GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ac3H11_1695 in Desulfovibrio vulgaris Hildenborough

Align ABC transporter permease (characterized, see rationale)
to candidate 209487 DVU0548 high-affinity branched-chain amino acid ABC transporter, permease protein

Query= uniprot:A0A165KC95
         (309 letters)



>MicrobesOnline__882:209487
          Length = 302

 Score =  271 bits (694), Expect = 1e-77
 Identities = 143/297 (48%), Positives = 200/297 (67%), Gaps = 11/297 (3%)

Query: 8   IINGLVLGSMYALIALGYTMVYGIIQLINFAHGEVLMIGALTSWSCIGMMQGAMPGAPGW 67
           +  GL  GS+YALIALGYTMVYGII+LINFAHGEV MIGA T+    G++   + G P  
Sbjct: 10  LFGGLTRGSIYALIALGYTMVYGIIELINFAHGEVYMIGAFTALIVAGVL--GIYGFPEA 67

Query: 68  VILLLATIIACVVAATLNFVIEKVAYRPLRSSPRLAPLITAIGMSILLQTLAMIIWKPNY 127
            IL++A I+A +  A   F +EKVAY+PLR +PRL+PLI+AIGMSI LQ   ++    ++
Sbjct: 68  GILIIAAIVAVIYCAAYGFTLEKVAYKPLRDAPRLSPLISAIGMSIFLQNYVILAQTSDF 127

Query: 128 KPYPTMLPSSPFEIGGAFITPTQ-ILILGVTAVALASLVYLVNHTNLGRAMRATAENPRV 186
            P+P ++P        A IT T  +LI+  +A+ +  L   + +T +G+AMRATA+N ++
Sbjct: 128 VPFPRLVPDLAILEPIAHITGTSDVLIIVTSAITMVGLTLFIKYTRMGKAMRATAQNRKM 187

Query: 187 ASLMGVKPDMVISATFIIGAVLAAIAGIMYASNYGTAQHTMGFLPGLKAFTAAVFGGIGN 246
           A L+G+  D VIS TFIIG+ LAAI G++ AS+ G     +GF+ G+KAFTAAV GGIG+
Sbjct: 188 AMLLGIDADRVISLTFIIGSSLAAIGGVLIASHIGQVNFAIGFIAGIKAFTAAVLGGIGS 247

Query: 247 LAGAVVGGILLGLIEAIGSGYIGTLTGGLLGSHYTDIFAFIVLIIILTLRPSGLLGE 303
           + GA+ GG++LGL E+  +GY+         S Y D  AF +L++IL  RPSG+LG+
Sbjct: 248 IPGAMAGGLVLGLCESFATGYV--------SSDYEDALAFALLVLILIFRPSGILGK 296


Lambda     K      H
   0.327    0.142    0.419 

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: 262
Number of extensions: 14
Number of successful extensions: 5
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: 309
Length of database: 302
Length adjustment: 27
Effective length of query: 282
Effective length of database: 275
Effective search space:    77550
Effective search space used:    77550
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 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