-methylcitrate synthase (EC 2.3.3.5) (characterized)
to candidate WP_044411821.1 NA59_RS09995 citrate synthase

Query= BRENDA::P31660
         (389 letters)



>NCBI__GCF_000934765.1:WP_044411821.1
          Length = 397

 Score =  243 bits (620), Expect = 7e-69
 Identities = 134/379 (35%), Positives = 220/379 (58%), Gaps = 13/379 (3%)

Query: 22  LSGVPAGNTALCTVGKSGNDLHYRGYDILDLAKHCEFEEVAHLLIHGKLPTRDELAAYKT 81
           L+GVPA  + +  +      L YRGYDI++LA+   FEE   LL+ G+LPT  ELA +  
Sbjct: 7   LAGVPATESKISYIDGQKGVLTYRGYDIMELAEKSSFEETTLLLLFGELPTTSELADFDQ 66

Query: 82  KLKALRGLPANVRTVLEALPAASHPMDVMRTGVSALGCTLPEKE---GHTVSGA--RDIA 136
           +L+  R +  N+R +++ LP  +HPM +++  V++L    P  E   G T +     D+ 
Sbjct: 67  QLRDHRRVKYNIREIMKNLPETTHPMHMLQVVVASLASFYPSTEYMKGGTENQGYINDVT 126

Query: 137 DKLLASLSSILLYWYHYSHNGERIQPETDDDSIGGHFLHLLHGEKPSQSWEKAMHISLVL 196
            K++A +++++  W H  +  + I+P  D +    +FL+++ GE+P   W + +   L+L
Sbjct: 127 VKIIAHMATLVASWEHMRNGYDPIEPRKDLN-YAENFLYMVTGEEPDPDWARLLDACLIL 185

Query: 197 YAEHEFNASTFTSRVIAGTGSDMYSAIIGAIGALRGPKHGGANEVSLEIQQRYETPDEAE 256
           +AEH  NASTFT+ V   T ++  S I  AI +L GP HGGAN++ +E+ ++   P+ A 
Sbjct: 186 HAEHTINASTFTTMVTGSTLANPCSVISSAIASLSGPLHGGANQMVIEMLEKIGRPENAR 245

Query: 257 ADIRKRVENKEVVIGFGHPVYTIADPRHQVIKRVAKQL----SQEGGSLKMYNIADRLET 312
           A I  R+ NK+V+ G GH  Y   DPR  ++++++++L    S+ G    M+  A  +E 
Sbjct: 246 AYIEDRLANKKVIWGMGHREYKTKDPRATILQKLSEKLLTKKSKSGELSVMFETALEVER 305

Query: 313 VMWE---SKKMFPNLDWFSAVSYNMMGVPTEMFTPLFVIARVTGWAAHIIEQRQDNKIIR 369
           +  E    K ++PN+D++S + Y  MG   +MFT +F +AR  GW AH  EQ Q+NKI R
Sbjct: 306 ICEELLGHKGVYPNVDFYSGILYKEMGFDPKMFTSIFAVARSAGWMAHWREQLQNNKIFR 365

Query: 370 PSANYVGPEDRPFVALDKR 388
           P+  Y G  +  ++ LD+R
Sbjct: 366 PTQVYTGAGNSCYLPLDQR 384


Lambda     K      H
   0.317    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: 389
Number of extensions: 19
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: 389
Length of database: 397
Length adjustment: 31
Effective length of query: 358
Effective length of database: 366
Effective search space:   131028
Effective search space used:   131028
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 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