GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc04256 in Desulfacinum hydrothermale DSM 13146

Align ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized)
to candidate WP_084058302.1 B9A12_RS12460 ABC transporter ATP-binding protein

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



>NCBI__GCF_900176285.1:WP_084058302.1
          Length = 361

 Score =  198 bits (503), Expect = 2e-55
 Identities = 119/312 (38%), Positives = 178/312 (57%), Gaps = 8/312 (2%)

Query: 27  DHGEFLVLLGSSGCGKSTLLNCIAGLLDVSDGQIFIKDRNVTWEEPKDRGIGMVFQSYAL 86
           + G    LLG SGCGK+T+LN I+GLL  + G++   DR+VT   P+ R I  VFQ   L
Sbjct: 33  EDGGAYALLGPSGCGKTTMLNIISGLLTPTRGRVLYDDRDVTELPPEQRNIAQVFQFPVL 92

Query: 87  YPQMTVEKNLSFGLKVAKIPPAEIEKRVKRASEILQIQPLLKRKPSELSGGQRQRVAIGR 146
           Y  M+V  NL+F L+   + P  I +RV+  +E+L +   LK+K + LS   +Q++++GR
Sbjct: 93  YDTMSVFDNLAFPLRNRGLDPQTIHRRVQEVAEVLDLTADLKKKAAGLSADAKQKISLGR 152

Query: 147 ALVR-DVDVFLFDEPLSNLDAKLRSELRVEIKRLHQSLKNTMIYVTHDQIEALTLADRIA 205
            LVR DV   LFDEPL+ +D  L+  LR ++K +H+ L+ T+IYVTHDQ+EALT AD++ 
Sbjct: 153 GLVREDVAAILFDEPLTVIDPHLKWHLRRKLKEIHEKLQLTLIYVTHDQVEALTFADKVL 212

Query: 206 VMKSGVIQQLADPMTIYNAPENLFVAGFIGSPSMNFFRGEVEPKDGRSFVRAGGIAFD-V 264
           VM  G + Q+  P  ++  P + FV  FIGSP MNF    +E    R+      +  D  
Sbjct: 213 VMYEGEMVQMGTPAELFEEPRHKFVGYFIGSPGMNFIPCRLE--GNRAVCDGASVVLDEE 270

Query: 265 TAYPAHTRLQPGQKVVLGLRPEHVKVDEARDGEPTHQAVVDIEEPMGADNLLWLTFAGQS 324
           T   A  +  P +   LG+RP +++V +   G+      V   E  G   +L +  A  +
Sbjct: 271 TVRRAQGKEGPFE---LGIRPMYLEVHD-EPGDDRIPVQVRKVEDQGIFRILTVQMASST 326

Query: 325 MSVRIAGQRRYP 336
           + VRI+ +R  P
Sbjct: 327 LKVRISEERPLP 338


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: 340
Number of extensions: 16
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: 361
Length of database: 361
Length adjustment: 29
Effective length of query: 332
Effective length of database: 332
Effective search space:   110224
Effective search space used:   110224
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 Apr 09 2024. 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