GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpT in Tistlia consotensis USBA 355

Align ABC transporter for Glycerol, ATPase component 2 (characterized)
to candidate WP_085123761.1 B9O00_RS16330 ABC transporter ATP-binding protein

Query= reanno::acidovorax_3H11:Ac3H11_792
         (358 letters)



>NCBI__GCF_900177295.1:WP_085123761.1
          Length = 361

 Score =  202 bits (513), Expect = 1e-56
 Identities = 123/335 (36%), Positives = 187/335 (55%), Gaps = 16/335 (4%)

Query: 19  DSDYALLPLKMEFEDGGAYALLGPSGCGKTTMLNIMSGLLVPSHGKVLFDGRDVTRASPQ 78
           D   AL    +E  DG     LGPSGCGKTT L + +GL  P+ G++ F  R V    P 
Sbjct: 15  DGSVALQDFSLEVADGEFLTFLGPSGCGKTTTLRMTAGLETPTSGEIFFGERPVVDLPPG 74

Query: 79  ERNIAQVFQFPVIYDTMTVAENLAFPLRNRKVPEGQIKQRVGVIAEMLEMSGQLNQRAAG 138
            RNIA VFQ   +Y  MTV +NL +PLR + V   +  +R   +A  L++   L++R   
Sbjct: 75  RRNIAMVFQSYALYPHMTVQQNLEYPLRKQGVARDERARRATALAATLQLDALLHRRPKH 134

Query: 139 LAADAKQKISLGRGLVRADVAAVLFDEPLTVIDPHLKWQLRRKLKQIHHELKLTLIYVTH 198
           L+   +Q+++LGR L+R +    L DEPL+ +D  L+ Q+R +L Q+H  +  T+IYVTH
Sbjct: 135 LSGGQQQRVALGRALIR-EPEVFLLDEPLSNLDAELRTQMRAELIQLHRRIGRTMIYVTH 193

Query: 199 DQVEALTFADQVVVMTRGKAVQVGSADALFERPAHTFVGHFIGSPGMNFLPAH---RDGE 255
           DQVEA+T + ++ VM++G+  QVG+   ++  P + FV  F+GSP MNF+      RDG 
Sbjct: 194 DQVEAMTMSTRIAVMSKGELQQVGTPLEIYREPRNRFVAAFVGSPAMNFVEGGIELRDGR 253

Query: 256 NL-SVAGHRLASPVGRA------LPAGALQVGIRPEYLALAQPQQAGALPGTVVQVQDIG 308
            +   AG  +A P  R+        A  +  GIRPE+L+L    + G+  G V+ V+ +G
Sbjct: 254 AVFRAAGLEVALPDARSARLAGLARASGVLAGIRPEHLSL----EPGSGEGRVLVVEAMG 309

Query: 309 TYQMLTAKVGEHTVKARFTPETRLPSSGDTAWLQV 343
              ++TA+     +  R +  T   ++GD   L+V
Sbjct: 310 HEDIVTAETPAGRIVVR-SAGTATAAAGDLVPLRV 343


Lambda     K      H
   0.320    0.136    0.395 

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: 325
Number of extensions: 13
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: 358
Length of database: 361
Length adjustment: 29
Effective length of query: 329
Effective length of database: 332
Effective search space:   109228
Effective search space used:   109228
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.

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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