GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Methylovulum miyakonense HT12

Align 2-methylcitrate synthase (EC 2.3.3.5) (characterized)
to candidate WP_019865043.1 METMI_RS0104475 citrate (Si)-synthase

Query= BRENDA::Q8NSL1
         (383 letters)



>NCBI__GCF_000384075.1:WP_019865043.1
          Length = 433

 Score =  194 bits (493), Expect = 4e-54
 Identities = 122/361 (33%), Positives = 184/361 (50%), Gaps = 12/361 (3%)

Query: 29  ETNSLTYRGYAVEDLVENCSFEEVFYLLWHGELPTAQQLAEFNERGRSYRSLDAGLISLI 88
           E   L YRGY +E L E C+F EV YL+ +GELP + +LAEF      +  +   L +  
Sbjct: 65  EEGVLLYRGYPIEQLAEQCNFLEVCYLILNGELPASGELAEFQYNVTMHTMVHDQLTNFF 124

Query: 89  HSLPKEAHPMDVMRTAVSYMGTKDSEYFTTDSEHIRKVGHT-LLAQLPMVLAMDIRRRKG 147
               ++AHPM +M   V  +     +     S+  R++    L+A++P ++AM  +   G
Sbjct: 125 KGFRRDAHPMAIMVGVVGALSAFYHDALDIRSKKDREISAIRLIAKVPTIVAMCHKYSTG 184

Query: 148 LDIIAPDSSKSVAENLLSMVFGTGPESPASNPADVRDFEKSLILYAEHSFNASTFTARVI 207
           +  + P +  S  EN L M+  T  +   +NP  VR  E+ LIL+A+H  NAST T R+ 
Sbjct: 185 MPFMYPQNKLSYVENFLRMMHATPCDDYQANPVLVRALERILILHADHEQNASTSTVRLA 244

Query: 208 TSTKSDVYSAITGAIGALKGPLHGGANEFVMHTMLAIDDPNKAAAWINNALDNKNV--VM 265
            S+ ++ ++ IT  I  L G  HGGANE V++ +  I D ++   +I  A D  +   +M
Sbjct: 245 GSSGANPFACITAGIACLWGSAHGGANEAVLNMLEKIGDVSRIPEFIKKAKDKNDPFRLM 304

Query: 266 GFGHRVYKRGDSRVPSMEKSFRELAAR---HDGEKWVAMYENMRDAMDARTGIK----PN 318
           GFGHRVYK  D R   M  +  E+      HD + +    E  R A++    I+    PN
Sbjct: 305 GFGHRVYKNHDPRAKLMRATCHEVLTELGLHDNKLFALALELERIALEDEYFIEKKLYPN 364

Query: 319 LDFPAGPAYHLLGFPVDFFTPLFVIARVAGWTAHIVEQYEN--NSLIRPLSEYNGEEQRE 376
           +DF +G   H LG P + FT +F + R  GW AH  E   +    + RP   Y G  +R+
Sbjct: 365 VDFYSGIVLHALGIPTNMFTAMFAMGRTVGWIAHWDEMIADPEQKIGRPRQLYTGAVRRD 424

Query: 377 V 377
           V
Sbjct: 425 V 425


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: 386
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: 433
Length adjustment: 31
Effective length of query: 352
Effective length of database: 402
Effective search space:   141504
Effective search space used:   141504
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