GapMind for catabolism of small carbon sources

 

Alignments for a candidate for AZOBR_RS08240 in Malonomonas rubra DSM 5091

Align Leucine/isoleucine/valine ABC transporter,permease component (characterized, see rationale)
to candidate WP_072908495.1 BUB13_RS09995 branched-chain amino acid ABC transporter permease

Query= uniprot:G8ALI9
         (505 letters)



>NCBI__GCF_900142125.1:WP_072908495.1
          Length = 318

 Score =  179 bits (453), Expect = 2e-49
 Identities = 107/343 (31%), Positives = 184/343 (53%), Gaps = 30/343 (8%)

Query: 144 VQHASRWLGPIAVVVALAFPFTPLADRQLLDIGILLLTYIMLGWGLNIVVGLAGLLDLGY 203
           +++  +++ P  + V    P   L + +   + I  L + ++    +I++G +G+ ++G 
Sbjct: 1   MKNYEKFVLPAFIAVMAVLPH--LLNERWQAVAITFLIFSVVALSQDIILGKSGMFNMGQ 58

Query: 204 VAFYAVGAYSYALLAHYFGFSFWVCLPLAGFLAAMSGVLLGFPVLRLRGDYFAIVTLGFG 263
             F+ +GAY+ A+L + +G+S    +PLA  + A+ G+LL  P++ LRGDY  +VT+GF 
Sbjct: 59  ALFFGMGAYTTAILNNEYGWSIVSTIPLAILIPAIFGILLAGPIVHLRGDYLLVVTIGFN 118

Query: 264 EI-IRIILINWYQFTGGPNGISGIPRPSFFGIADFTRTPAEGTAAFHEMFGLEFSPLHRI 322
            + ++++  N    TGGPNGI G+   S FG                      +  ++++
Sbjct: 119 IVFVQVLQNNLGGVTGGPNGIFGLDSLSIFG----------------------YDLMNQV 156

Query: 323 IFLYYLILVLALVVNLFTMRVRKLPLGRAWEALREDDIACASLGINRTNMKLAAFAIAAM 382
              Y+  +VL L + + +   +  P GRA   LRED +A  S+GIN    K+ AF + A 
Sbjct: 157 AVYYFAFIVLLLTLWIMSNLEKSKP-GRALHYLREDQLAAESIGINTRVYKIFAFGLGAG 215

Query: 383 FGGFAGSFFATRQGFISPESFTFIESAIILAIVVLGGMGSQIGVVVAAFLVIGLPEAFRE 442
             G AG+ FA +   +SPE+F FI+S +  +IV++GG  S  GV++  F++  +PE FRE
Sbjct: 216 IAGLAGTVFAVQYSAVSPEAFEFIQSVLFFSIVLVGG-SSIPGVMLGVFVMFVVPEIFRE 274

Query: 443 LADYRMLAFGMGMVLIMLWRPRGLLA---HRDPTILLHGRPKG 482
            A +R   FG  M+  M+ RPRG++     + P  L+ G   G
Sbjct: 275 FATWRYFIFGFAMIAAMILRPRGIVPATFGKIPKFLIKGGSHG 317


Lambda     K      H
   0.329    0.144    0.438 

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: 400
Number of extensions: 33
Number of successful extensions: 4
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: 505
Length of database: 318
Length adjustment: 31
Effective length of query: 474
Effective length of database: 287
Effective search space:   136038
Effective search space used:   136038
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 (21.8 bits)
S2: 50 (23.9 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