GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc04256 in Cupriavidus basilensis 4G11

Align ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized)
to candidate RR42_RS18590 RR42_RS18590 hypothetical protein

Query= reanno::Smeli:SMc04256
         (361 letters)



>FitnessBrowser__Cup4G11:RR42_RS18590
          Length = 359

 Score =  308 bits (790), Expect = 1e-88
 Identities = 173/366 (47%), Positives = 232/366 (63%), Gaps = 12/366 (3%)

Query: 1   MTSVSVRDLSLNFGAVTVLDRLNLDIDHGEFLVLLGSSGCGKSTLLNCIAGLLDVSDGQI 60
           M SV +R +   FG+  V+  +++DI  G+F VL+G SGCGKSTLL  IAGL +++ G+I
Sbjct: 1   MASVQIRGIQKYFGSTQVIRGVDIDIADGQFTVLVGPSGCGKSTLLRMIAGLEEITTGEI 60

Query: 61  FIKDRNVTWEEPKDRGIGMVFQSYALYPQMTVEKNLSFGLKVAKIPPAEIEKRVKRASEI 120
            I +R V    PK+R I MVFQ+YALYP MTV  N++F LK+AK    EI+++V +AS I
Sbjct: 61  AIGNRVVNRLPPKERDIAMVFQNYALYPHMTVYDNMAFSLKLAKGDKEEIKRKVAKASAI 120

Query: 121 LQIQPLLKRKPSELSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRSELRVEIKRLH 180
           L +  LL+R P +LSGGQRQRVA+GRA+VRD  VFLFDEPLSNLDAKLR ++R EIK LH
Sbjct: 121 LGLDSLLERYPRQLSGGQRQRVAMGRAIVRDPQVFLFDEPLSNLDAKLRVQMRAEIKELH 180

Query: 181 QSLKNTMIYVTHDQIEALTLADRIAVMKSGVIQQLADPMTIYNAPENLFVAGFIGSPSMN 240
           Q L+ T +YVTHDQIEA+T+AD+I VM+ G ++Q   P+ +Y+ P+NLFVAGFIGSP+MN
Sbjct: 181 QRLRTTSVYVTHDQIEAMTMADQIVVMRDGRVEQRGKPLALYDHPDNLFVAGFIGSPAMN 240

Query: 241 FFRGEVEPKDGRSFVRAGGIAFDVTAYPAHTRLQ-----PGQKVVLGLRPEHVKVDEARD 295
           F  G +    G + V       D T  PA  R        GQ+V+ G+RPEH+ +     
Sbjct: 241 FVPGVLRRSGGDAAVEFP----DGTRLPAPARFDATAGTDGQRVIYGVRPEHLTLGMPGQ 296

Query: 296 GEPTHQAVVDIEEPMGADNLLWLTFAGQSMSVRIAGQRRYPPGSTVRLSFDMGVASIFDA 355
           G  T  +VV   EP GA+  ++  F           +  +  G  + L  D     +FDA
Sbjct: 297 GLQTRVSVV---EPTGANTEIYSRFCEAEFISIFRERHDFAAGDILNLVPDHQHTHLFDA 353

Query: 356 ESENRL 361
           +S   L
Sbjct: 354 DSGQTL 359


Lambda     K      H
   0.320    0.137    0.392 

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: 411
Number of extensions: 14
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: 361
Length of database: 359
Length adjustment: 29
Effective length of query: 332
Effective length of database: 330
Effective search space:   109560
Effective search space used:   109560
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