GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS03635 in Beijerinckia indica ATCC 9039

Align ABC-type sugar transport system, periplasmic component protein (characterized, see rationale)
to candidate WP_012385980.1 BIND_RS15555 periplasmic binding protein/LacI transcriptional regulator

Query= uniprot:D8IZC6
         (316 letters)



>NCBI__GCF_000019845.1:WP_012385980.1
          Length = 309

 Score =  281 bits (719), Expect = 1e-80
 Identities = 147/303 (48%), Positives = 206/303 (67%), Gaps = 4/303 (1%)

Query: 13  LLLAAAAQPAMAAD---KPLKSVGVTVGDLANPFFVAIAKGAESGAHKINPDAKVTVVSS 69
           +L+AAAA   M A    K LKS+G+++  + NP+FVA+AKGA + A KINP+ K+  +  
Sbjct: 4   VLVAAAAVALMTAHASAKDLKSIGLSLASMDNPYFVAMAKGATASAQKINPNVKINTLDF 63

Query: 70  KYDLNTQVGQIENFIANKVDLIVLNAADSKGVGPAVKKAQKAGIVVVAVDVAAAGADVTV 129
            YDLN Q  QI++ IA+ VDLI+LN  D   + PA+++A  AGI V+AVD AA GAD+T+
Sbjct: 64  DYDLNKQATQIDSLIASGVDLILLNPGDPAALEPAIQRAHAAGIPVIAVDAAAKGADITI 123

Query: 130 MSDNTMAGAESCKFLAEKLQGKGNVVIVNGPPVSAVMDRVTGCKAEFKKSPGIKILSDNQ 189
            +DN  AG  +C+++ +KL GKGNV+I NGP VS+V +RV GCK     +P I +LS +Q
Sbjct: 124 TTDNRQAGEIACQYIVDKLGGKGNVIIQNGPQVSSVRERVEGCKKALANAPEIAVLSSDQ 183

Query: 190 NAGGSRDGGMTTMSNLLAAQPKIDAVFAINDPTAIGAELAIRQAKRSDIKWISGVDGAPD 249
           NA GS   GM  M + L+   KIDAVF IND  AIG++ A ++  R+D+  I+ VDGAPD
Sbjct: 184 NAKGSHRHGMNVMQDHLSQFAKIDAVFTINDRQAIGSDFAAQRLHRNDL-IITSVDGAPD 242

Query: 250 AERALKDSKSLFAASPAQDPYGMAAESVAIGYAVMNGRAPQQKVKLLPVKLITRDNVADY 309
            E ALK   +   AS +QDPY +A  +V +G  ++NG+ P+Q V L+  KL+TR+NVA+Y
Sbjct: 243 IEVALKAKNTCIHASASQDPYAIAQLAVDLGNDLLNGKKPEQDVILIAPKLVTRENVAEY 302

Query: 310 QGW 312
           +GW
Sbjct: 303 KGW 305


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: 253
Number of extensions: 6
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: 316
Length of database: 309
Length adjustment: 27
Effective length of query: 289
Effective length of database: 282
Effective search space:    81498
Effective search space used:    81498
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: 48 (23.1 bits)

This GapMind analysis is from Sep 24 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