GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xylF_Tm in Pseudovibrio axinellae Ad2

Align ABC-type transporter, integral membrane subunit, component of Xylose porter (Nanavati et al. 2006). Regulated by xylose-responsive regulator XylR (characterized)
to candidate WP_068009667.1 PsAD2_RS19325 ribose ABC transporter permease

Query= TCDB::Q9WXW7
         (317 letters)



>NCBI__GCF_001623255.1:WP_068009667.1
          Length = 314

 Score =  206 bits (525), Expect = 5e-58
 Identities = 116/297 (39%), Positives = 179/297 (60%), Gaps = 6/297 (2%)

Query: 16  LVALVSLAVFTAILNPRFLTAFNLQALGRQIAIFGLLAIGETFVIISGGGAIDLSPGSMV 75
           L+ L+ L    +  N  FL   N+  + RQ +I  ++A+G TFVI++ G  IDLS GS++
Sbjct: 13  LIGLIILMAAVSFANANFLGVDNMLNILRQTSINAVIAMGMTFVILTSG--IDLSVGSIL 70

Query: 76  ALTGVMVAWLMTHGVPVWISVILILLFSIGAGAWHGLFVTKLRVPAFIITLGTLTIARGM 135
           A  G + A L+    P+ +++   ++   G GA  G+ ++   V  FI TL  +T+ RG 
Sbjct: 71  AFAGAICASLIGMDTPLVVALFATIMVGAGLGATSGVIISYFNVQPFIATLVGMTMIRGA 130

Query: 136 AAVITKGWPII----GLPSSFLKIGQGEFLKIPIPVWILLAVALVADFFLRKTVYGKHLR 191
             V T+G P+      +  SF + G G    IP PV +++ +  +  F L +T +G+++ 
Sbjct: 131 TLVYTQGRPVSTGSHDVAESFYQFGAGYIFGIPHPVILMIVIFAICWFILSQTRFGRYVY 190

Query: 192 ASGGNEVAARFSGVNVDRVRMIAFMVSGFLAGVVGIIIAARLSQGQPGVGSMYELYAIAS 251
           A GGNE  AR SG+NV +V+++ + +SG LA + GII+ ARL   QP  G  YEL AIA+
Sbjct: 191 AIGGNENVARLSGINVKKVKILVYALSGALAALAGIILTARLESAQPTAGLGYELDAIAA 250

Query: 252 TVIGGTSLTGGEGSVLGAIVGASIISLLWNALVLLNVSTYWHNVVIGIVIVVAVTLD 308
            V+GGTSL GG+G V G I+GA II +L NAL +++VS+Y+  +  G VI++AV +D
Sbjct: 251 VVLGGTSLAGGKGRVFGTIIGALIIGVLNNALNIMDVSSYYQMIAKGAVILLAVVVD 307


Lambda     K      H
   0.328    0.143    0.424 

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: 295
Number of extensions: 23
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: 317
Length of database: 314
Length adjustment: 27
Effective length of query: 290
Effective length of database: 287
Effective search space:    83230
Effective search space used:    83230
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 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