GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpS in Rhizobium freirei PRF 81

Align ABC transporter for Glycerol, ATPase component 1 (characterized)
to candidate WP_004112319.1 RHSP_RS07740 ABC transporter ATP-binding protein

Query= reanno::acidovorax_3H11:Ac3H11_791
         (363 letters)



>NCBI__GCF_000359745.1:WP_004112319.1
          Length = 351

 Score =  195 bits (495), Expect = 2e-54
 Identities = 124/354 (35%), Positives = 191/354 (53%), Gaps = 11/354 (3%)

Query: 1   MQLALDSISKKVGAQTWLYDMSLALQSGAVTVLLGATQAGKTSLMRIMAGLDAPTAGRVT 60
           M++ LD+ SK  G+   + +M L + SG +  LLG +  GK++ +  + G+  PT GR+ 
Sbjct: 1   MRILLDNFSKSFGSTKVIENMRLEVGSGEMLALLGPSGCGKSTTLFAVCGIHRPTGGRIL 60

Query: 61  VDGKDVTGMPVRDRNVAMVYQQFINYPSMKVAANIASPLKLRGEKNIDAR--VREIASRL 118
              +DVT +P + RNV +V+Q +  YP M VA NI  PLK++G    + R  V  IA+ +
Sbjct: 61  FGDRDVTDLPSQVRNVGVVFQSYALYPHMTVAENIGFPLKVKGMPTAEIRKEVDRIAALV 120

Query: 119 HIDMFLDRYPAELSGGQQQRVALARALAKGAPLMLLDEPLVNLDYKLREELREELTQLFA 178
            I   + R PAELSGGQQQRVALARAL +   ++LLDEPL NLD KLR E+R E+ +L  
Sbjct: 121 QIGNLMGRRPAELSGGQQQRVALARALIRKPDVLLLDEPLANLDAKLRLEMRSEIRRLQR 180

Query: 179 AGQSTVVYATTEPGEALLLGGYTAVLDEGQLLQYGPTAEVFHAPNSLRVARAFSDPPMNL 238
               T +  T +  EA+ +    A++ EG+++Q    AE+++ P +  VA    +PP+  
Sbjct: 181 ETGITAILVTHDQVEAMSMCDRIAIMKEGEIVQIATPAEMYNDPKTAFVAGFLGNPPITF 240

Query: 239 MAASATAQGVRLQGGAELTLPLPQGAATAAG--LTVGVRASALRVHARP-GDVSVAGVVE 295
           +      +G  +   +E+ +PLP     + G  L +GVR      H  P GDV+V+G + 
Sbjct: 241 L-RGVMDKGAFVVPESEIRVPLPDAVDASEGTKLMLGVRPE----HFTPTGDVAVSGKIT 295

Query: 296 LAEISGSDTFVHASTPWGDLVAQLTGV-HYFELGTAITLHLDPAQAYVFGADGR 348
            AE  G +         G L+  +  V +   +G  +   +D     VF  +GR
Sbjct: 296 FAETQGRENLYDVLLAGGPLLRSIQPVRNDIHVGDDVRWAIDSRSVLVFDENGR 349


Lambda     K      H
   0.318    0.133    0.375 

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: 271
Number of extensions: 9
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: 363
Length of database: 351
Length adjustment: 29
Effective length of query: 334
Effective length of database: 322
Effective search space:   107548
Effective search space used:   107548
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 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