GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Methylococcus capsulatus Bath

Align 2-methylcitrate synthase (EC 2.3.3.5) (characterized)
to candidate WP_010960169.1 MCA_RS04175 citrate synthase

Query= reanno::pseudo6_N2E2:Pf6N2E2_6062
         (375 letters)



>NCBI__GCF_000008325.1:WP_010960169.1
          Length = 429

 Score =  203 bits (517), Expect = 6e-57
 Identities = 125/371 (33%), Positives = 198/371 (53%), Gaps = 23/371 (6%)

Query: 26  GQSGAGLTYRGYDVRDLAADAQFEEVAYLLLYGELPTQAQLDAYTGKLRQLRDLPQALKE 85
           G+ G  L YRG D+ +L   + F EV+YLL+YG+LPT  Q   +  K+     + + +K 
Sbjct: 61  GEQGI-LRYRGIDIAELCEKSTFVEVSYLLIYGQLPTVEQYARFKEKIHHHSLIHEDMKS 119

Query: 86  VLERIPADAHPMDVMRTGCSFLGN-----LEPEQDFSQQHDKTDRLLAAFPAIMCYWYRF 140
                P  AHPM ++ +    L       L+P+Q   ++ +   RLL+    +  + Y+ 
Sbjct: 120 FFTSYPGHAHPMAILSSMVCSLSVYHPELLKPDQTIDERDETISRLLSKVRVLAAFAYKR 179

Query: 141 SHQGQRIECVTDEVSIGGHFLHLL-----HGKKPSELHVKVMNVSLILYAEHEFNASTFT 195
           S  G+       E+    +FLH++      G  P EL  KV++V  IL+A+HE N ST T
Sbjct: 180 S-VGEAFVYTRPELDYISNFLHMMFTRPMRGYVPDELIRKVLDVLFILHADHEQNCSTST 238

Query: 196 ARVCASTLSDLFSCITAAIGSLRGPLHGGANEAAMEMIERFSSPQEAIEGTLGMLARKD- 254
            R+  S+ ++LF+ I+A I +L GPLHGGAN+A +EM+E         +  +     K+ 
Sbjct: 239 VRMVGSSKANLFAAISAGICALWGPLHGGANQAVIEMLEEIHRAGGCYKKYIERAKDKND 298

Query: 255 --KIMGFGHAIYKDNDPRNEVIKGWSKKLADEVG-DTVLFPVSEAIDKT-----MWEQKK 306
             ++MGFGH +YK  DPR +++K +  ++ + +G D  +  +++ +++       + ++K
Sbjct: 299 PYRLMGFGHRVYKSYDPRAQILKKYCDEVLNYLGIDDPILEIAKGLEEVALTDPYFIERK 358

Query: 307 LFPNADFYHASAYHFMGIPTKLFTPIFVCSRLTGWAAHVFE--QRANNRIIRPSAEYTGV 364
           L+PN DFY    Y  + IPT +FT +F   RL GW AH  E  +    RI RP   Y G 
Sbjct: 359 LYPNVDFYSGIIYRALKIPTNMFTVMFALGRLPGWIAHWKEMLEDPGMRIARPRQIYIGE 418

Query: 365 EQRKFVPIEQR 375
            QR +VPI QR
Sbjct: 419 RQRPYVPIAQR 429


Lambda     K      H
   0.321    0.135    0.406 

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: 385
Number of extensions: 23
Number of successful extensions: 6
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: 429
Length adjustment: 31
Effective length of query: 344
Effective length of database: 398
Effective search space:   136912
Effective search space used:   136912
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 (21.9 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