GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS03635 in Paraburkholderia bryophila 376MFSha3.1

Align ABC-type sugar transport system, periplasmic component protein (characterized, see rationale)
to candidate H281DRAFT_02705 H281DRAFT_02705 monosaccharide ABC transporter substrate-binding protein, CUT2 family

Query= uniprot:D8IZC6
         (316 letters)



>FitnessBrowser__Burk376:H281DRAFT_02705
          Length = 365

 Score =  121 bits (304), Expect = 2e-32
 Identities = 94/276 (34%), Positives = 133/276 (48%), Gaps = 19/276 (6%)

Query: 16  AAAAQPAMAADKPLKSVGVTVGDLANPFFVAIAKGAESGAHKINPDAKVTVVSSKYDLNT 75
           A A+ P   A      VG +V  L N FFV +  G E GA +   D   T  ++  D   
Sbjct: 50  APASAPVANASGGKTKVGFSVSTLNNAFFVGLKAGVEKGAKEQGFDLVQT--NANGDAQQ 107

Query: 76  QVGQIENFIANKVDLIVLNAADSKGVGPAVKKAQKAGIVVVAVDVAAAGADVT--VMSDN 133
           QV    N ++  V  +VLN  DSK + PAV+KA    I V  +D  + G  VT  V SDN
Sbjct: 108 QVNDAINLLSQGVTALVLNPIDSKAIIPAVEKANSMNIPVFMLDRGSDGGKVTSFVASDN 167

Query: 134 TMAGAESCKFLAEKL-----QGKGNVV-IVNGPPVSAVMDRVTGCKAEFKKSPGIKILSD 187
              G  + K++A++L       KGNVV ++     +A  DR  G   E  K P IK+++ 
Sbjct: 168 VALGQTAAKWIADQLTKRYGSAKGNVVDLIGLVGTTAATDREKGFSDEIAKYPDIKVVA- 226

Query: 188 NQNAGGSRDGGMTTMSNLLAAQPKIDAVFAINDPTAIGAELAIRQAKR------SDIKWI 241
            Q     ++  +  M+N+L   P+IDAVF  ND   +GAE AI  A R           +
Sbjct: 227 RQEGAFDQEKSLNAMTNILQKYPQIDAVFGANDDNTVGAEKAIDNAGRYKPLGDKQHILV 286

Query: 242 SGVDGAPDAERALKDSKSLFAASPAQDPYGMAAESV 277
            G DG   A  A++  K    A+ +Q+P  MAA+S+
Sbjct: 287 IGADGTAQALSAIRAGKQ--DATISQNPIQMAAKSL 320


Lambda     K      H
   0.314    0.129    0.360 

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: 242
Number of extensions: 7
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 316
Length of database: 365
Length adjustment: 28
Effective length of query: 288
Effective length of database: 337
Effective search space:    97056
Effective search space used:    97056
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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