GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Paraburkholderia phymatum STM815

Align 2-methylcitrate synthase (EC 2.3.3.5) (characterized)
to candidate WP_012405891.1 BPHY_RS33390 2-methylcitrate synthase

Query= BRENDA::Q2Z1A8
         (398 letters)



>NCBI__GCF_000020045.1:WP_012405891.1
          Length = 389

 Score =  669 bits (1727), Expect = 0.0
 Identities = 325/384 (84%), Positives = 348/384 (90%)

Query: 14  DATASEPAAPRVKKSVALSGVTAGNTALCTVGRTGNDLHYRGYDILDIAETCEFEEIAHL 73
           D       A + KKSVALSGVTAGNTALCTVG+TGNDLHYRGYDILDIA  CEFEE+A+L
Sbjct: 5   DNVTQSAGAFKPKKSVALSGVTAGNTALCTVGKTGNDLHYRGYDILDIAGACEFEEVAYL 64

Query: 74  LVHGKLPTKSELAAYKAKLKSLRGLPANVKAALEWVPASAHPMDVMRTGVSVLGTVLPEK 133
           LVHGKLP  +ELAAYK KLK+LRGLPANVKAALEW+PA+AHPMDVMRTGVSVLGTVLPEK
Sbjct: 65  LVHGKLPNVAELAAYKTKLKALRGLPANVKAALEWIPAAAHPMDVMRTGVSVLGTVLPEK 124

Query: 134 EDHNTPGARDIADRLMASLGSMLLYWYHYSHNGRRIEVETDDDSIGGHFLHLLHGEKPSA 193
           +DHN PGARDIAD+LMASLGSMLLYWYHYSHNG+RIEVETDDDSIGGHFLHLLHG +P  
Sbjct: 125 DDHNLPGARDIADKLMASLGSMLLYWYHYSHNGKRIEVETDDDSIGGHFLHLLHGVEPPK 184

Query: 194 LWERAMHTSLNLYAEHEFNASTFTARVIAGTGSDMYSSISGAIGALRGPKHGGANEVAFE 253
            W  AMH SLNLYAEHEFNASTFT RVIAGTGSDMYS+I+GAIGALRGPKHGGANEVAFE
Sbjct: 185 SWVDAMHVSLNLYAEHEFNASTFTGRVIAGTGSDMYSAITGAIGALRGPKHGGANEVAFE 244

Query: 254 IQKRYDNPDEAQADITRRVGNKEVVIGFGHPVYTTGDPRNQVIKEVAKKLSKDAGSMKMF 313
           IQ RY  PDEA+ADI RRV NKEVVIGFGHPVYT  DPRN+VIKEVAKKLSK+  +MK+F
Sbjct: 245 IQSRYQTPDEAEADIRRRVDNKEVVIGFGHPVYTISDPRNKVIKEVAKKLSKEQSNMKLF 304

Query: 314 DIAERLETVMWDIKKMFPNLDWFSAVSYHMMGVPTAMFTPLFVIARTSGWAAHIIEQRID 373
           DIAERLETVM D+KKMFPNLDWFSAVSYHMMGVPTAMFTPLFVI+RTSGWAAHIIEQRID
Sbjct: 305 DIAERLETVMADVKKMFPNLDWFSAVSYHMMGVPTAMFTPLFVISRTSGWAAHIIEQRID 364

Query: 374 NKIIRPSANYTGPENLKFVPIGKR 397
           NKIIRPSANYTGP+NL F P+ KR
Sbjct: 365 NKIIRPSANYTGPDNLAFAPLAKR 388


Lambda     K      H
   0.317    0.133    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: 619
Number of extensions: 12
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: 398
Length of database: 389
Length adjustment: 31
Effective length of query: 367
Effective length of database: 358
Effective search space:   131386
Effective search space used:   131386
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 Apr 09 2024. 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