GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galactonolactonase in Paraburkholderia phymatum STM815

Align D-galactono-lactonase (EC 3.1.1.-) (characterized)
to candidate WP_012406047.1 BPHY_RS34215 lactonase family protein

Query= reanno::pseudo13_GW456_L13:PfGW456L13_3314
         (389 letters)



>NCBI__GCF_000020045.1:WP_012406047.1
          Length = 414

 Score =  160 bits (406), Expect = 5e-44
 Identities = 113/351 (32%), Positives = 174/351 (49%), Gaps = 30/351 (8%)

Query: 30  VGSYTAGQ----SQGIYRLAFDSRTGQIDASPLQVIKS-ANPSWLTLSKDQRHLFVVNEN 84
           VGS T  +     +GI     D+ TG ++   +Q++K   NPS+L LS++   L+ V+ +
Sbjct: 66  VGSRTTRERNAHGEGISVYQVDTETGALEL--VQLVKDLVNPSFLALSRNGERLYTVHGD 123

Query: 85  GPGQTDPVGRVSSFAIDPKTHALSLISQVQSLGNEPTHSSLSIDGSHLFVSNYSVAEDPG 144
                     +S+F +D  +  L+ +++  + G  P H ++   G ++ VSN+      G
Sbjct: 124 ASD-------ISAFKVDKASGKLTFLNRQSTQGKNPVHLAIDPLGRYIVVSNHI-----G 171

Query: 145 GTLAVLPVAADGKLKAVVQMSSHPASRVNPER--QASAHVHSTIPSPDGRYVFANDLGAD 202
            +LAVLP+AADG L+ + Q+  H    V P R  Q  A  H     P G +V   D G D
Sbjct: 172 ASLAVLPIAADGSLQELTQLV-HLEGPVGPHRVEQKQAKPHFNPFDPTGEFVIVPDKGLD 230

Query: 203 KVFAYRFDPKANPELPLTPATPAFVQLPPGSGPRHLLFSADGKHAWLTMEMSAQVAVFDY 262
           +VF +RF      +  LTPATP FV     +GPRH+ F   G +A++  E+ + V  + Y
Sbjct: 231 RVFTFRFK-----DGQLTPATPGFVVSRETAGPRHVAFHPKGAYAYVVNELDSTVTTYRY 285

Query: 263 HDGQ--LEQTQMVDLAAGQPVSDKAAAALHASADGKFLYVSNRGTANQLLVFAIDPATGH 320
             G   L   Q+V         +  A+ +     G+F+Y SNRG  + + VF ID ATGH
Sbjct: 286 SSGNGALTPVQIVSSLPDTYTGNSRASEIEVDPSGRFVYASNRGF-DSIAVFRIDQATGH 344

Query: 321 LSELQRRAVEGDHPREFSLDPSGKFLLIANQKSNQIVVVERDARTGLLGKT 371
           L+ +      G  PR  +  P G+F+   N+ S+ IV    +A TG L  T
Sbjct: 345 LTFIDAEPTLGRTPRFMTGTPDGRFMYALNEDSDTIVAFAVNAATGQLKPT 395


Lambda     K      H
   0.316    0.132    0.382 

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: 524
Number of extensions: 41
Number of successful extensions: 13
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: 389
Length of database: 414
Length adjustment: 31
Effective length of query: 358
Effective length of database: 383
Effective search space:   137114
Effective search space used:   137114
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 (21.6 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