GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TT_C0327 in Pseudomonas fluorescens GW456-L13

Align Glucose transport system permease protein aka TT_C0327, component of The glucose/mannose porter TTC0326-8 plus MalK1 (ABC protein, shared with 3.A.1.1.25) (characterized)
to candidate PfGW456L13_1895 Glucose ABC transport system, inner membrane component 1

Query= TCDB::Q72KX3
         (369 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1895
          Length = 302

 Score =  116 bits (290), Expect = 9e-31
 Identities = 58/129 (44%), Positives = 88/129 (68%), Gaps = 1/129 (0%)

Query: 237 VILAAVWQMSGYTMALYLAGLRGIPVEVLEAARVDGASEWQLFRRVIFPMLAPITLSAMI 296
           +++AAVWQ SG+ MA++LAGLRG+   ++ AA+VDGAS   ++ +++ P L P+  SA +
Sbjct: 169 LVIAAVWQASGFVMAMFLAGLRGVDQSIIRAAQVDGASLPTIYLKIVLPSLRPVFFSAFM 228

Query: 297 VLGHIALKIFDLVFAM-AGLDYAPTDVPAIYMYLLAFRGNQFAKGAAIGILLLLLVAVVV 355
           +L HIA+K FDLV AM AG     +D+PA++MY   F   Q   G+A  +L+L  V  ++
Sbjct: 229 ILAHIAIKSFDLVAAMTAGGPGYSSDLPAMFMYSFTFSRGQMGIGSASAMLMLGAVLTIL 288

Query: 356 VPYLATQLR 364
           VPYL ++LR
Sbjct: 289 VPYLYSELR 297



 Score = 94.0 bits (232), Expect = 5e-24
 Identities = 60/160 (37%), Positives = 89/160 (55%), Gaps = 11/160 (6%)

Query: 4   RILAFLVLLPSVLAVGVFVYGFIGQNLWVSLTDWGKDPAQALALRPELRFVGLENYRELF 63
           R L  LVL PS+L V V  YG+I     +S T+         +  P  ++VGL+ Y  L 
Sbjct: 18  RWLPKLVLAPSMLIVLVGFYGYIIWTFILSFTN--------SSFMPSYKWVGLQQYMRLM 69

Query: 64  TGFVDVRFRQSVVNLIFFTLFFMAGSLGLGLLLALAVDKAPRGEGFFRTVFLFPMALSFV 123
               + R+  +  NL  F   F++ SL LG+ LA+ +D+  R EGF RTV+L+PMALS +
Sbjct: 70  D---NDRWWVASKNLALFGGMFISISLVLGVFLAVLLDQRIRKEGFIRTVYLYPMALSMI 126

Query: 124 VTGTIWRWLLQPQGGVNVLPTLFGLPPLSFPWLATREQVL 163
           VTGT W+WLL P  G++ +   +G       WL  +++V+
Sbjct: 127 VTGTAWKWLLNPGLGLDKMLRDWGWEGFRLDWLVDQDRVV 166


Lambda     K      H
   0.331    0.146    0.458 

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: 340
Number of extensions: 12
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: 369
Length of database: 302
Length adjustment: 28
Effective length of query: 341
Effective length of database: 274
Effective search space:    93434
Effective search space used:    93434
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.9 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