GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcE in Pandoraea thiooxydans ATSB16

Align D-lactate oxidase, FAD binding subunit (EC 1.1.3.15) (characterized)
to candidate WP_047215943.1 PATSB16_RS00555 glycolate oxidase subunit GlcE

Query= reanno::Cup4G11:RR42_RS17310
         (374 letters)



>NCBI__GCF_001931675.1:WP_047215943.1
          Length = 357

 Score =  452 bits (1163), Expect = e-132
 Identities = 225/363 (61%), Positives = 274/363 (75%), Gaps = 10/363 (2%)

Query: 12  LTAFRDAIRHATGTRTPLRLRGGGSKDFYGQHPQGTLLDTRAYSGIVDYDPPELVITARC 71
           L  FR AI  AT T  PL+LRGGG+K +YGQ   G +LDTR Y G++ YDP ELVITARC
Sbjct: 5   LEQFRAAIETATATHQPLQLRGGGTKQWYGQQLVGQVLDTRPYRGVIAYDPAELVITARC 64

Query: 72  GTPLAQIEAALAERRQMLAFEPPHFSTGADGSDVATIGGAVAAGLSGPRRQAVGALRDFV 131
           GTPLA+IEA LAE+ Q+L FEPP+F   A      T GG VAAGLSGPRRQA GA+RDFV
Sbjct: 65  GTPLAEIEAVLAEKNQLLPFEPPYFGPHA------TFGGCVAAGLSGPRRQAAGAVRDFV 118

Query: 132 LGTRVMDGRGDVLSFGGQVMKNVAGYDVSRLMSGSLGTLGLILEVSLKVLPVPFDDATLR 191
           LG  +MDG+G VL FGGQVMKNVAGYDV+RL++GSLG LGLIL+VS+KV+P PF + TLR
Sbjct: 119 LGAALMDGKGQVLHFGGQVMKNVAGYDVARLLAGSLGILGLILDVSIKVMPQPFAELTLR 178

Query: 192 FALDEAAALDRLNDWGGQPLPIAASAWHDGVLHLRLSGAAAALRAARARLGGEAVDAAQA 251
           F ++   A+ +LN+WGGQPLPI+ASAW+D +L +RLSGA+AA++AAR +LGGE VDA  A
Sbjct: 179 FEMNAVDAVRKLNEWGGQPLPISASAWYDDMLAVRLSGASAAIKAARVKLGGELVDAIHA 238

Query: 252 DALWRALREHSHAFFAPVQAGRALWRIAVPTTAAPLALPGGQLIEWGGGQRWWLGGSDSA 311
              W+ +REH+  FFA     RALWR+++P    P  LPG QLIEWGG QRWW+    + 
Sbjct: 239 AKFWQGVREHTDPFFADAGPERALWRLSLPPITEPHRLPGKQLIEWGGAQRWWI----TD 294

Query: 312 ADSAIVRAAAKAAGGHATLFRNGDKAVGVFTPLSAPVAAIHQRLKATFDPAGIFNPQRMY 371
           AD+  VR+AA+ AGGHATLFR G+ + GVFTPL+ P+  IH+ LKA FDPAGIFNP RMY
Sbjct: 295 ADAQSVRSAARQAGGHATLFRYGEASAGVFTPLAVPLMRIHRNLKAAFDPAGIFNPGRMY 354

Query: 372 AGL 374
             L
Sbjct: 355 PEL 357


Lambda     K      H
   0.321    0.136    0.414 

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: 448
Number of extensions: 16
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: 374
Length of database: 357
Length adjustment: 30
Effective length of query: 344
Effective length of database: 327
Effective search space:   112488
Effective search space used:   112488
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 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