GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Bacillus altitudinis 41KF2b

Align 2-methylcitrate synthase; 2-MCS; MCS; Citrate synthase; EC 2.3.3.5; EC 2.3.3.16 (characterized)
to candidate WP_008346063.1 BA79_RS07510 citrate synthase

Query= SwissProt::Q8EJW2
         (375 letters)



>NCBI__GCF_000691145.1:WP_008346063.1
          Length = 372

 Score =  291 bits (745), Expect = 2e-83
 Identities = 156/369 (42%), Positives = 230/369 (62%), Gaps = 7/369 (1%)

Query: 11  GLRGQSAGETALSTVGVSGSGLTYRGYDVKDLAENATFEEVAYLILYGELPTTAQLAAYK 70
           GL G  A  +++S++      LTY GY++ DL E ATFEE+ YL+ + +LP   +L+  K
Sbjct: 6   GLEGIVATTSSVSSI--IDDTLTYVGYNIDDLTEKATFEEIVYLLWHLKLPNEQELSELK 63

Query: 71  TKLKGMRGLPQALKEVLERIPADA-HPMDVMRTGCSMLGNLEAEHSFSEQS---QIADRL 126
            +L     +PQ + E  +    D  HPM  +RT  S+LG L+ E    ++    + A RL
Sbjct: 64  QQLNENAHIPQEIIEHFKSYSLDGVHPMSAIRTAVSLLGLLDDESEIMDKEANYRKAIRL 123

Query: 127 LAAFPSIICYWYRFSHDGVRIDTETDDDQIGAHFLHLLHGKAPSALHTKVMDVSLILYAE 186
            A    ++  + R    G+      ++    A+FL++L+G+ PS +  + +D +LIL+A+
Sbjct: 124 QAKISGLVAAFSRI-RKGLEPVQPKEEYSYAANFLYMLNGEEPSPVEIEAIDKALILHAD 182

Query: 187 HEFNASTFTARVCASTLSDMHSCVTGAIGSLRGPLHGGANEAAMELIQDMKDEADARDVL 246
           HE NASTFTARVC +TLSD++S VT AIG+L+GPLHGGANE  M+++ ++ +  +    +
Sbjct: 183 HELNASTFTARVCVATLSDIYSGVTAAIGALKGPLHGGANEGVMKMLSEIGEVENVDSYI 242

Query: 247 MGKLERKEKIMGFGHAIYRDSDPRNAIIKEWSEKLAADYGDDRLYRVSVACEALMWEQKK 306
            GKLE+KEKIMGFGH +YR  DPR   +KE S++L    G+ + Y +SV  E ++  +K 
Sbjct: 243 HGKLEKKEKIMGFGHRVYRQGDPRAKHLKEMSQRLTNLTGEPKWYEMSVRAEEIVTSEKN 302

Query: 307 LFCNADFFHASAYHFMGIPTKLFTPIFVCSRVTGWTAHVMEQRSNNRIIRPSADYVGVSP 366
           L  N DF+ AS YH +GI   LFTPIFV SR +GW AH++EQ  NNR+IRP ADY+G   
Sbjct: 303 LPPNVDFYSASVYHSLGIDHDLFTPIFVISRFSGWIAHILEQYDNNRLIRPRADYIGPDL 362

Query: 367 RKVIPIANR 375
           +  +PI+ R
Sbjct: 363 QTFVPISER 371


Lambda     K      H
   0.320    0.134    0.401 

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: 321
Number of extensions: 13
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: 375
Length of database: 372
Length adjustment: 30
Effective length of query: 345
Effective length of database: 342
Effective search space:   117990
Effective search space used:   117990
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 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