GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PfGW456L13_1897 in Phaeobacter inhibens BS107

Align ABC transporter for D-Galactose and D-Glucose, ATPase component (characterized)
to candidate GFF776 PGA1_c07900 alpha-glucoside transport ATP-binding protein AglK

Query= reanno::pseudo13_GW456_L13:PfGW456L13_1897
         (386 letters)



>FitnessBrowser__Phaeo:GFF776
          Length = 363

 Score =  296 bits (757), Expect = 8e-85
 Identities = 171/361 (47%), Positives = 227/361 (62%), Gaps = 11/361 (3%)

Query: 1   MATLELRNVNKTYGPGLPDTLKNIELKIDDGEFLILVGPSGCGKSTLMNCIAGLETISGG 60
           MA L+L NV KTYG G+ + L++I L I  GE ++ VGPSGCGKSTL+  IAGLE ISGG
Sbjct: 1   MANLKLTNVAKTYGGGV-EVLRDINLDIKQGELIVFVGPSGCGKSTLLRMIAGLERISGG 59

Query: 61  AILVDDADISGMSPKDRDIAMVFQSYALYPTMSVRDNIAFGLKIRKMPTAEIDEEVARVS 120
            + +D+A ++ + P  R IAMVFQSYALYP M+VRDN+AF LKI K    EID  + R +
Sbjct: 60  TLEIDNAVMNDIPPAQRGIAMVFQSYALYPHMTVRDNMAFALKIAKKSKDEIDAAIDRAA 119

Query: 121 KLLQIEHLLSRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKL 180
           K+LQ+E  L R P  LSGGQ+QRVA+GR++ R PK+YLFDEPLSNLDA LRV  R E+  
Sbjct: 120 KILQLEPYLDRLPKALSGGQRQRVAIGRSIVRDPKVYLFDEPLSNLDAALRVATRIEIAQ 179

Query: 181 MHQRL-KTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKDIYNNPANLFVASFIGSP 239
           + + +  +T +YVTHDQ+EAMTL  ++ V+ D  I Q GTP D+Y  P N FVA FIGSP
Sbjct: 180 LKEAMPDSTMIYVTHDQVEAMTLASRIVVLADKGIAQVGTPLDLYQRPENEFVAQFIGSP 239

Query: 240 PMNFIPLRLQRKDGRLLALLDSG-QARCELPLGMQDAGLEDREVILGIRPEQIILANGEA 298
            MN IP  +     R    L SG +   E+P    D GL    V +G+RPE ++    E 
Sbjct: 240 AMNLIPGTVVATGPRTTVRLTSGEEVVAEIPTTDADQGL---AVNVGVRPEDLV---EEG 293

Query: 299 NGLPTIRAEVQVTEPTGPDTLVFVNLNDTK--VCCRLAPDVAPAVGETLTLQFDPAKVLL 356
            G   I + V + E  G  T++++   + K  +  +L        G ++ L  DPA++ L
Sbjct: 294 TGGALIDSRVDIVEALGEVTVLYIAAGEGKDPLIAKLPGIHKGLRGSSVRLYADPARLHL 353

Query: 357 F 357
           F
Sbjct: 354 F 354


Lambda     K      H
   0.319    0.138    0.393 

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: 392
Number of extensions: 20
Number of successful extensions: 2
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: 386
Length of database: 363
Length adjustment: 30
Effective length of query: 356
Effective length of database: 333
Effective search space:   118548
Effective search space used:   118548
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 (21.7 bits)
S2: 50 (23.9 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