GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livM in Rhodobacter sphaeroides ATCC 17029

Align High-affinity branched-chain amino acid transport system permease protein LivM; LIV-I protein M (characterized)
to candidate WP_011841104.1 RSPH17029_RS07950 branched-chain amino acid ABC transporter permease

Query= SwissProt::P22729
         (425 letters)



>NCBI__GCF_000015985.1:WP_011841104.1
          Length = 431

 Score =  107 bits (268), Expect = 5e-28
 Identities = 92/343 (26%), Positives = 147/343 (42%), Gaps = 53/343 (15%)

Query: 110 GTVDIATLTMIYIILGLGLNVVVGLSGLLVLGYGGFYA-----------IGAYTFALLNH 158
           G   I     ++  +  G    V L  +L+   GGF+A           I A   AL  +
Sbjct: 95  GAATIGAAVAVWRRMAKGWARTVALLAVLI---GGFFAYRAIFDPAVAAIEAINPALYGN 151

Query: 159 YYGLGFWTCL--PIAGLMAAAAGFLLGFPVLRLRGDYLAIVTLGFGEIVRILLLNNTEIT 216
             GLG    L  P  GL+AA A + +G   L LR DYLAI TLG  EI+  ++ N   + 
Sbjct: 152 IGGLGLPVLLAWPAGGLLAALAAWAIGKTALGLRSDYLAIATLGIAEIIIAVMKNEDWLA 211

Query: 217 GGPNGISQIPKPTLFGLEFSRTAREGGWDTFSNFFGLKYDP---SDRVIFLYLVALLLVV 273
            G   +  +P+P  + ++  ++A    W       G  YDP   S  V+ L   AL + V
Sbjct: 212 RGVKNMISLPRPVPYEVDLQQSAGFVAWAQ-----GWGYDPVTASAIVVKLCYAALFVAV 266

Query: 274 LSLFVI--NRLLRMPLGRAWEALREDEIACRSLGLSPRRIKLTAFTISAAFAGFAGTLFA 331
           L++ V      LR P GR   A+R++E+A  ++G    R  L  F + AA  G AG +  
Sbjct: 267 LAIIVTLSELALRSPWGRMMRAIRDNEVAAEAMGKDVTRRHLQIFVLGAAVIGIAGAMMT 326

Query: 332 ARQGFVSPESFTFAESAF-VLAIVVLGGMGSQFAVILAAILL------------------ 372
                ++P ++      F V  +V++GG GS +  +L   L+                  
Sbjct: 327 TLDSQLTPGTYNPLRFTFLVWVMVIVGGSGSNWGAVLGGFLIWWLWVMVEPIGLSLLGAI 386

Query: 373 --------VVSRELMRDFNEYSMLMLGGLMVLMMIWRPQGLLP 407
                    +   L        +L +G +++L++ + P+GL+P
Sbjct: 387 TAGMADGSWLKAHLQDSAAHMRLLTMGLILLLVLRFSPRGLIP 429


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: 362
Number of extensions: 20
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 425
Length of database: 431
Length adjustment: 32
Effective length of query: 393
Effective length of database: 399
Effective search space:   156807
Effective search space used:   156807
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: 51 (24.3 bits)

This GapMind analysis is from Sep 24 2021. 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