GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc02869 in Pseudomonas simiae WCS417

Align N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized)
to candidate GFF4321 PS417_22130 sugar ABC transporter ATPase

Query= reanno::Phaeo:GFF2754
         (331 letters)



>FitnessBrowser__WCS417:GFF4321
          Length = 386

 Score =  306 bits (784), Expect = 5e-88
 Identities = 172/366 (46%), Positives = 228/366 (62%), Gaps = 36/366 (9%)

Query: 1   MTALQLTNVCKSFGP--VEVLKDINLTVEDGEFVVFVGPSGCGKSTLLRVISGLEDATAG 58
           M  L+L NV K++G    + LK+I L++++GEF++ VGPSGCGKSTL+  I+GLE  T G
Sbjct: 1   MATLELRNVNKTYGAGLPDTLKNIELSIKEGEFLILVGPSGCGKSTLMNCIAGLETITGG 60

Query: 59  EISIGGQTVTTTPPAKRGIAMVFQSYALYPHLSVRENMALALKQERQPKEEIAARVAEAS 118
            I IG Q V+   P  R IAMVFQSYALYP +SVREN+   LK  + P+ +I A VA  +
Sbjct: 61  AIMIGDQDVSGMSPKDRDIAMVFQSYALYPTMSVRENIEFGLKIRKMPQADIDAEVARVA 120

Query: 119 RMLSLEDYLDRRPSELSGGQRQRVAIGRAVVREPKLFLFDEPLSNLDAALRMNTRLEIAR 178
           ++L +E  L+R+P +LSGGQ+QRVA+GRA+ R PK++LFDEPLSNLDA LR+  R E+  
Sbjct: 121 KLLQIEHLLNRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKL 180

Query: 179 LHRQLSASMIYVTHDQIEAMTLADKIVVLRDGRIEQVGTPMELYNNPANRFVAEFIGAPA 238
           +H++L  + +YVTHDQIEAMTL DK+ V++DG I+Q GTP E+YNNPAN+FVA FIG+P 
Sbjct: 181 MHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKEIYNNPANQFVASFIGSPP 240

Query: 239 MNFVP--AQRLGG------NPGQ-------------------FIGIRPEYARIS-----P 266
           MNFVP   QR  G      + GQ                    +G+RPE   ++      
Sbjct: 241 MNFVPLRLQRKDGRLVALLDSGQARCELALNTTEAGLEDRDVILGLRPEQIMLAAGEGDS 300

Query: 267 VGPLAGEVIHVEKLGGDTNILVDMGEDLTFTARLFGQHDTNVGETLQFDFDPANCLSFD- 325
              +  EV   E  G DT + V +  D     RL       VGETL   FDP+  L FD 
Sbjct: 301 ASSIRAEVQVTEPTGPDTLVFVQL-NDTKVCCRLAPDVAPQVGETLTLQFDPSKVLLFDA 359

Query: 326 EAGQRI 331
             G+R+
Sbjct: 360 NTGERL 365


Lambda     K      H
   0.320    0.137    0.391 

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: 372
Number of extensions: 17
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: 331
Length of database: 386
Length adjustment: 29
Effective length of query: 302
Effective length of database: 357
Effective search space:   107814
Effective search space used:   107814
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.

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