GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Pseudomonas benzenivorans DSM 8628

Align 2-methylcitrate synthase; 2-MCS; MCS; Citrate synthase; EC 2.3.3.5; EC 2.3.3.16 (characterized)
to candidate WP_090438375.1 BLS63_RS00670 2-methylcitrate synthase

Query= SwissProt::Q937N9
         (385 letters)



>NCBI__GCF_900100495.1:WP_090438375.1
          Length = 387

 Score =  651 bits (1679), Expect = 0.0
 Identities = 318/387 (82%), Positives = 345/387 (89%), Gaps = 2/387 (0%)

Query: 1   MSEAQPLVTP--KPKKSVALSGVTAGNTALCTVGRTGNDLHYRGYDILDIAETCEFEEIA 58
           MS      TP  KPKKSVALSG TAGNTALCTVGRTGNDLHYRGYD+LD A  CEFEEIA
Sbjct: 1   MSTTPETTTPGFKPKKSVALSGTTAGNTALCTVGRTGNDLHYRGYDVLDFANRCEFEEIA 60

Query: 59  HLLVHGKLPTKSELAAYKAKLKSLRGLPANVKAALEWVPASAHPMDVMRTGVSVLGTVLP 118
           HLLVHGKLP  +ELA YKAKLK+LRG+PA +KA+LE +P SAHPMDVMRT VSVLG + P
Sbjct: 61  HLLVHGKLPNVAELAGYKAKLKALRGIPAALKASLEQLPPSAHPMDVMRTAVSVLGCMSP 120

Query: 119 EKEDHNTPGARDIADRLMASLGSMLLYWYHYSHNGRRIEVETDDDSIGGHFLHLLHGEKP 178
           EKEDHN PGARDIAD+LMASLGS LLYWYH+SHNG+RI+VETDDDSIGGHFLHLLHGEKP
Sbjct: 121 EKEDHNHPGARDIADKLMASLGSALLYWYHFSHNGKRIDVETDDDSIGGHFLHLLHGEKP 180

Query: 179 SALWERAMNTSLNLYAEHEFNASTFTARVIAGTGSDMYSSISGAIGALRGPKHGGANEVA 238
              W RAM+TSLNLYAEHEFNASTFT+RVIAGTGSDM+S I+GAIGALRGPKHGGANEVA
Sbjct: 181 RESWVRAMHTSLNLYAEHEFNASTFTSRVIAGTGSDMFSCIAGAIGALRGPKHGGANEVA 240

Query: 239 FEIQKRYDNPDEAQADITRRVENKEVVIGFGHPVYTTGDPRNQVIKEVAKKLSKDAGSMK 298
           FEIQKRYDNPDEA+ADI  RVE KEVVIGFGHPVYT  DPRN+VIKEVA++LS +  + K
Sbjct: 241 FEIQKRYDNPDEAEADIRARVEKKEVVIGFGHPVYTVADPRNKVIKEVARELSAEQSNTK 300

Query: 299 MFDIAEALETVMWDIKKMFPNLDWFSAVSYHMMGVPTAMFTALFVIARTSGWAAHIIEQR 358
           MFDIAE LE+VMWDIKKMFPNLDWFSAVSYHMMGVPTAMFT LFVIARTSGW++H+IEQR
Sbjct: 301 MFDIAERLESVMWDIKKMFPNLDWFSAVSYHMMGVPTAMFTPLFVIARTSGWSSHVIEQR 360

Query: 359 IDNKIIRQSANYTGPENLKFVPLKDRK 385
           ID KIIR SANY GPE+LKFVPLKDRK
Sbjct: 361 IDGKIIRPSANYVGPEDLKFVPLKDRK 387


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: 587
Number of extensions: 10
Number of successful extensions: 1
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: 385
Length of database: 387
Length adjustment: 30
Effective length of query: 355
Effective length of database: 357
Effective search space:   126735
Effective search space used:   126735
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