GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Rhodomicrobium vannielii ATCC 17100

Align 2-methylcitrate synthase (EC 2.3.3.5) (characterized)
to candidate WP_013419463.1 RVAN_RS09210 2-methylcitrate synthase

Query= BRENDA::Q2Z1A8
         (398 letters)



>NCBI__GCF_000166055.1:WP_013419463.1
          Length = 397

 Score =  616 bits (1588), Expect = 0.0
 Identities = 296/381 (77%), Positives = 338/381 (88%)

Query: 17  ASEPAAPRVKKSVALSGVTAGNTALCTVGRTGNDLHYRGYDILDIAETCEFEEIAHLLVH 76
           A++ A P+ KKSVALSG+ AGNTALCTVGRTGNDLHYRGYDILD+AETCEFEEIAHLL+H
Sbjct: 5   ATKAAGPKPKKSVALSGIIAGNTALCTVGRTGNDLHYRGYDILDVAETCEFEEIAHLLIH 64

Query: 77  GKLPTKSELAAYKAKLKSLRGLPANVKAALEWVPASAHPMDVMRTGVSVLGTVLPEKEDH 136
           G LPT +EL AYK KLK+LRGLP+ V+ ALE +PA++HPMDV+R+GVS LG VLPE  DH
Sbjct: 65  GALPTPTELHAYKTKLKALRGLPSAVRTALEALPAASHPMDVLRSGVSALGCVLPEPADH 124

Query: 137 NTPGARDIADRLMASLGSMLLYWYHYSHNGRRIEVETDDDSIGGHFLHLLHGEKPSALWE 196
           N P ARD+ADRL+ASLGSMLLYW+H++HNGRRI+V TDDDSIGGHFLHLLHGE+P     
Sbjct: 125 NHPAARDVADRLLASLGSMLLYWHHFAHNGRRIDVHTDDDSIGGHFLHLLHGERPRESHV 184

Query: 197 RAMHTSLNLYAEHEFNASTFTARVIAGTGSDMYSSISGAIGALRGPKHGGANEVAFEIQK 256
           RAMHTSL LYAEHEFNASTFTAR IA TGSD+YS+++GAIGALRGPKHGGANE AFEIQK
Sbjct: 185 RAMHTSLILYAEHEFNASTFTARSIASTGSDLYSAVTGAIGALRGPKHGGANEAAFEIQK 244

Query: 257 RYDNPDEAQADITRRVGNKEVVIGFGHPVYTTGDPRNQVIKEVAKKLSKDAGSMKMFDIA 316
           RY++ DEA+ADI RRV  KEVVIGFGHPVYT  DPRN+VIKEVA++LS++ G+ KMF+IA
Sbjct: 245 RYNSADEAEADIRRRVEAKEVVIGFGHPVYTVADPRNKVIKEVARRLSREVGATKMFEIA 304

Query: 317 ERLETVMWDIKKMFPNLDWFSAVSYHMMGVPTAMFTPLFVIARTSGWAAHIIEQRIDNKI 376
           ER+E+VM + K+MFPNLDWFSAVSYH MGVPTAMFTPLFVIARTSGWAAHIIEQR DNKI
Sbjct: 305 ERIESVMAETKRMFPNLDWFSAVSYHQMGVPTAMFTPLFVIARTSGWAAHIIEQRQDNKI 364

Query: 377 IRPSANYTGPENLKFVPIGKR 397
           IRPSANY GPEN+ FVP+  R
Sbjct: 365 IRPSANYVGPENVAFVPLEDR 385


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: 588
Number of extensions: 13
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: 397
Length adjustment: 31
Effective length of query: 367
Effective length of database: 366
Effective search space:   134322
Effective search space used:   134322
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