GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xylE in Paraburkholderia bryophila 376MFSha3.1

Align Metapyrocatechase 2; MPC; EC 1.13.11.2; CatO2ase; Catechol 2,3-dioxygenase II (uncharacterized)
to candidate H281DRAFT_00703 H281DRAFT_00703 Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily protein

Query= curated2:P17296
         (320 letters)



>FitnessBrowser__Burk376:H281DRAFT_00703
          Length = 356

 Score =  115 bits (287), Expect = 2e-30
 Identities = 95/315 (30%), Positives = 132/315 (41%), Gaps = 19/315 (6%)

Query: 17  ARPRHAVHSIDHYALEVPDLAVAERFLDAFGLTVARTPECLEVYAADQRCWARFYEGERK 76
           A P     ++ +  LE PDL  AERFL+ FGL      E L +          +   + +
Sbjct: 12  ANPTAKATALSYLMLERPDLEQAERFLNDFGLLTVSRDEALLLLRGTGASHFCYAVRKAQ 71

Query: 77  RLAYLSFSCFEGDFAGIRQQLAASGATLVE-DPRYGDESGVWFFDPDGNLVQVKIGPKTS 135
           +  +  F    G  A +       GA+ V+     G    V   DP G  V    G   S
Sbjct: 72  KARFAGFGLQVGSLAELDALANLPGASQVQASALVGGGYVVQLTDPSGFRVDAIWGQ--S 129

Query: 136 PSSKSPARLEGAPGGQRGAVVRSQVQRVLPR-----RLSHVLLFTPSVQRALDFYRDALG 190
           P+   P R   +      AV  +  QR   +     RL HV+L     Q    +Y    G
Sbjct: 130 PAEALPHRQPLSFNSVDAAVRINDTQRPPEQPPEVIRLGHVVLELADYQETCAWYTRHFG 189

Query: 191 LRLSD-----RSDDVIAFTHAPYG---SDHHLLALVKSSARGWHHAAWDVADVNEVGQGA 242
           L  SD          +AF     G   +DHH LAL +     + H+A++V D + VG G 
Sbjct: 190 LIPSDIQVLPDGSPAVAFLRLDLGDEPADHHTLALAQGFVATYSHSAYEVVDADAVGMGQ 249

Query: 243 SQMAKAGYTQGWGTGRHVLGSNYFFYVLDPWGSFCEYSADIDYIPAGQAWPAGDFA-AED 301
             +   G+T  WG GRH+LGS  F Y  DPWG   E+  D D   +  A P G  A + +
Sbjct: 250 RVLRDKGWTHAWGIGRHILGSQIFDYWQDPWGDKHEHYCDGDLFTS--AAPTGIHAVSRE 307

Query: 302 SLYQWGPDVPEYFVR 316
           ++ QWGP +P  F R
Sbjct: 308 AMAQWGPTMPRSFTR 322


Lambda     K      H
   0.320    0.136    0.430 

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: 367
Number of extensions: 19
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: 320
Length of database: 356
Length adjustment: 28
Effective length of query: 292
Effective length of database: 328
Effective search space:    95776
Effective search space used:    95776
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: 49 (23.5 bits)

This GapMind analysis is from Sep 17 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