GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Thiomicrorhabdus arctica DSM 13458

Align 2-methylcitrate synthase (EC 2.3.3.5) (characterized)
to candidate WP_083917336.1 F612_RS0106990 citrate synthase

Query= BRENDA::Q8X694
         (389 letters)



>NCBI__GCF_000381085.1:WP_083917336.1
          Length = 392

 Score =  235 bits (600), Expect = 1e-66
 Identities = 135/380 (35%), Positives = 213/380 (56%), Gaps = 17/380 (4%)

Query: 22  LSGVPAGNTALCTVGKSGNDLHYRGYDILDLAEHCEFEEVAHLLIHGKLPTRDELAAYKT 81
           L+GVPA  + +  +      L YRGYDI +LAEH  FEE   LL+ G+LPT +ELA + T
Sbjct: 7   LAGVPATESKISFIDGQKGILTYRGYDIQELAEHSSFEETTLLLLFGELPTAEELANFDT 66

Query: 82  KLKALRGLPANVRTVLEALPAASHPMDVMRTGVSALGCTLPEKEGHTVSGARDIAD---- 137
           +L+  R +  N+R +++ LP  +HPM +++  V++L    P  E   + GA +  D    
Sbjct: 67  ELRNNRRVKYNIREIMKNLPPTTHPMHMLQVVVASLASFYPSTE--YMKGATENQDYINS 124

Query: 138 ---KLLASLSSILLYWYHYSHNGERIQPETDDDSIGGHFLHLLHGEKPSQSWEKAMHISL 194
              K++A + +++  W H  +  + I P  D +    +FL+++ GE+P + W + +    
Sbjct: 125 VTVKIIAHMGTLVAMWEHMRNGYDPIPPRKDLN-YAENFLYMVTGEEPDKDWARLLDAIF 183

Query: 195 VLYAEHEFNASTFTSRVIAGTGSDMYSAIIGAIGALRGPKHGGANEVSLEIQQRYETPDE 254
           +L+AEH  NASTFT+ V   T ++  S I  AI +L GP HGGAN+  +E+ +    P+ 
Sbjct: 184 ILHAEHTINASTFTTMVTGSTLANPCSVISSAIASLSGPLHGGANQKVIEMLEEIGAPEN 243

Query: 255 AEADIRKRVESKEVVIGFGHPVYTIADPRHQVIKRVAKQLSQEGGSLKM---YNIADRLE 311
           A A I  R+    V+ G GH  Y   DPR  ++++++  L  EG S K+   +  A  +E
Sbjct: 244 ARAYIEDRLAKNRVIWGMGHREYKTKDPRASILQKLSSSL-LEGKSDKLSMAFQTALEVE 302

Query: 312 TVMWE---SKKMFPNLDWFSAVSYNMMGVPTEMFTPLFVIARVTGWAAHIIEQRQDNKII 368
            V  E    K ++PN+D++S + Y  MG    +FTP+F +AR  GW AH  EQ Q+NKI 
Sbjct: 303 KVCEELLGHKGVYPNVDFYSGILYKEMGFDVGIFTPIFAVARSAGWMAHWREQLQNNKIF 362

Query: 369 RPSANYVGPEDRQFVALDKR 388
           RP+  Y G  D  ++ ++ R
Sbjct: 363 RPTQIYSGSGDLCYLPVELR 382


Lambda     K      H
   0.317    0.133    0.394 

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: 377
Number of extensions: 18
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: 389
Length of database: 392
Length adjustment: 31
Effective length of query: 358
Effective length of database: 361
Effective search space:   129238
Effective search space used:   129238
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