GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livM in Malonomonas rubra DSM 5091

Align High-affinity branched-chain amino acid transport system permease protein LivM; LIV-I protein M (characterized)
to candidate WP_072908495.1 BUB13_RS09995 branched-chain amino acid ABC transporter permease

Query= SwissProt::P22729
         (425 letters)



>NCBI__GCF_900142125.1:WP_072908495.1
          Length = 318

 Score =  187 bits (476), Expect = 3e-52
 Identities = 111/335 (33%), Positives = 188/335 (56%), Gaps = 28/335 (8%)

Query: 89  QKLFLVALLVLAVAWPFMVSRGTVDIATLTMIYIILGLGLNVVVGLSGLLVLGYGGFYAI 148
           +K  L A + +    P +++     +A   +I+ ++ L  ++++G SG+  +G   F+ +
Sbjct: 5   EKFVLPAFIAVMAVLPHLLNERWQAVAITFLIFSVVALSQDIILGKSGMFNMGQALFFGM 64

Query: 149 GAYTFALLNHYYGLGFWTCLPIAGLMAAAAGFLLGFPVLRLRGDYLAIVTLGFGEI-VRI 207
           GAYT A+LN+ YG    + +P+A L+ A  G LL  P++ LRGDYL +VT+GF  + V++
Sbjct: 65  GAYTTAILNNEYGWSIVSTIPLAILIPAIFGILLAGPIVHLRGDYLLVVTIGFNIVFVQV 124

Query: 208 LLLNNTEITGGPNGISQIPKPTLFGLEFSRTAREGGWDTFSNFFGLKYDPSDRVIFLYLV 267
           L  N   +TGGPNGI  +   ++FG                      YD  ++V  +Y  
Sbjct: 125 LQNNLGGVTGGPNGIFGLDSLSIFG----------------------YDLMNQVA-VYYF 161

Query: 268 ALLLVVLSLFVINRLLRMPLGRAWEALREDEIACRSLGLSPRRIKLTAFTISAAFAGFAG 327
           A ++++L+L++++ L +   GRA   LRED++A  S+G++ R  K+ AF + A  AG AG
Sbjct: 162 AFIVLLLTLWIMSNLEKSKPGRALHYLREDQLAAESIGINTRVYKIFAFGLGAGIAGLAG 221

Query: 328 TLFAARQGFVSPESFTFAESAFVLAIVVLGGMGSQFAVILAAILLVVSRELMRDFNEYSM 387
           T+FA +   VSPE+F F +S    +IV++GG  S   V+L   ++ V  E+ R+F  +  
Sbjct: 222 TVFAVQYSAVSPEAFEFIQSVLFFSIVLVGG-SSIPGVMLGVFVMFVVPEIFREFATWRY 280

Query: 388 LMLGGLMVLMMIWRPQGLLPMT---RPQLKLKNGA 419
            + G  M+  MI RP+G++P T    P+  +K G+
Sbjct: 281 FIFGFAMIAAMILRPRGIVPATFGKIPKFLIKGGS 315


Lambda     K      H
   0.330    0.145    0.436 

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: 324
Number of extensions: 15
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: 425
Length of database: 318
Length adjustment: 30
Effective length of query: 395
Effective length of database: 288
Effective search space:   113760
Effective search space used:   113760
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: 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